methionine has been researched along with Abnormalities, Congenital in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (44.44) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 1 (11.11) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 1 (11.11) | 2.80 |
Authors | Studies |
---|---|
Elder, K; Ménézo, Y | 1 |
Arning, E; Bottiglieri, T; Caudill, MA; Christensen, KE; Deng, L; Greene, ND; Jerome-Majewska, L; Krupenko, NI; Leung, KY; MacKenzie, RE; Malysheva, OV; Rozen, R | 1 |
HAYASHI, K; KAGEYAMA, M; NISHIMURA, H | 1 |
ANTENER, I; HOOFT, C; OYAERT, W; SNOECK, J; TIMMERMANS, J; VANDENHENDE, C | 1 |
CARSON, NA; DENT, CE; FIELD, CM; GAULL, GE | 1 |
Allen, WP | 1 |
Brent, RL; Fawcett, LB; Pugarelli, JE | 1 |
Carone, FA; Dalecki, TM; Kanwar, YS; Lelongt, B; Liu, ZZ; Wallner, EI | 1 |
Chiang-Teng, C; Clark, SH; Dassell, SW; Scott, CR; Swedberg, KR | 1 |
2 review(s) available for methionine and Abnormalities, Congenital
Article | Year |
---|---|
Epigenetic remodeling of chromatin in human ART: addressing deficiencies in culture media.
Topics: Amino Acids; Blastocyst; Chromatin; Chromatin Assembly and Disassembly; Congenital Abnormalities; Culture Media; DNA Methylation; DNA Repair; Embryo Culture Techniques; Embryonic Development; Endocrine Disruptors; Female; Genomic Imprinting; Glucose; Humans; Infant, Newborn; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oocytes; Oxidative Stress; Pregnancy; Reproductive Techniques, Assisted; S-Adenosylmethionine | 2020 |
Folic acid in the prevention of birth defects.
Topics: Congenital Abnormalities; Female; Folic Acid; Homocysteine; Humans; Methionine; Neural Tube Defects; Preconception Care; Pregnancy; Prenatal Care | 1996 |
7 other study(ies) available for methionine and Abnormalities, Congenital
Article | Year |
---|---|
A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development.
Topics: Aminohydrolases; Animals; Cell Proliferation; Cells, Cultured; Choline; Congenital Abnormalities; Embryo Loss; Embryonic Development; Female; Folic Acid; Formate-Tetrahydrofolate Ligase; Gene Knock-In Techniques; Genetic Variation; Humans; Leucovorin; Leukocyte Count; Male; Methionine; Methylenetetrahydrofolate Dehydrogenase (NADP); Methylenetetrahydrofolate Reductase (NADPH2); Mice; Mice, Inbred C57BL; Models, Animal; Multienzyme Complexes; Multifunctional Enzymes; Mutagenesis, Site-Directed; Polymorphism, Single Nucleotide; Pregnancy; Pregnancy Complications; Purines | 2013 |
Teratogenic effect of the methionine derivatives upon the mouse embryos.
Topics: Animals; Congenital Abnormalities; Methionine; Mice; Teratogenesis | 1962 |
METHIONINE MALABSORPTION IN A MENTALLY DEFECTIVE CHILD.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Congenital Abnormalities; Diarrhea; Diarrhea, Infantile; Feces; Hair; Humans; Hydroxybutyrates; Intellectual Disability; Intestines; Methionine; Proteins; Respiration Disorders; Respiratory Tract Diseases; Seizures; Urine | 1964 |
HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Bone Diseases; Brain; Brain Diseases; Cardiovascular Diseases; Cerebrospinal Fluid; Child; Chromatography; Congenital Abnormalities; Eye Diseases; Facial Expression; Fatty Liver; Foot Diseases; Genetics, Medical; Homocystinuria; Humans; Hydro-Lyases; Infant; Intellectual Disability; Lens, Crystalline; Liver; Metabolism; Methionine; Urine | 1965 |
Effects of supplemental methionine on antiserum-induced dysmorphology in rat embryos cultured in vitro.
Topics: Animals; Congenital Abnormalities; Culture Techniques; Dose-Response Relationship, Drug; Embryo, Mammalian; Female; Folic Acid; Immune Sera; Lethal Dose 50; Leucine; Maternal Exposure; Methionine; Rats; Rats, Wistar; Yolk Sac | 2000 |
Mannose-induced dysmorphogenesis of metanephric kidney. Role of proteoglycans and adenosine triphosphate.
Topics: Adenosine Triphosphate; Animals; Autoradiography; Congenital Abnormalities; Immunohistochemistry; Kidney; Mannose; Methionine; Mice; Proteoglycans | 1992 |
Cystathioninemia: a benign genetic condition.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Butyrates; Child; Child, Preschool; Congenital Abnormalities; Cysteine; Female; Homozygote; Humans; Intellectual Disability; Keto Acids; Male; Methionine; Pyridoxine | 1970 |