Compounds > 1-carboxyglutamic acid
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1-carboxyglutamic acid and Deficiency, Protein C

1-carboxyglutamic acid has been researched along with Deficiency, Protein C in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hatada, T; Hayashi, T; Ido, M; Nishioka, J; Ohiwa, M; Shirakawa, S; Suzuki, K; Wada, H; Watanabe, Y1
Bignell, P; Cooper, DN; Grundy, CB; Kakkar, VV; Martin, R; Millar, DS; Moffat, EH1

Other Studies

2 other study(ies) available for 1-carboxyglutamic acid and Deficiency, Protein C

ArticleYear
A compound heterozygous protein C deficiency with a single nucleotide G deletion encoding Gly-381 and an amino acid substitution of Lys for Gla-26.
    Thrombosis and haemostasis, 1993, Oct-18, Volume: 70, Issue:4

    Topics: 1-Carboxyglutamic Acid; Antigens; Base Sequence; Exons; Fathers; Genetic Code; Glycine; Guanine; Heterozygote; Humans; Infant, Newborn; Lysine; Male; Molecular Sequence Data; Mutation; Pedigree; Protein C; Protein C Deficiency; Reference Values

1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1993, Volume: 4, Issue:2

    Topics: 1-Carboxyglutamic Acid; Arginine; Base Sequence; Conserved Sequence; Humans; Molecular Sequence Data; Mutation; Pedigree; Protein C; Protein C Deficiency; Recurrence; Thrombosis; Tryptophan

1993