Compounds > histidine
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histidine and Ataxias, Hereditary

histidine has been researched along with Ataxias, Hereditary in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Advincula, J; Ashizawa, T; Lee, LV; Perlman, S; Rosales, RL; Subramony, SH; Waters, MF1
Bannykh, S; Bickford, JS; Fernandez-Funez, P; Gallego-Iradi, C; Hall, A; Huynh, DP; Khare, S; Nick, HS; Nick, JA; Pulst, SM; Rincon-Limas, DE; Salmasinia, D; Waters, MF; Wawrowsky, K1
Brunt, ER; Ferrari, MD; Frants, RR; Haan, J; Keeling, S; Kors, EE; Pascual, J; Ravine, D; Terwindt, GM; van den Maagdenberg, AM; van Paesschen, W; Vanmolkot, KR; Vermeulen, FL1
Brahmachari, SK; Pasha, S; Sharma, D; Sharma, S1

Other Studies

4 other study(ies) available for histidine and Ataxias, Hereditary

ArticleYear
Comprehensive phenotype of the p.Arg420his allelic form of spinocerebellar ataxia type 13.
    Cerebellum (London, England), 2013, Volume: 12, Issue:6

    Topics: Adult; Arginine; Cerebellum; Family Health; Female; Genetic Linkage; Genotype; Histidine; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Phenotype; Philippines; Shaw Potassium Channels; Spinocerebellar Ataxias; Spinocerebellar Degenerations

2013
KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking.
    Neurobiology of disease, 2014, Volume: 71

    Topics: Animals; Animals, Genetically Modified; Arginine; Biotinylation; Cadherins; Chlorocebus aethiops; COS Cells; Cytoplasm; Drosophila; Drosophila Proteins; Endoplasmic Reticulum; Female; Histidine; Humans; Intracellular Fluid; Male; Mutation; Oocytes; Protein Processing, Post-Translational; Protein Transport; Shaw Potassium Channels; Spinocerebellar Ataxias; Spinocerebellar Degenerations; Transfection

2014
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene.
    Journal of neurology, 2002, Volume: 249, Issue:11

    Topics: Adult; Amino Acid Sequence; Calcium Channels; Calcium Channels, P-Type; Cerebellum; Chromosome Mapping; Chromosomes, Human, Pair 19; DNA Mutational Analysis; Exons; Female; Genetic Testing; Histidine; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Protein Structure, Tertiary; Spinocerebellar Degenerations; Trinucleotide Repeat Expansion

2002
Peptide models for inherited neurodegenerative disorders: conformation and aggregation properties of long polyglutamine peptides with and without interruptions.
    FEBS letters, 1999, Jul-30, Volume: 456, Issue:1

    Topics: Ataxin-1; Ataxins; Circular Dichroism; Histidine; Humans; Models, Molecular; Nerve Tissue Proteins; Nuclear Proteins; Peptides; Protein Conformation; Solubility; Spectroscopy, Fourier Transform Infrared; Spinocerebellar Degenerations

1999