Artykuły w czasopismach na temat „MTHFR”
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Thompson, Henry R., Gayle M. Jones i Michael R. Narkewicz. "Ontogeny of hepatic enzymes involved in serine- and folate-dependent one-carbon metabolism in rabbits". American Journal of Physiology-Gastrointestinal and Liver Physiology 280, nr 5 (1.05.2001): G873—G878. http://dx.doi.org/10.1152/ajpgi.2001.280.5.g873.
Pełny tekst źródłaElsadig Babiker, Nihad. "Detection of Mthfr (C667t) and Mthfd (G1958a) Polymorphisms Among Sudanese Women with The Recurrent Miscarriages". Archives of Gynaecology and Women Health 1, nr 1 (6.02.2023): 01–04. http://dx.doi.org/10.58489/2836-497x/006.
Pełny tekst źródłaCole, Leslie, Alina Cernasev, Katie Webb, Santosh Kumar i A. Shaun Rowe. "A Study of the MTHFR Gene Prevalence in a Rural Tennessee Opioid Use Disorder Treatment Center Population". International Journal of Environmental Research and Public Health 19, nr 6 (10.03.2022): 3255. http://dx.doi.org/10.3390/ijerph19063255.
Pełny tekst źródłaKaragur, Ege, Mustafa Alay, Aydin Demiray, Nedim Karagenc, Onur Tokgün, Taner Durak i Hakan Akca. "The impact of hereditary thrombophilias in recurrent pregnancy loss". Genetika 54, nr 3 (2022): 1399–410. http://dx.doi.org/10.2298/gensr2203399k.
Pełny tekst źródłaMarosi, Krisztina, Annamária Ágota, Veronika Végh, József Gábor Joó, Zoltán Langmár, Ildikó †Kriszbacher i Zsolt B. Nagy. "The role of homocysteine and methylenetetrahydrofolate reductase, methionine synthase, methionine synthase reductase polymorphisms in the development of cardiovascular diseases and hypertension". Orvosi Hetilap 153, nr 12 (marzec 2012): 445–53. http://dx.doi.org/10.1556/oh.2012.29326.
Pełny tekst źródłaLiu, Zhiping, Hong Jiang, Justin H. Townsend i Jianhua Wang. "Effects of Ocufolin on retinal microvasculature in patients with mild non-proliferative diabetic retinopathy carrying polymorphisms of the MTHFR gene". BMJ Open Diabetes Research & Care 9, nr 1 (wrzesień 2021): e002327. http://dx.doi.org/10.1136/bmjdrc-2021-002327.
Pełny tekst źródłaLu, Mong-Liang, Wei-Chi Ku, Nailis Syifa, Shu-Chin Hu, Chia-Te Chou, Yi-Hsio Wu, Po-Hsiu Kuo, Chun-Hsin Chen, Wei J. Chen i Tzu-Hua Wu. "Developing a Sensitive Platform to Measure 5-Methyltetrahydrofolate in Subjects with MTHFR and PON1 Gene Polymorphisms". Nutrients 14, nr 16 (13.08.2022): 3320. http://dx.doi.org/10.3390/nu14163320.
Pełny tekst źródłaTsaousidou, Maria M. K. T., Fotis F. I. G. Girtovitis, Afroditi A. K. Boutou, Elefteria E. P. Pithara i Pantelis M. E. P. Makris. "Appliance of the DNA-Micro Array Technique for the Identification of Patients with Thrombophilic Diathesis. I-Comparison to the Classic PCR Analysis." Blood 104, nr 11 (16.11.2004): 4049. http://dx.doi.org/10.1182/blood.v104.11.4049.4049.
Pełny tekst źródłaSimonian, Rebecca, Emanuela Pannia, Rola Hammoud, Xiucheng Cui, Ruslan Kubant, Brandi Wasek, Terry Bottiglieri, James Dowling, Ramil Noche i G. Harvey Anderson. "Methylenetetrahydrofolate Reductase Deficiency Reduces Brain Microglia in Zebrafish During Embryonic Development and Is Not Corrected by Folic Acid". Current Developments in Nutrition 5, Supplement_2 (czerwiec 2021): 925. http://dx.doi.org/10.1093/cdn/nzab049_038.
Pełny tekst źródłaDevlin, Angela M., Erland Arning, Teodoro Bottiglieri, Frank M. Faraci, Rima Rozen i Steven R. Lentz. "Effect of Mthfr genotype on diet-induced hyperhomocysteinemia and vascular function in mice". Blood 103, nr 7 (1.04.2004): 2624–29. http://dx.doi.org/10.1182/blood-2003-09-3078.
