A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex-Reference-Cited by-同舟云学术

A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex

Published:2008-04-23 Issue:10 Volume:16 Page:1245-1253
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Horvath Anelia,Giatzakis Christoforos,Tsang Kitman,Greene Elizabeth,Osorio Paulo,Boikos Sosipatros,Libè Rossella,Patronas Yianna,Robinson-White Audrey,Remmers Elaine,Bertherat Jerôme,Nesterova Maria,Stratakis Constantine A

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg200885.pdf

Reference25 articles.

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2. Gunther DF, Bourdeau I, Matyakhina L et al: Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity? J Clin Endocrinol Metab 2004; 89: 3173–3182.

3. Stratakis CA : Adrenocortical tumors, primary pigmented adrenocortical disease (PPNAD)/Carney complex, and other bilateral hyperplasias: the NIH studies. Horm Metab Res 2007; 39: 467–473.

4. Weinstein LS, Yu S, Warner DR, Liu J : Endocrine manifestations o stimulatory G protein-subunit mutations and the role of genomic imprinting. Endocr Rev 2001; 22: 675–705.

5. Kirschner LS, Carney JA, Pack SD et al: Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet 2000; 26: 89–92.

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