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Works by Messika-Zeitoun, Liza

Results: 3

1

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

Published in:

Human Molecular Genetics, 2009, v. 18, n. 16, p. 3002, doi. 10.1093/hmg/ddp238

By:

Belville, Corinne;
Maréchal, Jean-Didier;
Pennetier, Sophie;
Carmillo, Paul;
Masgrau, Laura;
Messika-Zeitoun, Liza;
Galey, Julie;
Machado, Gabrielle;
Treton, Dominique;
Gonzalès, Jacques;
Picard, Jean-Yves;
Josso, Nathalie;
Cate, Richard L.;
di Clemente, Nathalie

Publication type:

Article

2

A 27 Base-Pair Deletion of the Anti-Müllerian Type Ii Receptor Gene is the Most Common Cause of the Persistent MüLlerian Duct Syndrome.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 9, p. 1269, doi. 10.1093/hmg/5.9.1269

By:

Imbeaud, Sandrine;
Belville, Corinne;
Messika-Zeitoun, Liza;
Rey, Rodolfo;
di Clemente, Nathalie;
Josso, Nathalie;
Picard, Jean-Yves

Publication type:

Article

3

Autosomal Recessive Segregation of a Truncating Mutation of Anti-Müllerian Type II Receptor in a Family Affected by the Persistent Müllerian Duct Syndrome Contrasts with Its Dominant Negative Activity in Vitro.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4390, doi. 10.1210/jcem.86.9.7839

By:

MESSIKA-ZEITOUN, LIZA;
GOUÉDARD, LUCILE;
BELVILLE, CORINNE;
DUTERTRE, MARTIN;
LINS, LAURENCE;
IMBEAUD, SANDRINE;
HUGHES, IEUAN A.;
PICARD, JEAN-YVES;
JOSSO, NATHALIE;
DI CLEMENTE, NATHALIE

Publication type:

Article