methionine has been researched along with Parkinsonian Disorders in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Charlton, CG; Darling-Reed, S; Lamango, N; Lee, ES; Reuben, JS; Shepherd, KR; Soliman, KF; Williams, Z; Zhao, WQ | 1 |
Dawson, TM; Dawson, VL; Moore, DJ; Zhang, L | 1 |
Gollamudi, S; Jeon, BS; Kim, JY; Lee, JY; Ozelius, LJ | 1 |
Binelli, S; Bugiani, O; Capobianco, R; Di Fede, G; Fociani, P; Giaccone, G; Grisoli, M; Limido, L; Mangieri, M; Suardi, S; Tagliavini, F | 1 |
4 other study(ies) available for methionine and Parkinsonian Disorders
Article | Year |
---|---|
S-adenosyl-methionine-induced apoptosis in PC12 cells.
Topics: Animals; Apoptosis; bcl-2-Associated X Protein; Brain; Cell Differentiation; Culture Media, Conditioned; DNA Fragmentation; Intracellular Fluid; L-Lactate Dehydrogenase; Methionine; Neurons; Parkinsonian Disorders; PC12 Cells; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Proteins; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-bcl-2; Rats; S-Adenosylhomocysteine; S-Adenosylmethionine | 2002 |
A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization.
Topics: Autoantigens; Blotting, Northern; Blotting, Western; Cell Line, Tumor; Cycloheximide; Electrophoresis, Gel, Pulsed-Field; Humans; In Vitro Techniques; Intracellular Signaling Peptides and Proteins; Leucine; Methionine; Mutation, Missense; Oncogene Proteins; Parkinsonian Disorders; Phenylalanine; Precipitin Tests; Protein Deglycase DJ-1; Protein Synthesis Inhibitors; Proteins; Proto-Oncogene Proteins c-myc; Ribonucleoproteins; RNA, Messenger; SS-B Antigen; Sulfur Isotopes; Transfection | 2003 |
ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.
Topics: Adult; Dystonic Disorders; Humans; Korea; Male; Methionine; Mutation; Parkinsonian Disorders; Sodium-Potassium-Exchanging ATPase; Threonine | 2007 |
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Topics: Aged; Antibodies; Antibodies, Monoclonal; Antiparkinson Agents; Blotting, Western; Brain; Codon; Creutzfeldt-Jakob Syndrome; Female; Humans; Immunohistochemistry; Levodopa; Magnetic Resonance Imaging; Methionine; Parkinsonian Disorders; Phenotype; Polymorphism, Genetic; PrPSc Proteins; Valine | 2007 |