Related references
Note: Only part of the references are listed.Minireview: Roles of the Forkhead Transcription Factor FOXL2 in Granulosa Cell Biology and Pathology
Margareta D. Pisarska et al.
ENDOCRINOLOGY (2011)
Differential apoptotic activities of wild-type FOXL2 and the adult-type granulosa cell tumor-associated mutant FOXL2 (C134W)
J-H Kim et al.
ONCOGENE (2011)
Evolutionary genomics of the Fox genes: Origin of gene families and the ancestry of gene clusters
Sebastian M. Shimeld et al.
GENOMICS (2010)
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)
Berenice A. Benayoun et al.
PLOS ONE (2010)
Microarray analysis of Foxl2 mediated gene regulation in the mouse ovary derived KK1 granulosa cell line: Over-expression of Foxl2 leads to activation of the gonadotropin releasing hormone receptor gene promoter
Jean M. Escudero et al.
JOURNAL OF OVARIAN RESEARCH (2010)
Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations
Berenice A. Benayoun et al.
HUMAN MOLECULAR GENETICS (2009)
Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems
Aurelie Dipietromaria et al.
HUMAN MOLECULAR GENETICS (2009)
Mutation of FOXL2 in Granulosa-Cell Tumors of the Ovary
Sohrab P. Shah et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
The Specificity of the FOXL2 c.402C>G Somatic Mutation: A Survey of Solid Tumors
Kasmintan A. Schrader et al.
PLOS ONE (2009)
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
Diane Beysen et al.
HUMAN MOLECULAR GENETICS (2008)
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
Berenice A. Benayoun et al.
HUMAN MOLECULAR GENETICS (2008)
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)
Functional genetic analysis of mutations implicated in a human speech and language disorder
Sonja C. Vernes et al.
HUMAN MOLECULAR GENETICS (2006)
The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis
FB Berry 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)
Serum antimullerian hormone levels best reflect the reproductive decline with age in normal women with proven fertility: a longitudinal study
IAJ van Rooij et al.
FERTILITY AND STERILITY (2005)
Classification of amino acids induced by their associated matrices
JG Esteve et al.
BIOPHYSICAL CHEMISTRY (2005)
The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
D Schmidt et al.
DEVELOPMENT (2004)
Essential structural and functional determinants within the forkhead domain of FOXC1
RA Saleem et al.
NUCLEIC ACIDS RESEARCH (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)
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
RA Saleem et al.
HUMAN MOLECULAR GENETICS (2003)
The gonadotropin releasing hormone (GnRH) receptor activating sequence (GRAS) is a composite regulatory element that interacts with multiple classes of transcription factors including Smads, AP-1 and a forkhead DNA binding protein
BS Ellsworth et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (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)
Letter to the Editor: Assignment of a 15 kDa protein complex formed between the p160 coactivator ACTR and CREB binding protein
SJ Demarest et al.
JOURNAL OF BIOMOLECULAR NMR (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)
Share Paper
