Literature DB >> 29159234

Gene expression microarray data from mouse cerebrum treated with rTMS for 30 days.

Tetsurou Ikeda1,2, Satoru Kobayashi3, Chikao Morimoto2.   

Abstract

This data article contains complementary tables related to the research article entitled, 'Effects of repetitive transcranial magnetic stimulation on ER stress-related genes and glutamate, γ-aminobutyric acid, and glycine transporter genes in mouse brain' (Ikeda et al. (2017) [1]), which showed that rTMS modulates glutamate, GABA and glycine transporters and regulates ER stress-related genes. Here we provide accompanying data collected using Affymetrix GeneChip microarrays to identify changes in gene expression in mouse cerebrum treated with rTMS for 30 days (Tables 1-10).

Entities:  

Year:  2017        PMID: 29159234      PMCID: PMC5683740          DOI: 10.1016/j.dib.2017.10.034

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Value of the Data A global gene expression analysis of mouse cerebrum treated with rTMS for 30 days. These data may be useful for comparison with microarray data obtained from rTMS of different durations. Genes identified as differentially expressed in this data set could be useful in further studies on the effects of rTMS on mouse brain.

1. Data

Affymetrix GeneChip microarray analyses of mRNA isolated from mouse cerebrum after 30 days of rTMS revealed altered expression of several genes (Table 1, Table 2, Table 3, Table 4, Table 5, Table 6, Table 7, Table 8, Table 9, Table 10), including glutamatergic genes (e.g., glutamate transporter), dopaminergic genes, cholinergic genes, genes of adrenergic signaling in cardiomyocytes and so on.
Table 1

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
93320_atCpt1a0.44I0.15I0.3I0.17I40carnitine palmitoyltransferase 1a, liver
93372_atAnp32a1.75I2.28I1.59I1.91I40acidic (leucine-rich) nuclear phosphoprotein 32 family, member A
95466_atCotl12.41I1.11I2.03I0.83I40coactosin-like 1 (Dictyostelium)
103012_atCcl21a0.27I3.54I-1.5D1.6I31chemokine (C-C motif) ligand 21A (serine); chemokine (C-C motif)
ligand 21B (leucine); chemokine (C-C motif) ligand 21C (leucine);
predicted gene 10591; predicted gene 13304; predicted gene 1987;
predicted gene, 21541; C-C motif chemokine 21c



























100307_atNfix1.12I0.62I0.41I-0.05NC30nuclear factor I/X
101883_s_atXlr3a0.03NC1.16I0.74I1.79I30X-linked lymphocyte-regulated 3A; X-linked lymphocyte-regulated
3B; X-linked lymphocyte-regulated 3C



























101921_atRab4a0.46I0.27I-0.01NC0.07I30RAB4A, member RAS oncogene family
104175_atDlg41.09I1.46I0.41I1.15NC30discs, large homolog 4 (Drosophila)
93253_atMapk1-0.04NC0.34I0.34I0.71I30mitogen-activated protein kinase 1
93924_f_atTuba3b0.4I0.15I0.11I-0.09NC30tubulin, alpha 3B
96295_atPsat10.09NC0.11I0.28I0.44I30phosphoserine aminotransferase 1
96590_f_atOtud7b0.59NC0.7I0.33I0.32I30OTU domain containing 7B
99598_g_atGnai20.33I0.67I-0.1NC0.2MI30guanine nucleotide binding protein (G protein), alpha inhibiting 2
102009_atCyfip20.53I0.21I-0.33NC-0.6D21cytoplasmic FMR1 interacting protein 2
103275_atAtp6v0a10.52I-1.05D1.2I-0.31NC21ATPase, H+ transporting, lysosomal V0 subunit A1
104486_atA2m0.27I-0.91D0.83I-0.91NC21alpha-2-macroglobulin
104564_atScg30.47I0.32I-0.49D-0.52NC21secretogranin III
104643_atWwc10.72I0.47I-0.34NC-0.69D21WW, C2 and coiled-coil domain containing 1
160189_atNudt4-0.2NC-0.84D0.63I0.4I21nudix (nucleoside diphosphate linked moiety X)-type motif 4
162138_s_atCbx60.21I0.27I-0.54D-0.71NC21chromobox 6
93660_atCamk2a1.53I-0.93D2.09I-0.27NC21calcium/calmodulin-dependent protein kinase II alpha
95301_atS100a50.6I0.96I-0.86D-0.45NC21S100 calcium binding protein A5
95785_s_atRab7-0.36NC-0.91D0.91I0.4I21RAB7, member RAS oncogene family
96583_s_atKif5a-0.13NC-1.32D1.6I0.36I21kinesin family member 5A
97458_atGnb10.61I0.8I-0.58D-0.62NC21guanine nucleotide binding protein (G protein), beta 1
97560_atPsap-0.28NC-1.49D1.74I0.37I21prosaposin
98457_atSlc4a40.72I0.35I-0.62NC-0.92D21solute carrier family 4 (anion exchanger), member 4
99458_i_atMark20.28I0.46I-0.66D-0.5NC21MAP/microtubule affinity regulating kinase 2
99481_atAtp1a20.86I0.45I-0.49NC-0.82D21ATPase, Na+/K+ transporting, alpha 2 polypeptide
99882_atIds-0.75NC-1.24D0.55I-0.19MI21iduronate 2-sulfatase
100012_atLaptm50.63I0.07NC0.34MI-0.35NC20lysosomal-associated protein transmembrane 5
100068_atAldh1a10.21I0.16I-0.42NC-0.31NC20aldehyde dehydrogenase family 1, subfamily A1
100133_atFyn0.35I0.55I-0.22NC0.06NC20Fyn proto-oncogene
100154_atTapbp0.8I0.21I0.28NC-0.19NC20TAP binding protein
100380_atGm102570.06NC0.26I-0.21NC0.02I20predicted gene 10257; predicted gene 12657; H3 histone, family 3A;
H3 histone, family 3B; H3 histone, family 3C; histone H3.3-like;
uncharacterized LOC105242736
100494_atFgf10.48NC-0.23NC0.71I0.29I20fibroblast growth factor 1
100573_f_atGpi10.35I0.41I-0.13NC-0.05NC20glucose phosphate isomerase 1
100727_atRpl280.36I0.6I-0.26NC-0.02NC20ribosomal protein L28
100762_atSema6a2.15I-0.09NC0.39MI-1.7NC20sema domain, transmembrane domain (TM), and cytoplasmic
domain, (semaphorin) 6A

Gnb1, Gnai2, Dlg4 and Mapk1 are glutamatergic genes. Fyn, Camk2a and Mapk1 are cholinergic genes. Kif5a is Dopaminergic gene. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 2

