Works matching DE "METHYLENETETRAHYDROFOLATE reductase"
Results: 988
Quorum sensing in Vibrio controls carbon metabolism to optimize growth in changing environmental conditions.
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- PLoS Biology, 2024, v. 22, n. 11, p. 1, doi. 10.1371/journal.pbio.3002891
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- Article
Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease.
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- Molecular & Cellular Biochemistry, 2009, v. 325, n. 1/2, p. 199, doi. 10.1007/s11010-009-0038-0
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- Article
MTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension in Indians.
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- Molecular & Cellular Biochemistry, 2007, v. 302, n. 1/2, p. 125, doi. 10.1007/s11010-007-9434-5
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- Article
The MTHFR 677CâT polymorphism and risk of prostate cancer: results from the CAPS study.
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- Cancer Causes & Control, 2007, v. 18, n. 10, p. 1169, doi. 10.1007/s10552-007-9055-z
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- Article
Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and the risk of primary Hepatocellular Carcinoma (HCC) in a Chinese population.
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- Cancer Causes & Control, 2007, v. 18, n. 6, p. 665
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- Article
Study on Maternal SNPs of MTHFR Gene and HCY Level Related to Congenital Heart Diseases.
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- Pediatric Cardiology, 2021, v. 42, n. 1, p. 42, doi. 10.1007/s00246-020-02449-1
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- Article
A Genetic Variant in FIGN Gene Reduces the Risk of Congenital Heart Disease in Han Chinese Populations.
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- Pediatric Cardiology, 2017, v. 38, n. 6, p. 1169, doi. 10.1007/s00246-017-1636-3
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- Article
Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation (Communicated by Jan P. Kraus).
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- Human Mutation, 2003, v. 21, n. 5, p. 509, doi. 10.1002/humu.10193
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- Article
Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD‐responsive mutationCommunicated by Jan P. Kraus.
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- Human Mutation, 2003, v. 21, n. 5, p. 509, doi. 10.1002/humu.10193
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- Article
Genetic polymorphism of MTHFR C677T with preterm birth and low birth weight susceptibility: a meta-analysis.
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- 2017
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- journal article
The association between MTHFR polymorphisms and cervical cancer risk: a system review and meta analysis.
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- 2016
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- journal article
Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation.
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- 2016
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- journal article
Methylenetetrahydrofolate reductase gene polymorphisms and recurrent pregnancy loss in China: a systematic review and meta-analysis.
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- 2016
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- journal article
The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
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- Archives of Gynecology & Obstetrics, 2015, v. 291, n. 6, p. 1303, doi. 10.1007/s00404-014-3561-5
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- Article
Investigation of the effects of MTHFR gene variations and homocysteine levels in hypertensive patients.
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- Northern Clinics of Istanbul, 2025, v. 12, n. 1, p. 55, doi. 10.14744/nci.2023.84770
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- Article
The frequency of Raynaud's phenomenon in patients with methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemia.
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- Turkish Journal of Medical Sciences, 2019, v. 49, n. 5, p. 1444, doi. 10.3906/sag-1903-206
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- Article
Distribution of prothrombin G20210A, factor V Leiden, and MTHFR C677T mutations in the middle Black Sea area (Tokat) of Turkey.
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- Turkish Journal of Medical Sciences, 2012, v. 42, n. 6, p. 1093, doi. 10.3906/sag-1107-51
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- Article
Gender-Specific Effect of Mthfr Genotype and Neonatal Vigabatrin Interaction on Synaptic Proteins in Mouse Cortex.
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- Neuropsychopharmacology, 2011, v. 36, n. 8, p. 1714, doi. 10.1038/npp.2011.52
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- Article
Mthfr polymorphisms as possible markers of treatment response in first-episode psychosis.
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- European Psychiatry, 2020, v. 63, p. S22
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- Article
Detection of the relationship between clinical features consist of psychopathy levels and MTHFR mutation among subjects with antisocial personality disorder.
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- European Psychiatry, 2016, v. 33, p. S249, doi. 10.1016/j.eurpsy.2016.01.503
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- Article
Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and antipsychotic-induced metabolic disturbances in first-episode schizophrenia patients.
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- European Psychiatry, 2016, v. 33, p. S106, doi. 10.1016/j.eurpsy.2016.01.086
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- Article
Distribution of 1298A>C polymorphism of methylenetetrahydrofolate reductase gene in patients with bipolar disorder and schizophrenia
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- European Psychiatry, 2007, v. 22, n. 1, p. 39, doi. 10.1016/j.eurpsy.2006.11.003
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- Article
ДОСЛІДЖЕННЯ ВЗАЄМОЗВ'ЯЗКІВ ПОЛІМОРФІЗМІВ ГЕНІВ ФЕРМЕНТІВ ФОЛАТНОГО ЦИКЛУ З РІВНЯМИ ГОМОЦИСТЕЇНУ ТА ФОЛІЄВОЇ КИСЛОТИ ЯК ФАКТОРІВ РИЗИКУ СЕРЦЕВО-СУДИННИХ ПОРУШЕНЬ У ПОСТКОВІДНОМУ ПЕРІОДІ.
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- Medical Perspectives / Medičnì Perspektivi, 2024, v. 29, n. 3, p. 4, doi. 10.26641/2307-0404.2024.3.313071
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- Article
СLINICAL CASE OF FUNICULAR MYELOSIS IN COMBINATION WITH A CONCOMITANT GENETIC PREDISPOSITION TO FOLATE CYCLE DISORDER.
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- Medical Perspectives / Medičnì Perspektivi, 2024, v. 29, n. 2, p. 229, doi. 10.26641/2307-0404.2024.2.307773
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- Article
Differentiated Thyroid Cancer Genetic Mechanisms - Focus on Vitamin D Receptor and Methylenetetrahydrofolate Reductase Gene Polymorphisms.
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- Medicina Moderna, 2022, v. 29, n. 1, p. 7, doi. 10.31689/rmm.2021.29.1.7
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- Article
High incidence of MTHFR, CBS, and MTRR polymorphisms in vitiligo patients. Preliminary report in a retrospective study.
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- European Review for Medical & Pharmacological Sciences, 2019, v. 23, n. 2, p. 471, doi. 10.26355/eurrev_201901_16858
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- Article
Methylenetetraydrofolate Reductase Gene Polymorphisms In Saudi Patients with Schizophrenia.
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- Arab Journal of Psychiatry, 2014, v. 25, n. 2, p. 180, doi. 10.12816/0006766
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- Article
Evaluation of pai-1 polymorphisms in central and peripheral thromboembolies.
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- Journal of Experimental & Clinical Medicine / Deneysel ve Klinik Tip Dergisi, 2021, v. 38, n. 2, p. 167, doi. 10.52142/omujecm.38.2.20
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- Article
Association of the plasm homocysteine levels and methylenetetrahydrofolate reductase C677T polymorphisms with essential hypertension in Han nationality in Xinjiang.
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- Journal of Xi'an Jiaotong University (Medical Sciences), 2014, v. 35, n. 1, p. 59, doi. 10.7652/jdyxb201401013
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- Article
Study on the association between the MTHFR gene C677T polymorphism and venous thromboembolism (VTE) in the Chinese population.
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- Journal of Xi'an Jiaotong University (Medical Sciences), 2013, v. 34, n. 6, p. 818, doi. 10.7652/jdyxb201306024
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- Article
Pharmacogenetic profiling of paediatric oncology patients: a single-centre experience.
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- Paediatria Croatica, 2024, v. 68, n. 2, p. 55, doi. 10.13112/PC.2024.8
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- Article
Association between the A1298C Polymorphism of the Methylenetetrahydrofolate Reductase Gene and Recurrent Spontaneous Abortion.
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- Iranian Journal of Neonatology, 2014, v. 5, n. 2, p. 7
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- Article
Co-Occurring Methylenetetrahydrofolate Reductase (MTHFR) rs1801133 and rs1801131 Genotypes as Associative Genetic Modifiers of Clinical Severity in Rett Syndrome.
