Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. - Wikidata - wikimedia - TriplyDB

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

http://www.wikidata.org/entity/Q34959002

about

A genome-wide association study identifies five loci influencing facial morphology in Europeans Cleft lip and palate: understanding genetic and environmental influences A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 Testing reported associations of genetic risk factors for oral clefts in a large Irish study population Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate Current Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency.Palatogenesis and cutaneous repair: A two-headed coin Developments in our understanding of the genetic basis of birth defects Cleft lip - a comprehensive review Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities Tooth agenesis and orofacial clefting: genetic brothers in arms?New insights into craniofacial malformations Neighborhood-Based Socioeconomic Position and Risk of Oral Clefts Among Offspring A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting MicroRNA-17-92, a direct Ap-2α transcriptional target, modulates T-box factor activity in orofacial clefting Multidisciplinary approach to genomics research in Africa: the AfriCRAN model Genome-wide association study identifies five susceptibility loci for glioma 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 Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.Joint testing of genotypic and gene-environment interaction identified novel association for BMP4 with non-syndromic CL/P in an Asian population using data from an International Cleft Consortium.The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.The power of protein interaction networks for associating genes with diseases.Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate.Multiple loci are associated with white blood cell phenotypes.The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.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 The FaceBase Consortium: a comprehensive program to facilitate craniofacial research.PVRL1 as a candidate gene for nonsyndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in southern Han Chinese patients.BMP4 was associated with NSCL/P in an Asian population.Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.Enhancing the prioritization of disease-causing genes through tissue specific protein interaction networks.

P2860

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P2860

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

http://www.wikidata.org/entity/Q34959002

description

2009 nî lūn-bûn

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2009 թուականի Մարտին հրատարակուած գիտական յօդուած

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2009 թվականի մարտին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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type

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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prefLabel

Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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P2860

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P1433

Nature Genetics

P1476

Key susceptibility locus for n ...... eft palate on chromosome 8q24.

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P2093

Alexander Hemprich

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Bernd Pötzsch

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Bernhard Horsthemke

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Bert Braumann

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Carlotta Baluardo

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Carola Lauster

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Elisabeth Mangold

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Franz-Josef Kramer

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Franziska Schiefke

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Gül Schmidt

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P2860

Population structure and eigenanalysis

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

Large recurrent microdeletions associated with schizophrenia

A haplotype map of the human genome

Haploview: analysis and visualization of LD and haplotype maps

A human genome diversity cell line panel

The future of genetic studies of complex human diseases

A genome-wide association study of global gene expression

P2888

P304

473-477

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scholarly article

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10.1038/NG.333

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P433

4

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P478

41

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P50

Markus M Nöthen

Michael Steffens

Melissa Ferrian

P577

2009-03-08T00:00:00Z

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P5875

24186105

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19270707

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P921

susceptibility locus