222 related articles for article (PubMed ID: 9448292)
1. Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene.
Miyoshi N; Kuroiwa Y; Kohda T; Shitara H; Yonekawa H; Kawabe T; Hasegawa H; Barton SC; Surani MA; Kaneko-Ishino T; Ishino F
Proc Natl Acad Sci U S A; 1998 Feb; 95(3):1102-7. PubMed ID: 9448292
[TBL] [Abstract][Full Text] [Related]
2. Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation.
Shiura H; Nakamura K; Hikichi T; Hino T; Oda K; Suzuki-Migishima R; Kohda T; Kaneko-ishino T; Ishino F
Hum Mol Genet; 2009 Apr; 18(8):1424-38. PubMed ID: 19174477
[TBL] [Abstract][Full Text] [Related]
3. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.
Monk D; Wakeling EL; Proud V; Hitchins M; Abu-Amero SN; Stanier P; Preece MA; Moore GE
Am J Hum Genet; 2000 Jan; 66(1):36-46. PubMed ID: 10631135
[TBL] [Abstract][Full Text] [Related]
4. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.
Monk D; Smith R; Arnaud P; Preece MA; Stanier P; Beechey CV; Peters J; Kelsey G; Moore GE
Mamm Genome; 2003 Dec; 14(12):805-16. PubMed ID: 14724735
[TBL] [Abstract][Full Text] [Related]
5. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.
Yoshihashi H; Maeyama K; Kosaki R; Ogata T; Tsukahara M; Goto Y; Hata J; Matsuo N; Smith RJ; Kosaki K
Am J Hum Genet; 2000 Aug; 67(2):476-82. PubMed ID: 10856193
[TBL] [Abstract][Full Text] [Related]
6. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.
Joyce CA; Sharp A; Walker JM; Bullman H; Temple IK
Hum Genet; 1999 Sep; 105(3):273-80. PubMed ID: 10987657
[TBL] [Abstract][Full Text] [Related]
7. DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
Hitchins MP; Bentley L; Monk D; Beechey C; Peters J; Kelsey G; Ishino F; Preece MA; Stanier P; Moore GE
Mamm Genome; 2002 Dec; 13(12):686-91. PubMed ID: 12514746
[TBL] [Abstract][Full Text] [Related]
8. Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.
Hitchins MP; Monk D; Bell GM; Ali Z; Preece MA; Stanier P; Moore GE
Eur J Hum Genet; 2001 Feb; 9(2):82-90. PubMed ID: 11313740
[TBL] [Abstract][Full Text] [Related]
9. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.
Caspary T; Cleary MA; Baker CC; Guan XJ; Tilghman SM
Mol Cell Biol; 1998 Jun; 18(6):3466-74. PubMed ID: 9584186
[TBL] [Abstract][Full Text] [Related]
10. Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism.
Charalambous M; Smith FM; Bennett WR; Crew TE; Mackenzie F; Ward A
Proc Natl Acad Sci U S A; 2003 Jul; 100(14):8292-7. PubMed ID: 12829789
[TBL] [Abstract][Full Text] [Related]
11. Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10.
Eggermann T; Begemann M; Gogiel M; Palomares M; Vallespín E; Fernández L; Cazorla R; Spengler S; García-Miñaúr S
Am J Med Genet A; 2012 Nov; 158A(11):2815-9. PubMed ID: 22987336
[TBL] [Abstract][Full Text] [Related]
12. Imprinting disorders: non-Mendelian mechanisms affecting growth.
Butler MG
J Pediatr Endocrinol Metab; 2002 Dec; 15 Suppl 5(Suppl 5):1279-88. PubMed ID: 12510981
[TBL] [Abstract][Full Text] [Related]
13. Evidence against GRB10 as the gene responsible for Silver-Russell syndrome.
McCann JA; Zheng H; Islam A; Goodyer CG; Polychronakos C
Biochem Biophys Res Commun; 2001 Sep; 286(5):943-8. PubMed ID: 11527390
[TBL] [Abstract][Full Text] [Related]
14. Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays.
Kim Y; Kim SS; Kim G; Park S; Park IS; Yoo HW
Clin Genet; 2005 Mar; 67(3):267-9. PubMed ID: 15691366
[No Abstract] [Full Text] [Related]
15. Meg1/Grb10 overexpression causes postnatal growth retardation and insulin resistance via negative modulation of the IGF1R and IR cascades.
Shiura H; Miyoshi N; Konishi A; Wakisaka-Saito N; Suzuki R; Muguruma K; Kohda T; Wakana S; Yokoyama M; Ishino F; Kaneko-Ishino T
Biochem Biophys Res Commun; 2005 Apr; 329(3):909-16. PubMed ID: 15752742
[TBL] [Abstract][Full Text] [Related]
16. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.
Hannula K; Lipsanen-Nyman M; Kontiokari T; Kere J
Am J Hum Genet; 2001 Jan; 68(1):247-53. PubMed ID: 11112662
[TBL] [Abstract][Full Text] [Related]
17. Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations.
Eggermann T; Begemann M; Kurth I; Elbracht M
Eur J Med Genet; 2019 Jul; 62(7):103671. PubMed ID: 31100449
[TBL] [Abstract][Full Text] [Related]
18. Grb10 exceeding the boundaries of a common signaling adapter.
Riedel H
Front Biosci; 2004 Jan; 9():603-18. PubMed ID: 14766395
[TBL] [Abstract][Full Text] [Related]
19. Ribonucleic acid expression of the clustered imprinted genes, p57KIP2, insulin-like growth factor II, and H19, in adrenal tumors and cultured adrenal cells.
Liu J; Kahri AI; Heikkilä P; Voutilainen R
J Clin Endocrinol Metab; 1997 Jun; 82(6):1766-71. PubMed ID: 9177379
[TBL] [Abstract][Full Text] [Related]
20. The search for the gene for Silver-Russell syndrome.
Moore GE; Abu-Amero S; Wakeling E; Hitchins M; Monk D; Stanier P; Preece M
Acta Paediatr Suppl; 1999 Dec; 88(433):42-8. PubMed ID: 10626544
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]