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histidine and Hereditary Sensory and Autonomic Neuropathies

histidine has been researched along with Hereditary Sensory and Autonomic Neuropathies in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cunningham, JM; Dyck, PJ; Kilfoyle, DH; Klein, CJ; Klein, DM; Kumar, N; Litchy, WJ; Wu, Y1
Bacikova, D; Dunn, TM; Gable, K; Han, G; Monaghan, E; Natarajan, M; Williams, R1
Cohen, AS; Milunsky, A; Milunsky, JM; Skare, IB; Skare, JC; Skinner, M1

Other Studies

3 other study(ies) available for histidine and Hereditary Sensory and Autonomic Neuropathies

ArticleYear
Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis.
    Journal of neurology, neurosurgery, and psychiatry, 2006, Volume: 77, Issue:8

    Topics: Adult; Age of Onset; Child, Preschool; DNA Mutational Analysis; Female; Hearing Loss; Hereditary Sensory and Autonomic Neuropathies; Histidine; Humans; Male; Middle Aged; Multiple Sclerosis; Myelin P0 Protein; Pedigree; Phenotype; Proline; Restless Legs Syndrome

2006
Mutations in the yeast LCB1 and LCB2 genes, including those corresponding to the hereditary sensory neuropathy type I mutations, dominantly inactivate serine palmitoyltransferase.
    The Journal of biological chemistry, 2002, Mar-22, Volume: 277, Issue:12

    Topics: Acyltransferases; Alleles; Amino Acid Sequence; Binding Sites; Blotting, Western; Calcium; Catalysis; Chromatography, Liquid; Dimerization; Diploidy; Hereditary Sensory and Autonomic Neuropathies; Histidine; Lysine; Microsomes, Liver; Models, Chemical; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Plasmids; Precipitin Tests; Protein Binding; Protein Structure, Tertiary; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Serine C-Palmitoyltransferase; Sphingolipids

2002
A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90.
    Clinical genetics, 1991, Volume: 39, Issue:1

    Topics: Amino Acid Sequence; Amyloidosis; Asparagine; Base Sequence; Female; Hereditary Sensory and Autonomic Neuropathies; Histidine; Humans; Ion Exchange; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Prealbumin

1991