Compounds > histidine
Page last updated: 2024-08-17

histidine and Hemophilia A

histidine has been researched along with Hemophilia A in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's2 (28.57)18.2507
2000's2 (28.57)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fay, PJ; Nogami, K; Shima, M; Wakabayashi, H; Yada, K1
Griffiths, AB; Nath, SV; Revesz, T; Williams, VK1
Buhot, C; Burny, W; Chaux, P; Demotte, N; Jacquemin, M; Lavend'homme, R; Maillere, B; Peerlinck, K; Saint-Remy, JM; van der Bruggen, P; Vantomme, V; Vermylen, J1
Fay, PJ; Nogami, K; Wakabayashi, H; Zhou, Q1
Eickhorst, AN; Kaufman, RJ; McKinley, SH; Pipe, SW; Saenko, EL1
Antonarakis, SE; Enayat, MS; Higuchi, M; Hill, FG; Kazazian, HH; Theophilus, BD1
Antonarakis, SE; Arai, M; Fujimaki, M; Higuchi, M; Hoyer, LW; Inaba, H; Kazazian, HH1

Other Studies

7 other study(ies) available for histidine and Hemophilia A

ArticleYear
The mild phenotype in severe hemophilia A with Arg1781His mutation is associated with enhanced binding affinity of factor VIII for factor X.
    Thrombosis and haemostasis, 2013, Volume: 109, Issue:6

    Topics: Adult; Arginine; Factor VIII; Factor X; Factor Xa; Gene Expression Regulation; Genotype; Hemophilia A; Hemostasis; Histidine; Humans; Kinetics; Male; Mutagenesis; Mutation; Phenotype; Protein Binding; Recombinant Proteins; Thrombelastography; Thrombin

2013
Discrepancy in factor VIII 1-stage/2-stage activity in a child with Arg(531)--> His mutation.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2010, Volume: 21, Issue:5

    Topics: Amino Acid Substitution; Arginine; Child; Factor VIII; Hemophilia A; Histidine; Humans; Male; Mutation, Missense

2010
CD4+ T-cell clones specific for wild-type factor VIII: a molecular mechanism responsible for a higher incidence of inhibitor formation in mild/moderate hemophilia A.
    Blood, 2003, Feb-15, Volume: 101, Issue:4

    Topics: Antibodies; Antigen Presentation; Arginine; CD4-Positive T-Lymphocytes; Clone Cells; Epitope Mapping; Factor VIII; Hemophilia A; Histidine; Histocompatibility Antigens Class II; HLA-DR Antigens; HLA-DRB1 Chains; HLA-DRB4 Chains; Humans; Lymphocyte Activation; Middle Aged; Mutation; Peptide Fragments; Recombinant Proteins

2003
Thrombin-catalyzed activation of factor VIII with His substituted for Arg372 at the P1 site.
    Blood, 2005, Jun-01, Volume: 105, Issue:11

    Topics: Amino Acid Substitution; Arginine; Catalysis; Factor VIII; Factor Xa; Hemophilia A; Histidine; Humans; Hydrolysis; Kinetics; Thrombin

2005
Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation: evidence for nonproteolytic inactivation of factor VIIIa in vivo.
    Blood, 1999, Jan-01, Volume: 93, Issue:1

    Topics: Amino Acid Substitution; Animals; Arginine; COS Cells; Factor VIIIa; Hemophilia A; Histidine; Humans; Hydrolysis; Mutagenesis, Site-Directed; Peptide Hydrolases; Phenotype; Protein Binding; Recombinant Proteins; Thrombin

1999
Independent occurrence of the novel Arg2163 to His mutation in the factor VIII gene in three unrelated families with haemophila A with different phenotypes. Mutations in brief no. 126. Online.
    Human mutation, 1998, Volume: 11, Issue:4

    Topics: Amino Acid Substitution; Arginine; Factor VIII; Hemophilia A; Histidine; Humans; Mutation; Phenotype

1998
Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).
    Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:11

    Topics: Arginine; Base Sequence; Factor VIII; Genes; Hemophilia A; Histidine; Humans; Immunoblotting; Molecular Sequence Data; Mutation; Thrombin

1989