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
100774_atSynj2bp0.34I-0.15I-0.28NC-0.08NC20synaptojanin 2 binding protein
100892_atNdufaf10.4NC0.31I0.26NC0.29I20NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly
factor 1
100992_atPhc10.43I0.24I-0.07NC-0.28NC20polyhomeotic-like 1 (Drosophila)
101113_atRhoa0.31I0.16MI0.18NC-0.26NC20ras homolog gene family, member A
101419_atTubb4a0.35I0.51I-0.27NC-0.01NC20tubulin, beta 4 A class IVA
101441_i_atItpr20.32I0.25MI-0.18NC-0.57NC20inositol 1,4,5-triphosphate receptor 2
101467_atS100b0.06NC0.04NC0.53I0.44I20S100 protein, beta polypeptide, neural
101510_atPsme10.21NC0.27I0.08NC0.19I20proteasome (prosome, macropain) activator subunit 1 (PA28 alpha)
101578_f_atActb0.92I0.99I-0.4NC-0.47NC20actin, beta
101587_atEphx10.9I0.99I-1.13NC-1.27NC20epoxide hydrolase 1, microsomal
101855_atMap60.3I0.15I-0.01NC-0.35NC20microtubule-associated protein 6
101923_atPla2g70.47I0.42I-0.08NC-0.18NC20phospholipase A2, group VII (platelet-activating factor
acetylhydrolase, plasma)
101930_atNfix0.63I0.34MI-0.11NC-0.34NC20nuclear factor I/X
101960_atRtcb0.24NC0.3I-0.18NC0.04I20RNA 2',3'-cyclic phosphate and 5'-OH ligase
102007_atHccs0.02NC-0.35NC0.41I0.48I20holocytochrome c synthetase
102033_atTesk10.42I0.4I0.09NC-0.05NC20testis specific protein kinase 1
102063_atPdpk10.87I0.2I-0.2NC-0.46NC203-phosphoinositide dependent protein kinase 1
102095_f_atSpock20.32I0.18MI-0.53NC-0.73NC20sparc/osteonectin, cwcv and kazal-like domains proteoglycan 2
102252_atPfdn20.42I0.24I-0.03NC-0.14NC20prefoldin 2
102271_atZmiz20.58I0.54I-0.32NC-0.52NC20zinc finger, MIZ-type containing 2
102374_atRcan30.27NC-0.03NC0.29I0.12I20regulator of calcineurin 3
102384_atSmarca20.42I0.59I-0.31NC-0.04NC20SWI/SNF related, matrix associated, actin dependent regulator of
chromatin, subfamily a, member 2
102639_atChst20.47I0.4I-0.04NC-0.21NC20carbohydrate sulfotransferase 2
102691_atZfp385a0.88I0.67I-0.18NC-0.56NC20zinc finger protein 385A
102700_atTbr10.43I0.41I-0.37NC-0.43NC20T-box brain gene 1
102752_atCyfip10.43I0.31I-0.17NC-0.32NC20cytoplasmic FMR1 interacting protein 1
102787_atAdgrg10.79I0.26I0.52NC-0.42NC20adhesion G protein-coupled receptor G1
102815_atAnxa110.28I0.5I-0.86NC-0.55NC20annexin A11; predicted gene 2260; predicted gene 2274
102856_atSox100.39I0.45I-0.08NC-0.14NC20SRY (sex determining region Y)-box 10
102912_atTnks20.28I0.34I-0.4NC-0.2NC20tankyrase, TRF1-interacting ankyrin-related ADP-ribose
polymerase 2
102942_atSpecc10.3I0.28I-0.35NC-0.43NC20sperm antigen with calponin homology and coiled-coil domains 1
103001_atVegfb0.46MI0.15I-0.13NC-0.02NC20vascular endothelial growth factor B
103029_atPdcd40.76I0.61I-0.17NC-0.02NC20programmed cell death 4
103040_atCd830.02NC0.43I-0.12NC0.11I20CD83 antigen
103054_atPolr2a0.43I0.07NC0.23I-0.06NC20polymerase (RNA) II (DNA directed) polypeptide A
103090_atUqcc1-0.41NC-0.09NC0.21I0.33I20ubiquinol-cytochrome c reductase complex assembly factor 1
103299_atPld40.88I0.03NC1.18I0.36NC20phospholipase D family, member 4
103300_atAbcb70.64I-0.12NC0.41I-0.48NC20ATP-binding cassette, sub-family B (MDR/TAP), member 7
103305_atItgb40.83I2.63I0.51NC2.83NC20integrin beta 4
103369_atKlf130.77I0.36I-0.36NC-0.43NC20Kruppel-like factor 13
103370_atLin7c0.35I0.27I0NC-0.21NC20lin-7 homolog C (C. elegans)
103404_atRere0.6I0.19I0.05NC-0.15NC20arginine glutamic acid dipeptide (RE) repeats
103411_atGna110.23NC0.48I0.1NC0.13I20guanine nucleotide binding protein, alpha 11
103584_atCmip0.32I0.46I-0.37NC-0.37NC20c-Maf inducing protein

Actb, Itpr2 and Rho are oxytocin signaling pathway genes. Cyfip1and Itgb4 are actin cytoskeleton regulation genes. Pdpk1 and Pdcd4 are genes of proteoglycans in cancer. Pla2g7 amd Pld4 are ether lipid metabolism genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 3

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
103611_atCd470.55I0.59I-0.22NC-0.18NC20CD47 antigen (Rh-related antigen, integrin-associated signal
transducer)
103613_atAldoart21.82I1.52I1.42NC1.55NC20aldolase 1 A, retrogene 2
103624_atUrm10.25NC-0.2NC0.54I0.36I20ubiquitin related modifier 1 homolog (S. cerevisiae)
103663_atPomgnt10.35I0.32I-0.16NC0.07NC20protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
103682_atUri1-0.04NC0.65I-0.23NC0.27I20URI1, prefoldin-like chaperone
103748_atCmip0.78I0.34I-0.03NC-0.27NC20c-Maf inducing protein
103771_atRnf2080.48I0.17I-0.16NC-0.32NC20ring finger protein 208
104032_atMast30.6I0.36I-0.39NC-0.51NC20microtubule associated serine/threonine kinase 3
104034_atAI4641310.63I0.66I-0.77NC-0.4NC20expressed sequence AI464131
104214_atSlc7a80.63I0.33I0.09NC0.16NC20solute carrier family 7 (cationic amino acid transporter,
y+ system).member 8
104244_atMark20.95I0.63I-0.35NC-0.5NC20MAP/microtubule affinity regulating kinase 2
104250_atLrrc8a0.53I0.12I-0.36NC-0.64NC20leucine rich repeat containing 8A
104316_atGna130.64I0.59I-0.02NC-0.01NC20guanine nucleotide binding protein, alpha 13
104352_atBrd40.2MI0.41I-0.37NC-0.33NC20bromodomain containing 4
104368_atMapre30.23MI0.56I-0.22NC-0.09NC20microtubule-associated protein, RP/EB family, member 3
104380_atSlc35a1-0.23NC0.34I0.02NC0.7I20solute carrier family 35 (CMP-sialic acid transporter), member 1
104409_atGrik50.49I0.37I-0.16NC-0.25NC20glutamate receptor, ionotropic, kainate 5 (gamma 2)
104415_atFoxp10.47I0.2I-0.12NC-0.18NC20forkhead box P1
104514_atEpn10.3I0.11I-0.17NC-0.39NC20epsin 1
104546_g_atCsnk2a11.1I-0.1NC0.97I0.13NC20casein kinase 2, alpha 1 polypeptide; predicted pseudogene 10031
104634_atLims10.49NC0.73I-0.16NC0.5I20LIM and senescent cell antigen-like domains 1
104650_atAche0.48I0.38I0.19NC-0.12NC20acetylcholinesterase
104725_atRhoq0.81I0.61I0.37NC0.02NC20ras homolog gene family, member Q
104739_atTcta0.18NC-0.34NC0.66I0.31I20T cell leukemia translocation altered gene
104741_atZdhhc90.8I0.14I0.75NC-0.1NC20zinc finger, DHHC domain containing 9
104747_atSlc1a10.42I0.44I-0.28NC-0.35NC20solute carrier family 1 (neuronal/epithelial high affinity glutamate
transporter, system Xag), member 1
160111_atEif1ax-0.38NC-0.47NC0.48I0.31I20eukaryotic translation initiation factor 1A, X-linked
160181_atSyp0.37I0.45I-0.43NC-0.42NC20synaptophysin
160184_atErgic10.75I0.12NC0.75I-0.22NC20endoplasmic reticulum-golgi intermediate compartment (ERGIC) 1
160190_atSyt40.5I0.68I-0.09NC-0.01NC20synaptotagmin IV
160196_atSmap10.37I0.42I-0.59NC-0.48NC20small ArfGAP 1
160272_atCbx30.55I0.55I-0.41NC-0.13NC20chromobox 3
160414_atSlc38a100.42I-0.17NC0.28I-0.26NC20solute carrier family 38, member 10
160417_atKif5b0.34I0.7I-0.23NC0.08NC20kinesin family member 5B
160502_atCreg1-0.03NC-0.22NC0.52MI0.14I20cellular repressor of E1A-stimulated genes 1
160614_atPten0.6I0.39I-0.13NC-0.36NC20phosphatase and tensin homolog
160667_atEvl0.58I0.56I-0.2NC-0.34NC20Ena-vasodilator stimulated phosphoprotein
160743_atPole30.41I-0.13NC0.15I-0.44NC20polymerase (DNA directed), epsilon 3 (p17 subunit)
160754_atPygm0.66I0.83I-0.34NC-0.1NC20muscle glycogen phosphorylase
160942_atCbx60.63I0.23I-0.06NC-0.36NC20chromobox 6
161015_atClvs10.11NC0.7I-0.06NC0.71I20clavesin 1
161054_atSpock10.62I0.44I-0.13NC-0.05NC20sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1
161057_atActr100.35I0.33I-0.36NC-0.41NC20ARP10 actin-related protein 10

