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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 11115855)

  • 1. 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]  

  • 2. 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; 18(2):248-60. PubMed ID: 18930956
    [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. 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; 5(5):324-32. PubMed ID: 9412790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 9302265
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 9354807
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 28(7):1745-55. PubMed ID: 18272695
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 213(1-2):65-72. PubMed ID: 9630521
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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; 25(30):7090-9. PubMed ID: 16049186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis.
    Bush JR; Wevrick R
    Gene; 2012 Apr; 497(1):45-51. PubMed ID: 22305984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.