arginine has been researched along with Amyloidosis in 16 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (6.25) | 18.7374 |
| 1990's | 8 (50.00) | 18.2507 |
| 2000's | 5 (31.25) | 29.6817 |
| 2010's | 1 (6.25) | 24.3611 |
| 2020's | 1 (6.25) | 2.80 |
| Authors | Studies |
|---|---|
| Annibal, A; Antebi, A; Braumann, M; Göbel, H; Kubacki, T; Laasch, V; Laboy, R; Müller, RU; Späth, MR; Steiner, JD | 1 |
| Amero, C; Gil-Rodriguez, P; Maya-Martinez, R | 1 |
| Furuya, R; Hishida, A; Kumagai, H; Sano, K; Takahashi, M | 1 |
| Arici, M; Bakkaloglu, A; Berdeli, A; Besbas, N; Kutlay, S; Ozen, S; Türel, B; Yalcinkaya, F; Yilmaz, E | 1 |
| Axelsson, J; Caglar, K; Cakir, E; Carrero, JJ; Eyileten, T; Lindholm, B; Oguz, Y; Qureshi, AR; Saglam, M; Sonmez, A; Stenvinkel, P; Vural, A; Yenicesu, M; Yilmaz, MI | 1 |
| Ando, M; Ando, Y; Gotoh, T; Sakashita, N; Tanaka, Y; Tashima, K; Uchino, M; Yamashita, T; Yonehara, T | 1 |
| Benson, MD; Correa, R; Liepnieks, J; Uemichi, T; Wheeler, G | 1 |
| Argilés, A; Friedlander, MA; Gouin-Charnet, A; Mourad, G; Wu, YC | 1 |
| Billerey, C; Chevet, D; Delpech, M; Droz, D; Fournier, V; Grateau, G; Hamidi Asl, L; Justrabo, E; Pécheux, C | 1 |
| Biadi, O; Conigli, P; D'Alessandro, M; Ferlini, A; Manzati, E; Mazzaferro, V; Merlini, G; Obici, L; Salvi, F; Tarantino, E; Tassinari, CA | 1 |
| Fujiki, K; Hirano, K; Hotta, Y; Kanai, A; Nakamura, M; Yamamoto, N | 1 |
| Fujimura, H; Takahashi, N; Tarui, S; Uemichi, T; Ueno, S; Yorifuji, S | 1 |
| Booth, SE; Feest, TG; Hawkins, PN; Hsuan, JJ; Hutton, T; Nguyen, O; Soutar, AK; Tennent, GA; Totty, NF; Vigushin, DM | 1 |
| Benson, MD; Brewer, HB; Gregg, RE; Meng, MS; Rader, DJ; Schaefer, JR; Zech, LA | 1 |
| Almeida, MR; Altland, K; Costa, PP; Gawinowicz, M; Moreira, P; Rauh, S; Saraiva, MJ | 1 |
| Garner, A | 1 |
16 other study(ies) available for arginine and Amyloidosis
| Article | Year |
|---|---|
A novel TNFRSF1A mutation associated with TNF-receptor-associated periodic syndrome and its metabolic signature.
Topics: Amyloidosis; Arginine; Cysteine; Familial Mediterranean Fever; Humans; Methionine; Mutation; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Tryptophan | 2023 |
Solution structure of 6aJL2 and 6aJL2-R24G amyloidogenics light chain proteins.
Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Arginine; Entropy; Glycine; Humans; Immunoglobulin lambda-Chains; Molecular Sequence Data; Point Mutation; Protein Folding; Protein Structure, Secondary; Solutions | 2015 |
Ultrapure dialysate reduces plasma levels of beta2-microglobulin and pentosidine in hemodialysis patients.
Topics: Aged; Amyloidosis; Arginine; beta 2-Microglobulin; C-Reactive Protein; Endotoxins; Female; Hemodialysis Solutions; Humans; Interleukin-6; Kidney Failure, Chronic; Lysine; Male; Middle Aged; Renal Dialysis | 2005 |
Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease.
