MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
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Medical sequencing of candidate genes for nonsyndromic cleft lip and palateA nonsense mutation in MSX1 causes Witkop syndromeMSX1 and TGFB3 contribute to clefting in South AmericaMutations in IRF6 cause Van der Woude and popliteal pterygium syndromesCleft lip and palate: understanding genetic and environmental influencesEndogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammalsThe role of MSX1 in human tooth agenesisA genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defectsMissense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palateContributions of PTCH gene variants to isolated cleft lip and palateDefining the role of essential genes in human diseaseRoles of BMP signaling pathway in lip and palate developmentTooth agenesis and orofacial clefting: genetic brothers in arms?A missense mutation in PAX9 in a family with distinct phenotype of oligodontiaDistal 5q deletion syndrome: phenotypic correlationsA mutation in RYK is a genetic factor for nonsyndromic cleft lip and palateSatb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw developmentA specific requirement for PDGF-C in palate formation and PDGFR-alpha signalingDisruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palateMsx1 disruption leads to diencephalon defects and hydrocephalusMsx2 is a repressor of chondrogenic differentiation in migratory cranial neural crest cellsA comparative examination of odontogenic gene expression in both toothed and toothless amniotes.Development of the upper lip: morphogenetic and molecular mechanismsThe genetic basis of modularity in the development and evolution of the vertebrate dentition.Coordinately Co-opted Multiple Transposable Elements Constitute an Enhancer for wnt5a Expression in the Mammalian Secondary PalateA genome-wide association study of third molar agenesis in Japanese and Korean populationsMutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type IGREMLIN 2 Mutations and Dental Anomalies.Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.Fine tuning of craniofacial morphology by distant-acting enhancersAvian facial morphogenesis is regulated by c-Jun N-terminal kinase/planar cell polarity (JNK/PCP) wingless-related (WNT) signaling.Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers.Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.Identification and functional analysis of two novel PAX9 mutations.Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature reviewDifferential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.
P2860
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P2860
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
description
2000 nî lūn-bûn
@nan
2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@ast
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en-gb
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@nl
type
label
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@ast
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en-gb
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@nl
prefLabel
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@ast
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en-gb
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@nl
P2093
P3181
P356
P1433
P1476
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
@en
P2093
F A Beemer
H K van Amstel
M J van den Boogaard
P2888
P3181
P356
10.1038/74155
P407
P577
2000-04-01T00:00:00Z
P5875
P6179
1006219974