methionine has been researched along with Abnormalities, Autosome in 22 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 15 (68.18) | 18.7374 |
1990's | 1 (4.55) | 18.2507 |
2000's | 4 (18.18) | 29.6817 |
2010's | 1 (4.55) | 24.3611 |
2020's | 1 (4.55) | 2.80 |
Authors | Studies |
---|---|
Binz, RL; Garg, S; Hauer-Jensen, M; Koturbash, I; Miousse, IR; Pathak, R; Sadhukhan, R; Zhou, D | 1 |
Cho, YW; Kim, DK; Lim, JG; Motamedi, GK; Yi, SD | 1 |
Boonen, S; Dubois, B; Goris, A; Hersmus, N; Lemmens, R; Matthijs, G; Race, V; Robberecht, W; Van Damme, P; Van Den Bosch, L | 1 |
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC | 1 |
Apter, A; Burg, M; Carmel, M; Frisch, A; Gothelf, D; Inbar, D; Korostishevsky, M; Michaelovsky, E; Steinberg, T; Weizman, A | 1 |
Giraudier, S; Michot, JM; Papo, T; Sedel, F; Smiejan, JM | 1 |
Rozynkowa, D; Stepień, J | 1 |
Bonassi, S; De Biase, A; Deeva, IB; Degan, P; Doronin, YK; Iaccarino, M; Korkina, LG; Oral, R; Pagano, G; Warnau, M | 1 |
Hitachi, PM; Takayama, S; Yamada, K | 1 |
Gebhart, E | 3 |
Azevedo, JL; Menezes, EM | 1 |
Butenandt, O | 1 |
Becher, R; Gebhart, E | 1 |
Leder, P | 1 |
André, F; Aschkenasy, A | 2 |
van der Horst, JL; Wadman, SK | 1 |
Berger, R; Broyer, M | 1 |
Hansen, S; Hardwick, DF; Perry, TL; Pohlmann, L; Warrington, PD | 1 |
Nakagawa, H; Sato, T; Tada, K; Yokoyama, Y; Yoshida, T | 1 |
1 review(s) available for methionine and Abnormalities, Autosome
Article | Year |
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The elongation reactions in protein synthesis.
Topics: Alanine; Amino Acyl-tRNA Synthetases; Bacterial Proteins; Binding Sites; Chromosome Aberrations; Lysine; Methionine; Models, Biological; Peptide Chain Elongation, Translational; Peptide Elongation Factors; Peptide Initiation Factors; Protein Binding; Protein Biosynthesis; Puromycin; Ribosomes; RNA, Bacterial; RNA, Messenger; RNA, Transfer | 1973 |
21 other study(ies) available for methionine and Abnormalities, Autosome
Article | Year |
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Dietary Methionine Deficiency Enhances Genetic Instability in Murine Immune Cells.
Topics: Animals; Bone Marrow Cells; Chromosome Aberrations; Diet; DNA Damage; DNA Repair; Macrophages; Male; Malnutrition; Methionine; Mice; Mice, Inbred CBA; Monocytes; RAW 264.7 Cells | 2021 |
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 |
TDP-43 M311V mutation in familial amyotrophic lateral sclerosis.
Topics: Adult; Aged; Alleles; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Belgium; Chromosome Aberrations; Codon; DNA Mutational Analysis; DNA-Binding Proteins; Exons; Female; Genes, Dominant; Humans; Male; Methionine; Middle Aged; Pedigree; Sequence Analysis, DNA; Superoxide Dismutase; Superoxide Dismutase-1; Valine | 2009 |
Precancerous and non-cancer disease endpoints of chronic arsenic exposure: the level of chromosomal damage and XRCC3 T241M polymorphism.
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 |
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
Topics: Adolescent; Adult; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, Pair 22; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single-Stranded Conformational; Valine | 2008 |
Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Catatonia; Chromosome Aberrations; Chromosomes, Human, Pair 1; Coma; Dementia; Exons; Folic Acid; Genes, Recessive; Homocysteine; Humans; Magnetic Resonance Imaging; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Neurologic Examination; Paraplegia; Polymorphism, Genetic; Psychotic Disorders | 2008 |
[Search for phenotypic expression of Philadelphia chromosome aberration in leukemic cell cultures in a medium without methionine].
