arginine has been researched along with Afibrinogenemia, Congenital in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (33.33) | 18.7374 |
| 1990's | 3 (25.00) | 18.2507 |
| 2000's | 4 (33.33) | 29.6817 |
| 2010's | 1 (8.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Okumura, N; Soya, K; Takezawa, Y; Terasawa, F | 1 |
| Brennan, SO; Fellowes, AP; George, PM; Maghzal, GJ; Spearing, R | 1 |
| Dai, J; Ding, Q; Fang, Y; Qi, H; Wang, H; Wang, W; Wang, X; Wu, W; Xie, S; Zhou, R | 1 |
| Malé, PJ; Neerman-Arbez, M; Rougemont, AL; Rubbia-Brandt, L; Spahr, L | 1 |
| Brennan, SO; Dear, A; Dolan, G; Hill, MB; Nejim, T; Strong, J | 1 |
| Beck, EA; Furlan, M; Rupp, C; Sievi, R | 1 |
| Higgins, DL; Shafer, JA | 1 |
| Kanbayashi, J; Matsuda, M; Sakon, M; Terukina, S; Tsujinaka, T; Yamazumi, K | 1 |
| Beck, EA; Furlan, M; Jungo, M; Lämmle, B; Steinmann, C | 1 |
| Hayashida, N; Kitano, K; Lord, ST; Okazaki, M; Okumura, N; Shimosaka, M; Terasawa, F | 1 |
| Alving, BM; Henschen, AH | 1 |
| Bell, WR; Ebert, RF; Schreiler, WE | 1 |
12 other study(ies) available for arginine and Afibrinogenemia, Congenital
| Article | Year |
|---|---|
[Functional analysis for dysfibrinogenemias, Toyama and Adachi, which have a mutation of Aalpha16Arg-->His (CGT-->CAT) with aberrant fibrinopeptide A release].
Topics: Adolescent; Adult; Afibrinogenemia; Arginine; Batroxobin; Catalysis; Child, Preschool; Female; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Mutation; Polymerization; Thrombin | 2012 |
Familial hypofibrinogenaemia associated with heterozygous substitution of a conserved arginine residue; Bbeta255 Arg-->His (Fibrinogen Merivale).
Topics: Afibrinogenemia; Amino Acid Sequence; Arginine; Child; Electrophoresis, Polyacrylamide Gel; Fibrinogen; Fibrinogens, Abnormal; Genotype; Heterozygote; Histidine; Humans; Male; Molecular Sequence Data; Pedigree; Peptide Fragments; Point Mutation; Sequence Analysis, DNA; Spectrometry, Mass, Electrospray Ionization | 2003 |
[Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
Topics: Adult; Afibrinogenemia; Amino Acid Substitution; Arginine; DNA Mutational Analysis; Female; Fibrinogen; Histidine; Humans; Male; Pedigree; Phenotype | 2005 |
Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis.
Topics: Adult; Afibrinogenemia; Amino Acid Sequence; Amino Acid Substitution; Arginine; Endoplasmic Reticulum; Family Health; Fibrinogen; Hepatocytes; Humans; Inclusion Bodies; Liver; Liver Cirrhosis; Male; Middle Aged; Molecular Sequence Data; Mutation, Missense; Point Mutation; Tryptophan | 2006 |
Fibrinogen Nottingham II: a novel Bbeta Arg264gly substitution causing hypofibrinogenaemia.
Topics: Adult; Afibrinogenemia; Arginine; Binding Sites; Calcium; Crystallography, X-Ray; Female; Fibrinogen; Humans; Models, Molecular; Mutation; Peptides; Protein Structure, Tertiary; Spectrometry, Mass, Electrospray Ionization | 2006 |
[Fibrinogen Bern II: hereditary fibrinogen variant with amino acid substitution of arginine replaced by histidine in position 16 of the A alpha chain].
Topics: Afibrinogenemia; Amino Acids; Arginine; Chemical Phenomena; Chemistry; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Genetic Variation; Histidine; Humans; Male; Switzerland; Thrombin | 1983 |
Fibrinogen Petoskey, a dysfibrinogenemia characterized by replacement of Arg-A alpha 16 by a histidyl residue. Evidence for thrombin-catalyzed hydrolysis at a histidyl residue.
Topics: Afibrinogenemia; Amino Acids; Arginine; Carboxypeptidases; Fibrinogen; Fibrinogens, Abnormal; Histidine; Humans; Peptide Fragments; Thrombin | 1981 |
Fibrinogen Osaka IV: a congenital dysfibrinogenemia found in a patient originally reported in relation to surgery, now defined to have an A alpha arginine-16 to histidine substitution.
Topics: Afibrinogenemia; Amino Acid Sequence; Ancrod; Arginine; Chromatography, High Pressure Liquid; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data | 1993 |
Fibrinogen Claro--another dysfunctional fibrinogen variant with gamma 275 arginine-->histidine substitution.
Topics: Adult; Afibrinogenemia; Arginine; Base Sequence; Blood Protein Electrophoresis; DNA Mutational Analysis; Female; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Histidine; Humans; Male; Molecular Sequence Data; Pedigree; Point Mutation | 1996 |
Hypofibrinogenemia associated with a heterozygous missense mutation gamma153Cys to arg (Matsumoto IV): in vitro expression demonstrates defective secretion of the variant fibrinogen.
Topics: Adult; Afibrinogenemia; Animals; Arginine; Base Sequence; CHO Cells; Cricetinae; Cysteine; Female; Fibrinogen; Gene Expression; Heterozygote; Humans; Molecular Sequence Data; Mutation, Missense | 1999 |
Fibrinogen giessen I: a congenital homozygously expressed dysfibrinogenemia with A alpha 16 Arg----His substitution.
Topics: Adult; Afibrinogenemia; Amino Acid Sequence; Arginine; Base Sequence; Chromatography, High Pressure Liquid; Female; Fibrinogen; Fibrinogens, Abnormal; Histidine; Homozygote; Humans | 1987 |
Fibrinogen Seattle II: congenital dysfibrinogenemia with an Arg (A alpha 16)----his substitution.
Topics: Afibrinogenemia; Amino Acids; Arginine; Chromatography, High Pressure Liquid; Fibrinogen; Fibrinogens, Abnormal; Fibrinopeptide A; Fibrinopeptide B; Histidine; Humans; Thrombin; Time Factors | 1986 |