Ache is Cholinergic gene. Grik5 and Slc1a1 are Glutamatergic gene. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 4

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
161070_atSpred20.28I0.38I-0.74NC-0.5NC20sprouty-related, EVH1 domain containing 2
161167_r_atUck12.05I-0.84NC2.47I-0.66NC20uridine-cytidine kinase 1
161371_r_atPtprk1.29NC1.29NC3.1I2.98I20protein tyrosine phosphatase, receptor type, K
161819_f_atLaptm50.73I0.48I-0.11NC-0.05NC20lysosomal-associated protein transmembrane 5
162134_r_at2010111I01Rik0.47I-0.14NC0.47I-0.47NC20RIKEN cDNA 2010111I01 gene
162182_f_atKcnab20.54I0.17I-0.22NC-0.73NC20potassium voltage-gated channel, shaker-related subfamily,
beta member 2
162332_f_atMapre30.9I1.08I0.08NC-0.03NC20microtubule-associated protein, RP/EB family, member 3
162499_f_atUbe2d2a0.48I0.38I-0.17NC-0.17NC20ubiquitin-conjugating enzyme E2D 2A
92180_atH1fx0.42I0.37I-0.38NC-0.51NC20H1 histone family, member X
92196_f_atSf3a20.37I0.29I-0.16NC-0.27NC20splicing factor 3a, subunit 2
92202_g_atZbtb160.72I0.66I-0.61NC-0.73NC20zinc finger and BTB domain containing 16
92227_s_atCtnna20.08NC0.36I-0.25NC-0.01I20catenin (cadherin associated protein), alpha 2
92241_atNfic0.68I0.88I-0.58NC-0.43NC20nuclear factor I/C
92247_atArhgap50.6I-0.02NC0.31MI-0.43NC20Rho GTPase activating protein 5
92350_atMapre10.82I0.42I0.09NC-0.44NC20microtubule-associated protein, RP/EB family, member 1
92379_f_atPtprz10.27MI0.49I-0.55NC-0.2NC20protein tyrosine phosphatase, receptor type Z, polypeptide 1
92397_atAgap10.52I0.2I0.06NC-0.46NC20ArfGAP with GTPase domain, ankyrin repeat and PH domain 1
92411_atHs1bp30.44I0.12I0.3NC-0.02NC20HCLS1 binding protein 3
92426_atTspan50.33I0NC0.33I-0.14NC20tetraspanin 5
92484_atHivep20.5I-0.2NC0.36I-0.45NC20human immunodeficiency virus type I enhancer binding protein 2
92525_i_atNacc20.33I0.82I-0.03NC0.4NC20nucleus accumbens associated 2, BEN and BTB (POZ) domain
containing
92528_atAdgrb10.37I0.17I-0.43NC-0.55NC20adhesion G protein-coupled receptor B1
92586_atGlud10.36NC0.39I-0.13NC0.24I20glutamate dehydrogenase 1
92621_atPcbp20.43I0.09I-0.08NC-0.49NC20poly(rC) binding protein 2
92659_atRapgef4-0.28NC-0.73NC0.98I0.66I20Rap guanine nucleotide exchange factor (GEF) 4
92678_atDdx250.22NC-0.07NC0.17I0.12I20DEAD (Asp-Glu-Ala-Asp) box polypeptide 25
92795_atMap40.56I0.5I-0.07NC-0.28NC20microtubule-associated protein 4
92817_atImp3-0.22NC-0.46NC0.23I-0.03MI20IMP3, U3 small nucleolar ribonucleoprotein, homolog (yeast)
92820_atUsp20.64I0.54I-0.28NC-0.34NC20ubiquitin specific peptidase 2
92821_atUsp20.42I0.29I-0.25NC-0.27NC20ubiquitin specific peptidase 2
92838_atFscn10.73I0.2NC0.35I-0.16NC20fascin homolog 1, actin bundling protein (Strongylocentrotus
purpuratus)
92871_atSel1l0.79I0.4I-0.19NC-0.36NC20sel-1 suppressor of lin-12-like (C. elegans)
92927_atEtv10.66I0.27NC0.49I0.26NC20ets variant 1
92949_atPacsin10.31I0.33I-0.23NC-0.29NC20protein kinase C and casein kinase substrate in neurons 1
92958_atFoxo30.43I0.11I-0.44NC-0.54NC20forkhead box O3
93006_atNfic0.33I0.35MI-0.39NC-0.58NC20nuclear factor I/C
93047_atNup500.48I-0.61NC0.81I-0.38NC20nucleoporin 50
93055_atAnkrd46-0.16NC-0.14NC0.28I0.28I20ankyrin repeat domain 46
93058_atEif1a0.02NC0.35I-0.04NC0.26I20eukaryotic translation initiation factor 1A
93069_atUbe2d2a0.04NC0.41I-0.04NC0.2I20ubiquitin-conjugating enzyme E2D 2A
93129_atCux20.51I0.43I0NC-0.28NC20cut-like homeobox 2
93147_f_atCelf40.43I0.23I-0.2NC-0.39NC20CUGBP, Elav-like family member 4
93246_atNaa150.22I0.55I-0.27NC-0.35NC20N(alpha)-acetyltransferase 15, NatA auxiliary subunit
93284_atCirbp-0.27NC0.42I-0.02NC0.54I20cold inducible RNA binding protein
93288_atArpc20.23MI0.44I-0.31NC-0.01NC20actin related protein 2/3 complex, subunit 2

