A human MSX1 homeodomain missense mutation causes selective tooth agenesis
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A nonsense mutation in MSX1 causes Witkop syndromeMutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancerMutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouseTranscriptional autorepression of Msx1 gene is mediated by interactions of Msx1 protein with a multi-protein transcriptional complex containing TATA-binding protein, Sp1 and cAMP-response-element-binding protein-binding protein (CBP/p300)Msx3 protein recruits histone deacetylase to down-regulate the Msx1 promoterAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansRegulation of dental enamel shape and hardnessEndogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammalsThe role of MSX1 in human tooth agenesisCtip2/Bcl11b controls ameloblast formation during mammalian odontogenesisComplete sequencing shows a role for MSX1 in non-syndromic cleft lip and palatePalatogenesis and cutaneous repair: A two-headed coinMSX2 in ameloblast cell fate and activityGenes and dental disordersTooth agenesis and orofacial clefting: genetic brothers in arms?Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth AgenesisMutation of PAX9 is associated with oligodontiaFunctional analysis of a mutation in PAX9 associated with familial tooth agenesis in humansA missense mutation in PAX9 in a family with distinct phenotype of oligodontiaThe role of DNA insertions in phenotypic differentiation between humans and other primatesCloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeMsx1 disruption leads to diencephalon defects and hydrocephalusMsx2 is a repressor of chondrogenic differentiation in migratory cranial neural crest cellsMorphoregulation of teeth: modulating the number, size, shape and differentiation by tuning Bmp activityThe genetic basis of modularity in the development and evolution of the vertebrate dentition.Development and evolution occlude: evolution of development in mammalian teethA genome-wide association study of third molar agenesis in Japanese and Korean populationsHypodontia: An Update on Its Etiology, Classification, and Clinical Management.Late development of a mandibular second premolar.Fine tuning of craniofacial morphology by distant-acting enhancersCandidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers.Transcription factors in dysmorphology.Phenotypic analysis of Dlx5 overexpression in post-natal bone.Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature reviewThe impact of molecular genetics on oral health paradigms.Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome.The molecular basis for developmental disorders of the pituitary gland in man.
P2860
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P2860
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
description
1996 nî lūn-bûn
@nan
1996 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@ast
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en-gb
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@nl
type
label
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@ast
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en-gb
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@nl
prefLabel
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@ast
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en-gb
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@nl
P2093
P3181
P356
P1433
P1476
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
@en
P2093
C E Seidman
H Vastardis
J G Seidman
N Karimbux
S W Guthua
P2888
P304
P3181
P356
10.1038/NG0896-417
P407
P577
1996-08-01T00:00:00Z
P6179
1047735800