tyrosine and Autosomal Dominant Hereditary Spastic Paraplegia

tyrosine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Bonifacino, JS; De Pace, R; Mattera, R1
Baas, PW; D'Rozario, M; Davidson, MW; Jean, DC; Marenda, DR; Solowska, JM1
Bernardi, G; Hase, Y; Iseki, K; Kawarai, T; Matsui, M; Orlacchio, A; Rogaeva, E; St George-Hyslop, P; Takahashi, R; Tomimoto, H1

Reviews

1 review(s) available for tyrosine and Autosomal Dominant Hereditary Spastic Paraplegia

ArticleYear
The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia.
    Biochemical Society transactions, 2020, 10-30, Volume: 48, Issue:5

    Topics: Adaptor Proteins, Signal Transducing; Adenosine Triphosphatases; Animals; Autophagosomes; Autophagy; Autophagy-Related Proteins; Binding Sites; Caenorhabditis elegans; Cryptococcus neoformans; Drosophila melanogaster; Fungi; Humans; Lysosomes; Membrane Proteins; Membrane Transport Proteins; Mice; Mutation; Protein Binding; Protein Conformation; Protein Transport; Spastic Paraplegia, Hereditary; trans-Golgi Network; Transport Vesicles; Tyrosine; Vesicular Transport Proteins

2020

Other Studies

2 other study(ies) available for tyrosine and Autosomal Dominant Hereditary Spastic Paraplegia

ArticleYear
Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014, Jan-29, Volume: 34, Issue:5

    Topics: Adenosine Triphosphatases; Animals; Animals, Genetically Modified; Cells, Cultured; Cysteine; Disease Models, Animal; Drosophila; Drosophila Proteins; Female; Gene Expression Regulation; Green Fluorescent Proteins; Haploinsufficiency; Humans; Locomotion; Male; Microtubules; Mutation; Neurons; Nocodazole; Rats; Spastic Paraplegia, Hereditary; Spastin; Transfection; Tubulin Modulators; Tyrosine

2014
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia.
    Journal of neurology, 2007, Volume: 254, Issue:7

    Topics: Adult; Cysteine; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Japan; Membrane Proteins; Polymorphism, Genetic; Spastic Paraplegia, Hereditary; Tyrosine

2007