Kcnab2 and Pacsin1 are Synaptosome genes. Rapgef4, Arhgap5 and Ctnna2 are Leukocyte transendothelial migration genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 5

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
93374_atJph30.44I0.38I-0.25NC-0.17NC20junctophilin 3
93382_atPde1b0.61I0.29I0.04NC-0.27NC20phosphodiesterase 1B, Ca2+-calmodulin dependent
93423_atLdoc1l0.51I0.31I0.21NC-0.14NC20leucine zipper, down-regulated in cancer 1-like
93548_atSec. 61b-0.12NC-0.3NC0.29I0.11I20Sec. 61 beta subunit
93645_atRgs7-0.02NC0.53I-0.03NC0.45I20regulator of G protein signaling 7
93659_atCamk2a1.66I-0.95NC1.5I-0.55NC20calcium/calmodulin-dependent protein kinase II alpha
93664_atAtp1b20.78I-0.28NC0.76I-0.15NC20ATPase, Na+/K+ transporting, beta 2 polypeptide
93720_atAgpat10.27MI-0.71NC0.51I-0.23NC201-acylglycerol-3-phosphate O-acyltransferase 1
(lysophosphatidic acid acyltransferase, alpha)
93793_atLasp10.43I0.28I-0.14NC-0.24NC20LIM and SH3 protein 1
93852_atMef2a0.2I0.25I-0.04NC-0.12NC20myocyte enhancer factor 2A
93861_f_atLOC1052473280.29I-0.33NC0.56I-0.05NC20MLV-related proviral Env polyprotein-like
93964_s_atDdx60.81I0.36I0.14NC-0.46NC20DEAD (Asp-Glu-Ala-Asp) box polypeptide 6
93965_r_atDdx60.88I0.59I0.23NC-0.17NC20DEAD (Asp-Glu-Ala-Asp) box polypeptide 6
93994_atChpt10.4I0.27I0.15NC0.16NC20choline phosphotransferase 1
94057_g_atScd10.32I0.43I-0.12NC-0.03NC20stearoyl-Coenzyme A desaturase 1
94077_f_atRpn20.49MI0.29I-0.13NC-0.27NC20ribophorin II
94194_s_atHcn20.84I0.33I-0.23NC-0.61NC20hyperpolarization-activated, cyclic nucleotide-gated K+ 2
94218_atTcp10.27I0.49I-0.05NC0.35NC20t-complex protein 1
94245_atVimp0.08NC0.26I0.04NC0.09I20VCP-interacting membrane protein
94257_atRraga0.08NC-0.07NC0.47I0.17I20Ras-related GTP binding A
94335_r_atIna0.45I0.14I-0.25NC-0.63NC20internexin neuronal intermediate filament protein, alpha
94336_atOtub10.76I0.43I0NC-0.55NC20OTU domain, ubiquitin aldehyde binding 1
94353_atEif4ebp21.04MI-0.37NC0.4I-0.98NC20eukaryotic translation initiation factor 4E binding protein 2
94374_atWdr130.13NC0.03MI0.06NC0.09MI20WD repeat domain 13
94456_atSet-0.13NC0.77I-0.14NC0.79I20SET nuclear oncogene
94819_f_atCcni0.3I0.28I-0.4NC-0.28NC20cyclin I
94832_atHnrnph20.45NC0.95I0.21NC0.83I20heterogeneous nuclear ribonucleoprotein H2
94876_f_atGorasp20.29I0.27I-0.35NC-0.5NC20golgi reassembly stacking protein 2
94986_atGng30.34I0.27I-0.13NC-0.17NC20guanine nucleotide binding protein (G protein), gamma 3
95010_atTraf30.29I-0.08NC0.31I-0.02NC20TNF receptor-associated factor 3
95159_atGm135520.1NC0.35I-0.15NC0.22I20predicted gene 13552; mitochondrial ribosomal protein S18B
95397_atD430019H16Rik0.45I0.28I0.04NC-0.3NC20RIKEN cDNA D430019H16 gene
95432_f_atTomm70a0.01NC0.35I-0.32NC0.13MI20translocase of outer mitochondrial membrane
70 homolog A (yeast)
95447_atMdp1-0.4NC-0.23NC0.43MI0.41I20magnesium-dependent phosphatase 1
95468_atEgln10.4I0.11NC0.26I0.1NC20egl-9 family hypoxia-inducible factor 1
95530_atGtf2a10.13NC-0.1NC0.29I0.13I20general transcription factor II A, 1
95721_atMapkapk20.36I-0.21NC0.6I-0.02NC20MAP kinase-activated protein kinase 2
95883_atJade10.25MI0.54I-0.54NC-0.14NC20jade family PHD finger 1
95927_f_at0.55MI0.65I-0.2NC-0.14NC20
96007_atSsr3-0.12NC-0.3NC0.24I0.16I20signal sequence receptor, gamma
96056_atRhoc0.57I-0.23NC0.46I-0.12NC20ras homolog gene family, member C
96065_atLxn0.55I0.73I-0.43NC0.12NC20latexin
96088_atNdrg20.44I0.48I-0.28NC-0.34NC20N-myc downstream regulated gene 2
96102_i_atRad23b-0.07NC0.26I-0.26NC0.12I20RAD23b homolog (S. cerevisiae)
96186_atLrp100.58I-0.1NC0.42I-0.28NC20low-density lipoprotein receptor-related protein 10

Rad23b, Sec. 61b, Vimp, Rpn2 and Ssr3 are genes of protein processing in endoplasmic reticulum. Atp1b2 and Camk2a are cAMP signaling pathway genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 6

