Functional characterization of two naturally occurring mutations V 221 G and T 449 N in the follicle stimulating hormone receptor-Reference-Cited by-同舟云学术

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Functional characterization of two naturally occurring mutations V 221 G and T 449 N in the follicle stimulating hormone receptor

Published:2017-01 Issue: Volume:440 Page:69-79
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Banerjee Antara A.,Achrekar Swati K.,Joseph Shaini,Pathak Bhakti R.,Mahale Smita D.

Funder

Indian Council of Medical Research

Government of India

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference48 articles.

1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Aittomäki;Cell,1995

2. A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergondotrophic hypogonadism: clinical and molecular characteristics;Allen;Hum. Reprod.,2003

3. FSH receptor-specific residues L501 and I505 in extracellular loop 2 are essential for its function;Banerjee;J. Mol. Endocrinol.,2015

4. A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor;Beau;J. Clin. Invest.,1998

5. Spontaneous ovarian hyperstimulation in a pregnant woman with hypothyroidism;Borna;Fertil. Steril.,2007

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