enkephalin, leucine has been researched along with Ataxias, Hereditary in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 8 (88.89) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Fisher, SE; Ma, KY; Smeets, CJLM; Verbeek, DS | 1 |
| Goto, J; Hirano, M; Ichikawa, Y; Kusunoki, S; Mitsui, J; Saigoh, K; Samukawa, M; Shioyama, M; Tsuji, S | 1 |
| Smeets, CJ; Verbeek, DS | 1 |
| Barsottini, OG; Freua, F; Kok, F; Pedroso, JL; Vale, TC | 1 |
| Bakalkin, G; Dooley, C; Marrink, SJ; McLaughlin, J; Melo, MN; Reits, E; Sinke, RJ; Smeets, CJ; Stargardt, A; Verbeek, DS; Zmorzyńska, J | 1 |
| Artemenko, KA; Bakalkin, G; Bazov, I; Depoorter, C; Dooijes, D; Hauser, KF; Jezierska, J; Knapp, PE; Kremer, B; Nyberg, F; Sinke, RJ; Van de Warrenburg, BP; Verbeek, DS; Verschuuren-Bemelmans, C; Watanabe, H; Wijmenga, C; Yakovleva, T; Zubarev, RA | 1 |
| Beetz, C; Schicks, J; Schiele, F; Schöls, L; Synofzik, M | 1 |
| Guan, WJ; Jiang, H; Liu, YT; Shen, L; Shi, YT; Tang, BS; Wang, JL; Xia, K; Yan, XX; Zhou, Y | 1 |
| Elahi, E; Fawcett, K; Giunti, P; Hamed, S; Herscheson, J; Houlden, H; Koutsis, G; Liu, YT; Mehrabian, M; Morris, HR; Morrison, PJ; Revesz, T; Schottlaender, L; Wardle, M; Wood, N | 1 |
9 other study(ies) available for enkephalin, leucine and Ataxias, Hereditary
| Article | Year |
|---|---|
Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23.
Topics: Animals; Cerebellum; Enkephalins; Humans; Mice; Mice, Transgenic; Neurogenesis; Protein Precursors; Spinocerebellar Degenerations | 2021 |
The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.
Topics: Age of Onset; Brain Stem; Cerebellum; Enkephalins; Family Health; Female; Humans; Japan; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Protein Precursors; Spinocerebellar Degenerations | 2015 |
Reply: SCA23 and prodynorphin: is it time for gene retraction?
Topics: Enkephalins; Humans; Protein Precursors; RNA, Messenger; Spinocerebellar Degenerations | 2016 |
SCA23 and prodynorphin: is it time for gene retraction?
Topics: Enkephalins; Humans; Protein Precursors; Spinocerebellar Degenerations | 2016 |
Altered secondary structure of Dynorphin A associates with loss of opioid signalling and NMDA-mediated excitotoxicity in SCA23.
Topics: Amino Acid Sequence; Animals; Cell Culture Techniques; Computer Simulation; Dynorphins; Endorphins; Enkephalins; Mice; Mice, Inbred C57BL; N-Methylaspartate; Neurons; Neurotoxins; Protein Precursors; Protein Structure, Secondary; Receptors, N-Methyl-D-Aspartate; Signal Transduction; Spinal Cord; Spinocerebellar Degenerations | 2016 |
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.
Topics: Cerebellum; Dynorphins; Enkephalins; Female; Glutamate Plasma Membrane Transport Proteins; Humans; Male; Mutation, Missense; Pedigree; Protein Precursors; Purkinje Cells; Spinocerebellar Degenerations | 2010 |
Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe.
Topics: Enkephalins; Europe; Humans; Mutation; Protein Precursors; Spinocerebellar Degenerations | 2011 |
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.
Topics: Adolescent; Adult; Aged; Asian People; Base Sequence; Child; Child, Preschool; China; DNA Mutational Analysis; Enkephalins; Female; Humans; Male; Middle Aged; Mutation; Pedigree; Polymorphism, Single Nucleotide; Protein Precursors; Reverse Transcriptase Polymerase Chain Reaction; Spinocerebellar Degenerations; Young Adult | 2012 |
The frequency of spinocerebellar ataxia type 23 in a UK population.
Topics: Adult; Aged; Aged, 80 and over; Cohort Studies; Enkephalins; Female; Humans; Male; Middle Aged; Population Surveillance; Prevalence; Protein Precursors; Spinocerebellar Degenerations; United Kingdom | 2013 |