Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
about
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasiaVariation in WNT genes is associated with non-syndromic cleft lip with or without cleft palateCleft lip and palate: understanding genetic and environmental influencesWnt modulators in the biotech pipelineWnt/beta-catenin signaling: components, mechanisms, and diseasesThe Wnt-dependent signaling pathways as target in oncology drug discoveryIt's all in your head: new insights into craniofacial development and deformationLower urinary tract development and diseaseWNT signaling in bone development and homeostasisAnisotropic stress orients remodelling of mammalian limb bud ectoderm.Thalidomide-induced teratogenesis: history and mechanismsWNT signaling in bone homeostasis and disease: from human mutations to treatmentsGenetic evidence that SOST inhibits WNT signaling in the limbFrizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processesDistinct patterns of desynchronized limb regression in malagasy scincine lizards (squamata, scincidae)Canonical Wnt signalling regulates epithelial patterning by modulating levels of laminins in zebrafish appendagesDevelopment of the upper lip: morphogenetic and molecular mechanismsGenome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritisWNT and beta-catenin signalling: diseases and therapiesA biochemical screen for identification of small-molecule regulators of the Wnt pathway using Xenopus egg extracts.Ectodermal Wnt/β-catenin signaling shapes the mouse face.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.Elucidating the genetic basis of an oligogenic birth defect using whole genome sequence data in a non-model organism, Bubalus bubalis.Radiological imaging of teratological fetuses: what can we learn?Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosisThe canonical Wnt signaling activator, R-spondin2, regulates craniofacial patterning and morphogenesis within the branchial arch through ectodermal-mesenchymal interactionStudies with Wnt genes and nonsyndromic cleft lip and palate.Wnt signaling in disease and in development.Wnt/Frizzled signaling in the vasculature: new angiogenic factors in sight.Wnt signaling and the control of human stem cell fate.Gsk3β is required in the epithelium for palatal elevation in mice.Zebrafish wnt3 is expressed in developing neural tissue.The inductive role of Wnt-β-Catenin signaling in the formation of oral apparatus.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.Planar cell polarity signaling in craniofacial development.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 developmentWnt gene expression in the post-natal growth plate: regulation with chondrocyte differentiation.
P2860
Q24293212-C21BE9AC-83C6-4249-B437-27A8698AC012Q24321656-A2282B59-FAD5-4ABF-BD48-AEC12B6799BEQ24601804-5C8F250B-EA0D-4254-9E6F-68833EEE1835Q24618567-12CE2BDE-D32B-4AA2-8650-68652BBF9EC8Q24630938-185354D7-142F-4DB6-8E10-4C657C45380FQ24652979-6826F7B2-9C98-4855-A082-2DA090F556CBQ24675572-4CBC7171-A26A-4183-90C5-06F024B5CCFCQ27000375-9AF20CA0-D4E2-44D5-90E0-55C60B3FB620Q27008570-6A629D28-A22F-4D48-9096-464A9C448A73Q27313091-E524E7B5-4557-4D8E-9BAE-7A9E2CD0EB9EQ28085087-0E64A2D7-E6A5-4A34-B0F3-51090FA28297Q28285090-24B2EE23-8FFF-457C-BDC0-E73958A7AFADQ28509512-3BE95BDD-7AE7-49FF-9BE0-EDC438051322Q28586361-AF8C03C4-5558-4B93-B770-F0CB847D9E7CQ28645838-C2422033-0DA5-47DF-8F18-A46D77729A9DQ28651704-FBFA87CE-5291-4825-9734-EBC2FCC6D8FBQ28756916-4CA5970B-9D40-4443-A315-9EACE2F11BDFQ28943553-C6FF2D2B-4151-48F6-B575-B830B5B96752Q29616159-43DBEF7A-9B3A-4B63-8D7F-7FAA475C5886Q30453133-C4BC2B89-8380-4643-927D-EDBCDA66FE65Q30498676-9EF2D7E8-D3D6-4135-9C9A-708FB687BE75Q30825766-8C1C8E39-0E62-4901-A78E-C4B0E597C0DEQ31152378-3825029D-DAA4-4A77-BBB2-4392FD9867C4Q33708338-4BA9D5CD-33E1-4E80-9E60-69911A279933Q34058672-176644F7-DDE8-4AED-9AF6-11F49F4AF3CDQ34159158-FE085A78-4CDF-4999-A90A-2A01425A3C8AQ34349094-E5C7A79C-4DD3-4177-B410-7C9867D8D663Q34390198-2D9C3CAA-B7E1-4D0E-BCB2-8239DB18F346Q34528832-C798A365-2D60-4145-9596-C596672270C4Q34658275-597606A3-B551-49FE-8F9D-9DF36F8480F6Q34753930-DDF7CA78-6C94-40A2-91CC-549180C686BFQ34906920-8B4624FD-E112-4B0C-A89D-A0BC72A37029Q35089503-01BBE42A-2085-40B9-A4DF-55841DBAC71BQ35111595-AB2FD330-42E5-4E5E-BA04-8D5B0E84FE3CQ35119945-E99FA023-0D30-4A88-AA9A-5A31D6BE30ABQ35421119-4D0F57E9-ABCD-4467-9F72-DA9E89FC963FQ35693873-8083EBE8-DE54-4119-9F1D-39AFF7AB5F06Q35755034-7E4850EB-875B-474F-9840-D959E123C982Q35893650-CC7CBA0A-72B3-4431-A58C-BAE6437BD65EQ35928985-06CC2E43-A84A-4845-9497-BA1EA3925A31
P2860
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@ast
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en-gb
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@nl
type
label
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@ast
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en-gb
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@nl
prefLabel
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@ast
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en-gb
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@nl
P2093
P2860
P3181
P356
P1476
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
@en
P2093
Chengfeng Zhao
Filon Pascu
James L Weber
Stephan Niemann
Ulrich Müller
Ulrich Stahl
Ute Aulepp
P2860
P304
P3181
P356
10.1086/382196
P407
P577
2004-03-01T00:00:00Z