Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12)
about
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicleAnalyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1Differential activation of lung-specific genes by two forkhead proteins, FREAC-1 and FREAC-2Characterization of the human forkhead gene FREAC-4. Evidence for regulation by Wilms' tumor suppressor gene (WT-1) and p53A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani familyDedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilitiesAutosomal dominant iridogoniodysgenesis anomaly maps to 6p25Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regionsThe forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiationThe evolutionary origin of human subtelomeric homologies--or where the ends beginThe OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal deathA Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings.Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.Glaucoma genetics.BRCC2, a novel BH3-like domain-containing protein, induces apoptosis in a caspase-dependent manner.Mechanisms of FOXC2- and FOXD1-mediated regulation of the RI alpha subunit of cAMP-dependent protein kinase include release of transcriptional repression and activation by protein kinase B alpha and cAMP.The winged helix transcription factor Fkh10 is required for normal development of the inner ear.Exome sequencing reveals novel homozygous FOXE3 mutation in microphthalmos with staphylomatous malformation.Forkhead transcription factor FoxF2 is expressed in mesodermal tissues involved in epithelio-mesenchymal interactions.
P2860
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P2860
Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12)
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@ast
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en-gb
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@nl
type
label
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@ast
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en-gb
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@nl
prefLabel
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@ast
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en-gb
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@nl
P2093
P356
P1433
P1476
Chromosomal localization of si ...... , -6 (FKHL10), and -8 (FKHL12)
@en
P2093
P356
10.1006/GENO.1995.1266
P407
P577
1995-12-10T00:00:00Z