cysteine has been researched along with Deficiency, Protein C in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aoki, N; Hirosawa, S; Miura, O; Sugahara, Y | 1 |
Cooper, DN; Girolami, A; Henderson, SC; Kalafatis, M; Luni, S; Millar, DS; Simioni, P | 1 |
Choi, CR; Kim, HK; Kim, HS; Park, Q; Park, YS; Song, KS | 1 |
3 other study(ies) available for cysteine and Deficiency, Protein C
Article | Year |
---|---|
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.
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.
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).
Topics: Adult; Cysteine; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Recurrence; Threonine; Thrombosis | 1998 |