Page last updated: 2024-10-18

glycine and Deficiency, Protein C

glycine 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
Ireland, H1
Bayston, T1
Thompson, E1
Adami, A1
Gonçalves, C1
Lane, DA1
Finazzi, G1
Barbui, T1
Alhenc-Gelas, M1
Emmerich, J1
Gandrille, S1
Aubry, ML1
Benaily, N1
Fiessinger, JN1
Aiach, M1
Ido, M1
Ohiwa, M1
Hayashi, T1
Nishioka, J1
Hatada, T1
Watanabe, Y1
Wada, H1
Shirakawa, S1
Suzuki, K1

Reviews

1 review available for glycine and Deficiency, Protein C

ArticleYear
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1995, Volume: 6, Issue:1

    Topics: Arginine; Codon; DNA Mutational Analysis; Drug Therapy, Combination; Female; Genes; Glycine; Heparin

1995

Other Studies

2 other studies available for glycine and Deficiency, Protein C

ArticleYear
Apparent heterozygous type II protein C deficiency caused by the factor V 506 Arg to Gln mutation.
    Thrombosis and haemostasis, 1995, Volume: 73, Issue:4

    Topics: Arginine; Factor V; Family; Female; Glycine; Heterozygote; Humans; Male; Point Mutation; Protein C D

1995
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; Het

1993