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Similar articles for PubMed (Select 17893678)

1.

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.

Nat Genet. 2007 Oct;39(10):1266-72. Epub 2007 Sep 23.

PMID:
17893678
2.

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

Bischof JM, Stewart CL, Wevrick R.

Hum Mol Genet. 2007 Nov 15;16(22):2713-9. Epub 2007 Aug 29.

3.
4.

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.

Schaller F, Watrin F, Sturny R, Massacrier A, Szepetowski P, Muscatelli F.

Hum Mol Genet. 2010 Dec 15;19(24):4895-905. doi: 10.1093/hmg/ddq424. Epub 2010 Sep 28.

5.

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.

6.

Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.

Mercer RE, Kwolek EM, Bischof JM, van Eede M, Henkelman RM, Wevrick R.

Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1085-99. doi: 10.1002/ajmg.b.30934.

PMID:
19199291
7.

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.

Boccaccio I, Glatt-Deeley H, Watrin F, Ro√ęckel N, Lalande M, Muscatelli F.

Hum Mol Genet. 1999 Dec;8(13):2497-505.

8.
9.

Attenuated circadian rhythms in mice lacking the prokineticin 2 gene.

Li JD, Hu WP, Boehmer L, Cheng MY, Lee AG, Jilek A, Siegel JM, Zhou QY.

J Neurosci. 2006 Nov 8;26(45):11615-23.

10.

Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.

Mercer RE, Wevrick R.

PLoS One. 2009;4(1):e4291. doi: 10.1371/journal.pone.0004291. Epub 2009 Jan 27.

11.

Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice.

Mercer RE, Michaelson SD, Chee MJ, Atallah TA, Wevrick R, Colmers WF.

PLoS Genet. 2013;9(1):e1003207. doi: 10.1371/journal.pgen.1003207. Epub 2013 Jan 17.

12.
13.

Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.

Tennese AA, Wevrick R.

Endocrinology. 2011 Mar;152(3):967-78. doi: 10.1210/en.2010-0709. Epub 2011 Jan 19.

14.

Circadian and dark-pulse activation of orexin/hypocretin neurons.

Marston OJ, Williams RH, Canal MM, Samuels RE, Upton N, Piggins HD.

Mol Brain. 2008 Dec 3;1:19. doi: 10.1186/1756-6606-1-19.

15.

Paradoxical function of orexin/hypocretin circuits in a mouse model of Huntington's disease.

Williams RH, Morton AJ, Burdakov D.

Neurobiol Dis. 2011 Jun;42(3):438-45. doi: 10.1016/j.nbd.2011.02.006. Epub 2011 Feb 13.

PMID:
21324360
16.

Double-stranded RNA-mediated suppression of Period2 expression in the suprachiasmatic nucleus disrupts circadian locomotor activity in rats.

Gavrila AM, Robinson B, Hoy J, Stewart J, Bhargava A, Amir S.

Neuroscience. 2008 Jun 23;154(2):409-14. doi: 10.1016/j.neuroscience.2008.04.032. Epub 2008 Apr 29.

PMID:
18511208
18.

Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells.

Devos J, Weselake SV, Wevrick R.

J Circadian Rhythms. 2011 Dec 30;9(1):12. doi: 10.1186/1740-3391-9-12.

19.

Altered photic and non-photic phase shifts in 5-HT(1A) receptor knockout mice.

Smith VM, Sterniczuk R, Phillips CI, Antle MC.

Neuroscience. 2008 Dec 2;157(3):513-23. doi: 10.1016/j.neuroscience.2008.09.030. Epub 2008 Sep 27.

PMID:
18930788
20.

Temporal profile of circadian clock gene expression in a transplanted suprachiasmatic nucleus and peripheral tissues.

Sujino M, Nagano M, Fujioka A, Shigeyoshi Y, Inouye ST.

Eur J Neurosci. 2007 Nov;26(10):2731-8. Epub 2007 Oct 31.

PMID:
17973924
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