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Results: 1 to 20 of 201

1.

Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.

Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F.

BMC Dev Biol. 2006 Nov 20;6:56.

PMID:
17116257
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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.

PMID:
16049186
[PubMed - indexed for MEDLINE]
Free Article
3.

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
[PubMed - indexed for MEDLINE]
4.

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.

Tennese AA, Gee CB, Wevrick R.

Dev Dyn. 2008 Jul;237(7):1935-43. doi: 10.1002/dvdy.21615.

PMID:
18570257
[PubMed - indexed for MEDLINE]
Free Article
5.

Necdin protects embryonic motoneurons from programmed cell death.

Aebischer J, Sturny R, Andrieu D, Rieusset A, Schaller F, Geib S, Raoul C, Muscatelli F.

PLoS One. 2011;6(9):e23764. doi: 10.1371/journal.pone.0023764. Epub 2011 Sep 2.

PMID:
21912643
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.

Kurita M, Kuwajima T, Nishimura I, Yoshikawa K.

J Neurosci. 2006 Nov 15;26(46):12003-13.

PMID:
17108174
[PubMed - indexed for MEDLINE]
Free Article
7.

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.

PMID:
18272695
[PubMed - indexed for MEDLINE]
Free Article
8.

The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.

Watrin F, Roëckel N, Lacroix L, Mignon C, Mattei MG, Disteche C, Muscatelli F.

Eur J Hum Genet. 1997 Sep-Oct;5(5):324-32.

PMID:
9412790
[PubMed - indexed for MEDLINE]
9.

Necdin is required for terminal differentiation and survival of primary dorsal root ganglion neurons.

Takazaki R, Nishimura I, Yoshikawa K.

Exp Cell Res. 2002 Jul 15;277(2):220-32.

PMID:
12083804
[PubMed - indexed for MEDLINE]
10.

Differential effects of endogenous brain-derived neurotrophic factor on the survival of axotomized sensory neurons in dorsal root ganglia: a possible role for the p75 neurotrophin receptor.

Zhou XF, Li WP, Zhou FH, Zhong JH, Mi JX, Wu LL, Xian CJ.

Neuroscience. 2005;132(3):591-603.

PMID:
15837121
[PubMed - indexed for MEDLINE]
11.

Regulation of neuronal death and calcitonin gene-related peptide by fibroblast growth factor-2 and FGFR3 after peripheral nerve injury: evidence from mouse mutants.

Jungnickel J, Klutzny A, Guhr S, Meyer K, Grothe C.

Neuroscience. 2005;134(4):1343-50.

PMID:
16009496
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
Free Article
13.

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.

PMID:
12629158
[PubMed - indexed for MEDLINE]
Free Article
14.

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
[PubMed - indexed for MEDLINE]
Free Article
15.

Differential loss of spinal sensory but not motor neurons in the p75NTR knockout mouse.

Murray SS, Bartlett PF, Cheema SS.

Neurosci Lett. 1999 May 21;267(1):45-8.

PMID:
10400245
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
16707790
[PubMed - indexed for MEDLINE]
Free Article
17.

Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons.

Hasegawa K, Yoshikawa K.

J Neurosci. 2008 Aug 27;28(35):8772-84. doi: 10.1523/JNEUROSCI.3052-08.2008.

PMID:
18753379
[PubMed - indexed for MEDLINE]
Free Article
18.

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.

PMID:
14593116
[PubMed - indexed for MEDLINE]
Free Article
19.

Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy.

Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M.

Hum Mol Genet. 2006 Feb 1;15(3):511-8. Epub 2006 Jan 5.

PMID:
16396995
[PubMed - indexed for MEDLINE]
Free Article
20.

Dual roles of the retinoblastoma protein in cell cycle regulation and neuron differentiation.

Lee EY, Hu N, Yuan SS, Cox LA, Bradley A, Lee WH, Herrup K.

Genes Dev. 1994 Sep 1;8(17):2008-21.

PMID:
7958874
[PubMed - indexed for MEDLINE]
Free Article

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