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Fox's in development and disease
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Fox's in development and disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
author
Peter Carlsson
object named as
Peter Carlsson
series ordinal
3
0 references
Jane Sowden
object named as
Jane C Sowden
series ordinal
2
0 references
author name string
Ordan J Lehmann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
Tim Jordan
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
Shomi S Bhattacharya
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
publication date
1 June 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
volume
19
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
page(s)
339-344
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
cites work
The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo
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The fork head domain: a novel DNA binding motif of eukaryotic transcription factors?
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Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans
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reference URL
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Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein ILF
1 reference
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AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1
1 reference
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Forkhead transcription factors contribute to execution of the mitotic programme in mammals
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DNA repair pathway stimulated by the forkhead transcription factor FOXO3a through the Gadd45 protein
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reference URL
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7 January 2021
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Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5
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Initial sequencing and analysis of the human genome
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7 January 2021
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The Sequence of the Human Genome
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7 January 2021
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Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4.
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2.
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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HNF-3 beta is essential for node and notochord formation in mouse development
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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The winged-helix transcription factor HNF-3 beta is required for notochord development in the mouse embryo
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Fast1 is required for the development of dorsal axial structures in zebrafish
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FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice
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7 January 2021
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The winged helix transcription factor Hfh2 is expressed in neural crest and spinal cord during mouse development.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Congenital hypothyroidism, spiky hair, and cleft palate
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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
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Two genetically separable steps in the differentiation of thymic epithelium.
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The product of the mouse nude locus, Whn, regulates the balance between epithelial cell growth and differentiation.
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Exposing the human nude phenotype.
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The winged helix transcription factor Fkh10 is required for normal development of the inner ear.
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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A forkhead-domain gene is mutated in a severe speech and language disorder
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Molecular evolution of FOXP2, a gene involved in speech and language
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Foxn4--a new member of the forkhead gene family is expressed in the retina.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Visual projection map specified by topographic expression of transcription factors in the retina.
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Sequence and expression of zebrafish foxc1a and foxc1b, encoding conserved forkhead/winged helix transcription factors.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
based on heuristic
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A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
based on heuristic
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Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
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7 January 2021
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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
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7 January 2021
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Forkhead transcription factors: key players in development and metabolism
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
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7 January 2021
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Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiation
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
based on heuristic
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Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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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
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900111-2
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7 January 2021
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Identifiers
DOI
10.1016/S0168-9525(03)00111-2
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
PubMed ID
12801727
1 reference
stated in
Europe PubMed Central
PubMed ID
12801727
retrieved
31 July 2017
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