cysteine and Deficiency, Protein C

cysteine has been researched along with Deficiency, Protein C in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aoki, N; Hirosawa, S; Miura, O; Sugahara, Y1
Cooper, DN; Girolami, A; Henderson, SC; Kalafatis, M; Luni, S; Millar, DS; Simioni, P1
Choi, CR; Kim, HK; Kim, HS; Park, Q; Park, YS; Song, KS1

Other Studies

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

ArticleYear
Compound heterozygous protein C deficiency caused by two mutations, Arg-178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein C.
    Thrombosis and haemostasis, 1994, Volume: 72, Issue:6

    Topics: Alleles; Arginine; Base Sequence; Cysteine; Glutamine; Heterozygote; Humans; Molecular Sequence Data; Mutation; Protein C; Protein C Deficiency; Secretory Rate; Transfection

1994
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma.
    Blood, 1996, Sep-15, Volume: 88, Issue:6

    Topics: Adult; Asparagine; Cysteine; Enzyme Activation; Factor Va; Female; Glycosylation; Heterozygote; Humans; Isoenzymes; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Thrombin; Thrombophlebitis; Twins, Monozygotic

1996
Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).
    Journal of Korean medical science, 1998, Volume: 13, Issue:2

    Topics: Adult; Cysteine; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Recurrence; Threonine; Thrombosis

1998