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Items: 1 to 20 of 110

1.

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth.

Lee S, Walker CL, Karten B, Kuny SL, Tennese AA, O'Neill MA, Wevrick R.

Hum Mol Genet. 2005 Mar 1;14(5):627-37. Epub 2005 Jan 13.

PMID:
15649943
2.
3.

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.

Hum Mol Genet. 2000 Jul 22;9(12):1813-9.

PMID:
10915770
4.

Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.

Zanella S, Watrin F, Mebarek S, Marly F, Roussel M, Gire C, Diene G, Tauber M, Muscatelli F, Hilaire G.

J Neurosci. 2008 Feb 13;28(7):1745-55. doi: 10.1523/JNEUROSCI.4334-07.2008.

5.
6.

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

MacDonald HR, Wevrick R.

Hum Mol Genet. 1997 Oct;6(11):1873-8.

PMID:
9302265
7.
8.

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.

Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F.

Nat Genet. 1997 Nov;17(3):357-61.

PMID:
9354807
9.

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region.

Nakada Y, Taniura H, Uetsuki T, Inazawa J, Yoshikawa K.

Gene. 1998 Jun 15;213(1-2):65-72.

PMID:
9630521
10.

Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival.

Kuwako K, Hosokawa A, Nishimura I, Uetsuki T, Yamada M, Nada S, Okada M, Yoshikawa K.

J Neurosci. 2005 Jul 27;25(30):7090-9.

11.

Necdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptor.

Kuwako K, Taniura H, Yoshikawa K.

J Biol Chem. 2004 Jan 16;279(3):1703-12. Epub 2003 Oct 29.

12.

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Le Moal M, Cau P, Cremer H.

Hum Mol Genet. 2000 Dec 12;9(20):3101-10.

PMID:
11115855
13.
14.

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

Andrieu D, Watrin F, Niinobe M, Yoshikawa K, Muscatelli F, Fernandez PA.

Gene Expr Patterns. 2003 Dec;3(6):761-5.

PMID:
14643685
15.

Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis.

Bush JR, Wevrick R.

Gene. 2012 Apr 10;497(1):45-51. doi: 10.1016/j.gene.2012.01.027. Epub 2012 Jan 27.

PMID:
22305984
16.

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

Miller NL, Wevrick R, Mellon PL.

Hum Mol Genet. 2009 Jan 15;18(2):248-60. doi: 10.1093/hmg/ddn344. Epub 2008 Oct 17.

17.

The Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation.

Bush JR, Wevrick R.

Differentiation. 2008 Nov;76(9):994-1005. doi: 10.1111/j.1432-0436.2008.00281.x. Epub 2008 Jun 13.

PMID:
18557765
18.

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

Gérard M, Hernandez L, Wevrick R, Stewart CL.

Nat Genet. 1999 Oct;23(2):199-202.

PMID:
10508517
19.

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.

J Neurosci. 2003 Mar 1;23(5):1569-73.

20.

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

Kuwajima T, Nishimura I, Yoshikawa K.

J Neurosci. 2006 May 17;26(20):5383-92.

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