methionine has been researched along with Down Syndrome in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (17.65) | 18.7374 |
| 1990's | 5 (29.41) | 18.2507 |
| 2000's | 6 (35.29) | 29.6817 |
| 2010's | 3 (17.65) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, YQ; Guo, WY; Li, T; Su, FJ; Zhang, YX | 1 |
| Geisel, J; Gortner, L; Hartmuth, K; Herrmann, W; Nijhout, HF; Obeid, R; Reed, MC; Rohrer, TR | 1 |
| Duncan, TM; Nijhout, HF; Reed, MC | 1 |
| Bresolin, N; Castelli, E; Comi, GP; Crimi, M; Del Bo, R; Giorda, R; Locatelli, F; Martinelli-Boneschi, F; Pozzoli, U; Scarlato, G | 1 |
| Tapiero, H; Tew, KD; Townsend, DM | 1 |
| Eskes, TK | 1 |
| Coppus, AW; Egger, JI; Fekkes, D; Tuinier, S; van Duijn, CM; Verhoeven, WM | 1 |
| Andria, G; D'Angelo, S; D'Aniello, A; De Bonis, ML; Galletti, P; Ingrosso, D; Raimo, M; Scala, I; Sorrentino, A; Zappia, V | 1 |
| Sass, JO; Skladal, D; Viertler, E | 1 |
| Gaylor, DW; Gibson, JB; Hine, RJ; James, SJ; Melnyk, S; Pogribna, M; Pogribny, IP; Swenson, DH; Tafoya, DL; Wilson, VL; Yi, P | 1 |
| Chango, A; James, SJ; Melnyk, S; Pogribna, M; Pogribny, I; Yi, P | 1 |
| Emile, J; Houlgatte, R; Jabbour, W; Pouplard-Barthelaix, A | 1 |
| Gottfries, CG; Regland, B | 1 |
| Lejeune, J | 1 |
| Brattström, L; Hultberg, B; Israelsson, B; Tengborn, L | 1 |
| Borghi, E; Borowy, F; de Blois, MC; Lejeune, J; Maunoury-Burolla, C; Mir, M; Nicolle, L; Recan, D; Rethoré, MO | 1 |
| Allard, D; Ceballos, I; Chadefaux, B; Jérôme, H | 1 |
3 review(s) available for methionine and Down Syndrome
| Article | Year |
|---|---|
Sulfur containing amino acids and human disease.
Topics: Animals; Cysteine; Down Syndrome; Humans; Methionine; Neoplasms; Sulfur | 2004 |
Abnormal folate metabolism in mothers with Down syndrome offspring: review of the literature.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; DNA; Down Syndrome; Female; Ferredoxin-NADP Reductase; Folic Acid; Homocysteine; Homocystinuria; Humans; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mothers; Mutation | 2006 |
[The pathogenesis of mental retardation in trisomy 21].
Topics: Amyloid beta-Protein Precursor; Biopterins; Brain; Carbonic Acid; Cystathionine beta-Synthase; Down Syndrome; Folic Acid; Guanosine; Humans; Leucovorin; Mercaptopurine; Methionine; Neurons; Phosphofructokinase-1; Purines; Pyrimidines; S100 Proteins; Superoxide Dismutase; Thyroid Gland; Thyroxine | 1991 |
14 other study(ies) available for methionine and Down Syndrome
| Article | Year |
|---|---|
Identification of altered pathways in Down syndrome-associated congenital heart defects using an individualized pathway aberrance score.
Topics: Case-Control Studies; Dioxygenases; Down Syndrome; Gene Regulatory Networks; Heart Defects, Congenital; Humans; Membrane Glycoproteins; Metabolic Networks and Pathways; Methionine; NADPH Oxidase 2; NADPH Oxidases; Phagosomes | 2016 |
Blood biomarkers of methylation in Down syndrome and metabolic simulations using a mathematical model.
Topics: Adolescent; Adult; Betaine; Biomarkers; Case-Control Studies; Child; Child, Preschool; Choline; Cystathionine; Cysteine; Down Syndrome; Female; Glutathione; Humans; Infant; Male; Methionine; Methylation; Models, Theoretical; S-Adenosylhomocysteine; S-Adenosylmethionine; Sarcosine; Young Adult | 2012 |
The relationship between intracellular and plasma levels of folate and metabolites in the methionine cycle: a model.
Topics: Cystathionine beta-Synthase; Down Syndrome; Folic Acid; Folic Acid Deficiency; Half-Life; Homocysteine; Humans; Methionine; Methylation; Models, Theoretical; Nutrition Surveys; Nutritional Status; Oxidative Stress; S-Adenosylmethionine; Vitamin B 12 Deficiency; Vitamin B Complex; Vitamins | 2013 |
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.
