histidine has been researched along with Deficiency, Protein C in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (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 |
---|---|
Aiach, M; Alhenc-Gelas, M; Aubry, ML; Benaily, N; Emmerich, J; Fiessinger, JN; Gandrille, S | 1 |
Johnsen, AH; Lind, B; Thorsen, S | 1 |
Aiach, M; Akar, N; Alhenc-Gelas, M; Cin, S; Gandrille, S; Kemahli, S | 1 |
Zheng, Y; Zhou, B; Zhu, D | 1 |
1 review(s) available for histidine 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, Low-Molecular-Weight; Heterozygote; Histidine; Humans; Middle Aged; Pedigree; Protein C; Protein C Deficiency; Thrombophlebitis | 1995 |
3 other study(ies) available for histidine and Deficiency, Protein C
Article | Year |
---|---|
Naturally occurring Arg(-1) to His mutation in human protein C leads to aberrant propeptide processing and secretion of dysfunctional protein C.
Topics: Amino Acid Sequence; Antimicrobial Cationic Peptides; Arginine; Disease Susceptibility; Histidine; Humans; Male; Middle Aged; Peptides; Point Mutation; Protein C; Protein C Deficiency; Protein Precursors; Protein Processing, Post-Translational; Thromboembolism | 1997 |
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
Topics: Alanine; Amino Acid Substitution; Base Sequence; Consanguinity; Genetic Variation; Histidine; Homozygote; Humans; Infant, Newborn; Male; Mutation; Pedigree; Protein C; Protein C Deficiency; Threonine; Tyrosine | 1998 |
[Type I protein C deficiency caused by a novel protein C gene mutation].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antithrombin III; Aspartic Acid; Histidine; Humans; Middle Aged; Pedigree; Point Mutation; Protein C; Protein C Deficiency | 1998 |