tyrosine has been researched along with Amyloidosis in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (61.90) | 18.7374 |
| 1990's | 3 (14.29) | 18.2507 |
| 2000's | 2 (9.52) | 29.6817 |
| 2010's | 3 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Austin, GL; Butterfield, DA; Cuello, AC; Do Carmo, S; Foret, MK; Hall, H; Iulita, MF; Jia, DT; Malcolm, JC; Marks, AR; Wilson, EN | 1 |
| Adams, CM; Greicius, MD; Okumu, AN; Plowey, ED; Zhu, W; Ziskin, JL | 1 |
| Delekarte, A; Hammerschmidt, T; Heneka, MT; Hermes, M; Jessen, F; Klockgether, T; König, S; Korte, M; Kumar, S; Kummer, MP; Pape, HC; Roeber, S; Terwel, D; Walter, J | 1 |
| Benson, MD; Dupond, JL; Gil, H; Kantelip, B; Kluve-Beckerman, B; Liepnieks, JJ; Magy, N | 1 |
| Hayashi, A; Higa, S; Nakajima, A; Sakoda, S; Suzuki, T; Takaba, Y; Yamamura, Y | 1 |
| Groth, CG; Ringdén, O | 1 |
| Rewitzer, H; Stotz, R; Wegmann, W | 1 |
| François, J | 1 |
| Barone, V; Ceccherini, I; Loviselli, A; Martino, E; Pacini, F; Pinchera, A; Romei, C; Romeo, G | 1 |
| Berenguer, J; Berenguer, M; García-Herola, A; López-Viedma, B; Mir, J; Pascual, S; Prieto, M; Vilchez, JJ | 1 |
| Miranker, AD; Padrick, SB | 1 |
| Tarui, S; Uemichi, T; Ueno, S; Yorifuji, S | 1 |
| Benson, MD; Wallace, MR | 1 |
| Beneke, G; Rakow, AD; Rakow, L; Schmitt, W | 1 |
| Anderson, TJ; Ewen, SW | 1 |
| Ewen, SW; Pearse, AG; Polak, JM | 1 |
| Mantz, JM; Metais, P; Oberling, F; Storck, D; Warter, J | 1 |
| Franklin, EC; Rosenthal, CJ | 1 |
| Mantz, JM; Mètais, P; Warter, J | 1 |
| Clerici, E | 1 |
| Garner, A | 1 |
2 review(s) available for tyrosine and Amyloidosis
| Article | Year |
|---|---|
Transplantation in relation to the treatment of inherited disease.
Topics: alpha 1-Antitrypsin Deficiency; Amyloidosis; Bone Marrow Transplantation; Fabry Disease; Gaucher Disease; Genetic Diseases, Inborn; Gout; Granulomatous Disease, Chronic; Hemoglobinopathies; Hemophilia A; Hepatolenticular Degeneration; Humans; Immunologic Deficiency Syndromes; Kidney Transplantation; Leukodystrophy, Metachromatic; Liver Transplantation; Lymphocytes; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nephritis, Hereditary; Niemann-Pick Diseases; Osteopetrosis; Oxalates; Oxalic Acid; Transplantation; Tyrosine; Uremia | 1984 |
Genetic amyloidosis: recent advances.
Topics: Alanine; Amyloidosis; DNA Mutational Analysis; Humans; Methionine; Polymorphism, Restriction Fragment Length; Prealbumin; Serine; Tyrosine | 1989 |
19 other study(ies) available for tyrosine and Amyloidosis
| Article | Year |
|---|---|
Microdose Lithium NP03 Diminishes Pre-Plaque Oxidative Damage and Neuroinflammation in a Rat Model of Alzheimer's-like Amyloidosis.
Topics: Aldehydes; Alzheimer Disease; Amyloid beta-Protein Precursor; Amyloidosis; Animals; CA1 Region, Hippocampal; Cytokines; Disease Models, Animal; Encephalitis; Humans; Lithium; Mice, Transgenic; Mutation; Plaque, Amyloid; Rats; Tyrosine | 2018 |
Neuropathologic analysis of Tyr69His TTR variant meningovascular amyloidosis with dementia.
Topics: Aged; Amyloidosis; Dementia; DNA Mutational Analysis; Histidine; Humans; Male; Prealbumin; Tyrosine | 2015 |
Nitration of tyrosine 10 critically enhances amyloid β aggregation and plaque formation.
Topics: Age Factors; Alzheimer Disease; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Amyloidosis; Animals; Biophysics; Brain; Disease Models, Animal; Drug Combinations; Electric Stimulation; Enzyme-Linked Immunosorbent Assay; Gene Expression Regulation; Hippocampus; Humans; Immunoprecipitation; In Vitro Techniques; Long-Term Potentiation; Maze Learning; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurons; Nitric Oxide Synthase Type II; Patch-Clamp Techniques; Peptide Fragments; Peroxynitrous Acid; Plaque, Amyloid; Presenilin-1; Tyrosine | 2011 |
A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
Topics: Aged; Amyloidosis; Base Sequence; Carpal Tunnel Syndrome; Humans; Male; Pedigree; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Polymorphism, Single-Stranded Conformational; Prealbumin; Skin; Tyrosine | 2003 |
Orthostatic hypotension in familial amyloid polyneuropathy: treatment with DL-threo-3,4-dihydroxyphenylserine.
