(Q34519090)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

review article

1 reference

title

Foxl2 function in ovarian development (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author

Nina Henriette Uhlenhaut

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Mathias Treier

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

publication date

2 May 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

20 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

225-234

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

Multistep signaling requirements for pituitary organogenesis in vivo

20 January 2020

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7 January 2021

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7 January 2021

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Evolution and expression of FOXL2

7 January 2021

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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

7 January 2021

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Lessons from studies of complex genetic disorders: identification of FOXL2--a novel transcription factor on the wing to fertility

7 January 2021

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Alanine tracts: the expanding story of human illness and trinucleotide repeats

7 January 2021

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Associations between human disease genes and overlapping gene groups and multiple amino acid runs

7 January 2021

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A fork in the road to fertility.

7 January 2021

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Premature ovarian failure

7 January 2021

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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation

7 January 2021

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Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patients

7 January 2021

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FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

7 January 2021

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Diseases of unstable repeat expansion: mechanisms and common principles

7 January 2021

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Identification of novel mutations in FOXL2 associated with premature ovarian failure

7 January 2021

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A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report

7 January 2021

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Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure

7 January 2021

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FOXL2 mutation screening in a large panel of POF patients and XX males

7 January 2021

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The human FOXL2 mutation database.

7 January 2021

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Long-range control of gene expression: emerging mechanisms and disruption in disease

7 January 2021

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Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.

7 January 2021

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Molecular Cytogenetic Evaluation in a Patient with a Translocation (3;21) Associated with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (BPES)

7 January 2021

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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

7 January 2021

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FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

7 January 2021

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Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6.

7 January 2021

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Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats.

7 January 2021

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A 11.7-kb deletion triggers intersexuality and polledness in goats

7 January 2021

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Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman.

7 January 2021

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Expression studies of the PIS-regulated genes suggest different mechanisms of sex determination within mammals.

7 January 2021

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Pisrt1, a gene implicated in XX sex reversal, is expressed in gonads of both sexes during mouse development

7 January 2021

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Mammalian sex reversal and intersexuality: deciphering the sex-determination cascade

7 January 2021

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The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance

7 January 2021

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Role of growth factors in ovary organogenesis

7 January 2021

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Genetic control of early folliculogenesis in mice

7 January 2021

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Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

7 January 2021

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Molecular characterization of the follicle defects in the growth differentiation factor 9-deficient ovary.

7 January 2021

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Activin/inhibin beta B subunit gene disruption leads to defects in eyelid development and female reproduction.

7 January 2021

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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

7 January 2021

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StAR protein and the regulation of steroid hormone biosynthesis

7 January 2021

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Forkhead l2 is expressed in the ovary and represses the promoter activity of the steroidogenic acute regulatory gene

7 January 2021

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Triple layer control: phosphorylation, acetylation and ubiquitination of FOXO proteins.

7 January 2021

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Raf/MEK/MAPK signaling stimulates the nuclear translocation and transactivating activity of FOXM1c

7 January 2021

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Oocyte-dependent activation of mitogen-activated protein kinase (ERK1/2) in cumulus cells is required for the maturation of the mouse oocyte-cumulus cell complex

7 January 2021

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Foxl2 is required for commitment to ovary differentiation

7 January 2021

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Sox9 induces testis development in XX transgenic mice

7 January 2021

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A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation

7 January 2021

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Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation

7 January 2021

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One tissue, two fates: molecular genetic events that underlie testis versus ovary development

7 January 2021

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Structure, evolution and expression of the FOXL2 transcription unit

7 January 2021

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Characterization of Pisrt1/Foxl2 in Ellobius lutescens and exclusion as sex-determining genes

7 January 2021

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An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation

7 January 2021

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Molecular cloning and gene expression of Foxl2 in the Nile tilapia, Oreochromis niloticus

7 January 2021

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Sex determination: primitive Y chromosomes in fish

7 January 2021

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Sex chromosome evolution in non-mammalian vertebrates

7 January 2021

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Etiology of ovarian failure in blepharophimosis ptosis epicanthus inversus syndrome: FOXL2 is a conserved, early-acting gene in vertebrate ovarian development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.03.005

Different patterns of anti-Müllerian hormone expression, as related to DMRT1, SF-1, WT1, GATA-4, Wnt-4, and Lhx9 expression, in the chick differentiating gonads.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.03.005

Isolation of chicken homolog of the FOXL2 gene and comparison of its expression patterns with those of aromatase during ovarian development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.03.005

Homozygous inactivation of Sox9 causes complete XY sex reversal in mice

7 January 2021

1 reference

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A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development

7 January 2021

1 reference

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10.1016/J.YMGME.2006.03.005

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16647286%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference