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, M G; Malzac, P; Roëckel, N; Taviaux, S; Lefranc, J L; Cau, P; Berta, P; Lalande, M; Muscatelli, F

Jay, P; Rougeulle, C; Massacrier, A; Moncla, A; Mattei, M G; Malzac, P; Roëckel, N; Taviaux, S; Lefranc, J L; Cau, P; Berta, P; Lalande, M; Muscatelli, F.

Affiliation

Jay P; Centre de Recherches de Biochimie Macromoléculaire, CNRS ERS 115, INSERM U 249, Montpellier, France.

Nat Genet ; 17(3): 357-61, 1997 Nov.

Article in En | MEDLINE | ID: mdl-9354807

Subject(s)

Gene Expression Regulation, Developmental; Genomic Imprinting; Nerve Tissue Proteins/genetics; Nuclear Proteins/genetics; Prader-Willi Syndrome/genetics; Angelman Syndrome/genetics; Animals; Blotting, Northern; Chromosome Mapping; Chromosomes, Human, Pair 15; DNA Methylation; Deoxyribonucleases, Type II Site-Specific/genetics; Female; Humans; In Situ Hybridization/methods; In Situ Hybridization, Fluorescence; Male; Mice; Molecular Sequence Data; Nerve Tissue Proteins/metabolism; Nervous System Physiological Phenomena; Nuclear Proteins/metabolism; Tissue Distribution

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Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Nuclear Proteins / Genomic Imprinting / Gene Expression Regulation, Developmental / Nerve Tissue Proteins Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Year: 1997 Document type: Article

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