Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate - Test2 - elhamkhani - TriplyDB

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

http://www.wikidata.org/entity/Q24676916

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Medical sequencing of candidate genes for nonsyndromic cleft lip and palate Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate Cleft lip and palate: understanding genetic and environmental influences Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23 Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6 Impaired FGF signaling contributes to cleft lip and palate Contributions of PTCH gene variants to isolated cleft lip and palate Current Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency.Genomic expression in non syndromic cleft lip and palate patients: A review Palatogenesis and cutaneous repair: A two-headed coin Roles of BMP signaling pathway in lip and palate development A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development Development of the upper lip: morphogenetic and molecular mechanisms GREMLIN 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 enhancers Linkage disequilibrium between MSX1 and non-syndromic cleft lip/palate in the Chilean population.Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers.Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.Parent's age and the risk of oral clefts.Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance Folic acid and orofacial clefts: a review of the evidence Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population.Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12).In a Vietnamese population, MSX1 variants contribute to cleft lip and palate.Oral cleft prevention program (OCPP).Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34

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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

http://www.wikidata.org/entity/Q24676916

description

2003 nî lūn-bûn

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2003 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2003年の論文

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2003年論文

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name

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

@ast

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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type

label

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

@ast

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

@en

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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prefLabel

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

@ast

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

@en

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

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A R Vieira

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P2860

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

Evidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean population

A nonsense mutation in MSX1 causes Witkop syndrome

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Endogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammals

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism

A simple salting out procedure for extracting DNA from human nucleated cells

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

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399-407

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10.1136/JMG.40.6.399

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6

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Kaare Christensen

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