Compounds > cysteine

cysteine and Afibrinogenemia, Congenital

cysteine has been researched along with Afibrinogenemia, Congenital in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baudo, F; Bögli, C; Furlan, M; Heinemann, G; Jungo, M; Lämmle, B; Redaelli, R; Steinmann, C; Wermuth, B1
Hayashida, N; Kitano, K; Lord, ST; Okazaki, M; Okumura, N; Shimosaka, M; Terasawa, F1
Casetta, B; D'Angelo, F; Di Minno, G; Grandone, E; Margaglione, M; Papa, ML; Santacroce, R; Vecchione, G1

Other Studies

3 other study(ies) available for cysteine and Afibrinogenemia, Congenital

ArticleYear
Fibrinogen Milano V: a congenital dysfibrinogenaemia with a gamma 275 Arg-->Cys substitution.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1994, Volume: 5, Issue:4

    Topics: Afibrinogenemia; Amino Acid Sequence; Base Sequence; Blood Coagulation Tests; Cysteamine; Cysteine; Exons; Female; Fibrin; Fibrinogens, Abnormal; Humans; Middle Aged; Molecular Sequence Data; Nephelometry and Turbidimetry; Polymerase Chain Reaction; Sulfhydryl Compounds; Thrombin

1994
Hypofibrinogenemia associated with a heterozygous missense mutation gamma153Cys to arg (Matsumoto IV): in vitro expression demonstrates defective secretion of the variant fibrinogen.
    Blood, 1999, Dec-15, Volume: 94, Issue:12

    Topics: Adult; Afibrinogenemia; Animals; Arginine; Base Sequence; CHO Cells; Cricetinae; Cysteine; Female; Fibrinogen; Gene Expression; Heterozygote; Humans; Molecular Sequence Data; Mutation, Missense

1999
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Thrombosis and haemostasis, 2001, Volume: 86, Issue:6

    Topics: Afibrinogenemia; Amino Acid Sequence; Blood Coagulation Tests; Blood Protein Electrophoresis; Codon, Nonsense; Cysteine; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Exons; Fibrinogens, Abnormal; Frameshift Mutation; Heterozygote; Humans; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Protein Interaction Mapping; Protein Structure, Tertiary; Serum Albumin

2001