Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population. - Wikidata - wikimedia - TriplyDB

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

http://www.wikidata.org/entity/Q34446991

about

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 Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23 Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)Genomic expression in non syndromic cleft lip and palate patients: A review Addressing the challenges of cleft lip and palate research in India Association between IRF6 SNPs and oral clefts in West China IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign.Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12).Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate.Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.Ethnic heterogeneity of IRF6 AP-2a binding site promoter SNP association with nonsyndromic cleft lip and palate A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.TGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast China Tracing disease gene(s) in non-syndromic clefts of orofacial region: HLA haplotypic linkage by analyzing the microsatellite markers: MIB, C1_2_5, C1_4_1, and C1_2_A.Risk prediction models for oral clefts allowing for phenotypic heterogeneity.Genetics of nonsyndromic orofacial clefts Toward an orofacial gene regulatory network.Subclinical features in non-syndromic cleft lip with or without cleft palate (CL/P): review of the evidence that subepithelial orbicularis oris muscle defects are part of an expanded phenotype for CL/P.Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results Genetics of cleft lip and cleft palate.IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.The CRISPLD2 gene is involved in cleft lip and/or cleft palate in a Chinese population.Association between interferon regulatory factor 6 gene polymorphisms and nonsyndromic cleft lip with or without cleft palate in a chinese population.Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate.500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip

P2860

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P2860

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

http://www.wikidata.org/entity/Q34446991

description

2005 nî lūn-bûn

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2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2005年の論文

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Interferon regulatory factor-6 ...... ate in the Belgian population.

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SJ.EJHG.5201486

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European Journal of Human Genetics

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Interferon regulatory factor-6 ...... ate in the Belgian population.

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P2093

Benedicte Bayet

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Michella Ghassibé

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Nicole Revencu

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Romain Vanwijck

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Yves Gillerot

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P2860

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

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

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

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

The many faces and factors of orofacial clefts.

Identification of SATB2 as the cleft palate gene on 2q32-q33.

Gene/environment causes of cleft lip and/or palate.

Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.

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7629002

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