Literature DB >> 11170901

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

S Mergenthaler, M P Hitchins, N Blagitko-Dorfs, D Monk, H A Wollmann, M B Ranke, H H Ropers, S Apostolidou, P Stanier, M A Preece, T Eggermann, V M Kalscheuer, G E Moore.   

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Year:  2001        PMID： 11170901      PMCID： PMC1235290          DOI： 10.1086/318192

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  8 in total

1.  Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer.

Authors:  M Meguro; K Mitsuya; H Sui; K Shigenami; H Kugoh; M Nakao; M Oshimura
Journal:  Hum Mol Genet       Date:  1997-11       Impact factor: 6.150

2.  Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

Authors:  D Monk; E L Wakeling; V Proud; M Hitchins; S N Abu-Amero; P Stanier; M A Preece; G E Moore
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

3.  A model system to study genomic imprinting of human genes.

Authors:  J M Gabriel; M J Higgins; T C Gebuhr; T B Shows; S Saitoh; R D Nicholls
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-08       Impact factor: 11.205

4.  Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.

Authors:  H Yoshihashi; K Maeyama; R Kosaki; T Ogata; M Tsukahara; Y Goto; J Hata; N Matsuo; R J Smith; K Kosaki
Journal:  Am J Hum Genet       Date:  2000-06-12       Impact factor: 11.025

5.  Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.

Authors:  M P Hitchins; D Monk; G M Bell; Z Ali; M A Preece; P Stanier; G E Moore
Journal:  Eur J Hum Genet       Date:  2001-02       Impact factor: 4.246

6.  Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.

Authors:  C A Joyce; A Sharp; J M Walker; H Bullman; I K Temple
Journal:  Hum Genet       Date:  1999-09       Impact factor: 4.132

7.  Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.

Authors:  N Blagitko; S Mergenthaler; U Schulz; H A Wollmann; W Craigen; T Eggermann; H H Ropers; V M Kalscheuer
Journal:  Hum Mol Genet       Date:  2000-07-01       Impact factor: 6.150

8.  Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.

Authors:  M Angrist; S Bolk; K Bentley; S Nallasamy; M K Halushka; A Chakravarti
Journal:  Oncogene       Date:  1998-12-10       Impact factor: 9.867
  8 in total
  7 in total

Review 1.  Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Authors:  M P Hitchins; P Stanier; M A Preece; G E Moore
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

Review 2.  Silver-Russell syndrome: genetic basis and molecular genetic testing.

Authors:  Thomas Eggermann; Matthias Begemann; Gerhard Binder; Sabrina Spengler
Journal:  Orphanet J Rare Dis       Date:  2010-06-23       Impact factor: 4.123

Review 3.  Grb10 and Grb14: enigmatic regulators of insulin action--and more?

Authors:  Lowenna J Holt; Kenneth Siddle
Journal:  Biochem J       Date:  2005-06-01       Impact factor: 3.857

4.  Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.

Authors:  David Monk; Rachel Smith; Philippe Arnaud; Michael A Preece; Philip Stanier; Colin V Beechey; Jo Peters; Gavin Kelsey; Gudrun E Moore
Journal:  Mamm Genome       Date:  2003-12       Impact factor: 2.957

5.  LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.

Authors:  C Francks; S Maegawa; J Laurén; B S Abrahams; A Velayos-Baeza; S E Medland; S Colella; M Groszer; E Z McAuley; T M Caffrey; T Timmusk; P Pruunsild; I Koppel; P A Lind; N Matsumoto-Itaba; J Nicod; L Xiong; R Joober; W Enard; B Krinsky; E Nanba; A J Richardson; B P Riley; N G Martin; S M Strittmatter; H-J Möller; D Rujescu; D St Clair; P Muglia; J L Roos; S E Fisher; R Wade-Martins; G A Rouleau; J F Stein; M Karayiorgou; D H Geschwind; J Ragoussis; K S Kendler; M S Airaksinen; M Oshimura; L E DeLisi; A P Monaco
Journal:  Mol Psychiatry       Date:  2007-07-31       Impact factor: 15.992

6.  Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain.

Authors:  Xu Wang; Qi Sun; Sean D McGrath; Elaine R Mardis; Paul D Soloway; Andrew G Clark
Journal:  PLoS One       Date:  2008-12-04       Impact factor: 3.240

7.  Maternal 5mCpG Imprints at the PARD6G-AS1 and GCSAML Differentially Methylated Regions Are Decoupled From Parent-of-Origin Expression Effects in Multiple Human Tissues.

Authors:  Graziela de Sá Machado Araújo; Ronaldo da Silva Francisco Junior; Cristina Dos Santos Ferreira; Pedro Thyago Mozer Rodrigues; Douglas Terra Machado; Thais Louvain de Souza; Jozimara Teixeira de Souza; Cleiton Figueiredo Osorio da Silva; Antônio Francisco Alves da Silva; Claudia Caixeta Franco Andrade; Alan Tardin da Silva; Victor Ramos; Ana Beatriz Garcia; Filipe Brum Machado; Enrique Medina-Acosta
Journal:  Front Genet       Date:  2018-03-01       Impact factor: 4.599
  7 in total

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