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 *

191 related articles for article (PubMed ID: 15649943)

  • 21. 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. PubMed ID: 21912643
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. The Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation.
    Bush JR; Wevrick R
    Differentiation; 2008 Nov; 76(9):994-1005. PubMed ID: 18557765
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry.
    Sanderson MR; Badior KE; Fahlman RP; Wevrick R
    Hum Genet; 2020 Dec; 139(12):1513-1529. PubMed ID: 32529326
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism.
    Beneduzzi D; Iyer AK; Trarbach EB; Silveira-Neto AP; Silveira LG; Tusset C; Yip K; Mendonça BB; Mellon PL; Latronico AC
    Eur J Endocrinol; 2011 Jul; 165(1):145-50. PubMed ID: 21543378
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. [Necdin and Prader-Willi syndrome].
    Yoshikawa K
    Seikagaku; 2004 May; 76(5):460-3. PubMed ID: 15212237
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Necdin and neurotrophin receptors: interactors of relevance for neuronal resistance to oxidant stress.
    Ingraham CA; Wertalik L; Schor NF
    Pediatr Res; 2011 Apr; 69(4):279-84. PubMed ID: 21150695
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome.
    Tsai TF; Armstrong D; Beaudet AL
    Nat Genet; 1999 May; 22(1):15-6. PubMed ID: 10319852
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome.
    Sutcliffe JS; Han M; Christian SL; Ledbetter DH
    Lancet; 1997 Nov; 350(9090):1520-1. PubMed ID: 9388406
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Nogo-A inhibits necdin-accelerated neurite outgrowth by retaining necdin in the cytoplasm.
    Liu X; Wang Y; Zhang Y; Zhu W; Xu X; Niinobe M; Yoshikawa K; Lu C; He C
    Mol Cell Neurosci; 2009 May; 41(1):51-61. PubMed ID: 19386232
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.