methionine has been researched along with Amyloidosis in 43 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 17 (39.53) | 18.7374 |
| 1990's | 18 (41.86) | 18.2507 |
| 2000's | 5 (11.63) | 29.6817 |
| 2010's | 1 (2.33) | 24.3611 |
| 2020's | 2 (4.65) | 2.80 |
| Authors | Studies |
|---|---|
| Bolakhrif, N; Gohlke, H; Gremer, L; Kaiser, J; Nagel-Steger, L; Pauly, T; Willbold, D | 1 |
| Annibal, A; Antebi, A; Braumann, M; Göbel, H; Kubacki, T; Laasch, V; Laboy, R; Müller, RU; Späth, MR; Steiner, JD | 1 |
| Ericzon, BG; Nowak, G; Suhr, OB; Westermark, P | 1 |
| Akaike, T; Ando, Y; Ishima, Y; Kim, J; Nakamura, M; Otagiri, M; Saito, S; Ueda, M | 1 |
| Adamski-Werner, SL; Buxbaum, JN; Kelly, JW; Koziol, J; Reixach, N | 1 |
| Furukawa, Y; Ishida, C; Kato-Motozaki, Y; Machiya, T; Morinaga, A; Nozaki, I; Ono, K; Sakajiri, K; Shibata-Hamaguchi, A; Shima, K; Yamada, M; Yanase, D | 1 |
| But, TS | 1 |
| Bell, J; de Silva, R; Dempster, M; Esmonde, T; Estibeiro, P; Ironside, JW; Lathe, R; McCardle, L; Will, R; Windl, O | 1 |
| Haettner, E; Holmgren, G; Lundgren, E; Sandgren, O; Thylén, C; Wahlqvist, J | 1 |
| Almeida, MR; Altland, K; Alves, IL; Coelho, T; Costa, PP; Divino, CM; Palha, JA; Saraiva, MJ; Schussler, GC | 1 |
| Bonifácio, MJ; Breakfield, XO; Ezzeddine, D; Sakaki, Y; Saraiva, MJ | 1 |
| Alves, IL; Blake, CC; Costa, PP; Damas, AM; Matias, PM; Oliveira, P; Sakaki, Y; Saraiva, MJ; Terry, CJ | 1 |
| el-Gewely, MR; Husby, G; Nordvåg, BY; Ranløv, I; Riise, HM | 1 |
| Adams, D; Delpech, M; Grateau, G; Malapert, D; Said, G; Viemont, M | 1 |
| Nordvåg, BY; Steensgaard-Hansen, F; Svendsen, IH | 2 |
| Connors, L; Costello, CE; Skare, J; Skinner, M; Théberge, R | 1 |
| Chen, X; Dagan, T; Danon, Y; Fischel-Ghodsian, N; Halpern, GJ; Kastner, D; Lotan, R; Magal, N; Mimouni, A; Ogur, G; Rotter, JI; Schlezinger, M; Schwabe, A; Shohat, M; Shohat, T; Sirin, A | 1 |
| Baba, T; Date, Y; Goto, Y; Nakamura, Y; Nakazato, M; Yutani, C | 1 |
| Fast, J; Håkansson, M; Linse, S; Svensson, A | 1 |
| Altland, K; Buttmann, M; Marziniak, M; Sommer, C; Toyka, KV | 1 |
| Gottfries, CG; Regland, B | 1 |
| el-Gewely, MR; Husby, G; Nordvåg, BY; Ranløv, I | 1 |
| Benson, MD | 1 |
| Alves, IL; Costa, PP; Husby, G; Ranløv, I; Ranløv, PJ; Saraiva, MJ | 1 |
| Husby, G; Kolset, SO; Magnus, JH; Stenstad, T | 1 |
| Cohen, A; Dede, H; Erken, E; Milunsky, A; Skare, J; Skinner, M; Yazici, H | 1 |
| Alves, IL; Costa, PP; Saraiva, MJ | 1 |
| Benson, MD; Wallace, MR | 1 |
| Cohen, AS; Connors, LH; Gertz, MA; Kyle, RA; Skinner, M | 1 |
| Benson, MD; Dwulet, FE | 1 |
| Goodman, DS; Saraiva, MJ; Sherman, W | 1 |
| Costa, PP; Munar-Bernat, C; Munar-Qués, M; Saraiva, MJ; Viader-Farré, C | 1 |
| Haettner, E; Holmgren, G; Lundgren, E; Nordenson, I; Sandgren, O; Steen, L | 1 |
| Costa, PP; Goodman, DS; Saraiva, MJ | 1 |
