Compounds > threonine

threonine and Abnormalities, Autosome

threonine has been researched along with Abnormalities, Autosome in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Amr, SS; Hedley-Whyte, ET; Kamakura, T; Nadol, JB; O Apos Malley, JT1
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC1
Fishman, GA; Gilbert, LD; Kenna, P; Sheffield, VC; Stone, EM1
Anagnostopoulos, C; Jamet, C1

Other Studies

4 other study(ies) available for threonine and Abnormalities, Autosome

ArticleYear
Histopathology of the Inner Ear in Charcot-Marie-Tooth Syndrome Caused by a Missense Variant (p.Thr65Ala) in the MPZ Gene.
    Audiology & neuro-otology, 2018, Volume: 23, Issue:6

    Topics: Aged; Alanine; Charcot-Marie-Tooth Disease; Chromosome Aberrations; Cochlear Nerve; Ear, Inner; Exome Sequencing; Facial Nerve; Genes, Dominant; Genetic Variation; Humans; Male; Mutation, Missense; Myelin P0 Protein; Myelin Sheath; Threonine; Vestibular Nerve

2018
Precancerous and non-cancer disease endpoints of chronic arsenic exposure: the level of chromosomal damage and XRCC3 T241M polymorphism.
    Mutation research, 2011, Jan-10, Volume: 706, Issue:1-2

    Topics: Adult; Alleles; Amino Acid Substitution; Arsenic; Carcinogens; Case-Control Studies; Chromosome Aberrations; Conjunctivitis; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Methionine; Mutagens; Odds Ratio; Peripheral Nervous System Diseases; Polymorphism, Genetic; Precancerous Conditions; Skin Diseases; Threonine; Water Pollutants, Chemical

2011
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.
    Archives of ophthalmology (Chicago, Ill. : 1960), 1991, Volume: 109, Issue:10

    Topics: Adult; Arginine; Base Sequence; Chromosome Aberrations; Chromosome Disorders; Codon; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Electroretinography; Female; Fundus Oculi; Gene Expression; Genes, Dominant; Humans; Male; Middle Aged; Molecular Sequence Data; Mutagenesis; Pedigree; Phenotype; Retinitis Pigmentosa; Rhodopsin; Threonine; Visual Fields

1991
[A very poorly transformable mutation at the threonine deaminase locus in Bacillu subtilis].
    Molecular & general genetics : MGG, 1969, Volume: 105, Issue:3

    Topics: Bacillus subtilis; Chromosome Aberrations; Chromosome Mapping; DNA, Bacterial; Drug Resistance, Microbial; Hydro-Lyases; Mitomycins; Mutation; Radiation Effects; Selection, Genetic; Threonine; Transduction, Genetic; Transformation, Genetic; Ultraviolet Rays

1969