glutamine and Ataxias, Hereditary

glutamine has been researched along with Ataxias, Hereditary in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's6 (75.00)18.2507
2000's2 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gomez, CM; Subramony, SH1
Sakai, K; Sato, T; Takahashi, H; Tsuji, S; Yamada, M1
Antalffy, B; Armstrong, D; Koshy, B; Orr, HT; Servadio, A; Zoghbi, HY1
Finch, JT; Johnson, T; Perutz, MF; Suzuki, M1
Johnson, T1
Cummings, CJ; Helin, K; Klement, IA; Koshy, BT; Orr, HT; Servadio, A; Skinner, PJ; Zoghbi, HY1
Cummings, CJ; Isobe, T; Koshy, BT; Matilla, A; Orr, HT; Zoghbi, HY1
Agid, Y; Brice, A; Cancel, G; Damier, P; Dürr, A; Duyckaerts, C; Faucheux, B; Gourfinkel-An, I; Hirsch, EC; Holmberg, M; Trottier, Y1

Reviews

1 review(s) available for glutamine and Ataxias, Hereditary

ArticleYear
Dominantly inherited ataxias.
    Seminars in pediatric neurology, 2003, Volume: 10, Issue:3

    Topics: Genes, Dominant; Glutamine; Humans; Point Mutation; Spinocerebellar Ataxias; Spinocerebellar Degenerations; Trinucleotide Repeat Expansion

2003

Other Studies

7 other study(ies) available for glutamine and Ataxias, Hereditary

ArticleYear
Neuronal atrophy and synaptic alteration in a mouse model of dentatorubral-pallidoluysian atrophy.
    Brain : a journal of neurology, 2006, Volume: 129, Issue:Pt 9

    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.
    Nature genetics, 1995, Volume: 10, Issue:1

    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.
    Proceedings of the National Academy of Sciences of the United States of America, 1994, Jun-07, Volume: 91, Issue:12

    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.
    Biomedical peptides, proteins & nucleic acids : structure, synthesis & biological activity, 1995, Volume: 1, Issue:4

    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.
    Nature, 1997, Oct-30, Volume: 389, Issue:6654

    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.
    Nature, 1997, Oct-30, Volume: 389, Issue:6654

    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.
    Human molecular genetics, 1998, Volume: 7, Issue:5

    Topics: Ataxin-7; Brain; Cell Nucleus; Child; Glutamine; Humans; Immunohistochemistry; Inclusion Bodies; Male; Nerve Tissue Proteins; Neurons; Neuropeptides; Nuclear Proteins; Spinocerebellar Degenerations

1998