Chromosomal localization of the human and mouse histidine decarboxylase genes by in situ hybridization. Exclusion of the HDC gene from the Prader-Willi syndrome region-Reference-Cited by-同舟云学术

Chromosomal localization of the human and mouse histidine decarboxylase genes by in situ hybridization. Exclusion of the HDC gene from the Prader-Willi syndrome region

Published:1996-03 Issue:3 Volume:97 Page:359-361
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Malzac Perrine,Mattei Marie-Geneviève,Thibault Jean,Bruneau Gilles

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF02185772.pdf

Reference16 articles.

1. Bruneau G, Nguyen VC, Gros F, Bernheim A, Thibault J (1992) Preparation of a rat brain histidine decarboxylase (HDC) cDNA probe by PCR and assignment of the human HDC gene to chromosome 15. Hum Genet 90:235–238

2. Donlon TA, Malcolm S (1991) Report of the committee on the genetic constitution of chromosome 15. Human gene mapping. Cytogenet Cell Genet 58:624–642

3. Ericson H, Watanabe T, Köhler C (1987) Morphological analysis of the tuberomammillary nucleus in the rat brain: delineation of subgroups with antibody against L-histidine decarboxylase as a marker. J Comp Neurol 263:1–24

4. Joseph DR, Sullivan PM, Wang YM, Kozak C, Fenstermacher DA, Behrendsen ME, Zahnow CA (1990) Characterization and expression of the complementary DNA encoding rat histidine decarboxylase. Proc Natl Acad Sci USA 87:733–737

5. Leff SE, Brannan CI, Reed ML, Özçelik T, Francke U, Copeland NG, Jenkins NA (1992) Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi Syndrome region. Nature Genet 2: 259–264

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1. Mammalian histidine decarboxylase: from structure to function;BioEssays;2004-12-20