Topics: Bone Marrow; Cells, Cultured; Chromosome Aberrations; Chromosomes, Human, 21-22 and Y; Culture Media; Hematopoietic Stem Cells; Humans; In Vitro Techniques; Leukemia, Myeloid, Acute; Methionine; Mitosis; Phenotype | 1980 |
L-methionine induces stage-dependent changes of differentiation and oxidative activity in sea urchin embryogenesis.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Acetylcysteine; Animals; Anserine; Antioxidants; Carnosine; Chromosome Aberrations; Deoxyguanosine; Embryo, Nonmammalian; Free Radical Scavengers; Germ Cells; Luminescent Measurements; Methionine; Mitosis; Reactive Oxygen Species; Sea Urchins; Stereoisomerism | 1997 |
Cytologic changes induced in rat livers cells by short-term exposure to chemical substances.
Topics: 2-Acetylaminofluorene; Aflatoxins; Animals; Butanes; Carcinogens; Chromosome Aberrations; DDT; Diethylnitrosamine; Diploidy; Hepatectomy; Hexachlorocyclohexane; Hydrazines; Liver; Liver Neoplasms; Liver Regeneration; Male; Methionine; Mitosis; Nitroso Compounds; Rats | 1975 |
The anticlastogenic effect of various combinations of cysteamine, AET, HCT, and amino acids on chromosome damage by trenimon and bleomycin in human lymphocytes in vitro.
Topics: Alkylating Agents; Amino Acids, Sulfur; Aspartic Acid; beta-Aminoethyl Isothiourea; Bleomycin; Chromosome Aberrations; Chromosomes; Cysteamine; Cysteine; Lactones; Methionine; Mutagens; Serine; Triaziquone | 1978 |
Reversion in variants from a duplication strain of Aspergillus nidulans.
Topics: Aspergillus nidulans; Chromosome Aberrations; Gene Frequency; Genes; Methionine; Mitosis; Mutation; Suppression, Genetic; Ultraviolet Rays | 1978 |
[Growth disorders. Classification, diagnosis, therapy. 3. Excessive growth: constitutional tallness, endocrine tallness, chromosome abnormalities, tallness with unusual proportions, tallness in metabolic diseases].
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Endocrine System Diseases; Growth Disorders; Homocystinuria; Humans; Marfan Syndrome; Methionine; Obesity; Puberty, Precocious | 1979 |
Comparative studies on the specificity of anticlastogenic action in human lymphocytes in culture.
Topics: Asparagine; beta-Aminoethyl Isothiourea; Busulfan; Cells, Cultured; Chromosome Aberrations; Chromosomes; Culture Media; Cysteamine; Cysteine; Dose-Response Relationship, Drug; Humans; Lymphocytes; Methionine; Mutagens; Oxyquinoline; Triaziquone | 1976 |
[Studies on the influence of some amino acids on the chromosome-damaging activity of Trenimon in human lymphocytes in vitro].
Topics: Alanine; Amino Acids; Arginine; Asparagine; Cells, Cultured; Chromosome Aberrations; Genetic Techniques; Glutamates; Histidine; Humans; Lymphocytes; Methionine; Time Factors; Triaziquone | 1973 |
[Protective effect of methionine against cytogenetic abnormalities of leukocytes and spermatocytes induced by ethionine in rats].
Topics: Animals; Chromosome Aberrations; DNA; Drug Antagonism; Ethionine; Injections, Intraperitoneal; Leukocytes; Male; Methionine; Mitosis; Molecular Biology; Rats; Spermatozoa | 1972 |
[Comparative study of cytogenetic anomalies and hematologic, hepatic and testicular effects of ethionine in rats. Protective power of methionine].
Topics: Animals; Body Weight; Bone Marrow; Bone Marrow Cells; Chromosome Aberrations; Chromosomes; Ethionine; Liver; Male; Methionine; Mitosis; Neutrophils; Organ Size; Rats; Testis | 1972 |
[Comparative studies on the influence of radioprotectors and amino acids on the chromosome-damaging activity of 8-hydroxyquinoline sulfate in human lymphocytes in vitro].
Topics: Alanine; Amino Acids; Arginine; Asparagine; beta-Aminoethyl Isothiourea; Cells, Cultured; Chromatids; Chromosome Aberrations; Chromosomes; Cysteamine; Cysteine; Dose-Response Relationship, Drug; Glutamates; Histidine; Humans; Lymphocytes; Methionine; Quinolines | 1973 |
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 |
[Cystathioninuria].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Chromosome Aberrations; Chromosome Disorders; Humans; Intellectual Disability; Methionine; Pyridoxine | 1969 |
Methionine induction of experimental tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Chromosome Aberrations; Chromosome Disorders; Guinea Pigs; Methionine; Pancreas; Tyrosine | 1967 |
Cystathioninuria not associated with vitamin B6 dependency: a probably new type of cystathioninuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Child; Child, Preschool; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Cystine; Electroencephalography; Humans; Infant; Liver; Liver Function Tests; Male; Methionine; Pyridoxine; Riboflavin; Serine; Sulfates | 1968 |