Compounds > histidine
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histidine and Afibrinogenemia

histidine has been researched along with Afibrinogenemia in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19904 (40.00)18.7374
1990's2 (20.00)18.2507
2000's2 (20.00)29.6817
2010's2 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brennan, SO; Chitlur, M1
Okumura, N; Soya, K; Takezawa, Y; Terasawa, F1
Brennan, SO; Fellowes, AP; George, PM; Maghzal, GJ; Spearing, R1
Dai, J; Ding, Q; Fang, Y; Qi, H; Wang, H; Wang, W; Wang, X; Wu, W; Xie, S; Zhou, R1
Beck, EA; Furlan, M; Rupp, C; Sievi, R1
Higgins, DL; Shafer, JA1
Kanbayashi, J; Matsuda, M; Sakon, M; Terukina, S; Tsujinaka, T; Yamazumi, K1
Beck, EA; Furlan, M; Jungo, M; Lämmle, B; Steinmann, C1
Alving, BM; Henschen, AH1
Bell, WR; Ebert, RF; Schreiler, WE1

Other Studies

10 other study(ies) available for histidine and Afibrinogenemia

ArticleYear
Hypodysfibrinogenaemia and thrombosis in association with a new fibrinogen γ chain with two mutations (γ114Tyr→His, and γ320Asp deleted).
    Thrombosis and haemostasis, 2013, Volume: 109, Issue:6

    Topics: Afibrinogenemia; Aspartic Acid; Binding Sites; Chromatography, High Pressure Liquid; Dimerization; Fibrinogen; Gene Deletion; Genetic Variation; Histidine; Humans; Infant; Male; Mutation; Phenotype; Sequence Analysis, DNA; Thrombosis; Tyrosine

2013
[Functional analysis for dysfibrinogenemias, Toyama and Adachi, which have a mutation of Aalpha16Arg-->His (CGT-->CAT) with aberrant fibrinopeptide A release].
    Rinsho byori. The Japanese journal of clinical pathology, 2012, Volume: 60, Issue:6

    Topics: Adolescent; Adult; Afibrinogenemia; Arginine; Batroxobin; Catalysis; Child, Preschool; Female; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Mutation; Polymerization; Thrombin

2012
Familial hypofibrinogenaemia associated with heterozygous substitution of a conserved arginine residue; Bbeta255 Arg-->His (Fibrinogen Merivale).
    Biochimica et biophysica acta, 2003, Feb-21, Volume: 1645, Issue:2

    Topics: Afibrinogenemia; Amino Acid Sequence; Arginine; Child; Electrophoresis, Polyacrylamide Gel; Fibrinogen; Fibrinogens, Abnormal; Genotype; Heterozygote; Histidine; Humans; Male; Molecular Sequence Data; Pedigree; Peptide Fragments; Point Mutation; Sequence Analysis, DNA; Spectrometry, Mass, Electrospray Ionization

2003
[Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2005, Volume: 22, Issue:2

    Topics: Adult; Afibrinogenemia; Amino Acid Substitution; Arginine; DNA Mutational Analysis; Female; Fibrinogen; Histidine; Humans; Male; Pedigree; Phenotype

2005
[Fibrinogen Bern II: hereditary fibrinogen variant with amino acid substitution of arginine replaced by histidine in position 16 of the A alpha chain].
    Schweizerische medizinische Wochenschrift, 1983, Oct-08, Volume: 113, Issue:40

    Topics: Afibrinogenemia; Amino Acids; Arginine; Chemical Phenomena; Chemistry; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Genetic Variation; Histidine; Humans; Male; Switzerland; Thrombin

1983
Fibrinogen Petoskey, a dysfibrinogenemia characterized by replacement of Arg-A alpha 16 by a histidyl residue. Evidence for thrombin-catalyzed hydrolysis at a histidyl residue.
    The Journal of biological chemistry, 1981, Dec-10, Volume: 256, Issue:23

    Topics: Afibrinogenemia; Amino Acids; Arginine; Carboxypeptidases; Fibrinogen; Fibrinogens, Abnormal; Histidine; Humans; Peptide Fragments; Thrombin

1981
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.
    Surgery today, 1993, Volume: 23, Issue:1

    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.
    Thrombosis research, 1996, Jan-01, Volume: 81, Issue:1

    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
Fibrinogen giessen I: a congenital homozygously expressed dysfibrinogenemia with A alpha 16 Arg----His substitution.
    American journal of hematology, 1987, Volume: 25, Issue:4

    Topics: Adult; Afibrinogenemia; Amino Acid Sequence; Arginine; Base Sequence; Chromatography, High Pressure Liquid; Female; Fibrinogen; Fibrinogens, Abnormal; Histidine; Homozygote; Humans

1987
Fibrinogen Seattle II: congenital dysfibrinogenemia with an Arg (A alpha 16)----his substitution.
    Thrombosis research, 1986, Jul-01, Volume: 43, Issue:1

    Topics: Afibrinogenemia; Amino Acids; Arginine; Chromatography, High Pressure Liquid; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Fibrinopeptide B; Histidine; Humans; Thrombin; Time Factors

1986