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
96191_atArfgef10.59I0.17I0.24NC-0.28NC20ADP-ribosylation factor guanine nucleotide-exchange factor 1
(brefeldin A-inhibited)
96211_atDpp80.38I-0.08NC0.23MI-0.23NC20dipeptidylpeptidase 8
96255_atBnip3l-0.01NC0.37I-0.09NC0.15I20BCL2/adenovirus E1B interacting protein 3-like
96313_atRasgrf10.71I0.76I-0.25NC-0.19NC20RAS protein-specific guanine nucleotide-releasing factor 1
96360_atArhgdia0.33I0.13I-0.02NC-0.17NC20Rho GDP dissociation inhibitor (GDI) alpha
96518_atWwc10.33I0.31I-0.34NC-0.5NC20WW, C2 and coiled-coil domain containing 1
96593_atElk10.74I-0.53NC1.15I0.06NC20ELK1, member of ETS oncogene family
96674_atTnpo3-0.17NC0.57I-0.38NC0.14I20transportin 3
96725_atCic0.81I0.27I0.12NC-0.54NC20capicua homolog (Drosophila)
96731_atDdx60.39I0.38I-0.09NC-0.34NC20DEAD (Asp-Glu-Ala-Asp) box polypeptide 6
96741_atPhf120.46I0.48I-0.46NC-0.17NC20PHD finger protein 12
96784_atAnln-0.27NC-0.1NC0.7I0.32I20anillin, actin binding protein
96811_atRab31-0.01NC0.01NC0.16I0.04I20RAB31, member RAS oncogene family
96813_f_atOtud50.35I0.53I-0.33NC-0.1NC20OTU domain containing 5
96884_atCarhsp1-0.1NC0.06NC0.49I0.51I20calcium regulated heat stable protein 1
96920_atHtra10.68I0.29I-0.24NC-0.62NC20HtrA serine peptidase 1
96955_atAtp6v0e20.04NC0.03NC0.17I-0.01I20ATPase, H+ transporting, lysosomal V0 subunit E2
97210_at1700037H04Rik0.76I-0.13NC0.32I-0.16NC20RIKEN cDNA 1700037H04 gene
97243_atSlc9a3r10.51I0.39I-0.18NC-0.36NC20solute carrier family 9 (sodium/hydrogen exchanger), member 3
regulator 1
97365_atCoro2b0.46I0.26I-0.17NC-0.36NC20coronin, actin binding protein, 2B
97450_s_atAldh7a10.46I-0.07NC0.42I-0.22NC20aldehyde dehydrogenase family 7, member A1
97487_atSerpine20.32NC0.29I0.05NC0.1I20serine (or cysteine) peptidase inhibitor, clade E, member 2
97530_atUbe2i0.01NC0.18NC0.33I0.36I20ubiquitin-conjugating enzyme E2I
97536_atWdtc10.68I0.03I-0.03NC-0.49NC20WD and tetratricopeptide repeats 1
97740_atDusp160.46NC0.53I0.46NC0.69MI20dual specificity phosphatase 16
97770_s_atFam3c0.53I0.63I-0.43NC-0.49NC20family with sequence similarity 3, member C
97776_atDrd20.75I1.11I0.1NC0.27NC20dopamine receptor D2
97794_atSema7a2.38I-0.83NC4.45I0.15NC20sema domain, immunoglobulin domain (Ig), and GPI membrane
anchor, (semaphorin) 7A
97841_atChmp2a0.05NC0.37I-0.18NC0.28I20charged multivesicular body protein 2A
97974_atZfpm10.72I0.2I0.12NC-0.54NC20zinc finger protein, multitype 1
97998_atAtn10.7I0.44I0.19NC-0.03NC20atrophin 1
98004_atPkia0.11NC-0.53NC1.12I0.31I20protein kinase inhibitor, alpha
98011_atGabbr10.24I0.3I-0.21NC-0.23NC20gamma-aminobutyric acid (GABA) B receptor, 1
98026_g_atEvi2a-0.31NC-0.24NC0.28I0.6I20ecotropic viral integration site 2a
98073_atCux10.46I0.27I0.24NC-0.05NC20cut-like homeobox 1
98114_atNpc10.49I0.38I-0.11NC-0.24NC20Niemann-Pick type C1
98127_atCapza20.09NC0.5I-0.11NC0.22I20capping protein (actin filament) muscle Z-line, alpha 2
98129_atTmsb100.35I0.25MI-0.41NC-0.72NC20thymosin, beta 10
98141_atEif5b0.34I0.43I-0.58NC-0.29NC20eukaryotic translation initiation factor 5B
98150_atRab11b0.27I0.19I-0.23NC-0.31NC20RAB11B, member RAS oncogene family
98169_s_atFzd30.39I-0.49NC0.46I-0.41NC20frizzled homolog 3 (Drosophila)
98454_atPalm0.4I0.14MI0NC-0.25NC20paralemmin
98477_s_atAnk30.57I0.29I-0.29NC-0.51NC20ankyrin 3, epithelial

Arfgef1, Rab31, Rab11b, Capza2, and Chmp2a are genes of endocytosis. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 7

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
98543_atCtss-0.18NC0.3I-0.03NC0.25I20cathepsin S
98550_atSet-0.1NC0.46I-0.25NC0.09I20SET nuclear oncogene
98564_f_atGm66540.39I0.47I-0.29NC-0.2NC20predicted pseudogene 6654; 40S ribosomal protein S26-like;
ribosomal protein S26
98588_atFah-0.15NC-0.21NC0.21I0.58I20fumarylacetoacetate hydrolase
98590_atSdc40.69I0.12I-0.42NC-0.76NC20syndecan 4
98602_atRangap10.5I0.27I0.09NC-0.01NC20RAN GTPase activating protein 1
98616_f_atMyh70.64I0.16I-0.43NC-1.01NC20myosin, heavy polypeptide 7, cardiac muscle, beta
98827_i_atKif5a0.24NC-1.04NC1.74I0.33I20kinesin family member 5 A
98866_atDlx60.92I1.99I0.7NC2.14NC20distal-less homeobox 6
98925_atVamp20.91I0.33NC0.76I0.19NC20vesicle-associated membrane protein 2
98993_atPpp2r5c0.23MI0.35I0.08NC0.02NC20protein phosphatase 2, regulatory subunit B', gamma
99023_atPafah1b2-0.09NC-0.42NC0.66I0.26I20platelet-activating factor acetylhydrolase, isoform 1b, subunit 2
99045_atEno20.36I0.34I-0.38NC-0.49NC20enolase 2, gamma neuronal
99085_atUsp30.41NC0.22NC0.65I0.4I20ubiquitin specific peptidase 3
99378_f_atH2-Q4-0.42NC-0.42NC0.61MI0.53I20histocompatibility 2, Q region locus 4
99451_atFam102a0.36I0.16NC0.62I0.11NC20family with sequence similarity 102, member A
99465_atMecp20.69I0.59I0.08NC-0.04NC20methyl CpG binding protein 2
99504_atSt8sia30.38I0.2MI-0.22NC-0.3NC20ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3
99537_atRuvbl10.03NC-0.28NC0.48I0.1I20RuvB-like protein 1
99575_atUbqln10.52NC-0.16NC0.6I0.13I20ubiquilin 1
99597_atGnai20.45I0.23MI-0.11NC-0.34NC20guanine nucleotide binding protein (G protein), alpha inhibiting 2
99666_atCs0.39I0.14I0.06NC-0.21NC20citrate synthase
99893_atFgf130.07NC-0.57NC0.87I0.05I20fibroblast growth factor 13

Gnai2, Kif5a and Ppp2r5c are dopaminergic synapse genes. Gnai2, Myh7 and Ppp2r5c are genes of adrenergic signaling in cardiomyocytes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 8

