These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
209 related articles for article (PubMed ID: 15972963)
1. Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin. Pagliardini S; Ren J; Wevrick R; Greer JJ Am J Pathol; 2005 Jul; 167(1):175-91. PubMed ID: 15972963 [TBL] [Abstract][Full Text] [Related]
2. 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; 23(5):1569-73. PubMed ID: 12629158 [TBL] [Abstract][Full Text] [Related]
3. Necdin gene, respiratory disturbances and Prader-Willi syndrome. Zanella S; Barthelemy M; Muscatelli F; Hilaire G Adv Exp Med Biol; 2008; 605():159-64. PubMed ID: 18085265 [TBL] [Abstract][Full Text] [Related]
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; 28(7):1745-55. PubMed ID: 18272695 [TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 18570257 [TBL] [Abstract][Full Text] [Related]
6. Central respiratory rhythmogenesis is abnormal in lbx1- deficient mice. Pagliardini S; Ren J; Gray PA; Vandunk C; Gross M; Goulding M; Greer JJ J Neurosci; 2008 Oct; 28(43):11030-41. PubMed ID: 18945911 [TBL] [Abstract][Full Text] [Related]
7. 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; 6():56. PubMed ID: 17116257 [TBL] [Abstract][Full Text] [Related]
9. Neurodevelopmental abnormalities in the brainstem of prenatal mice lacking the Prader-Willi syndrome gene Necdin. Pagliardini S; Rent J; Wevrick R; Greer JJ Adv Exp Med Biol; 2008; 605():139-43. PubMed ID: 18085261 [No Abstract] [Full Text] [Related]
10. Breathing deficits of the Prader-Willi syndrome. Zanella S; Tauber M; Muscatelli F Respir Physiol Neurobiol; 2009 Aug; 168(1-2):119-24. PubMed ID: 19712904 [TBL] [Abstract][Full Text] [Related]
11. 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; 9(20):3101-10. PubMed ID: 11115855 [TBL] [Abstract][Full Text] [Related]
12. Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome. Matarazzo V; Caccialupi L; Schaller F; Shvarev Y; Kourdougli N; Bertoni A; Menuet C; Voituron N; Deneris E; Gaspar P; Bezin L; Durbec P; Hilaire G; Muscatelli F Elife; 2017 Oct; 6():. PubMed ID: 29087295 [TBL] [Abstract][Full Text] [Related]
13. Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome. Wu RN; Hung WC; Chen CT; Tsai LP; Lai WS; Min MY; Wong SB J Neurodev Disord; 2020 Jul; 12(1):21. PubMed ID: 32727346 [TBL] [Abstract][Full Text] [Related]
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; 14(5):627-37. PubMed ID: 15649943 [TBL] [Abstract][Full Text] [Related]
15. MafB deficiency causes defective respiratory rhythmogenesis and fatal central apnea at birth. Blanchi B; Kelly LM; Viemari JC; Lafon I; Burnet H; Bévengut M; Tillmanns S; Daniel L; Graf T; Hilaire G; Sieweke MH Nat Neurosci; 2003 Oct; 6(10):1091-100. PubMed ID: 14513037 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Loss of Necdin impairs myosin activation and delays cell polarization. Bush JR; Wevrick R Genesis; 2010 Sep; 48(9):540-53. PubMed ID: 20665884 [TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 10508517 [TBL] [Abstract][Full Text] [Related]