Page last updated: 2024-08-17

methionine and Parkinsonian Disorders

methionine has been researched along with Parkinsonian Disorders in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Charlton, CG; Darling-Reed, S; Lamango, N; Lee, ES; Reuben, JS; Shepherd, KR; Soliman, KF; Williams, Z; Zhao, WQ1
Dawson, TM; Dawson, VL; Moore, DJ; Zhang, L1
Gollamudi, S; Jeon, BS; Kim, JY; Lee, JY; Ozelius, LJ1
Binelli, S; Bugiani, O; Capobianco, R; Di Fede, G; Fociani, P; Giaccone, G; Grisoli, M; Limido, L; Mangieri, M; Suardi, S; Tagliavini, F1

Other Studies

4 other study(ies) available for methionine and Parkinsonian Disorders

ArticleYear
S-adenosyl-methionine-induced apoptosis in PC12 cells.
    Journal of neuroscience research, 2002, Aug-15, Volume: 69, Issue:4

    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.
    Journal of neurochemistry, 2003, Volume: 87, Issue:6

    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.
    Movement disorders : official journal of the Movement Disorder Society, 2007, Sep-15, Volume: 22, Issue:12

    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.
    Journal of neurology, neurosurgery, and psychiatry, 2007, Volume: 78, Issue:12

    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