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- Brain Sciences (2076-3425), 2024, v. 14, n. 7, p. 624, doi. 10.3390/brainsci14070624
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- Article
The Role of Folate Deficiency as a Potential Risk Factor for Nontraumatic Anterior Spinal Artery Syndrome in an Adolescent Girl.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 11, p. 1470, doi. 10.3390/brainsci12111470
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- Article
MTHFR Gene Polymorphisms Prevalence and Cardiovascular Risk Factors Involved in Cardioembolic Stroke Type and Severity.
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- Brain Sciences (2076-3425), 2020, v. 10, n. 8, p. 476, doi. 10.3390/brainsci10080476
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- Article
MTHFR SNPs (Methyl Tetrahydrofolate Reductase, Single Nucleotide Polymorphisms) C677T and A1298C Prevalence and Serum Homocysteine Levels in >2100 Hypofertile Caucasian Male Patients.
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- Biomolecules (2218-273X), 2022, v. 12, n. 8, p. 1086, doi. 10.3390/biom12081086
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- Article
MTHFR inhibits TRC8‐mediated HMOX1 ubiquitination and regulates ferroptosis in ovarian cancer.
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- Clinical & Translational Medicine, 2022, v. 12, n. 9, p. 1, doi. 10.1002/ctm2.1013
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- Article
Association Between MTHFR rs17367504 Polymorphism and Major Depressive Disorder in Taiwan: Evidence for Effect Modification by Exercise Habits.
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- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.821448
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- Article
Methylenetetrahydrofolate Reductase Genetic Polymorphisms in Patients with Primary Open-Angle Glaucoma.
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- Ophthalmic Genetics, 2007, v. 28, n. 2, p. 47, doi. 10.1080/13816810701329046
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- Article
The C677T Variant in the Methylenetetrahydrofolate Reductase Gene Is Not Associated with Disease in Cohorts of Pseudoexfoliation Glaucoma and Primary Open-Angle Glaucoma Patients from Iowa.
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- Ophthalmic Genetics, 2006, v. 27, n. 2, p. 39, doi. 10.1080/13816810600677883
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- Article
Case Report: Homozygous C677T MTHFR Gene Mutation in Male with Hypogonadism.
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- Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/6945124
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- Article
Case Report: Homozygous C677T MTHFR Gene Mutation in Male with Hypogonadism.
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- Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/6945124
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- Article
Arterial thrombosis associated with factor V Leiden and methylenetetrahydrofolate reductase C677T mutation in childhood membranous glomerulonephritis.
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- 2008
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- Report
Henoch–Schonlein purpura: polymorphisms in thrombophilia genes.
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- Pediatric Nephrology, 2006, v. 21, n. 8, p. 1117, doi. 10.1007/s00467-006-0155-x
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- Article
Polymorphism in ADH and MTHFR genes in oral squamous cell carcinoma of Indians.
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- Oral Diseases, 2008, v. 14, n. 7, p. 633, doi. 10.1111/j.1601-0825.2007.01437.x
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- Article
Association of c.+677 C>T (rs1801133) and c.+1298 A>C (rs1801131) MTHFR genetic variants with cardiometabolic and disease risk in systemic lupus erythematosus patients: A cross-sectional study.
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- Lupus, 2024, v. 33, n. 9, p. 918, doi. 10.1177/09612033241257158
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- Article
Influence of 677 C→T Polymorphism of Methylenetetrahydrofolate Reductase on Medium-Term Prognosis after Acute Coronary Syndromes.
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- Texas Heart Institute Journal, 2007, v. 34, n. 2, p. 142
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- Article
Methylenetetrahydrofolate Reductase C677T and A1298C Mutations in Women with Recurrent Spontaneous Abortions in the Northwest of Iran.
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- ISRN Obstetrics & Gynecology, 2012, p. 1, doi. 10.5402/2012/945486
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- Article
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy.
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- Genes, 2023, v. 14, n. 5, p. 980, doi. 10.3390/genes14050980
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- Article
Methylenetetrahydrofolate Reductase Polymorphism (rs1801133) and the Risk of Hypertension among African Populations: A Narrative Synthesis of Literature.
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- Genes, 2022, v. 13, n. 4, p. 631, doi. 10.3390/genes13040631
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- Article