213 related articles for article (PubMed ID: 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. PubMed ID: 17893678
[TBL] [Abstract][Full Text] [Related]
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; 16(22):2713-9. PubMed ID: 17728320
[TBL] [Abstract][Full Text] [Related]
3. 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; 19(24):4895-905. PubMed ID: 20876615
[TBL] [Abstract][Full Text] [Related]
4. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene.
Watrin F; Le Meur E; Roeckel N; Ripoche MA; Dandolo L; Muscatelli F
BMC Genet; 2005 Jan; 6():1. PubMed ID: 15634360
[TBL] [Abstract][Full Text] [Related]
5. Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty.
Fountain MD; Tao H; Chen CA; Yin J; Schaaf CP
Genes Brain Behav; 2017 Jul; 16(6):592-600. PubMed ID: 28296079
[TBL] [Abstract][Full Text] [Related]
6. Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome.
Pravdivyi I; Ballanyi K; Colmers WF; Wevrick R
Hum Mol Genet; 2015 Aug; 24(15):4276-83. PubMed ID: 25926624
[TBL] [Abstract][Full Text] [Related]
7. An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.
Meziane H; Schaller F; Bauer S; Villard C; Matarazzo V; Riet F; Guillon G; Lafitte D; Desarmenien MG; Tauber M; Muscatelli F
Biol Psychiatry; 2015 Jul; 78(2):85-94. PubMed ID: 25599930
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 23341784
[TBL] [Abstract][Full Text] [Related]
9. The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.
Wijesuriya TM; De Ceuninck L; Masschaele D; Sanderson MR; Carias KV; Tavernier J; Wevrick R
Hum Mol Genet; 2017 Nov; 26(21):4215-4230. PubMed ID: 28973533
[TBL] [Abstract][Full Text] [Related]
10. 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; 9(12):1813-9. PubMed ID: 10915770
[TBL] [Abstract][Full Text] [Related]
11. 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; Roëckel N; Lalande M; Muscatelli F
Hum Mol Genet; 1999 Dec; 8(13):2497-505. PubMed ID: 10556298
[TBL] [Abstract][Full Text] [Related]
12. Magel2 Modulates Bone Remodeling and Mass in Prader-Willi Syndrome by Affecting Oleoyl Serine Levels and Activity.
Baraghithy S; Smoum R; Drori A; Hadar R; Gammal A; Hirsch S; Attar-Namdar M; Nemirovski A; Gabet Y; Langer Y; Pollak Y; Schaaf CP; Rech ME; Gross-Tsur V; Bab I; Mechoulam R; Tam J
J Bone Miner Res; 2019 Jan; 34(1):93-105. PubMed ID: 30347474
[TBL] [Abstract][Full Text] [Related]
13. 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; 150B(8):1085-99. PubMed ID: 19199291
[TBL] [Abstract][Full Text] [Related]
14. Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.
Kamaludin AA; Smolarchuk C; Bischof JM; Eggert R; Greer JJ; Ren J; Lee JJ; Yokota T; Berry FB; Wevrick R
Hum Mol Genet; 2016 Sep; 25(17):3798-3809. PubMed ID: 27436578
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 19172181
[TBL] [Abstract][Full Text] [Related]
16. 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; 1():19. PubMed ID: 19055781
[TBL] [Abstract][Full Text] [Related]
17. Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes.
Ieda D; Negishi Y; Miyamoto T; Johmura Y; Kumamoto N; Kato K; Miyoshi I; Nakanishi M; Ugawa S; Oishi H; Saitoh S
PLoS One; 2020; 15(8):e0237814. PubMed ID: 32804975
[TBL] [Abstract][Full Text] [Related]
18. Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader-Willi syndrome.
Knani I; Earley BJ; Udi S; Nemirovski A; Hadar R; Gammal A; Cinar R; Hirsch HJ; Pollak Y; Gross I; Eldar-Geva T; Reyes-Capo DP; Han JC; Haqq AM; Gross-Tsur V; Wevrick R; Tam J
Mol Metab; 2016 Dec; 5(12):1187-1199. PubMed ID: 27900261
[TBL] [Abstract][Full Text] [Related]
19. Impaired melanocortin pathway function in Prader-Willi syndrome gene-Magel2 deficient mice.
Oncul M; Dilsiz P; Ates Oz E; Ates T; Aklan I; Celik E; Sayar Atasoy N; Atasoy D
Hum Mol Genet; 2018 Sep; 27(18):3129-3136. PubMed ID: 29878108
[TBL] [Abstract][Full Text] [Related]
20. Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production.
Chen H; Victor AK; Klein J; Tacer KF; Tai DJ; de Esch C; Nuttle A; Temirov J; Burnett LC; Rosenbaum M; Zhang Y; Ding L; Moresco JJ; Diedrich JK; Yates JR; Tillman HS; Leibel RL; Talkowski ME; Billadeau DD; Reiter LT; Potts PR
JCI Insight; 2020 Sep; 5(17):. PubMed ID: 32879135
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