| Benson, MD; Dwulet, FE; Greipp, P; Scheinberg, MA | 1 |
| Agnew, JE; Bouchier, IA; Melmed, RN | 1 |
| Cylwik, B; Duda, D; Nowak, HF | 2 |
| Korneeva, TS; Tareev, EM | 1 |
| Kornejewa, TS | 1 |
| Bladen, HA; Cuatrecasas, P; DeLellis, RA; Eanes, ED; Glenner, GG; Kanfer, JN; Keiser, HR; Ram, JS | 1 |
| Kennedy, JS | 1 |
2 review(s) available for methionine and Amyloidosis
| Article | Year |
|---|---|
[Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. A clinical, genetic and echocardiographic study of an affected Danish family].
Topics: Adolescent; Amyloidosis; Cardiomyopathies; Child; Denmark; Echocardiography, Doppler; Female; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Prealbumin | 1999 |
Genetic amyloidosis: recent advances.
Topics: Alanine; Amyloidosis; DNA Mutational Analysis; Humans; Methionine; Polymorphism, Restriction Fragment Length; Prealbumin; Serine; Tyrosine | 1989 |
1 trial(s) available for methionine and Amyloidosis
| Article | Year |
|---|---|
Characterization of transthyretin mutants from serum using immunoprecipitation, HPLC/electrospray ionization and matrix-assisted laser desorption/ionization mass spectrometry.
Topics: Amino Acid Sequence; Amyloidosis; Chromatography, High Pressure Liquid; Humans; Mass Spectrometry; Methionine; Molecular Sequence Data; Mutation; Prealbumin; Precipitin Tests; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Valine | 1999 |
40 other study(ies) available for methionine and Amyloidosis
| Article | Year |
|---|---|
Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation.
Topics: Amyloid; Amyloidosis; Creutzfeldt-Jakob Syndrome; Humans; Insomnia, Fatal Familial; Methionine; Polymorphism, Genetic; Prion Proteins; Protein Folding; Valine | 2022 |
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 |
Domino liver transplantation: full-length transthyretin in donor and recipient patients with ATTR Val30Met amyloidosis.
Topics: Adult; Aged; Amyloid Neuropathies; Amyloid Neuropathies, Familial; Amyloidosis; Female; Humans; Liver Transplantation; Male; Methionine; Middle Aged; Valine | 2017 |
Effect of nitric oxide in amyloid fibril formation on transthyretin-related amyloidosis.
Topics: Amino Acid Substitution; Amyloid; Amyloidosis; Endothelial Cells; Humans; Methionine; Myocytes, Smooth Muscle; Nitric Oxide; Oxidation-Reduction; Point Mutation; Prealbumin; Protein Structure, Quaternary; Protein Structure, Tertiary; Valine | 2005 |
Cell based screening of inhibitors of transthyretin aggregation.
Topics: Amyloidosis; Anti-Inflammatory Agents, Non-Steroidal; Cell Line, Tumor; Cell Lineage; Cell Survival; Diflunisal; Drug Evaluation, Preclinical; Humans; Methionine; Microfibrils; Neurons; Prealbumin; Resveratrol; Stilbenes; Valine | 2006 |
Epidemiology of familial amyloid polyneuropathy in Japan: Identification of a novel endemic focus.
