isoleucine has been researched along with Abnormalities, Autosome in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cho, YW; Kim, DK; Lim, JG; Motamedi, GK; Yi, SD | 1 |
| Baal, C; Hemmer, W; Jarisch, R; Litschauer-Poursadrollah, M; Mayer, DE | 1 |
| Eguchi, H; Hayashi, S; Kawajiri, K; Watanabe, J | 1 |
| Casto, BC; DiPaolo, JA; Popescu, NC | 1 |
| van der Horst, JL; Wadman, SK | 1 |
1 review(s) available for isoleucine and Abnormalities, Autosome
| Article | Year |
|---|---|
Genetic polymorphisms of drug-metabolizing enzymes and lung cancer susceptibility.
Topics: Chromosome Aberrations; Cytochrome P-450 Enzyme System; Deoxyribonuclease HpaII; Genetic Predisposition to Disease; Genotype; Glutathione Transferase; Humans; Isoenzymes; Isoleucine; Lung Neoplasms; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Smoking; Valine | 1995 |
4 other study(ies) available for isoleucine and Abnormalities, Autosome
| Article | Year |
|---|---|
Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor.
Topics: Adult; Alleles; Amino Acid Substitution; Chromosome Aberrations; Codon; Diagnosis, Differential; DNA Mutational Analysis; Epilepsy, Frontal Lobe; Female; Frontal Lobe; Genes, Dominant; Genetic Carrier Screening; Genetic Testing; Gyrus Cinguli; Humans; Isoleucine; Membrane Proteins; Memory Disorders; Methionine; Middle Aged; Mutation, Missense; Neuropsychological Tests; Nocturnal Paroxysmal Dystonia; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Polysomnography; Receptors, Nicotinic; Regional Blood Flow; Video Recording | 2008 |
Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.
Topics: Amino Acid Substitution; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Dental Enamel Hypoplasia; Dental Pulp Cavity; Dermatitis, Atopic; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Genes, Dominant; Hair; Homeodomain Proteins; Humans; Isoleucine; Microscopy, Electron; Phenotype; Serine; Syndrome; Tooth Abnormalities; Transcription Factors | 2010 |
Infrequent chromosome aberrations in Syrian hamster cells following partial synchrony by amino-acid deprivation.
Topics: Arginine; Cell Division; Cells, Cultured; Chromosome Aberrations; Culture Media; DNA; Isoleucine; Mitotic Index | 1975 |
A variant form of branched-chain keto aciduria.
Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine | 1971 |