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Cleft lip and palate: understanding genetic and environmental influences

Cleft lip and palate: understanding genetic and environmental influences

http://www.wikidata.org/entity/Q24601804

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Maternal occupational exposure to organic solvents during early pregnancy and risks of neural tube defects and orofacial clefts Epidemiology, Etiology, and Treatment of Isolated Cleft Palate The Roles of Hedgehog Signaling in Upper Lip Formation Current Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency.Roles of BMP signaling pathway in lip and palate development Evaluation and diagnosis of the dysmorphic infant Cleft lip - a comprehensive review Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics Signaling networks in palate development Dental phenomics: advancing genotype to phenotype correlations in craniofacial research SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination Accelerated wound closure in vitro by fibroblasts from a subgroup of cleft lip/palate patients: role of transforming growth factor-α Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities Tooth agenesis and orofacial clefting: genetic brothers in arms?What is the Risk of Having Offspring with Cleft Lip/Palate in Pre-Maternal Obese/Overweight Women When Compared to Pre-Maternal Normal Weight Women? A Systematic Review and Meta-Analysis The 19-bp deletion polymorphism of dihydrofolate reductase (DHFR) and nonsyndromic cleft lip with or without cleft palate: evidence for a protective role Examining factors associated with oral health-related quality of life for youth with cleft 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 Cleft Palate, Moderate Lung Developmental Retardation and Early Postnatal Lethality in Mice Deficient in the Kir7.1 Inwardly Rectifying K+ Channel The splicing regulators Esrp1 and Esrp2 direct an epithelial splicing program essential for mammalian development Genetic disruption of the sh3pxd2a gene reveals an essential role in mouse development and the existence of a novel isoform of tks5 Recent insights into the morphological diversity in the amniote primary and secondary palates Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family Embryonic bauplans and the developmental origins of facial diversity and constraint Insights into neural crest development and evolution from genomic analysis Coordinately Co-opted Multiple Transposable Elements Constitute an Enhancer for wnt5a Expression in the Mammalian Secondary Palate Precision Dentistry in Early Childhood: The Central Role of Genomics.Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.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 Avian facial morphogenesis is regulated by c-Jun N-terminal kinase/planar cell polarity (JNK/PCP) wingless-related (WNT) signaling.Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled-analysis.Pdgfra and Pdgfrb genetically interact during craniofacial development 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 Pierre Robin sequence: Subdivision, data, theories, and treatment - Part 2: Syndromic and nonsyndromic Pierre Robin sequence.A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk A Combined PLS and Negative Binomial Regression Model for Inferring Association Networks from Next-generation Sequencing Count Data.

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Cleft lip and palate: understanding genetic and environmental influences

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Cleft lip and palate: understanding genetic and environmental influences

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Nature Reviews Genetics

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Cleft lip and palate: understanding genetic and environmental influences

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Jeffrey C Murray

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Mary L Marazita

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Michael J Dixon

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Terri H Beaty

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P2860

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Genomic views of distant-acting enhancers

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

Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family

Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate

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

Vax1, a novel homeobox-containing gene, directs development of the basal forebrain and visual system

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Exome sequencing identifies the cause of a mendelian disorder

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10.1038/NRG2933

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1027918713

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