arginine has been researched along with Deficiency, Protein C in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 10 (90.91) | 18.2507 |
| 2000's | 1 (9.09) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mattson, JC; Smythe, MA; Stephens, JL; Warkentin, TE; Zakalik, D | 1 |
| Adami, A; Barbui, T; Bayston, T; Finazzi, G; Gonçalves, C; Ireland, H; Lane, DA; Thompson, E | 1 |
| Aoki, N; Hirosawa, S; Miura, O; Sugahara, Y | 1 |
| Aiach, M; Alhenc-Gelas, M; Aubry, ML; Benaily, N; Emmerich, J; Fiessinger, JN; Gandrille, S | 1 |
| Bignell, P; Cooper, DN; Grundy, CB; Kakkar, VV; Martin, R; Millar, DS; Moffat, EH | 1 |
| Alving, BM; Carrington, LR; Gillespie, DL; Griffin, JH | 1 |
| Koide, T; Tokunaga, F; Tsukamoto, T | 1 |
| Bernardi, F; Hendricx, S; Jude, B; Strecker, A; Wolschies, E | 1 |
| Johnsen, AH; Lind, B; Thorsen, S | 1 |
| Cooper, DN; Grundy, CB; Kakkar, VV; Kobosko, J; Krawczak, M; Schulman, S | 1 |
| Cooper, DN; Grundy, CB; Kakkar, VV; Schulman, S; Tengborn, L | 1 |
1 review(s) available for arginine 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 |
10 other study(ies) available for arginine and Deficiency, Protein C
| Article | Year |
|---|---|
Venous limb gangrene during overlapping therapy with warfarin and a direct thrombin inhibitor for immune heparin-induced thrombocytopenia.
Topics: Aged; Aged, 80 and over; Amputation, Surgical; Anticoagulants; Arginine; Autoimmune Diseases; Catheterization, Central Venous; Contraindications; Drug Administration Schedule; Drug Therapy, Combination; Female; Gangrene; Heparin; Hirudin Therapy; Hirudins; Humans; International Normalized Ratio; Leg; Male; Middle Aged; Necrosis; Pipecolic Acids; Protein C Deficiency; Recombinant Proteins; Sulfonamides; Surgical Wound Infection; Thrombin; Thrombocytopenia; Thrombophlebitis; Warfarin | 2002 |
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 Deficiency | 1995 |
Compound heterozygous protein C deficiency caused by two mutations, Arg-178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein C.
Topics: Alleles; Arginine; Base Sequence; Cysteine; Glutamine; Heterozygote; Humans; Molecular Sequence Data; Mutation; Protein C; Protein C Deficiency; Secretory Rate; Transfection | 1994 |
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.
Topics: 1-Carboxyglutamic Acid; Arginine; Base Sequence; Conserved Sequence; Humans; Molecular Sequence Data; Mutation; Pedigree; Protein C; Protein C Deficiency; Recurrence; Thrombosis; Tryptophan | 1993 |
Resistance to activated protein C: a common inherited cause of venous thrombosis.
Topics: Adolescent; Adult; Anticoagulants; Antithrombin III; Arginine; Contraceptives, Oral; DNA; Drug Resistance; Factor V; Female; Glutamine; Humans; Male; Middle Aged; Mutation; Obesity; Pregnancy; Protein C; Protein C Deficiency; Protein S Deficiency; Recurrence; Risk Factors; Thromboembolism; Thrombophlebitis | 1996 |
Cellular basis for protein C deficiency caused by a single amino acid substitution at Arg15 in the gamma-carboxyglutamic acid domain.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Cell Line; Cricetinae; DNA Primers; Endoplasmic Reticulum; Humans; Molecular Structure; Mutagenesis, Site-Directed; Point Mutation; Protein C; Protein C Deficiency; Recombinant Proteins; Thrombophlebitis; Transfection | 1996 |
[Pulmonary embolism disclosing activated protein C resistance].
Topics: Adult; Arginine; Codon; Factor V; Glutamine; Humans; Male; Mutation; Partial Thromboplastin Time; Protein C; Protein C Deficiency; Pulmonary Embolism | 1996 |
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 |
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Exons; Female; Genetic Carrier Screening; Humans; Male; Molecular Sequence Data; Mutation; Oligodeoxyribonucleotides; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Protein C; Protein C Deficiency; Thromboembolism | 1992 |
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis.
Topics: Arginine; Base Sequence; Exons; Female; Heterozygote; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Protein C; Protein C Deficiency; Recurrence; Thrombophlebitis | 1992 |