Functional Evidence Implicating FOXL2 in Non-Syndromic Premature Ovarian Failure and in the Regulation of the Transcription Factor OSR2

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.2008.065086
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Recent Advances in the Study of Genes Involved in Non-Syndromic Premature Ovarian Failure

Molecular and Cellular Endocrinology
BiochemistryEndocrinologyMolecular Biology
2008English

Autoimmune Premature Ovarian Failure

Przeglad Menopauzalny
GynecologyEndocrinologyMetabolismObstetricsDiabetes
2016English

Genes Involved in Human Premature Ovarian Failure

Journal of Molecular Endocrinology
EndocrinologyMolecular Biology
2010English

Emotional Impacts of Premature Ovarian Failure in Kuwait

Health
2016English

Pregnancy in Patients With Premature Ovarian Failure

Expert Review of Obstetrics & Gynecology
2007English

A Recurrent Polyalanine Expansion in the Transcription Factor FOXL2 Induces Extensive Nuclear and Cytoplasmic Protein Aggregation

Journal of Medical Genetics
Genetics
2004English

The Screening of HELQ Gene in Chinese Patients With Premature Ovarian Failure

Reproductive BioMedicine Online
GynecologyReproductive MedicineDevelopmental BiologyObstetrics
2015English

The Therapeutic Potential of Bone Marrow Mesenchymal Stem Cells in Premature Ovarian Failure

Stem Cell Research and Therapy
GeneticsCell BiologyMolecular BiologyBiochemistryMedicineMolecular Medicine
2018English

Subtle Functional Defects in the Arf-Specific Guanine Nucleotide Exchange Factor IQSEC2 Cause Non-Syndromic X-Linked Intellectual Disability

Small GTPases
BiochemistryCell Biology
2010English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy