Moore GE - Search Results

1

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. Monk D, et al. Among authors: moore ge. Hum Genet. 2002 Oct;111(4-5):376-87. doi: 10.1007/s00439-002-0777-4. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384779

2

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.

Nakabayashi K, Bentley L, Hitchins MP, Mitsuya K, Meguro M, Minagawa S, Bamforth JS, Stanier P, Preece M, Weksberg R, Oshimura M, Moore GE, Scherer SW. Nakabayashi K, et al. Among authors: moore ge. Hum Mol Genet. 2002 Jul 15;11(15):1743-56. doi: 10.1093/hmg/11.15.1743. Hum Mol Genet. 2002. PMID: 12095916

3

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. Hitchins MP, et al. Among authors: moore ge. Mamm Genome. 2002 Dec;13(12):686-91. doi: 10.1007/s00335-002-3028-z. Mamm Genome. 2002. PMID: 12514746

4

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.

Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey CV, Peters J, Craigen W, Preece M, Stanier P, Moore GE, Kelsey G. Arnaud P, et al. Among authors: moore ge. Hum Mol Genet. 2003 May 1;12(9):1005-19. doi: 10.1093/hmg/ddg110. Hum Mol Genet. 2003. PMID: 12700169

5

Intrauterine growth restriction--genetic causes and consequences.

Monk D, Moore GE. Monk D, et al. Among authors: moore ge. Semin Fetal Neonatal Med. 2004 Oct;9(5):371-8. doi: 10.1016/j.siny.2004.03.002. Semin Fetal Neonatal Med. 2004. PMID: 15691772 Review.

6

Maternal uniparental disomy 7 in Silver-Russell syndrome.

Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE. Preece MA, et al. Among authors: moore ge. J Med Genet. 1997 Jan;34(1):6-9. doi: 10.1136/jmg.34.1.6. J Med Genet. 1997. PMID: 9032641 Free PMC article.

7

Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver Russell syndrome probands and their families.

Abu-Amero S, Price S, Wakeling E, Stanier P, Trembath R, Preece MA, Moore GE. Abu-Amero S, et al. Among authors: moore ge. Eur J Hum Genet. 1997 Jul-Aug;5(4):235-41. Eur J Hum Genet. 1997. PMID: 9359045

8

Genetics of Silver-Russell syndrome.

Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA. Wakeling EL, et al. Among authors: moore ge. Horm Res. 1998;49 Suppl 2:32-6. doi: 10.1159/000053085. Horm Res. 1998. PMID: 9730670 Review.

9

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.

Wakeling EL, Abu-Amero SN, Stanier P, Preece MA, Moore GE. Wakeling EL, et al. Among authors: moore ge. Eur J Hum Genet. 1998 Mar-Apr;6(2):158-64. doi: 10.1038/sj.ejhg.5200179. Eur J Hum Genet. 1998. PMID: 9781061

10

The search for the gene for Silver-Russell syndrome.

Moore GE, Abu-Amero S, Wakeling E, Hitchins M, Monk D, Stanier P, Preece M. Moore GE, et al. Acta Paediatr Suppl. 1999 Dec;88(433):42-8. doi: 10.1111/j.1651-2227.1999.tb14402.x. Acta Paediatr Suppl. 1999. PMID: 10626544 Review.

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