glutamine has been researched along with Ataxias, Hereditary in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 6 (75.00) | 18.2507 |
2000's | 2 (25.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gomez, CM; Subramony, SH | 1 |
Sakai, K; Sato, T; Takahashi, H; Tsuji, S; Yamada, M | 1 |
Antalffy, B; Armstrong, D; Koshy, B; Orr, HT; Servadio, A; Zoghbi, HY | 1 |
Finch, JT; Johnson, T; Perutz, MF; Suzuki, M | 1 |
Johnson, T | 1 |
Cummings, CJ; Helin, K; Klement, IA; Koshy, BT; Orr, HT; Servadio, A; Skinner, PJ; Zoghbi, HY | 1 |
Cummings, CJ; Isobe, T; Koshy, BT; Matilla, A; Orr, HT; Zoghbi, HY | 1 |
Agid, Y; Brice, A; Cancel, G; Damier, P; Dürr, A; Duyckaerts, C; Faucheux, B; Gourfinkel-An, I; Hirsch, EC; Holmberg, M; Trottier, Y | 1 |
1 review(s) available for glutamine and Ataxias, Hereditary
Article | Year |
---|---|
Dominantly inherited ataxias.
Topics: Genes, Dominant; Glutamine; Humans; Point Mutation; Spinocerebellar Ataxias; Spinocerebellar Degenerations; Trinucleotide Repeat Expansion | 2003 |
7 other study(ies) available for glutamine and Ataxias, Hereditary
Article | Year |
---|---|
Neuronal atrophy and synaptic alteration in a mouse model of dentatorubral-pallidoluysian atrophy.
Topics: Animals; Atrophy; Axons; Cerebral Cortex; Corpus Callosum; Dendrites; Dendritic Spines; Disease Models, Animal; Glutamine; Immunohistochemistry; Mice; Mice, Transgenic; Microscopy, Electron; Microtubules; Neurons; Peptides; Pyramidal Tracts; Spinocerebellar Degenerations; Synapses | 2006 |
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals.
Topics: Animals; Ataxin-1; Ataxins; Brain; Cell Nucleus; Cells, Cultured; Cerebellar Cortex; Cytoplasm; Female; Gene Expression Regulation; Glutamine; Humans; Immunoblotting; Immunohistochemistry; Lymphocytes; Male; Mice; Nerve Tissue Proteins; Nuclear Proteins; Purkinje Cells; Rats; Recombinant Fusion Proteins; Repetitive Sequences, Nucleic Acid; Spinocerebellar Degenerations | 1995 |
Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases.
Topics: Amino Acid Sequence; Genes, Dominant; Glutamine; Humans; Huntingtin Protein; Huntington Disease; Hydrogen Bonding; Molecular Sequence Data; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Nuclear Proteins; Protein Binding; Protein Structure, Secondary; Receptors, Androgen; Repetitive Sequences, Nucleic Acid; Spinocerebellar Degenerations | 1994 |
Chemical synthesis of polar zipper peptides: motifs for potential protein association in inherited neurodegenerative diseases.
Topics: Amino Acid Sequence; Brain Diseases; Chromatography, High Pressure Liquid; Glutamine; Humans; Huntington Disease; Indicators and Reagents; Machado-Joseph Disease; Molecular Sequence Data; Muscular Dystrophies; Nerve Degeneration; Nerve Tissue Proteins; Peptides; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Spinocerebellar Degenerations | 1995 |
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures.
Topics: Animals; Ataxin-1; Ataxins; Brain; COS Cells; Glutamine; Humans; Immunohistochemistry; Mice; Mice, Transgenic; Mutation; Nerve Tissue Proteins; Nuclear Matrix; Nuclear Proteins; Purkinje Cells; Spinocerebellar Degenerations | 1997 |
The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1.
Topics: Animals; Ataxin-1; Ataxins; Binding Sites; Cell Nucleus; Cerebellum; Cloning, Molecular; COS Cells; Glutamine; Humans; Immunohistochemistry; Mice; Microscopy, Confocal; Mutation; Nerve Tissue Proteins; Neuropeptides; Nuclear Matrix; Nuclear Proteins; Purkinje Cells; Rats; Saccharomyces cerevisiae; Spinocerebellar Degenerations | 1997 |
Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.
Topics: Ataxin-7; Brain; Cell Nucleus; Child; Glutamine; Humans; Immunohistochemistry; Inclusion Bodies; Male; Nerve Tissue Proteins; Neurons; Neuropeptides; Nuclear Proteins; Spinocerebellar Degenerations | 1998 |