Topics: Adolescent; Adult; Age Factors; Alleles; Amino Acid Substitution; Apolipoprotein E4; Apolipoproteins E; Child; Child, Preschool; Codon; Cognition Disorders; Down Syndrome; Female; Follow-Up Studies; Gene Frequency; Genotype; Humans; Intelligence Tests; Male; Methionine; Mutation; Polymorphism, Genetic; Prions; Valine | 2003 |
Plasma amino acids and neopterin in healthy persons with Down's syndrome.
Topics: Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biomarkers; Comorbidity; Dopamine; Down Syndrome; Female; Homocysteine; Homovanillic Acid; Humans; Immune System Diseases; Immunity, Cellular; Male; Methionine; Middle Aged; Neopterin; Taurine; Up-Regulation | 2007 |
Accumulation of altered aspartyl residues in erythrocyte proteins from patients with Down's syndrome.
Topics: Case-Control Studies; Child; Down Syndrome; Erythrocyte Aging; Erythrocyte Membrane; Herpesvirus 4, Human; Humans; Isoaspartic Acid; Lymphocytes; Membrane Proteins; Methemoglobin; Methionine; Methylation; Oxidative Stress; Protein D-Aspartate-L-Isoaspartate Methyltransferase; Recombinant Proteins; S-Adenosylhomocysteine | 2007 |
Methionine loading in a Down's syndrome patient with cerebral infarction.
Topics: Adult; Cerebral Infarction; Down Syndrome; Homocysteine; Humans; Male; Methionine; Thiobarbituric Acid Reactive Substances | 1999 |
Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome.
Topics: Adult; Alcohol Drinking; Case-Control Studies; Chromatography, High Pressure Liquid; Deoxyribonucleases, Type II Site-Specific; Diet Surveys; Diet, Reducing; Dietary Supplements; DNA; Down Syndrome; Electrophoresis, Agar Gel; Female; Folic Acid; Genotype; Homocysteine; Humans; Methionine; Methotrexate; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Polymerase Chain Reaction; Risk Factors; Surveys and Questionnaires | 1999 |
Homocysteine metabolism in children with Down syndrome: in vitro modulation.
Topics: Adenosine; Case-Control Studies; Child; Chromatography, High Pressure Liquid; Cystathionine; Cystathionine beta-Synthase; Cysteine; DNA Methylation; Down Syndrome; Glutathione; Homocysteine; Humans; Leucovorin; Lymphocytes; Methionine; Oxidative Stress; S-Adenosylhomocysteine; S-Adenosylmethionine; Sarcosine; Superoxide Dismutase; Thymidine; Vitamin B 12 | 2001 |
Abnormal expression of actin in lymphocytes of Alzheimer's disease and Down's syndrome patients.
Topics: Actins; Aged; Aged, 80 and over; Alzheimer Disease; Culture Media; Down Syndrome; Electrophoresis, Gel, Two-Dimensional; Female; Humans; Immunoblotting; Lymphocytes; Male; Methionine; Middle Aged; Peptide Mapping | 1992 |
Slowed synthesis of DNA and methionine is a pathogenetic mechanism common to dementia in Down's syndrome, AIDS and Alzheimer's disease?
Topics: AIDS Dementia Complex; Alzheimer Disease; Amyloidosis; Cell Death; Dementia; DNA; DNA Repair; DNA Replication; Down Syndrome; Humans; Methionine; Models, Biological | 1992 |
Homocysteine, factor VII and antithrombin III in subjects with different gene dosage for cystathionine beta-synthase.
Topics: Antithrombin III; Cystathionine beta-Synthase; Dosage Compensation, Genetic; Down Syndrome; Factor VII; Female; Homocysteine; Homozygote; Humans; Hydro-Lyases; Male; Methionine | 1989 |
[Metabolism of monocarbons and trisomy 21: sensitivity to methotrexate].
Topics: Cells, Cultured; Dose-Response Relationship, Drug; Down Syndrome; Homocysteine; Humans; Lymphocytes; Methionine; Methotrexate; Mitotic Index; Purines | 1986 |
[Effects of gene localization and its metabolic significance in trisomy 21].
Topics: Chromosome Mapping; Chromosomes, Human, 21-22 and Y; Cystathionine; Cystathionine beta-Synthase; Down Syndrome; Fibroblasts; Homocysteine; Homocystinuria; Humans; Methionine | 1985 |