Literature DB >> 12955587

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

Tomohiko Kayashima1,2, Tohru Ohta3,2, Norio Niikawa1,2, Tatsuya Kishino4,5.   

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Year:  2003        PMID： 12955587     DOI： 10.1007/s10038-003-0061-z

Source DB:  PubMed          Journal:  J Hum Genet        ISSN： 1434-5161            Impact factor:   3.172


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  6 in total

1.  The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.

Authors:  S J Chamberlain; C I Brannan
Journal:  Genomics       Date:  2001-05-01       Impact factor: 5.736

2.  A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

Authors:  M Meguro; A Kashiwagi; K Mitsuya; M Nakao; I Kondo; S Saitoh; M Oshimura
Journal:  Nat Genet       Date:  2001-05       Impact factor: 38.330

3.  Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.

Authors:  K Yamasaki; K Joh; T Ohta; H Masuzaki; T Ishimaru; T Mukai; N Niikawa; M Ogawa; J Wagstaff; T Kishino
Journal:  Hum Mol Genet       Date:  2003-04-15       Impact factor: 6.150

4.  Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.

Authors:  Akiko Kashiwagi; Makiko Meguro; Hidetoshi Hoshiya; Masayuki Haruta; Fumitoshi Ishino; Toshiyuki Shibahara; Mitsuo Oshimura
Journal:  J Hum Genet       Date:  2003-03-12       Impact factor: 3.172

5.  Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

Authors:  S Jiang; M A Hemann; M P Lee; A P Feinberg
Journal:  Genomics       Date:  1998-11-01       Impact factor: 5.736

6.  Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting.

Authors:  Tomohiko Kayashima; Kentaro Yamasaki; Keiichiro Joh; Takahiro Yamada; Tohru Ohta; Koh-ichiro Yoshiura; Naomichi Matsumoto; Yoshibumi Nakane; Tsunehiro Mukai; Norio Niikawa; Tatsuya Kishino
Journal:  Genomics       Date:  2003-06       Impact factor: 5.736
  6 in total
  8 in total

1.  Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

Authors:  Yong-Hui Jiang; Yanzhen Pan; Li Zhu; Luis Landa; Jong Yoo; Corinne Spencer; Isabel Lorenzo; Murray Brilliant; Jeffrey Noebels; Arthur L Beaudet
Journal:  PLoS One       Date:  2010-08-20       Impact factor: 3.240

2.  Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

Authors:  Amanda J DuBose; Karen A Johnstone; Emily Y Smith; Ryan A E Hallett; James L Resnick
Journal:  Neurogenetics       Date:  2009-11-06       Impact factor: 2.660

Review 3.  The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.

Authors:  Amber Hogart; David Wu; Janine M LaSalle; N Carolyn Schanen
Journal:  Neurobiol Dis       Date:  2008-09-18       Impact factor: 5.996

4.  Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

Authors:  A Hogart; K N Leung; N J Wang; D J Wu; J Driscoll; R O Vallero; N C Schanen; J M LaSalle
Journal:  J Med Genet       Date:  2008-10-07       Impact factor: 6.318

5.  The neurobiology of mouse models syntenic to human chromosome 15q.

Authors:  Toru Takumi
Journal:  J Neurodev Disord       Date:  2011-07-26       Impact factor: 4.025

6.  Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans.

Authors:  Miguel Landers; Margaret A Calciano; Dan Colosi; Heather Glatt-Deeley; Joseph Wagstaff; Marc Lalande
Journal:  Nucleic Acids Res       Date:  2005-07-18       Impact factor: 16.971

7.  Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.

Authors:  Noelle D Germain; Pin-Fang Chen; Alex M Plocik; Heather Glatt-Deeley; Judith Brown; James J Fink; Kaitlyn A Bolduc; Tiwanna M Robinson; Eric S Levine; Lawrence T Reiter; Brenton R Graveley; Marc Lalande; Stormy J Chamberlain
Journal:  Mol Autism       Date:  2014-08-20       Impact factor: 7.509

8.  Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation.

Authors:  Arne W Mould; Zhenyi Pang; Miha Pakusch; Ian D Tonks; Mitchell Stark; Dianne Carrie; Pamela Mukhopadhyay; Annica Seidel; Jonathan J Ellis; Janine Deakin; Matthew J Wakefield; Lutz Krause; Marnie E Blewitt; Graham F Kay
Journal:  Epigenetics Chromatin       Date:  2013-07-02       Impact factor: 4.954
  8 in total

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