tyrosine and Autosomal Dominant Hereditary Spastic Paraplegia

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

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	1 (33.33)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Bonifacino, JS; De Pace, R; Mattera, R	1
Baas, PW; D'Rozario, M; Davidson, MW; Jean, DC; Marenda, DR; Solowska, JM	1
Bernardi, G; Hase, Y; Iseki, K; Kawarai, T; Matsui, M; Orlacchio, A; Rogaeva, E; St George-Hyslop, P; Takahashi, R; Tomimoto, H	1

Reviews

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

Article	Year
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

Article

Year

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

Article	Year
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

Article

Year

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