Topics: Adult; Amyloidosis; Blood Pressure; Droxidopa; Female; Humans; Hypotension, Orthostatic; Male; Middle Aged; Norepinephrine; Peripheral Nervous System Diseases; Serine; Tyrosine | 1981 |
[Intestinal pseudo-obstruction in primary amyloidosis of the intestinal tract].
Topics: Aged; Amyloid; Amyloidosis; Colectomy; Colon; Colonic Diseases; Humans; Intestinal Obstruction; Male; Tryptophan; Tyrosine | 1984 |
Metabolic disorders and corneal changes.
Topics: Amino Acid Metabolism, Inborn Errors; Amyloidosis; Cornea; Corneal Dystrophies, Hereditary; Dysautonomia, Familial; Fabry Disease; Glycogen Storage Disease; Humans; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidoses; Tyrosine | 1981 |
Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis.
Topics: Amyloidosis; Base Sequence; Cysteine; Exons; Genetic Carrier Screening; Humans; Lichen Planus; Molecular Sequence Data; Multiple Endocrine Neoplasia; Mutation; Pedigree; Polymerase Chain Reaction; Proto-Oncogene Mas; Proto-Oncogenes; Tyrosine | 1994 |
Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant.
Topics: Amyloid Neuropathies; Amyloidosis; Cardiomyopathies; Disease Progression; Humans; Liver Transplantation; Male; Middle Aged; Mutation; Prealbumin; Tyrosine | 1999 |
Islet amyloid polypeptide: identification of long-range contacts and local order on the fibrillogenesis pathway.
Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Animals; Diabetes Mellitus, Type 2; Energy Transfer; Fluorescence Polarization; Fluorescent Dyes; Humans; Hydrogen-Ion Concentration; Islet Amyloid Polypeptide; Kinetics; Light; Molecular Sequence Data; Osmolar Concentration; Protein Denaturation; Protein Structure, Quaternary; Rats; Rotation; Scattering, Radiation; Sequence Alignment; Solvents; Static Electricity; Titrimetry; Tyrosine | 2001 |
A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases.
Topics: Adult; Amyloidosis; Base Sequence; Cysteine; DNA; Exons; Humans; Male; Molecular Sequence Data; Mutation; Peripheral Nervous System Diseases; Polymerase Chain Reaction; Prealbumin; Tyrosine | 1990 |
[Demonstration of fibrin and amyloid using morphological methods in tissue sections].
Topics: Amyloid; Amyloidosis; Biopsy; Fibrin; Fluorescent Antibody Technique; Histocytochemistry; Humans; Intestinal Mucosa; Microscopy, Electron; Rectum; Staining and Labeling; Tryptophan; Tyrosine | 1970 |
Amyloid in normal and pathological parathyroid glands.
Topics: Aging; Amyloid; Amyloidosis; Autopsy; Histocytochemistry; Humans; Parathyroid Glands; Staining and Labeling; Thyroidectomy; Tryptophan; Tyrosine | 1974 |
The genesis of apudamyloid in endocrine polypeptide tumours: histochemical distinction from immunamyloid.
Topics: Adenocarcinoma, Scirrhous; Adenoma, Islet Cell; Adrenal Gland Neoplasms; Amyloidosis; Arthritis, Rheumatoid; Carcinoma; Endocrine System Diseases; Histocytochemistry; Humans; Microscopy, Electron; Neoplasm Proteins; Neoplasms; Pancreatic Neoplasms; Pheochromocytoma; Thyroid Neoplasms; Tryptophan Oxygenase; Tyrosine | 1972 |
[Greenish blue man. Primary amyloidosis. Tyrosinuria].
Topics: Amino Acid Metabolism, Inborn Errors; Amyloidosis; Ascorbic Acid Deficiency; Autopsy; Digestive System; Humans; Malabsorption Syndromes; Male; Microscopy, Fluorescence; Middle Aged; Muscles; Myocardium; Phenylpyruvic Acids; Pigmentation Disorders; Syndrome; Tyrosine | 1972 |
Age-associated changes of an amyloid related serum component.
Topics: Acute Disease; Adolescent; Adult; Aged; Aging; Amyloid; Amyloidosis; Arteriosclerosis; Child; Child, Preschool; Chromatography, Gel; Chronic Disease; Diabetes Mellitus; Female; Follow-Up Studies; Humans; Infant; Infant, Newborn; Iodine Radioisotopes; Middle Aged; Osteoarthritis; Pregnancy; Radioimmunoassay; Tyrosine | 1974 |
[Primary amyloidosis, tyrosinuria and blue-green pigmentation].
Topics: Amyloidosis; Ascorbic Acid Deficiency; Humans; Male; Metabolic Diseases; Middle Aged; Pigmentation Disorders; Tyrosine | 1972 |
Induction of amyloidosis in mice upon treatment with polypeptidyl-caseins and DNP-casein. Relation to antigenicity.
Topics: Alanine; Amyloidosis; Animals; Antigens; Caseins; Female; Hemagglutination Tests; Male; Mice; Nitrobenzenes; Peptides; Tyrosine | 1972 |
Hereditary amyloidosis of the cornea.
Topics: Amyloid; Amyloidosis; Arginine; Cornea; Corneal Dystrophies, Hereditary; Humans; Sulfur; Tyrosine | 1970 |