Fox's in development and disease (Q34205134)

31 July 2017

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title

Fox's in development and disease (English)

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31 July 2017

Peter Carlsson

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Jane C Sowden

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Ordan J Lehmann

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31 July 2017

Tim Jordan

series ordinal

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31 July 2017

Shomi S Bhattacharya

series ordinal

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31 July 2017

publication date

1 June 2003

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31 July 2017

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

339-344

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The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The fork head domain: a novel DNA binding motif of eukaryotic transcription factors?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein ILF

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Forkhead transcription factors contribute to execution of the mitotic programme in mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

DNA repair pathway stimulated by the forkhead transcription factor FOXO3a through the Gadd45 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Initial sequencing and analysis of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The Sequence of the Human Genome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

HNF-3 beta is essential for node and notochord formation in mouse development

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The winged-helix transcription factor HNF-3 beta is required for notochord development in the mouse embryo

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Fast1 is required for the development of dorsal axial structures in zebrafish

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The winged helix transcription factor Hfh2 is expressed in neural crest and spinal cord during mouse development

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Congenital hypothyroidism, spiky hair, and cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Two genetically separable steps in the differentiation of thymic epithelium.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The product of the mouse nude locus, Whn, regulates the balance between epithelial cell growth and differentiation.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Exposing the human nude phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The winged helix transcription factor Fkh10 is required for normal development of the inner ear.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Molecular evolution of FOXP2, a gene involved in speech and language

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Foxn4--a new member of the forkhead gene family is expressed in the retina.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Visual projection map specified by topographic expression of transcription factors in the retina

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Sequence and expression of zebrafish foxc1a and foxc1b, encoding conserved forkhead/winged helix transcription factors.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Forkhead transcription factors: key players in development and metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

Structural changes in the region directly adjacent to the DNA-binding helix highlight a possible mechanism to explain the observed changes in the sequence-specific binding of winged helix proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2

7 January 2021

10.1016/S0168-9525(03)00111-2

Identifiers

DOI

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31 July 2017

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