cysteine and Deficiency, Protein S

cysteine has been researched along with Deficiency, Protein S in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chan, LC; Chan, NP; Chan, TL; Fan, YH; Lam, CW; Lam, WW; Leung, TW; Liu, HS; Siu, DY; Wong, KS; Yip, SF	1
Hamaguchi, M; Kagami, K; Katsumi, A; Kojima, T; Okamoto, Y; Saito, H; Sugiura, I; Takamatsu, J; Yamazaki, T	1

Other Studies

2 other study(ies) available for cysteine and Deficiency, Protein S

Article	Year
Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation. Neurology, 2010, Dec-14, Volume: 75, Issue:24 Topics: Adolescent; Adult; Aged; Arginine; Brain; Cerebral Infarction; Child; Cysteine; Female; Genetic Predisposition to Disease; Haplotypes; Hong Kong; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Molecular Sequence Annotation; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Protein S; Protein S Deficiency; Risk Factors; Young Adult	2010
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474. Blood, 1996, Jun-01, Volume: 87, Issue:11 Topics: Androgen-Binding Protein; Animals; Arginine; Base Sequence; Binding Sites; Cattle; Cell Line, Transformed; Chlorocebus aethiops; CHO Cells; Consanguinity; Cricetinae; Cysteine; DNA, Complementary; Female; Genetic Predisposition to Disease; Genetic Vectors; Humans; Laminin; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein S; Protein S Deficiency; Rabbits; Rats; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thrombosis	1996

Article

Year

Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation.

Neurology, 2010, Dec-14, Volume: 75, Issue:24

Topics: Adolescent; Adult; Aged; Arginine; Brain; Cerebral Infarction; Child; Cysteine; Female; Genetic Predisposition to Disease; Haplotypes; Hong Kong; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Molecular Sequence Annotation; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Protein S; Protein S Deficiency; Risk Factors; Young Adult

2010

Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.

Blood, 1996, Jun-01, Volume: 87, Issue:11

Topics: Androgen-Binding Protein; Animals; Arginine; Base Sequence; Binding Sites; Cattle; Cell Line, Transformed; Chlorocebus aethiops; CHO Cells; Consanguinity; Cricetinae; Cysteine; DNA, Complementary; Female; Genetic Predisposition to Disease; Genetic Vectors; Humans; Laminin; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein S; Protein S Deficiency; Rabbits; Rats; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thrombosis

1996