A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
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Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancerGenes and dental disordersMorphoregulation of teeth: modulating the number, size, shape and differentiation by tuning Bmp activityCandidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.Non-syndromic tooth agenesis in two Chinese families associated with novel missense mutations in the TNF domain of EDA (ectodysplasin A)Identification and functional analysis of two novel PAX9 mutations.Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature reviewClinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.Novel mutation of the initiation codon of PAX9 causes oligodontia.Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.Msx1 mutations: how do they cause tooth agenesis?Multidisciplinary treatment of non-syndromic oligodontiaA Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of PAX9-A Clinical and Genetic Report.Novel MSX1 frameshift causes autosomal-dominant oligodontia.Phenotype characterization and sequence analysis of BMP2 and BMP4 variants in two Mexican families with oligodontia.Multidisciplinary Management of OligodontiaPathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.Genetic basis for tooth malformations: from mice to men and back again.Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.The genetic basis of dental anomalies and its relation to orthodonticsPAX9 gene mutations and tooth agenesis: A review.Management of a child with severe hypodontia in the mixed dentition stage of development.The promise of human induced pluripotent stem cells in dental research.Congenitally missing primary mandibular lateral incisors: a case of rare occurrenceCharacterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis.Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.Complex analysis of multiple single nucleotide polymorphisms as putative risk factors of tooth agenesis in the Hungarian population.Novel missense mutation in PAX9 gene associated with familial tooth agenesis.Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies.Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis.Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?TGFB3 and BMP4 polymorphism are associated with isolated tooth agenesis.Dental transposition as a disorder of genetic origin.PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.Functional consequences of interactions between Pax9 and Msx1 genes in normal and abnormal tooth development.MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.A review on non-syndromic tooth agenesis associated with PAX9 mutations.Identification of Genetic Risk Factors for Maxillary Lateral Incisor Agenesis
P2860
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P2860
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
description
2003 nî lūn-bûn
@nan
2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@ast
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@en
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@nl
type
label
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@ast
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@en
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@nl
prefLabel
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@ast
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@en
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@nl
P2093
P2860
P356
P1476
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
@en
P2093
Katri Halonen
Laura Lammi
Pekka Nieminen
Sinikka Pirinen
Sirpa Arte
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201060
P407
P577
2003-11-01T00:00:00Z