The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator
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A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis.Identification of novel SHOX target genes in the developing limb using a transgenic mouse modelLarge Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland PoniesShox2 is required for chondrocyte proliferation and maturation in proximal limb skeletonCloning and functional analysis of hypothalamic homeobox gene Bsx1a and its isoform, Bsx1bThe Short-Stature Homeobox-Containing Gene (shox/SHOX) Is Required for the Regulation of Cell Proliferation and Bone Differentiation in Zebrafish Embryo and Human Mesenchymal Stem Cells.The homeobox transcription factor HOXA9 is a regulator of SHOX in U2OS cells and chicken micromass culturesAlternative splicing and nonsense-mediated RNA decay contribute to the regulation of SHOX expressionFunctional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function.Intratumoral decorin gene delivery by AAV vector inhibits brain glioblastomas and prolongs survival of animals by inducing cell differentiation.Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia.Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape.Genetic Diversity on the Human X Chromosome Does Not Support a Strict Pseudoautosomal BoundarySHOX at a glance: from gene to protein.Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiencyRecombinant human growth hormone in the treatment of Turner syndrome.A Track Record on SHOX: From Basic Research to Complex Models and TherapyShox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5.NPPB and ACAN, two novel SHOX2 transcription targets implicated in skeletal development.Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.Diagnosis of Lung Cancer by SHOX2 Gene Methylation Assay.Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region.FGFR3 is a target of the homeobox transcription factor SHOX in limb development.Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes.Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX.In vivo loss of function study reveals the short stature homeobox-containing (shox) gene plays indispensable roles in early embryonic growth and bone formation in zebrafish.Transactivation function of an approximately 800-bp evolutionarily conserved sequence at the SHOX 3' region: implication for the downstream enhancer.Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature.Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamentoBases Genéticas dos Distúrbios de CrescimentoShort stature homeoboxcontaining gene and idiopathic short stature
P2860
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P2860
The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
The Leri-Weill and Turner synd ...... ific transcriptional activator
@ast
The Leri-Weill and Turner synd ...... ific transcriptional activator
@en
The Leri-Weill and Turner synd ...... ific transcriptional activator
@nl
type
label
The Leri-Weill and Turner synd ...... ific transcriptional activator
@ast
The Leri-Weill and Turner synd ...... ific transcriptional activator
@en
The Leri-Weill and Turner synd ...... ific transcriptional activator
@nl
prefLabel
The Leri-Weill and Turner synd ...... ific transcriptional activator
@ast
The Leri-Weill and Turner synd ...... ific transcriptional activator
@en
The Leri-Weill and Turner synd ...... ific transcriptional activator
@nl
P2093
P3181
P356
P1476
The Leri-Weill and Turner synd ...... ific transcriptional activator
@en
P2093
P304
P3181
P356
10.1093/HMG/10.26.3083
P407
P577
2001-12-15T00:00:00Z