Topics: Adult; Age of Onset; Aged; Amyloid Neuropathies, Familial; Amyloidosis; Female; Humans; Japan; Male; Methionine; Middle Aged; Molecular Epidemiology; Mutation; Prealbumin; Registries; Retrospective Studies; Valine | 2008 |
[Role of thiols in amyloidogenesis].
Topics: Amyloid; Amyloidosis; Animals; Cysteine; Free Radicals; Humans; In Vitro Techniques; Methionine; Mice; Protein Binding; Sulfhydryl Compounds; Unithiol | 1980 |
Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease.
Topics: Aged; Aged, 80 and over; Amyloid; Amyloidosis; Creutzfeldt-Jakob Syndrome; DNA; Genotype; Humans; Methionine; Middle Aged; Open Reading Frames; Phenotype; Polymerase Chain Reaction; Polymorphism, Genetic; Prions; Valine | 1994 |
Modifications of transthyretin in amyloid fibrils: analysis of amyloid from homozygous and heterozygous individuals with the Met30 mutation.
Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Disulfides; Heterozygote; Homozygote; Humans; Methionine; Methylation; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Prealbumin; Vitreous Body | 1993 |
Thyroxine binding in a TTR Met 119 kindred.
Topics: Amyloidosis; Asparagine; Binding Sites; DNA; Female; Genotype; Heterozygote; Humans; Hyperthyroxinemia; Isoelectric Focusing; Male; Methionine; Nervous System Diseases; Pedigree; Point Mutation; Polymorphism, Restriction Fragment Length; Portugal; Prealbumin; Serum Albumin; Thyrotropin; Thyroxine; Triiodothyronine | 1993 |
Retrovirus-mediated gene transfer of transthyretin and transthyretin-methionine 30: a potential tool for the study of amyloidogenesis.
Topics: 3T3 Cells; Amyloid; Amyloidosis; Animals; Base Sequence; Carcinoma, Hepatocellular; Cell Line; DNA; Gene Transfer Techniques; Genetic Vectors; Humans; Liver Neoplasms; Methionine; Mice; Molecular Sequence Data; Molecular Weight; Moloney murine leukemia virus; Oligodeoxyribonucleotides; Plasmids; Point Mutation; Polymerase Chain Reaction; Prealbumin; Rats; Repetitive Sequences, Nucleic Acid; Retroviridae; Tumor Cells, Cultured | 1993 |
Structure of Met30 variant of transthyretin and its amyloidogenic implications.
Topics: Amino Acids; Amyloidosis; Computer Simulation; Disulfides; Methionine; Models, Molecular; Peripheral Nervous System Diseases; Prealbumin; Protein Conformation; X-Ray Diffraction | 1993 |
Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissues.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amyloidosis; Cardiomyopathies; Child, Preschool; Denmark; DNA-Cytosine Methylases; Female; Formaldehyde; Humans; Leucine; Male; Methionine; Middle Aged; Oligodeoxyribonucleotides; Paraffin Embedding; Point Mutation; Polymerase Chain Reaction; Prealbumin; Retrospective Studies; Tissue Fixation; Tissue Survival | 1993 |
Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France.
Topics: Aged; Aged, 80 and over; Amyloidosis; Base Sequence; Electrophoresis, Agar Gel; France; Hereditary Sensory and Autonomic Neuropathies; Humans; Methionine; Middle Aged; Molecular Sequence Data; Oligonucleotides; Point Mutation; Polymerase Chain Reaction; Prealbumin | 1993 |
A clinical, echocardiographic and genetic characterization of a Danish kindred with familial amyloid transthyretin methionine 111 linked cardiomyopathy.
Topics: Adolescent; Adult; Aged; Amyloidosis; Cardiomyopathies; Cardiomyopathy, Restrictive; Carpal Tunnel Syndrome; Child; DNA Mutational Analysis; Female; Genetic Carrier Screening; Genetic Linkage; Genotype; Humans; Male; Methionine; Middle Aged; Pedigree; Prealbumin; Ultrasonography; Ventricular Function, Left | 1998 |
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis.