Topics: Amyloidosis; Arginine; Environment; Familial Mediterranean Fever; Genetic Predisposition to Disease; Glutamine; Humans; Phenotype; Point Mutation; Polymorphism, Restriction Fragment Length; Toll-Like Receptor 2 | 2006 |
ADMA levels correlate with proteinuria, secondary amyloidosis, and endothelial dysfunction.
Topics: Adult; Amyloidosis; Arginine; Chronic Disease; Endothelium; Female; Glomerulonephritis; Humans; Male; Multivariate Analysis; Predictive Value of Tests; Proteinuria; Risk Factors | 2008 |
Role of nitric oxide in the peripheral vessels of patients with familial amyloidotic polyneuropathy (FAP) type I.
Topics: Adult; Amyloidosis; Arginine; Blood Vessels; Body Temperature; Female; Humans; Leg; Male; Middle Aged; Muscles; Nitrates; Nitric Oxide; Nitrites; omega-N-Methylarginine; Peripheral Nervous System Diseases; Regional Blood Flow | 1994 |
Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.
Topics: Adult; Amino Acid Sequence; Amyloidosis; Arginine; Base Sequence; DNA; Exons; Female; Fibrinogen; Genetic Variation; Humans; Kidney Diseases; Leucine; Macromolecular Substances; Male; Middle Aged; Molecular Sequence Data; Oligodeoxyribonucleotides; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length | 1993 |
Elevated pentosidine content in amyloid deposits and in insoluble amyloid fibrils from patients with beta 2-microglobulin amyloidosis.
Topics: Amyloidosis; Arginine; beta 2-Microglobulin; Humans; Lysine | 1996 |
Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family.
Topics: Adult; Aged; Amino Acid Substitution; Amyloidosis; Arginine; Base Sequence; DNA; Female; Fibrinogens, Abnormal; Humans; Immunohistochemistry; Kidney Diseases; Leucine; Male; Middle Aged; Mutation; Pedigree; Polymorphism, Restriction Fragment Length | 1998 |
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47.
Topics: Adolescent; Adult; Amyloidosis; Arginine; Codon; DNA Mutational Analysis; DNA Primers; Exons; Female; Humans; Italy; Male; Middle Aged; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Prealbumin; RNA, Messenger; Sequence Analysis, DNA; Transcription, Genetic | 2000 |
Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.
Topics: Aged; Aged, 80 and over; Amyloidosis; Arginine; Codon; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Extracellular Matrix Proteins; Humans; Leucine; Male; Neoplasm Proteins; Point Mutation; Polymerase Chain Reaction; Transforming Growth Factor beta | 2001 |
Amyloid polyneuropathy with transthyretin Arg50 in a Japanese case from Osaka.
Topics: Adult; Amyloidosis; Arginine; Chromatography, High Pressure Liquid; Humans; Immunohistochemistry; Male; Mutation; Pedigree; Peripheral Nervous System Diseases; Prealbumin; Sciatic Nerve | 1992 |
Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.
Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Apolipoprotein A-I; Arginine; Base Sequence; DNA; Female; Genes, Dominant; Humans; Macromolecular Substances; Male; Molecular Sequence Data; Mutation; Pedigree | 1992 |
In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosis.
Topics: Adult; Amyloidosis; Apolipoprotein A-I; Arginine; Electrophoresis, Gel, Two-Dimensional; Female; Glycine; Humans; Hypolipoproteinemias; Immunoblotting; Lipoproteins, HDL; Male; Mutation | 1992 |
Characterization of a basic transthyretin variant--TTR Arg 102--in the German population.
Topics: Amyloidosis; Arginine; Base Sequence; Exons; Female; Genetic Testing; Genetic Variation; Germany; Humans; Molecular Sequence Data; Mutation; Peptide Mapping; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Prealbumin; Pregnancy; Proline | 1991 |
Hereditary amyloidosis of the cornea.
Topics: Amyloid; Amyloidosis; Arginine; Cornea; Corneal Dystrophies, Hereditary; Humans; Sulfur; Tyrosine | 1970 |