Characterization of the gene for the a subunit of human factor XIII (plasma transglutaminase), a blood coagulation factor
about
Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genesPrimary structure of keratinocyte transglutaminaseOrganization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIIIOrganization and evolution of the human epidermal keratinocyte transglutaminase I geneDeficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon IIIIdentification of the calcium binding site and a novel ytterbium site in blood coagulation factor XIII by x-ray crystallographyCoagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII ActionExamining thrombin hydrolysis of the factor XIII activation peptide segment leads to a proposal for explaining the cardioprotective effects observed with the factor XIII V34L mutationEvolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase ZCrystallization of blood coagulation factor XIII by an automated procedureFactor XIII: novel structural and functional aspects.Factor XIIIA Calgary: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIIIA subunit.Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.Regulation of transglutaminases by nitric oxide.Role of calcium in the conformational dynamics of factor XIII activation examined by hydrogen-deuterium exchange coupled with MALDI-TOF MS.Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)Prenatal diagnosis in factor XIII-A deficiency.Regulation of type I (epidermal) transglutaminase mRNA levels during squamous differentiation: down regulation by retinoids.Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1).Purification and partial characterization of transglutaminase from Physarum polycephalum.Impaired dimer assembly and decreased stability of naturally recurring R260C mutant A subunit for coagulation factor XIII.Plasma factor XIII activity in patients with disseminated intravascular coagulation.Cloning and expression of chicken erythrocyte transglutaminase.Factor XIII: a coagulation factor with multiple plasmatic and cellular functions.Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.Acquired FXIII inhibitors: a systematic review.Transcriptional regulation of cell type-specific expression of the TATA-less A subunit gene for human coagulation factor XIII.A crucial sequence for transglutaminase type 2 extracellular trafficking in renal tubular epithelial cells lies in its N-terminal beta-sandwich domain.Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.Proteosomal degradation of naturally recurring R260C missense and exon-IV deletion mutants of factor XIII A-subunit expressed in mammalian cells.The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.Novel primer specific false terminations during DNA sequencing reactions: danger of inaccuracy of mutation analysis in molecular diagnostics.Molecular and cellular basis of deficiency of the b subunit for factor XIII secondary to a Cys430-Phe mutation in the seventh Sushi domain.Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.First trimester prenatal diagnosis of severe FXIII deficiency.Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.Molecular characterization of five Italian families with inherited severe factor XIII deficiency.Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family.
P2860
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P2860
Characterization of the gene for the a subunit of human factor XIII (plasma transglutaminase), a blood coagulation factor
description
1988 nî lūn-bûn
@nan
1988 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Characterization of the gene f ...... e), a blood coagulation factor
@ast
Characterization of the gene f ...... e), a blood coagulation factor
@en
Characterization of the gene f ...... e), a blood coagulation factor
@nl
type
label
Characterization of the gene f ...... e), a blood coagulation factor
@ast
Characterization of the gene f ...... e), a blood coagulation factor
@en
Characterization of the gene f ...... e), a blood coagulation factor
@nl
prefLabel
Characterization of the gene f ...... e), a blood coagulation factor
@ast
Characterization of the gene f ...... e), a blood coagulation factor
@en
Characterization of the gene f ...... e), a blood coagulation factor
@nl
P2860
P356
P1476
Characterization of the gene f ...... e), a blood coagulation factor
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.16.5829
P407
P577
1988-08-01T00:00:00Z