FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate - Wikidata - wikimedia - TriplyDB

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

http://www.wikidata.org/entity/Q24655358

about

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia Cleft lip and palate: understanding genetic and environmental influences Genomic expression in non syndromic cleft lip and palate patients: A review Definition of critical periods for Hedgehog pathway antagonist-induced holoprosencephaly, cleft lip, and cleft palate Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits.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.Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.Association between PAX7 and NTN1 gene polymorphisms and nonsyndromic orofacial clefts in a northern Chinese population.The effects of oral clefts on hospital use throughout the lifespan Association between single-nucleotide polymorphisms on chromosome 1p22 and 20q12 and nonsyndromic cleft lip with or without cleft palate: new data in Han Chinese and meta-analysis.A glance at methods for cleft palate repair.TGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast China Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.Digital imaging analysis to assess scar phenotype.Further evidence of association of the ABCA4 gene with cleft lip/palate.Meta-analysis of gene-based genome-wide association studies of bone mineral density in Chinese and European subjects.Palatogenesis: engineering, pathways and pathologies The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts.A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1 Association of AXIN2 with non-syndromic oral clefts in multiple populations.Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia.Genetics of nonsyndromic orofacial clefts Identification of susceptibility genes in non-syndromic cleft lip with or without cleft palate using whole-exome sequencing.GWAS reveals new recessive loci associated with non-syndromic facial clefting Irf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate Yap and Taz play a crucial role in neural crest-derived craniofacial development.Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study The evolution of human genetic studies of cleft lip and cleft palate.Genetics of cleft lip and cleft palate.Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.Zebrafish models of orofacial clefts.

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P2860

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

http://www.wikidata.org/entity/Q24655358

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

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

@zh-hk

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

FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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FOXE1 association with both is ...... ate, and isolated cleft palate

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Human Molecular Genetics

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FOXE1 association with both is ...... ate, and isolated cleft palate

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Ana Maria López

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Andrew C Lidral

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Anne Hing

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Astanand Jugessur

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Consuelo Valencia-Ramirez

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Dora Rivera

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Edward J Lammer

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Elizabeth Pugh

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Jamie L'heureux

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Jeffrey C Murray

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P2860

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

Sporadic and familial blepharophimosis -ptosis-epicanthus inversus syndrome: FOXL2 mutation screen and MRI study of the superior levator eyelid muscle

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest Colombia

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P

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

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4879-4896

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10.1093/HMG/DDP444

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24

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18

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Kaare Christensen

Mauricio Arcos-Burgos

Sandra Daack-Hirsch

Allen James Wilcox

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2009-09-24T00:00:00Z

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26836006

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19779022

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2778374

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