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Volumn 203, Issue 2, 1996, Pages 109-110

Association between a null mutation in the human ciliary neurotrophic factor (CNTF) gene and increased incidence of psychiatric diseases?

Author keywords

Ciliary neurotrophic factor; Genetics; Mutation; Neurodevelopment; Neurotrophic factor; Psychiatry; Psychoses

Indexed keywords

CILIARY NEUROTROPHIC FACTOR;

EID: 0030026455     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/0304-3940(95)12274-5     Document Type: Article
Times cited : (13)

References (10)
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    • Hattori, M.1    Nanko, S.2
  • 2
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    • Prenatal developmental disturbances in the limbic allocortex in schizophrenics
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  • 3
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    • The genetics of schizophrenia is the genetics of neurodevelopment
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    • Jones, P.1    Murray, R.M.2
  • 4
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    • The neurotrophic factor concept: A reexamination
    • Korsching, S., The neurotrophic factor concept: a reexamination, J. Neurosci., 13 (1993) 2739-2748.
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  • 5
    • 0025882856 scopus 로고
    • Sequence and structural organization of the human gene encoding ciliary neurotrophic factor
    • Lam, A., Fuller, F., Miller, J., Kloss, J., Manthorpe, M., Varon, S. and Cordell, B., Sequence and structural organization of the human gene encoding ciliary neurotrophic factor, Gene, 102 (1991) 271-276.
    • (1991) Gene , vol.102 , pp. 271-276
    • Lam, A.1    Fuller, F.2    Miller, J.3    Kloss, J.4    Manthorpe, M.5    Varon, S.6    Cordell, B.7
  • 6
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    • Human ciliary neurotrophic factor: Localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat
    • Lev, A.A., Rosen, D.R., Kos, C., Clifford, E., Landes, G., Hauser, S.L. and Brown, Jr., R.H., Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat, Genomics, 16 (1993) 539-541.
    • (1993) Genomics , vol.16 , pp. 539-541
    • Lev, A.A.1    Rosen, D.R.2    Kos, C.3    Clifford, E.4    Landes, G.5    Hauser, S.L.6    Brown R.H., Jr.7
  • 8
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    • A null mutation in the human CNTF gene is not causally related to neurological diseases
    • Takahashi, R., Yokoji, H., Misawa, H., Hayashi, M., Hu, J. and Deguchi, T., A null mutation in the human CNTF gene is not causally related to neurological diseases, Nature Genet., 7 (1994) 79-84.
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  • 9
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    • Cortical maldevelopment, anti-psychotic drugs, and schizophrenia: A search for common ground
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    • Weinberger, D.R.1    Lipska, B.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.