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Epidemiology, Etiology, and Treatment of Isolated Cleft PalateCurrent Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency.SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delaminationTooth agenesis and orofacial clefting: genetic brothers in arms?Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociFine tuning of craniofacial morphology by distant-acting enhancersAvian facial morphogenesis is regulated by c-Jun N-terminal kinase/planar cell polarity (JNK/PCP) wingless-related (WNT) signaling.Functional analysis of SPECC1L in craniofacial development and oblique facial cleft pathogenesis.Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS dataImputation 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.The Transcription Factor IRF6 Co-Represses PPARγ-Mediated Cytoprotection in Ischemic Cerebrovascular Endothelial Cells.Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral cleftsAssociation 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 combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.IRF6 Is Involved in the Regulation of Cell Proliferation and Transformation in MCF10A Cells Downstream of Notch SignalingBMP7 Gene involved in nonsyndromic orofacial clefts in Western Han Chinese.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.Cellular and Molecular Mechanisms of PalatogenesisClinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian populationSequencing 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 studyThe evolution of human genetic studies of cleft lip and cleft palate.MicroRNAs in Palatogenesis and Cleft Palate.The Role of Noncoding Genetic Variation in Isolated Orofacial Clefts.Genetic Screening in Patients with Craniofacial Malformations.Long-range enhancers regulating Myc expression are required for normal facial morphogenesis.Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen.Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts.Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population.Visualization of craniofacial development in the sox10: kaede transgenic zebrafish line using time-lapse confocal microscopy.Strong association of variants around FOXE1 and orofacial clefting.Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.Evaluating LINE-1 methylation in cleft lip tissues and its association with early pregnancy exposures.Genome-wide Chromatin Mapping Defines AP2α in the Etiology of Craniofacial Disorders.Enamel defects on the maxillary premolars in patients with cleft lip and/or palate: a retrospective case-control study.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Breakthroughs in the genetics of orofacial clefting.
@en
Breakthroughs in the genetics of orofacial clefting.
@nl
type
label
Breakthroughs in the genetics of orofacial clefting.
@en
Breakthroughs in the genetics of orofacial clefting.
@nl
prefLabel
Breakthroughs in the genetics of orofacial clefting.
@en
Breakthroughs in the genetics of orofacial clefting.
@nl
P1476
Breakthroughs in the genetics of orofacial clefting.
@en
P2093
Elisabeth Mangold
Kerstin U Ludwig
P304
P356
10.1016/J.MOLMED.2011.07.007
P407
P577
2011-08-30T00:00:00Z