Topics: Adolescent; Amyloidosis; Child; Child, Preschool; Cytoskeletal Proteins; Familial Mediterranean Fever; Female; Genotype; Humans; Male; Methionine; Phenotype; Proteins; Pyrin; Valine | 1999 |
A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
Topics: Aged; Amyloid Neuropathies; Amyloidosis; Base Sequence; Cardiomyopathies; Female; Giant Cells; Heart Ventricles; Humans; Methionine; Point Mutation; Prealbumin; Rectum | 1999 |
An extended hydrophobic core induces EF-hand swapping.
Topics: Amino Acid Substitution; Amyloidosis; Apoproteins; Binding Sites; Calbindins; Calcium; Chromatography, Gel; Crystallography, X-Ray; Dimerization; EF Hand Motifs; Kinetics; Methionine; Models, Molecular; Mutation; Proline; Protein Structure, Quaternary; Protein Structure, Tertiary; S100 Calcium Binding Protein G; Structure-Activity Relationship; Thermodynamics | 2001 |
"Sporadic" familial amyloidotic polyneuropathy in a German patient with B cell lymphocytic leukaemia.
Topics: Aged; Amyloidosis; Germany; Heterozygote; Humans; Immunohistochemistry; Leukemia, B-Cell; Male; Methionine; Mutation; Polyneuropathies; Prealbumin; Valine | 2002 |
Slowed synthesis of DNA and methionine is a pathogenetic mechanism common to dementia in Down's syndrome, AIDS and Alzheimer's disease?
Topics: AIDS Dementia Complex; Alzheimer Disease; Amyloidosis; Cell Death; Dementia; DNA; DNA Repair; DNA Replication; Down Syndrome; Humans; Methionine; Models, Biological | 1992 |
Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.
Topics: Amyloidosis; Base Sequence; Cardiomyopathies; Denmark; DNA-Cytosine Methylases; Heterozygote; Humans; Methionine; Molecular Sequence Data; Mutation; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Prealbumin | 1992 |
Hereditary amyloidosis and cardiomyopathy.
Topics: Amyloidosis; Cardiomyopathies; Genes, Dominant; Humans; Methionine; Mutation; Prealbumin | 1992 |
A Danish kindred with familial amyloid cardiomyopathy revisited: identification of a mutant transthyretin-methionine111 variant in serum from patients and carriers.
Topics: Adult; Aged; Aged, 80 and over; Amyloidosis; Cardiomyopathies; Denmark; Electrophoresis, Polyacrylamide Gel; Female; Heterozygote; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Peptide Fragments; Prealbumin; Sodium Dodecyl Sulfate | 1992 |
Glycosaminoglycans in extracts of cardiac amyloid fibrils from familial amyloid cardiomyopathy of Danish origin related to variant transthyretin Met 111.
Topics: Adult; Amyloidosis; Cardiomyopathies; Chromatography, Gel; Chromatography, Ion Exchange; Denmark; Glycosaminoglycans; Humans; Methionine; Polysaccharides; Prealbumin; Serum Amyloid A Protein | 1991 |
Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy.
Topics: Amyloidosis; Base Sequence; DNA; Exons; Female; Homozygote; Humans; Male; Methionine; Molecular Sequence Data; Mutation; Pedigree; Peripheral Nervous System Diseases; Polymerase Chain Reaction; Prealbumin; Turkey | 1990 |
Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
Topics: Amyloidosis; Electrophoresis, Polyacrylamide Gel; Humans; Hydrolysis; Methionine; Mutation; Peripheral Nervous System Diseases; Prealbumin; Risk Factors | 1989 |
Isolation and characterization of a kappa amyloid fibril protein.
Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Animals; Antibody Formation; Electrophoresis, Polyacrylamide Gel; Female; Glutamates; Glutamic Acid; Histidine; Humans; Immunodiffusion; Isoleucine; Methionine; Middle Aged; Rabbits; Serine | 1985 |
Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I.
