glycine 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 |
---|---|
Ireland, H | 1 |
Bayston, T | 1 |
Thompson, E | 1 |
Adami, A | 1 |
Gonçalves, C | 1 |
Lane, DA | 1 |
Finazzi, G | 1 |
Barbui, T | 1 |
Alhenc-Gelas, M | 1 |
Emmerich, J | 1 |
Gandrille, S | 1 |
Aubry, ML | 1 |
Benaily, N | 1 |
Fiessinger, JN | 1 |
Aiach, M | 1 |
Ido, M | 1 |
Ohiwa, M | 1 |
Hayashi, T | 1 |
Nishioka, J | 1 |
Hatada, T | 1 |
Watanabe, Y | 1 |
Wada, H | 1 |
Shirakawa, S | 1 |
Suzuki, K | 1 |
1 review available for glycine and Deficiency, Protein C
Article | Year |
---|---|
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.
Topics: Arginine; Codon; DNA Mutational Analysis; Drug Therapy, Combination; Female; Genes; Glycine; Heparin | 1995 |
2 other studies available for glycine and Deficiency, Protein C
Article | Year |
---|---|
Apparent heterozygous type II protein C deficiency caused by the factor V 506 Arg to Gln mutation.
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.
Topics: 1-Carboxyglutamic Acid; Antigens; Base Sequence; Exons; Fathers; Genetic Code; Glycine; Guanine; Het | 1993 |