Page last updated: 2024-08-17

histidine and Deficiency, Protein C

histidine has been researched along with Deficiency, Protein C in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aiach, M; Alhenc-Gelas, M; Aubry, ML; Benaily, N; Emmerich, J; Fiessinger, JN; Gandrille, S1
Johnsen, AH; Lind, B; Thorsen, S1
Aiach, M; Akar, N; Alhenc-Gelas, M; Cin, S; Gandrille, S; Kemahli, S1
Zheng, Y; Zhou, B; Zhu, D1

Reviews

1 review(s) available for histidine and Deficiency, Protein C

ArticleYear
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1995, Volume: 6, Issue:1

    Topics: Arginine; Codon; DNA Mutational Analysis; Drug Therapy, Combination; Female; Genes; Glycine; Heparin, Low-Molecular-Weight; Heterozygote; Histidine; Humans; Middle Aged; Pedigree; Protein C; Protein C Deficiency; Thrombophlebitis

1995

Other Studies

3 other study(ies) available for histidine and Deficiency, Protein C

ArticleYear
Naturally occurring Arg(-1) to His mutation in human protein C leads to aberrant propeptide processing and secretion of dysfunctional protein C.
    Blood, 1997, Apr-15, Volume: 89, Issue:8

    Topics: Amino Acid Sequence; Antimicrobial Cationic Peptides; Arginine; Disease Susceptibility; Histidine; Humans; Male; Middle Aged; Peptides; Point Mutation; Protein C; Protein C Deficiency; Protein Precursors; Protein Processing, Post-Translational; Thromboembolism

1997
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1998, Volume: 9, Issue:4

    Topics: Alanine; Amino Acid Substitution; Base Sequence; Consanguinity; Genetic Variation; Histidine; Homozygote; Humans; Infant, Newborn; Male; Mutation; Pedigree; Protein C; Protein C Deficiency; Threonine; Tyrosine

1998
[Type I protein C deficiency caused by a novel protein C gene mutation].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 1998, Volume: 19, Issue:3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antithrombin III; Aspartic Acid; Histidine; Humans; Middle Aged; Pedigree; Point Mutation; Protein C; Protein C Deficiency

1998