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Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate
by
Xu, Tianhui
, Gu, Zhiping
, Du, Mengmeng
, Yuan, Donglan
, Bu, Xinhua
, Yu, Pei
, Jin, Chunyan
, Chen, Jiao
, Li, Xuefang
in
Amino acids
/ Biomedical and Life Sciences
/ Biomedicine
/ Case Report
/ Causes of
/ Child, Preschool
/ Cleft lip
/ Cleft Lip - genetics
/ Cleft lip with or without cleft palate
/ Cleft lip/palate
/ Cleft palate
/ Cleft Palate - genetics
/ Cytogenetics
/ Deoxyribonucleic acid
/ DNA
/ DNA microarrays
/ Families & family life
/ Functional and structural genomics
/ Gene Expression
/ Gene mutations
/ Genes
/ Genetic aspects
/ Genetic research
/ Genomes
/ Genotype & phenotype
/ Human Genetics
/ Humans
/ Intelligence
/ Male
/ Microarrays
/ Mutation
/ Nonsense mutation
/ Nonsyndromic cleft lip with or without cleft palate
/ Oligomerization
/ Pathogenesis
/ Pedigree
/ Phenotype
/ Phenotypes
/ Proteins
/ Stop codon
/ TP63
/ Transcription Factors - genetics
/ Tumor proteins
/ Tumor Suppressor Proteins - genetics
/ Whole exome sequencing
2021
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Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate
by
Xu, Tianhui
, Gu, Zhiping
, Du, Mengmeng
, Yuan, Donglan
, Bu, Xinhua
, Yu, Pei
, Jin, Chunyan
, Chen, Jiao
, Li, Xuefang
in
Amino acids
/ Biomedical and Life Sciences
/ Biomedicine
/ Case Report
/ Causes of
/ Child, Preschool
/ Cleft lip
/ Cleft Lip - genetics
/ Cleft lip with or without cleft palate
/ Cleft lip/palate
/ Cleft palate
/ Cleft Palate - genetics
/ Cytogenetics
/ Deoxyribonucleic acid
/ DNA
/ DNA microarrays
/ Families & family life
/ Functional and structural genomics
/ Gene Expression
/ Gene mutations
/ Genes
/ Genetic aspects
/ Genetic research
/ Genomes
/ Genotype & phenotype
/ Human Genetics
/ Humans
/ Intelligence
/ Male
/ Microarrays
/ Mutation
/ Nonsense mutation
/ Nonsyndromic cleft lip with or without cleft palate
/ Oligomerization
/ Pathogenesis
/ Pedigree
/ Phenotype
/ Phenotypes
/ Proteins
/ Stop codon
/ TP63
/ Transcription Factors - genetics
/ Tumor proteins
/ Tumor Suppressor Proteins - genetics
/ Whole exome sequencing
2021
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Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate
by
Xu, Tianhui
, Gu, Zhiping
, Du, Mengmeng
, Yuan, Donglan
, Bu, Xinhua
, Yu, Pei
, Jin, Chunyan
, Chen, Jiao
, Li, Xuefang
in
Amino acids
/ Biomedical and Life Sciences
/ Biomedicine
/ Case Report
/ Causes of
/ Child, Preschool
/ Cleft lip
/ Cleft Lip - genetics
/ Cleft lip with or without cleft palate
/ Cleft lip/palate
/ Cleft palate
/ Cleft Palate - genetics
/ Cytogenetics
/ Deoxyribonucleic acid
/ DNA
/ DNA microarrays
/ Families & family life
/ Functional and structural genomics
/ Gene Expression
/ Gene mutations
/ Genes
/ Genetic aspects
/ Genetic research
/ Genomes
/ Genotype & phenotype
/ Human Genetics
/ Humans
/ Intelligence
/ Male
/ Microarrays
/ Mutation
/ Nonsense mutation
/ Nonsyndromic cleft lip with or without cleft palate
/ Oligomerization
/ Pathogenesis
/ Pedigree
/ Phenotype
/ Phenotypes
/ Proteins
/ Stop codon
/ TP63
/ Transcription Factors - genetics
/ Tumor proteins
/ Tumor Suppressor Proteins - genetics
/ Whole exome sequencing
2021
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Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate
Journal Article
Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate
2021
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Overview
Background
Cleft lip with or without cleft palate (CL/P) is the most common craniofacial anomaly with a high incidence of live births. The specific pathogenesis of CL/P is still unclear, although plenty of studies have been conducted. Variations of tumor protein 63 (
TP63
) was reported to be related to the phenotype of CL/P. The case discussed in this report involves a pedigree with mutation at
TP63
gene, and the variation was not reported before.
Case presentation
A Chinese pedigree with CL/P was collected in this study. The proband is a 3-year-old boy with the phenotype of CL/P, while his global development and intelligence are normal. After two CL/P repair operations, he looks almost normal. The proband's uncle and grandmother both have the phenotype of CL/P. Cytogenetic analysis and chromosomal microarray analysis (CMA) were performed, followed by whole exome sequencing (WES) and sanger validation. Analysis of WES revealed a variant of C>T at nucleotide position 1324 (1324C>T) of
TP63
gene, possibly producing a truncated protein with a premature stop codon at amino acid position 442 (p.Q442*). This mutation was localized at the oligomerization domain (OD) of
TP63
and might impair the capacity of p63 oligomerization.
Conclusion
The mutation in
TP63
was recognized to be the possible cause of the phenotype of CL/P in this pedigree. This report provides some evidence for the clinical diagnosis of CL/P. And our study also provides clinical evidence for the molecular mechanism of
TP63
gene causing nonsyndromic cleft lip with or without cleft palate (NSCL/P).
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Biomedical and Life Sciences
/ Cleft lip with or without cleft palate
/ DNA
/ Functional and structural genomics
/ Genes
/ Genomes
/ Humans
/ Male
/ Mutation
/ Nonsyndromic cleft lip with or without cleft palate
/ Pedigree
/ Proteins
/ TP63
/ Transcription Factors - genetics
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