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Volumn 13, Issue 10, 2005, Pages 1841-1842

Evaluation of Prader-Willi syndrome gene MAGEL2 in severe childhood-onset obesity

Author keywords

[No Author keywords available]

Indexed keywords

MURINAE;

EID: 33644788640     PISSN: 10717323     EISSN: None     Source Type: Journal    
DOI: 10.1038/oby.2005.224     Document Type: Article
Times cited : (6)

References (8)
  • 1
    • 0035098226 scopus 로고    scopus 로고
    • The role of genomic imprinting in human developmental disorders: Lessons from Prader-Willi syndrome
    • Hanel M, Wevrick R. The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome. Clin Genet. 2001;59:156-64.
    • (2001) Clin Genet , vol.59 , pp. 156-164
    • Hanel, M.1    Wevrick, R.2
  • 2
    • 2242447082 scopus 로고    scopus 로고
    • NRAGE, a p75 neurotrophin receptor-interacting protein, induces caspase activation and cell death through a JNK-dependent mitochondria! pathway
    • Salehi AH, Xanthoudakis S, Barker PA. NRAGE, a p75 neurotrophin receptor-interacting protein, induces caspase activation and cell death through a JNK-dependent mitochondria! pathway. J Biol Chem. 2002;277:48043-50.
    • (2002) J Biol Chem , vol.277 , pp. 48043-48050
    • Salehi, A.H.1    Xanthoudakis, S.2    Barker, P.A.3
  • 3
    • 14644391578 scopus 로고    scopus 로고
    • Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
    • Lee S, Walker CL, Karten B, et al. Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum Mol Genet. 2005;14:627-37.
    • (2005) Hum Mol Genet , vol.14 , pp. 627-637
    • Lee, S.1    Walker, C.L.2    Karten, B.3
  • 4
    • 0042786856 scopus 로고    scopus 로고
    • Prader-Willi Syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain
    • Lee S, Walker CL, Wevrick R. Prader-Willi Syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Exp Patterns. 2003;3: 599-609.
    • (2003) Gene Exp Patterns , vol.3 , pp. 599-609
    • Lee, S.1    Walker, C.L.2    Wevrick, R.3
  • 5
    • 0000067107 scopus 로고    scopus 로고
    • Genetics and pathophysiology of human obesity
    • Cummings DE, Schwartz MW. Genetics and pathophysiology of human obesity. Annu Rev Med. 2003;54:453-71.
    • (2003) Annu Rev Med , vol.54 , pp. 453-471
    • Cummings, D.E.1    Schwartz, M.W.2
  • 6
    • 0036325531 scopus 로고    scopus 로고
    • Genetic approaches to studying energy balance: Perception and integration
    • Barsh GS, Schwartz MW. Genetic approaches to studying energy balance: perception and integration. Nat Rev Genet. 2002;3:589-600.
    • (2002) Nat Rev Genet , vol.3 , pp. 589-600
    • Barsh, G.S.1    Schwartz, M.W.2
  • 8
    • 0034956226 scopus 로고    scopus 로고
    • Systematic screening for mutations in the human necdin gene (NDN): Identification of two naturally occurring polymorphisms and association analysis in body weight regulation
    • Oeffner F, Korn T, Roth H, et al. Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. Int J Obes Relat Metab Disord. 2001;25:767-9.
    • (2001) Int J Obes Relat Metab Disord , vol.25 , pp. 767-769
    • Oeffner, F.1    Korn, T.2    Roth, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.