threonine and Spinocerebellar Ataxias

threonine has been researched along with Spinocerebellar Ataxias in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Banoei, MM; Houshmand, M; Nafisi, S; Panahi, MS; Parivar, K; Rostami, M; Safaei, S; Shariati, P	1
Brice, A; Debeir, T; Lasbleiz, C; Latouche, M; Martin, E; Monnier, V; Morel, L; Mouatt-Prigent, A; Muriel, MP; Ruberg, M; Stevanin, G; Tricoire, H	1

Other Studies

2 other study(ies) available for threonine and Spinocerebellar Ataxias

Article	Year
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias. Neuro-degenerative diseases, 2009, Volume: 6, Issue:1-2 Topics: Alanine; Amino Acid Substitution; Ataxin-3; Ataxin-7; Ataxins; Calcium Channels; DNA; DNA Primers; Gene Amplification; Genetic Variation; Glycine; Humans; Methionine; Mitochondrial Proton-Translocating ATPases; Nerve Tissue Proteins; Nuclear Proteins; Repressor Proteins; RNA, Transfer, Leu; RNA, Transfer, Lys; Spinocerebellar Ataxias; Threonine; Trinucleotide Repeats; Valine	2009
A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, Mar-07, Volume: 27, Issue:10 Topics: Animals; Animals, Genetically Modified; Ataxin-7; Cell Death; Cells, Cultured; Disease Models, Animal; Drosophila; Dyskinesias; Glutamine; Humans; Intranuclear Inclusion Bodies; Longevity; Male; Mutation; Nerve Tissue Proteins; Neurons; Peptides; Phenotype; Rats; Spinocerebellar Ataxias; Threonine	2007

Article

Year

Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias.

Neuro-degenerative diseases, 2009, Volume: 6, Issue:1-2

Topics: Alanine; Amino Acid Substitution; Ataxin-3; Ataxin-7; Ataxins; Calcium Channels; DNA; DNA Primers; Gene Amplification; Genetic Variation; Glycine; Humans; Methionine; Mitochondrial Proton-Translocating ATPases; Nerve Tissue Proteins; Nuclear Proteins; Repressor Proteins; RNA, Transfer, Leu; RNA, Transfer, Lys; Spinocerebellar Ataxias; Threonine; Trinucleotide Repeats; Valine

2009

A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes.

The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, Mar-07, Volume: 27, Issue:10

Topics: Animals; Animals, Genetically Modified; Ataxin-7; Cell Death; Cells, Cultured; Disease Models, Animal; Drosophila; Dyskinesias; Glutamine; Humans; Intranuclear Inclusion Bodies; Longevity; Male; Mutation; Nerve Tissue Proteins; Neurons; Peptides; Phenotype; Rats; Spinocerebellar Ataxias; Threonine

2007