Pełny tekst źródłaSoydan, Ender A., Pervin Topcuoglu, Muhit Ozcan, Onder Arslan, Gunhan Gurman, Meral Beksac, Mutlu Arat i Osman Ilhan. "The Impact of Methylenetetrahydrofolate Reductase C677T Gene Polymorphism on Engraftment after Allogeneic Hematopoetic Cell Transplantation." Blood 106, nr 11 (16.11.2005): 5318. http://dx.doi.org/10.1182/blood.v106.11.5318.5318.
Pełny tekst źródłaXie, Xiong-wei, Mao-ren Wang i Yong-lian Zhang. "Methylenetetrahydrofolate reductase polymorphism and capecitabine-induced toxicity in patients with gastric cancer". Tropical Journal of Pharmaceutical Research 19, nr 1 (9.04.2020): 195–99. http://dx.doi.org/10.4314/tjpr.v19i1.28.
Pełny tekst źródłaStangler Herodež, Š., B. Zagradišnik, A. Erjavec Škerget, A. Zagorac, I. Takač, V. Vlaisavljević, L. Lokar i N. Kokalj Vokač. "MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions". Balkan Journal of Medical Genetics 16, nr 1 (1.06.2013): 31–39. http://dx.doi.org/10.2478/bjmg-2013-0015.
Pełny tekst źródłaHe, Wei, Minzhi Lu, Guoqing Li, Zhigang Sun, Dinghua Liu i Lujun Gu. "Methylene Tetrahydrofolate Reductase (MTHFR) rs868014 Polymorphism Regulated by miR-1203 Associates with Risk and Short Term Outcome of Ischemic Stroke". Cellular Physiology and Biochemistry 41, nr 2 (2017): 701–10. http://dx.doi.org/10.1159/000458429.
Pełny tekst źródłaSiraj, Abdul K., Rong Bu, Mona Ibrahim, Maha Al-Rasheed, Shahab Uddin, Adnan Ezzat i Khawla Al-Kuraya. "Genetic Polymorphisms of Methylenetetrahydrofolate Reductase Genes and Diffuse Large B-Cell Lymphoma Risk in Middle Eastern Population." Blood 108, nr 11 (16.11.2006): 4609. http://dx.doi.org/10.1182/blood.v108.11.4609.4609.
Pełny tekst źródłaLi, Zhen, Ji Zhang, Wei Zou, Qi Xu, Siyuan Li, Jie Wu, Li Zhu i in. "The methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism is associated with breast cancer subtype susceptibility in southwestern China". PLOS ONE 16, nr 7 (9.07.2021): e0254267. http://dx.doi.org/10.1371/journal.pone.0254267.
Pełny tekst źródłaSCHWAHN, Bernd C., Maurice D. LARYEA, Zhoutao CHEN, Stepan MELNYK, Igor POGRIBNY, Timothy GARROW, S. Jill JAMES i Rima ROZEN. "Betaine rescue of an animal model with methylenetetrahydrofolate reductase deficiency". Biochemical Journal 382, nr 3 (7.09.2004): 831–40. http://dx.doi.org/10.1042/bj20030822.
Pełny tekst źródłaLazic, Jelena, Nikola Kotur, Nada Krstovski, Lidija Dokmanovic, Branka Zukic, Jelica Predojevic-Samardzic, Maja Zivotic i in. "Importance of pharmacogenetic markers in the methylenetetrahydrofolate reductase gene during methotrexate treatment in pediatric patients with acute lymphoblastic leukemia". Archives of Biological Sciences 69, nr 2 (2017): 239–46. http://dx.doi.org/10.2298/abs160325091l.
Pełny tekst źródłaClark, Daniel F., Rachael Schmelz, Nicole Rogers, Nuri E. Smith i Kimberly R. Shorter. "Acute high folic acid treatment in SH-SY5Y cells with and without MTHFR function leads to gene expression changes in epigenetic modifying enzymes, changes in epigenetic marks, and changes in dendritic spine densities". PLOS ONE 16, nr 1 (7.01.2021): e0245005. http://dx.doi.org/10.1371/journal.pone.0245005.
Pełny tekst źródłaFÖDINGER, MANUELA, HEIDI BUCHMAYER, GOTFRIED HEINZ, MENELAOS PAPAGIANNOPOULOS, JOSEF KLETZMAYR, SUSANNE RASOUL-ROCKENSCHAUB, WALTER H. HÖRL i GERE SUNDER-PLASSMANN. "Effect of MTHFR 1298A→C and MTHFR 677C→T Genotypes on Total Homocysteine, Folate, and Vitamin B12 Plasma Concentrations in Kdiney Graft Recipients". Journal of the American Society of Nephrology 11, nr 10 (październik 2000): 1918–25. http://dx.doi.org/10.1681/asn.v11101918.
