proline has been researched along with Parkinsonian Disorders in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 4 (57.14) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Funayama, M; Hattori, N; Li, Y; Matsuura, E; Nishioka, K; Takanashi, M; Takashima, H; Tsuyama, S; Yoshino, H | 1 |
Barbe, MT; Coenen, HH; Fink, GR; Galldiks, N; Langen, KJ; Schroeter, M; Sommerauer, M; Stoffels, G; Timmermann, L; Willuweit, A | 1 |
Behari, M; Kirola, L; Shishir, C; Thelma, BK | 1 |
Cui, AM; Davenport, B; Garruto, RM; Go, RC; Heizer, JW; Hermosura, MC; Mocz, G; Perraud, AL; Schmitz, C; Shetler, CM | 1 |
Baekelandt, V; García-Horsman, JA; Gerard, M; Hannula, MJ; Lambeir, AM; Männistö, PT; Myöhänen, TT; Van Der Veken, P; Van Elzen, R | 1 |
Abramsky, O; Biran, I; Boher, M; Ekstein, D; Gal, A; Gomori, JM; Lossos, A; Meiner, Z; Newman, JP; Reches, A; Rosenmann, H; Soffer, D | 1 |
Epplen, JT; Krüger, R; Kuhn, W; Leenders, KL; Maguire, RP; Müller, T; Portman, AT; Przuntek, H; Riess, O; Schöls, L; Schröder, U; Sprengelmeyer, R; Veenma, L; Woitalla, D | 1 |
1 trial(s) available for proline and Parkinsonian Disorders
Article | Year |
---|---|
Cis-4-[18F]fluoro-D-proline detects neurodegeneration in patients with akinetic-rigid parkinsonism.
Topics: Aged; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Multimodal Imaging; Parkinsonian Disorders; Positron-Emission Tomography; Proline | 2019 |
6 other study(ies) available for proline and Parkinsonian Disorders
Article | Year |
---|---|
Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations.
Topics: Aged; alpha-Synuclein; Astrocytes; Autopsy; DNA-Binding Proteins; Female; Gene Expression Regulation; Histidine; Homozygote; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Neurodegenerative Diseases; Parkinsonian Disorders; Proline; Protein Aggregation, Pathological; Substantia Nigra; tau Proteins | 2018 |
Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism.
Topics: Adult; Arginine; DNA Mutational Analysis; Family Health; Female; Genes, Recessive; Humans; India; Magnetic Resonance Imaging; Male; Mutation; Parkinsonian Disorders; Phenotype; Phosphoric Monoester Hydrolases; Proline; Young Adult | 2016 |
Altered functional properties of a TRPM2 variant in Guamanian ALS and PD.
Topics: Adenosine Diphosphate Ribose; Amino Acid Sequence; Amino Acids, Diamino; Amyotrophic Lateral Sclerosis; Calcium; Calcium Signaling; Cell Membrane; Conserved Sequence; Cyanobacteria Toxins; Evolution, Molecular; Guam; Humans; Hydrogen Peroxide; Ion Channel Gating; Leucine; Magnesium; Models, Molecular; Molecular Sequence Data; Mutant Proteins; Mutation; Oxidative Stress; Parkinsonian Disorders; Proline; Temperature; TRPM Cation Channels | 2008 |
A prolyl oligopeptidase inhibitor, KYP-2047, reduces α-synuclein protein levels and aggregates in cellular and animal models of Parkinson's disease.
Topics: alpha-Synuclein; Animals; Blotting, Western; Brain; Cell Culture Techniques; Cell Line, Tumor; Cell Survival; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Fluorescence; Motor Activity; Oxidative Stress; Parkinsonian Disorders; Proline; Prolyl Oligopeptidases; Reverse Transcriptase Polymerase Chain Reaction; Serine Endopeptidases; Serine Proteinase Inhibitors; Transfection | 2012 |
Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.
Topics: Adult; Algeria; Cerebral Cortex; Dementia; DNA Mutational Analysis; Family Health; Female; Humans; Immunohistochemistry; Inclusion Bodies; Jews; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neurologic Examination; Neuropsychological Tests; Parkinsonian Disorders; Pedigree; Proline; Serine; tau Proteins; Tomography, Emission-Computed, Single-Photon | 2003 |
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.
Topics: Aged; Alanine; alpha-Synuclein; Amino Acid Sequence; Apolipoproteins E; Brain; DNA Mutational Analysis; Female; Genotype; Germany; Humans; Male; Middle Aged; Mutation; Nerve Tissue Proteins; Neuropsychological Tests; Parkinsonian Disorders; Pedigree; Proline; Synucleins; Thiolester Hydrolases; Tomography, Emission-Computed; Ubiquitin Thiolesterase | 2001 |