Immunoradiometric measurement of the factor VIII procoagulant antigen.
about
Cysteamine enhances the procoagulant activity of Factor VIII-East Hartford, a dysfunctional protein due to a light chain thrombin cleavage site mutation (arginine-1689 to cysteine)Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).Molecular basis of factor VIII inhibition by human antibodies. Antibodies that bind to the factor VIII light chain prevent the interaction of factor VIII with phospholipid.Two distinct forms of Factor VIII coagulant protein in human plasma. Cleavage by thrombin, and differences in coagulant activity and association with von Willebrand factor.Characterization of five partial deletions of the factor VIII gene.The molecular basis of hemophilia A.Molecular mechanisms of mild and moderate hemophilia A.Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII geneNonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides.Moderately severe hemophilia A resulting from Glu----Gly substitution in exon 7 of the factor VIII gene.Analysis of factor VIII coagulant antigen in normal, thrombin-treated, and hemophilic plasmaFactor VIII-East Hartford (arginine 1689 to cysteine) has procoagulant activity when separated from von Willebrand factor.Coexpression of factor VIII heavy and light chain adeno-associated viral vectors produces biologically active protein.Hemophilia A due to mutations that create new N-glycosylation sites.Combined functional and immunochemical analysis of normal and abnormal human factor X.Cysteamine revisited: repair of arginine to cysteine mutations.New methods in coagulation.Thrombin-catalyzed activation of factor VIII with His substituted for Arg372 at the P1 siteAssay of factor VIII antigen (VIII:CAg) in 294 haemophilia A patients by a new commercial ELISA using monoclonal antibodies.Assay discrepancy in mild haemophilia A due to a factor VIII missense mutation (Asn694Ile) in a large Danish family.
P2860
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P2860
Immunoradiometric measurement of the factor VIII procoagulant antigen.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh
1978年學術文章
@zh-hant
name
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@en
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@nl
type
label
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@en
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@nl
prefLabel
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@en
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@nl
P2860
P356
P1476
Immunoradiometric measurement of the factor VIII procoagulant antigen.
@en
P2093
Lazarchick J
P2860
P304
P356
10.1172/JCI109209
P407
P577
1978-11-01T00:00:00Z