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Literature DB >> 19286161

Mouse model for bilateral adrenal hyperplasia.

I Sahut-Barnola¹, C De Joussineau, P Val, S Lambert-Langlais, A-M Lefrançois-Martinez, J-C Pointud, G Marceau, V Sapin, B Ragazzon, J Bertherat, L S Kirschner, C A Stratakis, A Martinez.

Abstract

Entities: Chemical Disease Gene Species

Mesh：

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Year: 2009 PMID： 19286161 PMCID： PMC3130202 DOI： 10.1016/j.ando.2009.02.004

Source DB: PubMed Journal: Ann Endocrinol (Paris) ISSN： 0003-4266 Impact factor: 2.478

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6 in total

1. Increased basal cAMP-dependent protein kinase activity inhibits the formation of mesoderm-derived structures in the developing mouse embryo.

Authors: Paul S Amieux; Douglas G Howe; Heidi Knickerbocker; David C Lee; Thomas Su; George S Laszlo; Rejean L Idzerda; G Stanley McKnight
Journal: J Biol Chem Date: 2002-05-09 Impact factor: 5.157

2. Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

Authors: M Casey; C J Vaughan; J He; C J Hatcher; J M Winter; S Weremowicz; K Montgomery; R Kucherlapati; C C Morton; C T Basson
Journal: J Clin Invest Date: 2000-09 Impact factor: 14.808

3. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

Authors: L S Kirschner; J A Carney; S D Pack; S E Taymans; C Giatzakis; Y S Cho; Y S Cho-Chung; C A Stratakis
Journal: Nat Genet Date: 2000-09 Impact factor: 38.330

Mouse model for bilateral adrenal hyperplasia.

1. Increased basal cAMP-dependent protein kinase activity inhibits the formation of mesoderm-derived structures in the developing mouse embryo.

2. Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

3. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

4. The complex of myxomas, spotty pigmentation, and endocrine overactivity.

5. A transgenic mouse line with specific Cre recombinase expression in the adrenal cortex.

6. Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.