Human brain factor 1, a new member of the fork head gene family
about
Primary structure of hepatocyte nuclear factor/forkhead homologue 4 and characterization of gene expression in the developing respiratory and reproductive epitheliumA FOXG1 mutation in a boy with congenital variant of Rett syndrome.The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesPLU-1 nuclear protein, which is upregulated in breast cancer, shows restricted expression in normal human adult tissues: a new cancer/testis antigen?Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profilesGenetic and epigenetic factors: Role in male infertilityTransducin-like enhancer of Split-1 (TLE1) combines with Forkhead box protein G1 (FoxG1) to promote neuronal survival.FOXG1-Related Disorders: From Clinical Description to Molecular Genetics.FoxG1 promotes the survival of postmitotic neurons.Altered expression of neuropeptides in FoxG1-null heterozygous mutant miceGene expression profile in bone of diabetes-prone BB/OK rats fed a high-fat diet.Overproduction of a truncated hepatocyte nuclear factor 3 protein inhibits expression of liver-specific genes in hepatoma cells.14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.Patterns of hypothalamic regionalization in amphibians and reptiles: common traits revealed by a genoarchitectonic approach.FoxG1 and TLE2 act cooperatively to regulate ventral telencephalon formation.Transcription factor genes and the developing eye: a genetic perspective.Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation.Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions.Low FoxG1 and high Olig-2 labelling indices define a prognostically favourable subset in isocitrate dehydrogenase (IDH)-mutant gliomas.Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes.Microarray with micro- and nano-topographies enables identification of the optimal topography for directing the differentiation of primary murine neural progenitor cells.Wnt signal activation induces midbrain specification through direct binding of the beta-catenin/TCF4 complex to the EN1 promoter in human pluripotent stem cells.
P2860
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P2860
Human brain factor 1, a new member of the fork head gene family
description
1994 nî lūn-bûn
@nan
1994 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Human brain factor 1, a new member of the fork head gene family
@ast
Human brain factor 1, a new member of the fork head gene family
@en
Human brain factor 1, a new member of the fork head gene family
@en-gb
Human brain factor 1, a new member of the fork head gene family
@nl
type
label
Human brain factor 1, a new member of the fork head gene family
@ast
Human brain factor 1, a new member of the fork head gene family
@en
Human brain factor 1, a new member of the fork head gene family
@en-gb
Human brain factor 1, a new member of the fork head gene family
@nl
prefLabel
Human brain factor 1, a new member of the fork head gene family
@ast
Human brain factor 1, a new member of the fork head gene family
@en
Human brain factor 1, a new member of the fork head gene family
@en-gb
Human brain factor 1, a new member of the fork head gene family
@nl
P2093
P921
P356
P1433
P1476
Human brain factor 1, a new member of the fork head gene family
@en
P2093
Burfeind P
Schmundt D
Schulz-Schaeffer W
P304
P356
10.1006/GENO.1994.1313
P407
P50
P577
1994-06-01T00:00:00Z