histidine has been researched along with fibrinopeptide a in 11 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (36.36) | 18.7374 |
1990's | 4 (36.36) | 18.2507 |
2000's | 2 (18.18) | 29.6817 |
2010's | 1 (9.09) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bruhn, HD; Gram, J; Seydewitz, HH; Witt, I | 1 |
Carr, ME; Qureshi, GD | 1 |
Bell, WR; Ebert, RF; Schreiler, WE | 1 |
Beck, EA; Furlan, M; Rupp, C; Sievi, R | 1 |
Henschen, A; Kehl, M; Lane, DA; Southan, C | 1 |
Di Cera, E; Mathur, A; Schlapkohl, WA | 1 |
Kanbayashi, J; Matsuda, M; Sakon, M; Terukina, S; Tsujinaka, T; Yamazumi, K | 1 |
Beck, EA; Furlan, M; Jungo, M; Lämmle, B; Steinmann, C | 1 |
Akhavan, S; De Cristofaro, R; Landolfi, R; Lavoretano, S; Mannucci, PM; Peyvandi, F | 1 |
Nowak, P; Wachowicz, B; Zbikowska, HM | 1 |
Okumura, N; Soya, K; Takezawa, Y; Terasawa, F | 1 |
11 other study(ies) available for histidine and fibrinopeptide a
Article | Year |
---|---|
Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen.
Topics: Amino Acids; Arginine; Blood Coagulation Disorders; Chromatography, High Pressure Liquid; Coagulase; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Macromolecular Substances; Male; Middle Aged; Pedigree; Thrombin Time | 1991 |
The impact of delayed fibrinopeptide-A release on fibrin structure. Studies of an abnormal fibrinogen.
Topics: Arginine; Batroxobin; Blood Coagulation; Fibrin; Fibrinogen; Fibrinopeptide A; Histidine; Humans; Nephelometry and Turbidimetry; Osmolar Concentration; Thrombin | 1987 |
Fibrinogen Seattle II: congenital dysfibrinogenemia with an Arg (A alpha 16)----his substitution.
Topics: Afibrinogenemia; Amino Acids; Arginine; Chromatography, High Pressure Liquid; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Fibrinopeptide B; Histidine; Humans; Thrombin; Time Factors | 1986 |
[Fibrinogen Bern II: hereditary fibrinogen variant with amino acid substitution of arginine replaced by histidine in position 16 of the A alpha chain].
Topics: Afibrinogenemia; Amino Acids; Arginine; Chemical Phenomena; Chemistry; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Genetic Variation; Histidine; Humans; Male; Switzerland; Thrombin | 1983 |
Fibrinogen Manchester: identification of an abnormal fibrinopeptide A with a C-terminal arginine leads to histidine substitution.
Topics: Amino Acid Sequence; Amino Acids; Blood Coagulation Disorders; Chromatography, High Pressure Liquid; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male | 1983 |
Thrombin-fibrinogen interaction: pH dependence and effects of the slow-->fast transition.
Topics: Acylation; Amino Acid Sequence; Chromogenic Compounds; Fibrinogen; Fibrinopeptide A; Histidine; Humans; Hydrogen-Ion Concentration; Hydrolysis; Isoleucine; Kinetics; Molecular Sequence Data; Oligopeptides; Protons; Thrombin | 1993 |
Fibrinogen Osaka IV: a congenital dysfibrinogenemia found in a patient originally reported in relation to surgery, now defined to have an A alpha arginine-16 to histidine substitution.
Topics: Afibrinogenemia; Amino Acid Sequence; Ancrod; Arginine; Chromatography, High Pressure Liquid; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data | 1993 |
Fibrinogen Claro--another dysfunctional fibrinogen variant with gamma 275 arginine-->histidine substitution.
Topics: Adult; Afibrinogenemia; Arginine; Base Sequence; Blood Protein Electrophoresis; DNA Mutational Analysis; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Molecular Sequence Data; Pedigree; Point Mutation | 1996 |
Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype.
Topics: Arginine; Blood Coagulation Disorders; Cell Line; Consanguinity; Factor Va; Factor Xa; Female; Fibrinopeptide A; Hemorrhagic Disorders; Heparin Cofactor II; Histidine; Homozygote; Humans; Hydrolysis; Infant; Mutagenesis, Site-Directed; Mutation; Protein C; Prothrombin; Receptor, PAR-1; Receptors, Thrombin; Thrombin; Thrombomodulin; Thromboplastin; Transfection | 2002 |
The role of ascorbate and histidine in fibrinogen protection against changes following exposure to a sterilizing dose of gamma-irradiation.
Topics: Ascorbic Acid; Biological Products; Factor XIII; Fibrin; Fibrinogen; Fibrinopeptide A; Fibrinopeptide B; Gamma Rays; Histidine; Humans; In Vitro Techniques; Protein Carbonylation; Radiation-Protective Agents; Sterilization; Thrombin; Thrombin Time | 2007 |
[Functional analysis for dysfibrinogenemias, Toyama and Adachi, which have a mutation of Aalpha16Arg-->His (CGT-->CAT) with aberrant fibrinopeptide A release].
Topics: Adolescent; Adult; Afibrinogenemia; Arginine; Batroxobin; Catalysis; Child, Preschool; Female; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Mutation; Polymerization; Thrombin | 2012 |