Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palateCleft lip and palate: understanding genetic and environmental influencesFrizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processesRegulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American familyShape covariation between the craniofacial complex and first molars in humansEpigenetic integration of the developing brain and faceA pilot study: Screening target miRNAs in tissue of nonsyndromic cleft lip with or without cleft palateExpression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesisRole of GSK-3β in the osteogenic differentiation of palatal mesenchyme.The canonical Wnt signaling activator, R-spondin2, regulates craniofacial patterning and morphogenesis within the branchial arch through ectodermal-mesenchymal interactionExpression 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.Studies with Wnt genes and nonsyndromic cleft lip and palate.Discovery Genetics - The History and Future of Spontaneous Mutation Research.A glance at methods for cleft palate repair.Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage.Insights from studies with oral cleft genes suggest associations between WNT-pathway genes and risk of oral cancer.TGFβ-1 and Wnt-3a interact to induce unique gene expression profiles in murine embryonic palate mesenchymal cells.Palate morphogenesis: current understanding and future directions.Wnt/beta-catenin signaling in oral tissue development and disease.A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis.Palatogenesis: engineering, pathways and pathologiesPlanar cell polarity signaling in craniofacial development.Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios.A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.Wnt9b-dependent FGF signaling is crucial for outgrowth of the nasal and maxillary processes during upper jaw and lip developmentFurther evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.Genetics of nonsyndromic orofacial cleftsThe A-kinase Anchoring Protein GSKIP Regulates GSK3β Activity and Controls Palatal Shelf Fusion in Mice.Deciphering the Palimpsest: Studying the Relationship Between Morphological Integration and Phenotypic Covariation.Ectodermal Wnt controls nasal pit morphogenesis through modulation of the BMP/FGF/JNK signaling axis.Mouse resources for craniofacial research.Tissue engineering in cleft palate and other congenital malformations.Expression of Wnts in the developing murine secondary palate.Hear the Wnt Ror: how melanoma cells adjust to changes in Wnt.Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.Genetic and pathologic aspects of retinoic acid-induced limb malformations in the mouse.Zebrafish models of orofacial clefts.Examination of a palatogenic gene program in zebrafish.Influence of maternal metabolism and parental genetics on fetal maldevelopment in diabetic rat pregnancy.Expression of Wnt9, TCTP, and Bmp1/Tll in sea cucumber visceral regeneration.
P2860
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P2860
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
description
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
scientific journal article
@en
vedecký článok (publikovaný 2006/08/01)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/08/01)
@nl
наукова стаття, опублікована в серпні 2006
@uk
مقالة علمية (نشرت في أغسطس 2006)
@ar
name
Wnt9b is the mutated gene invo ...... a genetic complementation test
@ast
Wnt9b is the mutated gene invo ...... a genetic complementation test
@en
Wnt9b is the mutated gene invo ...... a genetic complementation test
@nl
type
label
Wnt9b is the mutated gene invo ...... a genetic complementation test
@ast
Wnt9b is the mutated gene invo ...... a genetic complementation test
@en
Wnt9b is the mutated gene invo ...... a genetic complementation test
@nl
prefLabel
Wnt9b is the mutated gene invo ...... a genetic complementation test
@ast
Wnt9b is the mutated gene invo ...... a genetic complementation test
@en
Wnt9b is the mutated gene invo ...... a genetic complementation test
@nl
P2093
P356
P1476
Wnt9b is the mutated gene invo ...... a genetic complementation test
@en
P2093
Andrew C. Lidral
Andrew P. McMahon
Diana M. Juriloff
Muriel J. Harris
Thomas J. Carroll
P2860
P304
P356
10.1002/BDRA.20302
P577
2006-08-01T00:00:00Z