Related references
Note: Only part of the references are listed.The mutations and potential targets of the forkhead transcription factor FOXL2
L. Moumne et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2008)
Structure/function relationships underlying regulation of FOXO transcription factors
T. Obsil et al.
ONCOGENE (2008)
The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways
Berenice A. Benayoun et al.
PROTEOMICS (2008)
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development
Lara Moumne et al.
HUMAN MOLECULAR GENETICS (2008)
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells
Chris Ottolenghi et al.
HUMAN MOLECULAR GENETICS (2007)
Crystal structure of the human FOXO3a-DBD/DNA complex suggests the effects of post-translational modification
Kuang-Lei Tsai et al.
NUCLEIC ACIDS RESEARCH (2007)
The emerging roles of forkhead box (Fox) proteins in cancer
Stephen S. Myatt et al.
NATURE REVIEWS CANCER (2007)
Foxe view of lens development and disease
Olga Medina-Martinez et al.
DEVELOPMENT (2007)
A novel polyalanine expansion in FOXL2:: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction
Jeyabalan Nallathambi et al.
HUMAN GENETICS (2007)
Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics
Frank Batista et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Crystal structure of the human FOXK1a-DNA complex and its implications on the diverse binding specificity of winged helix/forkhead proteins
Kuang-Lei Tsai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Structure of the forkhead domain of FOXP2 bound to DNA
JC Stroud et al.
STRUCTURE (2006)
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation
L Moumné et al.
HUMAN MOLECULAR GENETICS (2005)
FOXO transcription factors at the interface between longevity and tumor suppression
EL Greer et al.
ONCOGENE (2005)
Foxl2 is required for commitment to ovary differentiation
C Ottolenghi et al.
HUMAN MOLECULAR GENETICS (2005)
Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter
M Pannetier et al.
GENOMICS (2005)
The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
D Schmidt et al.
DEVELOPMENT (2004)
One tissue, two fates: Molecular genetic events that underlie testis versus ovary development
J Brennan et al.
NATURE REVIEWS GENETICS (2004)
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation
S Caburet et al.
JOURNAL OF MEDICAL GENETICS (2004)
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development
M Uda et al.
HUMAN MOLECULAR GENETICS (2004)
Structure and function of the feed-forward loop network motif
S Mangan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional Repressors
B Wang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Fox's in development and disease
OJ Lehmann et al.
TRENDS IN GENETICS (2003)
A sigmoidal transcriptional response: cooperativity, synergy and dosage effects
RA Veitia
BIOLOGICAL REVIEWS (2003)
FOXL2 and BPES:: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
E De Baere et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Structure, evolution and expression of the FOXL2 transcription unit
J Cocquet et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
Evolution and expression of FOXL2
J Cocquet et al.
JOURNAL OF MEDICAL GENETICS (2002)
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
E De Baere et al.
HUMAN MOLECULAR GENETICS (2001)
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
L Crisponi et al.
NATURE GENETICS (2001)