Pełny tekst źródłaZhang, Yong-lian, i Xiong-wei Xie. "Methylenetetrahydrofolate reductase C677T polymorphism and toxicity to 5-FU-based chemotherapy in colorectal cancer". Tropical Journal of Pharmaceutical Research 19, nr 1 (9.04.2020): 209–13. http://dx.doi.org/10.4314/tjpr.v19i1.30.
Pełny tekst źródłaChan, Donovan, Duncan W. Cushnie, Oana R. Neaga, Andrea K. Lawrance, Rima Rozen i Jacquetta M. Trasler. "Strain-Specific Defects in Testicular Development and Sperm Epigenetic Patterns in 5,10-Methylenetetrahydrofolate Reductase-Deficient Mice". Endocrinology 151, nr 7 (5.05.2010): 3363–73. http://dx.doi.org/10.1210/en.2009-1340.
Pełny tekst źródłaNguyễn, Thu Hằng, Thị Trang Nguyễn, Huy Thịnh Trần, Thị Huyền Vũ, Minh Tuấn Nguyễn, Thị Tình Phan, Hoàng Linh Dương i Thị Minh Lê. "KHẢO SÁT MỘT SỐ ĐA HÌNH GEN (MTHFR, MTR, MTRR) Ở PHỤ NỮ CÓ TIỀN SỬ SẢY THAI". Tạp chí Sinh lý học Việt Nam 25, nr 4 (13.06.2022): 23–29. http://dx.doi.org/10.54928/vjop.v25i4.35.
Pełny tekst źródłaHe, Yan, Zhengbao Zhu, Daoxia Guo, Huan Zhang, Xiaowei Zheng, Nimei Zeng, Qiu Zhang i in. "The U-shaped Relationship Between Serum Methylene Tetrahydrofolate Reductase and Large-artery Atherosclerotic Stroke". Current Neurovascular Research 16, nr 1 (13.05.2019): 82–88. http://dx.doi.org/10.2174/1567202616666190207161818.
Pełny tekst źródłaBagher, Amina M., Alexander P. Young, Thikryat Neamatallah, Reham M. Al-Amoudi, Sara M. Bagher i Eileen M. Denovan-Wright. "Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment". Annals of Saudi Medicine 41, nr 1 (styczeń 2021): 1–7. http://dx.doi.org/10.5144/0256-4947.2021.1.
Pełny tekst źródłaGupta, Akriti, Shubhangi Sharma, Saikrishna Lakkakula i Lakkakula VKS Bhaskar. "Association between the methylenetetrahydrofolate reductase (MTHFR) gene 677C>T and 1298A>C polymorphisms and the risk of diabetic nephropathy; a meta-analysis". Journal of Renal Injury Prevention 8, nr 3 (18.06.2019): 175–84. http://dx.doi.org/10.15171/jrip.2019.33.
Pełny tekst źródłaJadavji, Nafisa M., Lauren K. Murray, Joshua T. Emmerson, Chris A. Rudyk, Shawn Hayley i Patrice D. Smith. "Paraquat Exposure Increases Oxidative Stress Within the Dorsal Striatum of Male Mice With a Genetic Deficiency in One-carbon Metabolism". Toxicological Sciences 169, nr 1 (6.02.2019): 25–33. http://dx.doi.org/10.1093/toxsci/kfz034.
Pełny tekst źródłaShen, Yaqing, Zhujun Wang, Fen Zhou i Runming Jin. "The influence of MTHFR genetic polymorphisms on methotrexate therapy in pediatric acute lymphoblastic leukemia". Open Life Sciences 16, nr 1 (1.01.2021): 1203–12. http://dx.doi.org/10.1515/biol-2021-0121.
Pełny tekst źródłaCoppedè, Stoccoro, Tannorella, Gallo, Nicolì i Migliore. "Association of Polymorphisms in Genes Involved in One-Carbon Metabolism with MTHFR Methylation Levels". International Journal of Molecular Sciences 20, nr 15 (31.07.2019): 3754. http://dx.doi.org/10.3390/ijms20153754.