Topics: Adult; Amyloidosis; Cyanogen Bromide; Genetic Carrier Screening; Genetic Variation; Humans; Male; Methionine; Pedigree; Peptides; Peripheral Nervous System Diseases; Prealbumin; Sweden | 1985 |
Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
Topics: Amino Acid Sequence; Amyloidosis; Genetic Variation; Greece; Humans; Methionine; Pedigree; Peripheral Nervous System Diseases; Prealbumin; Valine | 1986 |
[Familial type I (Portuguese form) amyloidotic polyneuropathy in Majorca. Study using the TTR (Met30) genetic marker].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amyloidosis; Child; Child, Preschool; Female; Genetic Markers; Humans; Immunoblotting; Male; Methionine; Middle Aged; Nervous System Diseases; Pedigree; Prealbumin; Prospective Studies; Spain | 1988 |
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Topics: Adult; Amyloidosis; Female; Hereditary Sensory and Autonomic Neuropathies; Hereditary Sensory and Motor Neuropathy; Homozygote; Humans; Male; Methionine; Middle Aged; Mutation; Pedigree; Prealbumin; Sweden | 1988 |
Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy.
Topics: Adolescent; Adult; Aged; Amyloidosis; Child; Female; Humans; Male; Methionine; Middle Aged; Mutation; Nervous System Diseases; Pedigree; Portugal; Prealbumin | 1986 |
Chemical classification of hereditary amyloidosis in Brazilian families and identification of gene carriers.
Topics: Adult; Amyloidosis; Brazil; Chromatography, High Pressure Liquid; Female; Genetic Carrier Screening; Humans; Male; Methionine; Middle Aged; Pedigree; Prealbumin; Valine | 1986 |
The normal and abnormal pancreatic scan.
Topics: Adenoma, Islet Cell; Adult; Aged; Amyloidosis; Aneurysm; Cholelithiasis; Cystic Fibrosis; Diabetes Mellitus; Female; Gold Isotopes; Humans; Injections, Intravenous; Liver Function Tests; Male; Methionine; Middle Aged; Neoplasm Metastasis; Pancreas; Pancreatectomy; Pancreatic Diseases; Pancreatic Neoplasms; Pancreatitis; Peptic Ulcer; Radioisotopes; Radionuclide Imaging; Selenium | 1968 |
[Effect of cysteine and methionine on the course of experimental amyloidosis induced with sodium caseinate].
Topics: Amyloidosis; Animals; Caseins; Cysteine; Drug Synergism; Male; Methionine; Mice | 1974 |
[Histochemical studies of proteins, SH, S-S and NH-2 groups in experimental caseinate-induced amyloidosis with simultaneous administration of methionine and cysteine hydrochloride].
Topics: Amines; Amyloidosis; Animals; Caseins; Cysteine; Disulfides; Kidney; Liver; Methionine; Mice; Proteins; Spleen; Sulfhydryl Compounds | 1974 |
[Inhibitory action of L-cysteine and methionine on the formation of amyloid substance].
Topics: Amyloidosis; Animals; Cysteine; Male; Methionine; Mice | 1970 |
[Inhibitory effect of L-cysteine and methionine on amyloid formation].
Topics: Amyloid; Amyloidosis; Animals; Caseins; Cysteine; Depression, Chemical; Kidney; Liver; Male; Methionine; Mice; Spleen | 1970 |
Amyloid. VI. A comparison of two morphologic components of human amyloid deposits.
Topics: Acrylates; Amino Acids; Amyloid; Amyloidosis; Carbohydrates; Electrophoresis, Disc; Histocytochemistry; Humans; Kidney; Liver; Methionine; Methods; Microscopy, Electron; Peptides; Spleen; Tryptophan; X-Ray Diffraction | 1968 |
Sulfur-35 in experimental amyloidosis.
Topics: Amyloidosis; Animals; Autoradiography; Cricetinae; Kidney Glomerulus; Liver; Methionine; Spleen; Sulfur Isotopes | 1966 |