The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles-Reference-Cited by-同舟云学术

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The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles

Published:2008-07-16 Issue:20 Volume:17 Page:3118-3127
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Benayoun Bérénice A.,Caburet Sandrine,Dipietromaria Aurélie,Bailly-Bechet Marc,Batista Frank,Fellous Marc,Vaiman Daniel,Veitia Reiner A.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/17/20/3118/13940660/ddn209.pdf

Reference45 articles.

1. Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5;Clark;Nature,1993

2. Unified nomenclature for the winged helix/forkhead transcription factors;Kaestner;Genes Dev.,2000

3. Fox's in development and disease;Lehmann;Trends Genet.,2003

4. FOXO transcription factors at the interface between longevity and tumor suppression;Greer;Oncogene,2005

5. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome;Crisponi;Nat. Genet.,2001

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1. Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family;BMC Ophthalmology;2023-11-07

2. Reproductive System;In Utero Pediatrics;2023

3. Ovarian Reserve and ART Outcomes in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Patients With FOXL2 Mutations;Frontiers in Endocrinology;2022-04-28

4. Functional Studies of Novel FOXL2 Variants in Chinese Families With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome;Frontiers in Genetics;2021-03-16

5. Clinical Characteristics and Mutation Analyses of Ovarian Sertoli-Leydig Cell Tumors;The Oncologist;2020-08-11

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