Pełny tekst źródłaBisht, Shilpa, Bhavna Chawla i Rima Dada. "Oxidative Stress and Polymorphism in MTHFR SNPs (677 and 1298) in Paternal Sperm DNA is Associated with an Increased Risk of Retinoblastoma in Their Children: A Case–Control Study". Journal of Pediatric Genetics 07, nr 03 (11.07.2018): 103–13. http://dx.doi.org/10.1055/s-0038-1667037.
Pełny tekst źródłaWu, Ming-Tsung, Wei-Ting Ye, Yi-Cheng Wang, Po-Ming Chen, Jun-You Liu, Chien-Kuo Tai, Feng-Yao Tang, Jian-Rong Li, Chun-Chi Liu i En-Pei Isabel Chiang. "MTHFR Knockdown Assists Cell Defense against Folate Depletion Induced Chromosome Segregation and Uracil Misincorporation in DNA". International Journal of Molecular Sciences 22, nr 17 (30.08.2021): 9392. http://dx.doi.org/10.3390/ijms22179392.
Pełny tekst źródłaGoekkurt, Eray, Jan Stoehlmacher, Christian Stueber, Christine Wolschke, Tatjana Zabelina, Thomas Eiermann, Thomas Binder, Simona Iacobelli, Axel R. Zander i Nicolaus Kröger. "MTHFR-A1298C Polymorphism Is Associated with Veno-Occlusive Disease (VOD) and Liver Toxicity after Busulfan/Cyclophosphamide Conditioning Followed by Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)." Blood 106, nr 11 (16.11.2005): 2730. http://dx.doi.org/10.1182/blood.v106.11.2730.2730.
Pełny tekst źródłaPannia, Emanuela, Rebecca Simonian, Rola Hammoud, Xiucheng Cui, Ruslan Kubant, Brandi Wasek, Terry Bottiglieri, James Dowling, Ramil Noche i G. Harvey Anderson. "Development of a Zebrafish Model for Studies of the Interaction of Methylenetetrahydrofolate Reductase Deficiency and Dietary Folates on Metabolic Regulation". Current Developments in Nutrition 5, Supplement_2 (czerwiec 2021): 947. http://dx.doi.org/10.1093/cdn/nzab050_014.
Pełny tekst źródłaMosnier, Hannah, Erin Kelly, Kamaya Lawrence, Sarah Cruickshank, Sarah Stacey, Adelina McCall, Sunny Dhatt, Erland Arning, Teodoro Bottiglieri i Nafisa Jadavji. "The Role of One-Carbon Metabolism After Ischemic Stroke in an Aged Mouse Model". Current Developments in Nutrition 4, Supplement_2 (29.05.2020): 1226. http://dx.doi.org/10.1093/cdn/nzaa057_042.
Pełny tekst źródłaTrachtman, Joseph N., i Vincent Pagano. "Antifolates and MTHFR". Therapeutic Drug Monitoring 37, nr 6 (grudzień 2015): 697–98. http://dx.doi.org/10.1097/ftd.0000000000000215.
Pełny tekst źródłaBertsch, Johannes, Christian Öppinger, Verena Hess, Julian D. Langer i Volker Müller. "Heterotrimeric NADH-Oxidizing Methylenetetrahydrofolate Reductase from the Acetogenic Bacterium Acetobacterium woodii". Journal of Bacteriology 197, nr 9 (2.03.2015): 1681–89. http://dx.doi.org/10.1128/jb.00048-15.
Pełny tekst źródłaBulloch, Rhodi E., Clare R. Wall, Lesley M. E. McCowan, Rennae S. Taylor, Claire T. Roberts i John M. D. Thompson. "The Effect of Interactions between Folic Acid Supplementation and One Carbon Metabolism Gene Variants on Small-for-Gestational-Age Births in the Screening for Pregnancy Endpoints (SCOPE) Cohort Study". Nutrients 12, nr 6 (4.06.2020): 1677. http://dx.doi.org/10.3390/nu12061677.
Pełny tekst źródłaGadiyaram, V. K., M. A. Khan, T. Hogan, R. Altaha, E. Crowell, G. Hobbs i P. Perrota. "Significance of MTHFR gene mutation with normal homocysteine level in vascular events". Journal of Clinical Oncology 27, nr 15_suppl (20.05.2009): e20520-e20520. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.e20520.
Pełny tekst źródłaNam, Hee, Yeo-Kyeoung Kim, Il-Kwon Lee, Deok-Hwan Yang, Kyeong-Soo Park, Je-Jung Lee i Hyeoung-Joon Kim. "Methylenetetrahydrofolate Reductase and Methionine Synthase Polymorphism and Risk of Non-Hodgkin’s Lymphoma." Blood 106, nr 11 (16.11.2005): 4691. http://dx.doi.org/10.1182/blood.v106.11.4691.4691.
