The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.

作者: Philippe Jay , Claire Rougeulle , Annick Massacrier , Anne Moncla , Marie-Geneviève Mattel

DOI: 10.1038/NG1197-357

关键词:

摘要: … A hybridization signal of the correct size was detected on YACs 264A1 and 495D1 (CEPH … Tissue distribution of NDN mRNA was first analysed by northern hybridization with the cDNA …

参考文章(29)
Etsuko MARUYAMA, Biochemical characterization of mouse brain necdin. Biochemical Journal. ,vol. 314, pp. 895- 901 ,(1996) , 10.1042/BJ3140895
A Schinzel, W P Robinson, F Binkert, Y G Xie, J Balakrishman, A Prader, M Mächler, A Bottani, Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. American Journal of Human Genetics. ,vol. 49, pp. 1219- 1234 ,(1991)
Ann P. Walker, Jamel Chelly, Donald R. Love, Yumiko Ishikawa Brush, Dominique Récan, Jean-Louis Chaussain, Christine A. Oley, J.Michael Connor, John Yates, David A. Price, Maurice Super, Armand Bottani, Beat Steinman, Jean-Claude Kaplan, Kay E. Davies, Anthony P. Monaco, A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes Human Molecular Genetics. ,vol. 1, pp. 579- 585 ,(1992) , 10.1093/HMG/1.8.579
Y. Hayashi, K. Matsuyama, K. Takagi, H. Sugiura, K. Yoshikawa, Arrest of cell growth by necdin, a nuclear protein expressed in postmitotic neurons. Biochemical and Biophysical Research Communications. ,vol. 213, pp. 317- 324 ,(1995) , 10.1006/BBRC.1995.2132
Y Ning, A Roschke, S L Christian, J Lesser, J S Sutcliffe, D H Ledbetter, Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region. Genome Research. ,vol. 6, pp. 742- 746 ,(1996) , 10.1101/GR.6.8.742
Philippe Jay, Sylvie Diriong, Sylvie Taviaux, Nathalie Roeckel, Marie-Geneviève Mattéi, Muriel Audit, Jean-Louis Bergé-Lefranc, Michel Fontès, Philippe Berta, Isolation and Regional Mapping of cDNAs Expressed during Early Human Development Genomics. ,vol. 39, pp. 104- 108 ,(1997) , 10.1006/GENO.1996.4470
J Clayton-Smith, T Webb, S A Robb, I Dijkstra, P Willems, S Lam, X-J Cheng, M E Pembrey, S Malcolm, Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome. American Journal of Medical Genetics. ,vol. 44, pp. 256- 260 ,(1992) , 10.1002/AJMG.1320440236
Claire Rougeulle, Heather Glatt, Marc Lalande, The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nature Genetics. ,vol. 17, pp. 14- 15 ,(1997) , 10.1038/NG0997-14
Taichi Uetsuki, Keiich Takagi, Hiroko Sugiura, Kazuaki Yoshikawa, Structure and expression of the mouse necdin gene. Identification of a postmitotic neuron-restrictive core promoter. Journal of Biological Chemistry. ,vol. 271, pp. 918- 924 ,(1996) , 10.1074/JBC.271.2.918