Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport-Reference-Cited by-同舟云学术

Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport

Published:2009-05-20 Issue:16 Volume:18 Page:3002-3013
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Belville C.,Marechal J.-D.,Pennetier S.,Carmillo P.,Masgrau L.,Messika-Zeitoun L.,Galey J.,Machado G.,Treton D.,Gonzales J.,Picard J.-Y.,Josso N.,Cate R. L.,di Clemente N.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/16/3002/1463541/ddp238.pdf

Reference45 articles.

1. A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the mullerian duct

2. Cloning, expression, and alternative splicing of the receptor for anti- Mullerian hormone

3. Engagement of Bone Morphogenetic Protein Type IB Receptor and Smad1 Signaling by Anti-Müllerian Hormone and Its Type II Receptor

4. Mullerian Inhibiting Substance Signaling Uses a Bone Morphogenetic Protein (BMP)-Like Pathway Mediated by ALK2 and Induces Smad6 Expression

5. The Serine/Threonine Transmembrane Receptor ALK2 Mediates Mullerian Inhibiting Substance Signaling

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