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
102362_i_atJunb-2.26D-1.89D-1.91D-1.6D04jun B proto-oncogene
102371_atNr4a1-1.99D-1.81D-1.8D-1.72D04nuclear receptor subfamily 4, group A, member 1
102661_atEgr2-1.29D-1.33D-1.7D-1.69D04early growth response 2
102870_atDynlt1a-0.68D-1.04D-0.62D-0.91D04dynein light chain Tctex-type 1A
104598_atDusp1-1.41D-1.38D-1.51D-1.49D04dual specificity phosphatase 1
160172_atMeg3-1.61D-1.73D-0.68D-0.89D04maternally expressed 3
160173_atMeg3-0.91D-1.31D-0.79D-1.15D04maternally expressed 3
160901_atFos-2.14D-2.01D-2.08D-1.95D04FBJ osteosarcoma oncogene
160970_atOdf2-0.95D-1.24D-1.31D-1.54D04outer dense fiber of sperm tails 2
161666_f_atGadd45b-0.98D-0.99D-1.63D-1.51D04growth arrest and DNA-damage-inducible 45 beta
96302_atSrsf7-0.83D-0.73D-0.82D-0.74MD04serine/arginine-rich splicing factor 7
97752_atSnhg11-1.12D-0.63D-1.24D-0.71D04small nucleolar RNA host gene 11
97890_atSgk1-0.8D-1.04D-1.3D-1.59D04serum/glucocorticoid regulated kinase 1
99109_atIer2-0.92D-1.48D-0.87D-1.29D04immediate early response 2
101058_atAmy1-1.11D-0.83D-1.08MD-0.81NC03amylase 1, salivary
101583_atBtg2-0.58D-1.06D-0.6NC-1.04D03B cell translocation gene 2, anti-proliferative
104410_atMidn-0.72D-0.23NC-1.07D-0.77MD03midnolin
104639_i_atTaf1d-1.01D-0.74D-0.55D-0.63NC03TATA box binding protein (Tbp)-associated factor,
RNA polymerase I, D
160487_atMyl4-0.35MD-0.38NC-1.02D-0.96D03myosin, light polypeptide 4
92424_atZfp692-0.86D-0.94D-0.42NC-0.9D03zinc finger protein 692
92542_atRsrp1-1.25D-0.75D-0.96D-0.52NC03arginine/serine rich protein 1
93411_atSema7a-0.51D-0.1NC-1.37D-0.75D03sema domain, immunoglobulin domain (Ig), and GPI membrane
anchor, (semaphorin) 7A
93619_atPer1-0.9D-0.3NC-1.01D-0.8D03period circadian clock 1
98579_atEgr1-0.68D-0.57NC-1.42D-1.04D03early growth response 1
99347_f_atEml5-0.92D-1.48D-0.97NC-1.44D03echinoderm microtubule associated protein like 5
100002_atItih30.54I0.22NC-0.65D-0.82D12inter-alpha trypsin inhibitor, heavy chain 3
100592_atGhitm-0.56D-1.06D0.52I-0.01NC12growth hormone inducible transmembrane protein
100599_atAtf4-0.82D-0.58D-0.27NC-0.01MI12activating transcription factor 4
162457_f_atHba-a10.7I-1.46D-0.12NC-2.33D12hemoglobin alpha, adult chain 1; hemoglobin alpha, adult chain 2
93722_atEnsa-0.46MD-0.83D0.38I-0.03NC12endosulfine alpha
93909_f_atNoct-0.61D-0.84D0.35I0.08NC12nocturnin
94781_atHba-a10.35I-1.71D-0.38NC-2.42D12hemoglobin alpha, adult chain 1
97263_s_atCsnk1d-0.65D-1.23D0.13I-0.4NC12casein kinase 1, delta
99009_atNnt0.77I-0.6D-0.1NC-1.56D12nicotinamide nucleotide transhydrogenase
99095_atMax-0.62D0.36NC-0.98D0.01I12Max protein
100050_atId1-0.75D-0.55NC-0.64D-0.49NC02inhibitor of DNA binding 1
100064_f_atGja10.23NC-0.09NC-0.62D-0.7D02gap junction protein, alpha 1
100348_atGm40022-0.82D-0.93MD-1.22NC-1.12NC02predicted gene, 40022
100482_atZfp598-0.42D-0.81D-0.33NC-0.64NC02zinc finger protein 598
100536_atMobp-0.11NC-0.22NC-0.72D-0.66D02myelin-associated oligodendrocytic basic protein
100611_atLyz20.32NC-1.04D0.06NC-1.05D02lysozyme 2
101482_atPpp1cc0.08NC-0.04NC-0.59D-0.77D02protein phosphatase 1, catalytic subunit, gamma isoform
101580_atCox7b-0.62D-0.43NC-0.71D-0.43NC02cytochrome c oxidase subunit VIIb
101596_atC78859-0.96MD-0.8MD-0.66NC-0.91NC02expressed sequence C78859
101740_atAdra1a-0.04NC-2.3D-1.47NC-4.05D02adrenergic receptor, alpha 1a

Atf4, Adra1a, Myl4 and Ppp1cc are genes of adrenergic signaling in cardiomyocytes. Fos, Max, Atf4, Dusp1, Gadd45b and Nr4a1 are genes of MAPK signaling pathway. Fos, Atf4 and Ppp1cc are Dopaminergic genes. Csnk1d, Id1 and Ppp1cc are genes of hippo signaling pathway. Csnk1d and Per1 are circadian rhythm genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 9