Pełny tekst źródłaMarques, Manuel, Francisco Alves, Miguel Leitão, Catarina Rodrigues i Joana Tavares Ferreira. "Methylenetetrahydrofolate reductase polymorphisms as risk factors for retinal venous occlusive disease: A literature review". European Journal of Ophthalmology 31, nr 3 (9.03.2021): 884–91. http://dx.doi.org/10.1177/11206721211000647.
Pełny tekst źródłaLiu, Xinye, Lingxu Wang, Hao Chi, Jin Wang, Qian Zheng, Jingye Li, Yong Li i Dongwei Yang. "The SNP Rs915014 in MTHFR Regulated by MiRNA Associates with Atherosclerosis". Cellular Physiology and Biochemistry 45, nr 3 (2018): 1149–55. http://dx.doi.org/10.1159/000487355.
Pełny tekst źródłaDaugėlaitė, Klaudija, i Danielius Serapinas. "The importance of MTHFR gene mutation detection in patient with recurrent miscarriages". Genetika 47, nr 2 (2015): 609–16. http://dx.doi.org/10.2298/gensr1502609d.
Pełny tekst źródłaLiu, Nan, Xue Sheng Wang, Juan Cheng, Jing Wei Xiao i Bin Li. "Association between Genetic Polymorphisms of 5,10-Methylenetetrahydrofolate Reductase and Cytokinesis-Block Micronucleus in Peripheral Blood Lymphocyte among 1,3-Butadiene Workers". Applied Mechanics and Materials 273 (styczeń 2013): 478–82. http://dx.doi.org/10.4028/www.scientific.net/amm.273.478.
Pełny tekst źródłaTurkowski, Yana, Syed Razvi i Abdul Razzaque Ahmed. "Pyoderma gangrenosum-like lesion secondary to methylenetetrahydrofolate reductase mutation: an unusual presentation of a rare disease". BMJ Case Reports 12, nr 4 (kwiecień 2019): e228403. http://dx.doi.org/10.1136/bcr-2018-228403.
Pełny tekst źródłaJiang, Huafeng, i Yi Shen. "Methylene tetrahydrofolate reductase (MTHFR) gene rs1801133 C>T polymorphisms and response to 5-FU based chemotherapy in patients with colorectal cancer: a meta-analysis". Pteridines 30, nr 1 (1.01.2019): 126–32. http://dx.doi.org/10.1515/pteridines-2019-0015.
Pełny tekst źródłaMohamed Hefila, Nermeen. "Methylen tetrahydrofolate reductase enzyme gene C677T and A1298C mutations in primigravida with first trimester missed abortion: cross-sectional study". International Journal of Reproduction, Contraception, Obstetrics and Gynecology 10, nr 3 (24.02.2021): 836. http://dx.doi.org/10.18203/2320-1770.ijrcog20210492.
Pełny tekst źródłaDjurovic, Jelena, Oliver Stojkovic, Jelena Todorovic, Kristina Savic i Gorana Stamenkovic. "Should MTHFR 1298 A>C be tested together with MTHFR 677 C>T polymorphism in women with reproductive challenges?" Genetika 49, nr 2 (2017): 377–86. http://dx.doi.org/10.2298/gensr1702377d.
Pełny tekst źródłaShane, Barry, Faith Pangilinan, James L. Mills, Ruzong Fan, Tingting Gong, Cheryl D. Cropp, Yoonhee Kim i in. "The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population". American Journal of Clinical Nutrition 108, nr 6 (19.10.2018): 1334–41. http://dx.doi.org/10.1093/ajcn/nqy209.
Pełny tekst źródłaHashemi, Seyed, Nourollah Ramroodi, Hamed Amiri Fard, Sahar Talebian, Maryam Haghighi Rohani, Mahnaz Rezaei, Mehrangiz Noora i Saeedeh Salimi. "Common Variations in Prothrombotic Genes and Susceptibility to Ischemic Stroke in Young Patients: A Case-Control Study in Southeast Iran". Medicina 55, nr 2 (13.02.2019): 47. http://dx.doi.org/10.3390/medicina55020047.
Pełny tekst źródłaPanja, Amrita, Abhishek Abhinay i Antim Akash Pakhira. "Study on the polymorphism of methylenetetrahydrofolate reductase C677T gene as the genetic predisposition of congenital heart disease in North Indian population". Asian Journal of Medical Sciences 13, nr 2 (1.02.2022): 86–94. http://dx.doi.org/10.3126/ajms.v13i2.40766.
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