Wevrick R - Search Results

1

Disruption of the mouse necdin gene results in early post-natal lethality.

Gérard M, Hernandez L, Wevrick R, Stewart CL. Gérard M, et al. Among authors: wevrick r. Nat Genet. 1999 Oct;23(2):199-202. doi: 10.1038/13828. Nat Genet. 1999. PMID: 10508517

2

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.

MacDonald HR, Wevrick R. MacDonald HR, et al. Among authors: wevrick r. Hum Mol Genet. 1997 Oct;6(11):1873-8. doi: 10.1093/hmg/6.11.1873. Hum Mol Genet. 1997. PMID: 9302265

3

A mouse model for Prader-Willi syndrome imprinting-centre mutations.

Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI. Yang T, et al. Among authors: wevrick r. Nat Genet. 1998 May;19(1):25-31. doi: 10.1038/ng0598-25. Nat Genet. 1998. PMID: 9590284

4

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.

Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R. Lee S, et al. Among authors: wevrick r. Hum Mol Genet. 2000 Jul 22;9(12):1813-9. doi: 10.1093/hmg/9.12.1813. Hum Mol Genet. 2000. PMID: 10915770

5

Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice.

Ren J, Lee S, Pagliardini S, Gérard M, Stewart CL, Greer JJ, Wevrick R. Ren J, et al. Among authors: wevrick r. J Neurosci. 2003 Mar 1;23(5):1569-73. doi: 10.1523/JNEUROSCI.23-05-01569.2003. J Neurosci. 2003. PMID: 12629158 Free PMC article.

6

Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome.

Bischof JM, Stewart CL, Wevrick R. Bischof JM, et al. Among authors: wevrick r. Hum Mol Genet. 2007 Nov 15;16(22):2713-9. doi: 10.1093/hmg/ddm225. Epub 2007 Aug 29. Hum Mol Genet. 2007. PMID: 17728320

7

The imprinted gene Magel2 regulates normal circadian output.

Kozlov SV, Bogenpohl JW, Howell MP, Wevrick R, Panda S, Hogenesch JB, Muglia LJ, Van Gelder RN, Herzog ED, Stewart CL. Kozlov SV, et al. Among authors: wevrick r. Nat Genet. 2007 Oct;39(10):1266-72. doi: 10.1038/ng2114. Epub 2007 Sep 23. Nat Genet. 2007. PMID: 17893678

8

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

Miller NL, Wevrick R, Mellon PL. Miller NL, et al. Among authors: wevrick r. Hum Mol Genet. 2009 Jan 15;18(2):248-60. doi: 10.1093/hmg/ddn344. Epub 2008 Oct 17. Hum Mol Genet. 2009. PMID: 18930956 Free PMC article.

9

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

Wevrick R, Francke U. Wevrick R, et al. Hum Mol Genet. 1997 Feb;6(2):325-32. doi: 10.1093/hmg/6.2.325. Hum Mol Genet. 1997. PMID: 9063754

10

The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.

Hanel ML, Wevrick R. Hanel ML, et al. Among authors: wevrick r. Clin Genet. 2001 Mar;59(3):156-64. doi: 10.1034/j.1399-0004.2001.590303.x. Clin Genet. 2001. PMID: 11260224 Review.

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