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
101869_s_atHbb-b10.03NC-1.76D-0.05NC-1.94D02hemoglobin, beta adult major chain; hemoglobin, beta adult minor
chain; hemoglobin, beta adult s chain; hemoglobin, beta adult t chain
101936_atClk4-0.63D-0.73D-0.4NC-0.3NC02CDC like kinase 4
101962_atDdx17-0.73D-0.35NC-0.58D-0.19NC02DEAD (Asp-Glu-Ala-Asp) box polypeptide 17
102255_atOsmr0.04NC-1.08MD-3.48NC-3.02MD02oncostatin M receptor
102431_atMapt-0.01NC-0.04NC-0.61D-0.6D02microtubule-associated protein tau
102574_atFgf112.96NC-1.26D3.35NC-0.77D02fibroblast growth factor 11
102779_atGadd45b-1.04D-1.15D-0.64NC-0.62NC02growth arrest and DNA-damage-inducible 45 beta
102781_atCcnl2-0.78D-0.93D-0.72NC-0.79NC02cyclin L2
103253_atLin7b-0.46D-0.39NC-0.64D-0.56NC02lin-7 homolog B (C. elegans)
103427_atFbxl3-0.67D-0.63D-0.2NC-0.39NC02F-box and leucine-rich repeat protein 3
103448_atS100a82.13NC-2.11D1.42NC-2.74D02S100 calcium binding protein A8 (calgranulin A)
103460_atDdit4-0.34NC-0.5NC-1.1D-1.48D02DNA-damage-inducible transcript 4
103534_atHbb-b20.17NC-1.63D-0.09NC-2.34D02hemoglobin, beta adult minor chain
103811_atInvs-0.58NC-1.39D-1.34NC-2D02inversin
103863_atSft2d1-0.41D-0.66D-0.18NC-0.29NC02SFT2 domain containing 1
103990_atFosb0.08NC-1.24D-0.3NC-1.35D02FBJ osteosarcoma oncogene B
104155_f_atAtf3-1.59D-2.13D-0.47NC-1.05NC02activating transcription factor 3
104578_f_atActn10.08NC-0.05NC-0.69D-0.86D02actinin, alpha 1
104640_f_atTaf1d-0.02NC-0.47NC-0.68D-0.97D02TATA box binding protein (Tbp)-associated factor,
RNA polymerase I, D
104701_atBhlhe40-0.38NC-0.42NC-0.87D-0.9D02basic helix-loop-helix family, member e40
160140_atTbce-1.09D-0.66NC-0.92D-0.82NC02tubulin-specific chaperone E
160182_atSrsf6-0.6D-0.7D-0.45NC-0.56NC02serine/arginine-rich splicing factor 6
160316_atAI503316-0.89D-1.11D-0.01NC-0.74NC02expressed sequence AI503316; heterogeneous nuclear
ribonucleoprotein U
160407_atActr1a-1.42D-2.18D-0.11NC-0.68NC02ARP1 actin-related protein 1 A, centractin alpha
160547_s_atTxnip-0.6NC-1.07D-0.7NC-1.28D02thioredoxin interacting protein
160564_atLcn2-0.8NC-3.16D-0.92NC-3.84D02lipocalin 2
160791_atLuc7l3-0.9D-0.14NC-1.26D-0.37NC02LUC7-like 3 (S. cerevisiae)
160894_atCebpd-0.15NC-1.06D-0.34NC-1.37D02CCAAT/enhancer binding protein (C/EBP), delta
161462_r_at6820431F20Rik-1.44NC-2.05D-1.53NC-2.36D02cadherin 11 pseudogene; predicted gene, 21811
162093_atYars-0.87D-0.94D-0.07NC-0.35NC02tyrosyl-tRNA synthetase
162399_f_atAtxn2-0.14NC-0.23NC-0.94D-1.23D02ataxin 2
162424_f_atDdx17-0.58D-0.11NC-0.86D-0.23NC02DEAD (Asp-Glu-Ala-Asp) box polypeptide 17
162459_f_atCol6a1-0.11NC-0.78NC-3.33D-4.01D02collagen, type VI, alpha 1
92211_atBod1l-0.56D-0.69D-0.56NC-0.5NC02biorientation of chromosomes in cell division 1-like
92233_atPaxbp1-0.62D-0.93D-0.61NC-0.68NC02PAX3 and PAX7 binding protein 1
92523_atKcnj60.42NC-1.73D1.6NC-1.02MD02potassium inwardly-rectifying channel, subfamily J, member 6
92636_f_atGm10177-0.34D-0.09NC-0.52D-0.23NC02predicted gene 10177; predicted gene, 17756; predicted gene 4184;
protein transport protein Sec. 61 subunit gamma; protein transport
protein Sec. 61 subunit gamma-like; SEC. 61, gamma subunit
92642_atCar2-0.42MD-0.37NC-0.88D-0.72NC02carbonic anhydrase 2
92665_f_at3830403N18Rik-3.41D-3.56NC-3.93D-4.21NC02RIKEN cDNA 3830403N18 gene; X-linked lymphocyte-regulated
92751_i_atWnt10b0.49NC-1.75D-2.13NC-4.2D02wingless-type MMTV integration site family, member 10B
92768_s_atAlas2-0.01NC-1.89D-0.66NC-2.71D02aminolevulinic acid synthase 2, erythroid

Ddit4, Col6a1, Fgf11 and Osmr genes of PI3K-AKT signaling pathway. Fbxl3 and Bhlhe40 are circadian rhythm genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Table 10

Gene expression matrix after 30 days rTMS on cerebrum.

TC IDGSL1CL2CL3CL4C*#Description
92777_atCyr61-1.09NC-1.87D-1.21NC-2.36D02cysteine rich protein 61
92787_atAnkrd10-0.66D-1D-0.31NC-0.69NC02ankyrin repeat domain 10
92802_s_atPlp1-0.61D-0.99D0.03NC-0.42NC02proteolipid protein (myelin) 1
92945_atGria2-0.45NC-0.06NC-0.96D-0.82D02glutamate receptor, ionotropic, AMPA2 (alpha 2)
93009_atGstm2-2D-4.19D-0.85NC-2.44NC02glutathione S-transferase, mu 2
93126_atCkb-0.01NC-0.12NC-0.53D-0.56D02creatine kinase, brain
93274_atClk1-1.11D-1.04D-0.6NC-0.46NC02CDC-like kinase 1
93285_atDusp6-0.48NC-0.52NC-0.58D-0.83D02dual specificity phosphatase 6
93353_atLum-0.93D-0.76D0.22NC0.25NC02lumican
93390_g_atProm10.11NC0.05NC-1.44D-1.09D02prominin 1
93478_atDnajc21-0.14NC-0.07NC-1.02MD-1.39D02DnaJ (Hsp40) homolog, subfamily C, member 21
93486_atSlc27a10.53NC-0.65D-0.4NC-1.46D02solute carrier family 27 (fatty acid transporter), member 1
93615_atPbx30.26NC0.07NC-0.63D-0.94D02pre B cell leukemia homeobox 3
93666_atLmo2-0.51D-0.72D0.08NC-0.23NC02LIM domain only 2
93773_f_atZranb2-0.71D-0.4NC-0.61D-0.41NC02zinc finger, RAN-binding domain containing 2
93985_atTiparp-1.11D-0.46NC-0.74D-0.79NC02TCDD-inducible poly(ADP-ribose) polymerase
94155_atRgs4-0.56MD-0.96D0.49NC-0.31NC02regulator of G-protein signaling 4
94192_atGdap10-0.41NC-1.15D-0.66NC-1.24D02ganglioside-induced differentiation-associated-protein 10
94349_atKhdc1b-2.59NC-4.38D0.41NC-1.57D02KH domain containing 1B
94379_atKif1b-1.4NC-1.71D-1.62NC-2.65D02kinesin family member 1B
94395_atFubp1-0.48NC-0.78D-0.99D-1.05NC02far upstream element (FUSE) binding protein 1
94460_atStk38-0.43D-0.79D-0.04NC-0.37NC02serine/threonine kinase 38
94516_f_atPenk0.16NC0.02NC-0.78D-0.89D02preproenkephalin
94689_atGm39971-0.03NC-0.48NC-1.5D-2D02predicted gene, 39971
95001_atAkap8-0.88D-1MD-0.62NC-0.84NC02A kinase (PRKA) anchor protein 8
95081_atExosc8-1.38D-1.39D-0.8NC-0.95NC02exosome component 8
95134_atMid1ip1-0.92D-0.8D-0.3NC-0.2NC02Mid1 interacting protein 1 (gastrulation specific G12-like
(zebrafish))
95339_r_atMmp12-2.02MD-4.34D-1.71NC-4.09NC02matrix metallopeptidase 12
95418_atRasl11b0.02NC-0.09NC-0.76D-0.85D02RAS-like, family 11, member B
95674_r_atBasp1-0.37D-0.21NC-0.51D-0.3NC02brain abundant, membrane attached signal protein 1
95694_atTop1-0.2NC-0.4NC-0.56D-0.63D02topoisomerase (DNA) I
96464_atPlxnb2-0.41NC-1.64D0.19NC-0.78MD02plexin B2
96672_atHopx-0.45D-0.64D-0.29NC-0.52NC02HOP homeobox
96785_atKank3-0.55D-0.33NC-1.08D-0.92NC02KN motif and ankyrin repeat domains 3
96912_s_atCtla2a-0.8D-1.02D-0.38NC-0.77NC02cytotoxic T lymphocyte-associated protein 2 alpha; cytotoxic
T lymphocyte-associated protein 2 beta



























