The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

Author： Nakada Y.   Taniura H.   Uetsuki T.   Inazawa J.   Yoshikawa K.  

Publisher： Elsevier

ISSN： 0378-1119

Source： Gene, Vol.213, Iss.1, 1998-06, pp. : 65-72

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression

By Andrieu D.   Watrin F.   Niinobe M.   Yoshikawa K.   Muscatelli F.   Fernandez P.-A.  

Gene Expression Patterns, Vol. 3, Iss. 6, 2003-12 ,pp. : 761-765

Elsevier

Access to resources Recommend Favorite

Identification of a Testis-Specific Gene (C15orf2) in the Prader-Willi Syndrome Region on Chromosome 15

By Farber C.   Grosz S.   Neesen J.   Buiting K.   Horsthemke B.  

Genomics, Vol. 65, Iss. 2, 2000-04 ,pp. : 174-183

Elsevier

Access to resources Recommend Favorite

Prader-Willi Syndrome: Obesity due to Genomic Imprinting

By  

Current Genomics, Vol. 12, Iss. 3, 2011-05 ,pp. : 204-215

Bentham Science Publishers

Access to resources Recommend Favorite

p190-A, a human tumor suppressor gene, maps to the chromosomal region 19q13.3 that is reportedly deleted in some gliomas

By Tikoo A.   Czekay S.   Viars C.   White S.   Heath J.K.   Arden K.   Maruta H.  

Gene, Vol. 257, Iss. 1, 2000-10 ,pp. : 23-31

Elsevier

Access to resources Recommend Favorite

Characterization and chromosomal mapping of a human necdin pseudogene

By Nakada Y.   Taniura H.   Uetsuki T.   Yoshikawa K.  

Gene, Vol. 245, Iss. 1, 2000-03 ,pp. : 185-191

Elsevier

Access to resources Recommend Favorite