Page last updated: 2024-08-17

methionine and Abnormalities, Autosome

methionine has been researched along with Abnormalities, Autosome in 22 studies

Research

Studies (22)

TimeframeStudies, this research(%)All Research%
pre-199015 (68.18)18.7374
1990's1 (4.55)18.2507
2000's4 (18.18)29.6817
2010's1 (4.55)24.3611
2020's1 (4.55)2.80

Authors

AuthorsStudies
Binz, RL; Garg, S; Hauer-Jensen, M; Koturbash, I; Miousse, IR; Pathak, R; Sadhukhan, R; Zhou, D1
Cho, YW; Kim, DK; Lim, JG; Motamedi, GK; Yi, SD1
Boonen, S; Dubois, B; Goris, A; Hersmus, N; Lemmens, R; Matthijs, G; Race, V; Robberecht, W; Van Damme, P; Van Den Bosch, L1
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC1
Apter, A; Burg, M; Carmel, M; Frisch, A; Gothelf, D; Inbar, D; Korostishevsky, M; Michaelovsky, E; Steinberg, T; Weizman, A1
Giraudier, S; Michot, JM; Papo, T; Sedel, F; Smiejan, JM1
Rozynkowa, D; Stepień, J1
Bonassi, S; De Biase, A; Deeva, IB; Degan, P; Doronin, YK; Iaccarino, M; Korkina, LG; Oral, R; Pagano, G; Warnau, M1
Hitachi, PM; Takayama, S; Yamada, K1
Gebhart, E3
Azevedo, JL; Menezes, EM1
Butenandt, O1
Becher, R; Gebhart, E1
Leder, P1
André, F; Aschkenasy, A2
van der Horst, JL; Wadman, SK1
Berger, R; Broyer, M1
Hansen, S; Hardwick, DF; Perry, TL; Pohlmann, L; Warrington, PD1
Nakagawa, H; Sato, T; Tada, K; Yokoyama, Y; Yoshida, T1

Reviews

1 review(s) available for methionine and Abnormalities, Autosome

ArticleYear
The elongation reactions in protein synthesis.
    Advances in protein chemistry, 1973, Volume: 27

    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

Other Studies

21 other study(ies) available for methionine and Abnormalities, Autosome

ArticleYear
Dietary Methionine Deficiency Enhances Genetic Instability in Murine Immune Cells.
    International journal of molecular sciences, 2021, Feb-27, Volume: 22, Issue:5

    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.
    Epilepsy & behavior : E&B, 2008, Volume: 13, Issue:2

    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.
    Journal of neurology, neurosurgery, and psychiatry, 2009, Volume: 80, Issue:3

    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.
    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
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
    The international journal of neuropsychopharmacology, 2008, Volume: 11, Issue:3

    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.
    Journal of neurology, neurosurgery, and psychiatry, 2008, Volume: 79, Issue:8

    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].
    Medycyna doswiadczalna i mikrobiologia, 1980, Volume: 32, Issue:4

    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.
    Pharmacology & toxicology, 1997, Volume: 81, Issue:3

    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.
    Journal of the National Cancer Institute, 1975, Volume: 54, Issue:5

    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.
    Human genetics, 1978, Aug-31, Volume: 43, Issue:2

    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.
    Molecular & general genetics : MGG, 1978, Sep-08, Volume: 164, Issue:3

    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].
    Fortschritte der Medizin, 1979, Nov-22, Volume: 97, Issue:44

    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.
    Human genetics, 1976, Apr-15, Volume: 32, Issue:1

    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].
    Humangenetik, 1973, May-25, Volume: 18, Issue:3

    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].
    Journal de physiologie, 1972, Volume: 65

    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].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1972, Volume: 166, Issue:10

    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].
    Mutation research, 1973, Volume: 18, Issue:3

    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.
    Acta paediatrica Scandinavica, 1971, Volume: 60, Issue:5

    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].
    La Presse medicale, 1969, Oct-22, Volume: 77, Issue:44

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography; Chromosome Aberrations; Chromosome Disorders; Humans; Intellectual Disability; Methionine; Pyridoxine

1969
Methionine induction of experimental tyrosinaemia.
    Journal of mental deficiency research, 1967, Volume: 11, Issue:4

    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.
    The Tohoku journal of experimental medicine, 1968, Volume: 95, Issue:3

    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