96961_atPcgf2-0.35NC-1.18D-0.08NC-0.74D02polycomb group ring finger 2
97142_atDXErtd242e-1.93D-2.25D-2.93NC-3.23NC02DNA segment, Chr X, ERATO Doi 242, expressed
97358_atAdgrl10.02NC0.08NC-0.66D-0.5MD02adhesion G protein-coupled receptor L1
97759_atKcnma1-0.15NC-0.06NC-0.87D-0.65D02potassium large conductance calcium-activated channel,
subfamily M, alpha member 1
98474_r_atTnfaip6-1.14D-0.3NC-1.1MD0.04NC02tumor necrosis factor alpha induced protein 6
98475_atMatn2-0.17NC-0.29NC-0.76D-1.16D02matrilin 2
99089_atMal-0.28NC-0.61NC-0.92D-1.12D02myelin and lymphocyte protein, T cell differentiation protein
99622_atKlf4-0.81NC-0.52NC-2.7D-2.56D02Kruppel-like factor 4 (gut)
99830_atKalrn-0.16NC0.04NC-0.89D-0.69D02kalirin, RhoGEF kinase

Lmo2, Pbx3 and Prom1 are genes of transcriptional misregulation in cancer. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

Gene expression matrix after 30 days rTMS on cerebrum. Gnb1, Gnai2, Dlg4 and Mapk1 are glutamatergic genes. Fyn, Camk2a and Mapk1 are cholinergic genes. Kif5a is Dopaminergic gene. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Actb, Itpr2 and Rho are oxytocin signaling pathway genes. Cyfip1and Itgb4 are actin cytoskeleton regulation genes. Pdpk1 and Pdcd4 are genes of proteoglycans in cancer. Pla2g7 amd Pld4 are ether lipid metabolism genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Ache is Cholinergic gene. Grik5 and Slc1a1 are Glutamatergic gene. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Kcnab2 and Pacsin1 are Synaptosome genes. Rapgef4, Arhgap5 and Ctnna2 are Leukocyte transendothelial migration genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Rad23b, Sec. 61b, Vimp, Rpn2 and Ssr3 are genes of protein processing in endoplasmic reticulum. Atp1b2 and Camk2a are cAMP signaling pathway genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Arfgef1, Rab31, Rab11b, Capza2, and Chmp2a are genes of endocytosis. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Gnai2, Kif5a and Ppp2r5c are dopaminergic synapse genes. Gnai2, Myh7 and Ppp2r5c are genes of adrenergic signaling in cardiomyocytes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Atf4, Adra1a, Myl4 and Ppp1cc are genes of adrenergic signaling in cardiomyocytes. Fos, Max, Atf4, Dusp1, Gadd45b and Nr4a1 are genes of MAPK signaling pathway. Fos, Atf4 and Ppp1cc are Dopaminergic genes. Csnk1d, Id1 and Ppp1cc are genes of hippo signaling pathway. Csnk1d and Per1 are circadian rhythm genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Ddit4, Col6a1, Fgf11 and Osmr genes of PI3K-AKT signaling pathway. Fbxl3 and Bhlhe40 are circadian rhythm genes. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis. Gene expression matrix after 30 days rTMS on cerebrum. Lmo2, Pbx3 and Prom1 are genes of transcriptional misregulation in cancer. Mice cerebrum stimulated by rTMS for 30days were denoted as M1 and M2, sham control were denoted as C1 and C2. N=2. All expression ratios were converted into the log2(expression ratio) values. L1: Signal Log Ratio (M1/C1), L2: Signal Log Ratio (M2/C1), L3: Signal Log Ratio (M1/C2), L4: Signal Log Ratio (M1/C2). C1, C2 were used as a control and M1, M2 were normalized with respect to C1 and C2 to obtain expression ratios. Expression Console (EC) Ver.1.4 and Transcriptome Analysis Console (TAC) Ver.3. were used for Comparison Analysis as manufacture procedure. C means data analysis output for a Comparison Analysis illustrating Change p-values with the associated Increase (I) or Decrease (D) call. Increase calls have Change p-values closer to zero and Decrease calls have Change p-values closer to one. Finally, the Change algorithm assesses probe pair saturation, calculates a Change p-values, and assigns an (I), Marginal Increase (MI), No Change (NC), Marginal Decrease (MD), or (D) call for C. Gene with more than 2 significant difference calls was chosen. Abbreviations; TC ID: Transcript Cluster ID, GS: Gene Symbol, *: Total number of increase, #: Total number of decrease. TC ID is available for Pathway analysis.

2. Experimental design, materials and methods

We carried out a comprehensive analysis of altered gene expression in cerebrum following chronic rTMS using a high-density oligonucleotide array (GeneChip; Affymetrix, Santa Clara, CA, USA. MG_U74Av2 probe array), as described elsewhere [2]. Using the Affymetrix algorithm [3] and multiple analysis comparison software for assessing gene expression differences, mRNAs that increased or decreased in the mouse brain following chronic rTMS relative to levels in the control mouse brain were identified. Pathway analysis was used to identify the significant pathway of the differential genes according to KEGG. And also, Gene Ontology (GO) analysis was applied to analyze the main function of the differentially expressed genes according to the gene ontology, which is the key functional classification of NCBI that can organize genes into hierarchical categories and uncover the gene regulatory network based on biological process and molecular function [4]. Using these data, we indicated that rTMS modulates glutamate, GABA and glycine transporters and regulates ER stress-related genes [1].
Subject areaNeuroscience
More specific subject areaPsychiatric disorders
Type of dataTables
How data was acquiredAffymetrix GeneChip RNA microarray
Data formatFiltered, analysed
Experimental factorsMouse brain treated with rTMS for 30 days
Experimental featuresRNA isolation, global gene expression analyses
Data source locationWako, Saitama, Japan
Data accessibilityData are contained within this article
  3 in total

1.  Decreased expression of hypothalamic neuropeptides in Huntington disease transgenic mice with expanded polyglutamine-EGFP fluorescent aggregates.

Authors:  Svetlana Kotliarova; Nihar R Jana; Naoaki Sakamoto; Masaru Kurosawa; Haruko Miyazaki; Munenori Nekooki; Hiroshi Doi; Yoko Machida; Hon Kit Wong; Taishi Suzuki; Chiharu Uchikawa; Yuri Kotliarov; Kazuyo Uchida; Yoshiro Nagao; Utako Nagaoka; Akira Tamaoka; Kiyomitsu Oyanagi; Fumitaka Oyama; Nobuyuki Nukina
Journal:  J Neurochem       Date:  2005-05       Impact factor: 5.372

Review 2.  High density synthetic oligonucleotide arrays.

Authors:  R J Lipshutz; S P Fodor; T R Gingeras; D J Lockhart
Journal:  Nat Genet       Date:  1999-01       Impact factor: 38.330

3.  The Gene Ontology (GO) project in 2006.

Authors: 
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

  3 in total
  1 in total

1.  Effects of repetitive transcranial magnetic stimulation on ER stress-related genes and glutamate, γ-aminobutyric acid and glycine transporter genes in mouse brain.

Authors:  Tetsurou Ikeda; Satoru Kobayashi; Chikao Morimoto
Journal:  Biochem Biophys Rep       Date:  2018-11-12
  1 in total

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