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1رسالة جامعية
المساهمون: University/Department: Universitat Rovira i Virgili. Departament de Ciències Mèdiques Bàsiques
مرشدي الرسالة: Fernández i Ballart, Joan D., Murphy, Michelle
المصدر: TDX (Tesis Doctorals en Xarxa)
مصطلحات موضوعية: homocisteína, riboflavina, población, población de gestantes, MTHFR, MTRR, cobalamina
وصف الملف: application/pdf
الوصول الحر: http://hdl.handle.net/10803/129176Test
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2دورية أكاديمية
المؤلفون: Chih-Chia Huang
المصدر: Frontiers in Psychiatry, Vol 15 (2024)
مصطلحات موضوعية: hyperhomocysteinemia, folic acid, MTRR, MSR, delayed diagnosis, Psychiatry, RC435-571
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1353308/fullTest; https://doaj.org/toc/1664-0640Test
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3دورية أكاديمية
المؤلفون: T.L. Arkhypkina, V.A. Bondarenko, L.P. Lyubimovа, K.V. Misiura
المصدر: Mìžnarodnij Endokrinologìčnij Žurnal, Vol 19, Iss 7, Pp 529-535 (2023)
مصطلحات موضوعية: polycystic ovary syndrome, homocysteine, mthfr genes, mtr, mtrr, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
العلاقة: https://iej.zaslavsky.com.ua/index.php/journal/article/view/1331Test; https://doaj.org/toc/2224-0721Test; https://doaj.org/toc/2307-1427Test
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4دورية أكاديمية
المؤلفون: Yu. N. Reshetnikova, I. V. Ponomarenko, V. М. Churnosov, M. S. Ponomarenko, M. I. Churnosov, E. A. Reshetnikov, Ю. Н. Решетникова, И. В. Пономаренко, В. М. Чурносов, М. С. Пономаренко, М. И. Чурносов, Е. А. Решетников
المصدر: Obstetrics, Gynecology and Reproduction; Vol 18, No 1 (2024); 46-54 ; Акушерство, Гинекология и Репродукция; Vol 18, No 1 (2024); 46-54 ; 2500-3194 ; 2313-7347
مصطلحات موضوعية: масса тела новорожденного, FGR, single nucleotide polymorphism, SNP, folate cycle, MTRR gene, associations, neonatal birth weight, ЗРП, однонуклеотидный полиморфизм, фолатный цикл, ген MTRR, ассоциации
وصف الملف: application/pdf
العلاقة: https://www.gynecology.su/jour/article/view/1878/1173Test; Society for Maternal-Fetal Medicine (SMFM). Electronic address: pubs@smfm.org; Martins J.G., Biggio J.R., Abuhamad A. Society for Maternal-Fetal Medicine Consult Series #52: Diagnosis and management of fetal growth restriction: (Replaces Clinical Guideline Number 3, April 2012). Am J Obstet Gynecol. 2020;223(4):B2–B17. https://doi.org/10.1016/j.ajog.2020.05.010Test.; Головченко О.В. Молекулярно-генетические детерминанты преэклампсии. Научные результаты биомедицинских исследований. 2019;5(4):139–49. https://doi.org/10.18413/2658-6533-2019-5-4-0-11Test.; Решетников Е.А. Поиск ассоциаций генов-кандидатов, дифференциально экспрессирующихся в плаценте, с риском развития плацентарной недостаточности с синдромом задержки роста плода. Научные результаты биомедицинских исследований. 2020;6(3):338–49. https://doi.org/10.18413/2658-6533-2020-6-3-0-5Test.; Баев Т.О., Панова И.А., Кузьменко Г.Н. и др. Состояние микроциркуляции у беременных женщин с гипертензивными расстройствами в III триместре беременности. Научные результаты биомедицинских исследований. 2023;9(1):113–28. https://doi.org/10.18413/2658-6533-2023-9-1-0-8Test.; Pels A., Beune I.M., van Wassenaer-Leemhuis A.G. et al. Early-onset fetal growth restriction: A systematic review on mortality and morbidity. Acta Obstet Gynecol Scand. 2020;99(2):153–66. https://doi.org/10.1111/aogs.13702Test.; D'Agostin M., Di Sipio Morgia C., Vento G., Nobile S. Long-term implications of fetal growth restriction. World J Clin Cases. 2023;11(3):2855–863. https://doi.org/10.12998/wjcc.v11.i13.2855Test.; Anil K.C., Basel P.L., Singh S. Low birth weight and its associated risk factors: Health facility-based case-control study. PLoS ONE. 2020;15(6):e0234907. https://doi.org/10.1371/journal.pone.0234907Test.; Gaccioli F., Lager S. Placental nutrient transport and intrauterine growth restriction. Front Physiol. 2016;7:40. https://doi.org/10.3389/fphys.2016.00040Test.; Ducker G.S., Rabinowitz J.D. One-carbon metabolism in health and disease. Cell Metab. 2017;25(1):27–42. https://doi.org/10.1016/j.cmet.2016.08.009Test.; Jiang H.L., Cao L.Q., Chen H.Y. Blood folic acid, vitamin B12, and homocysteine levels in pregnant women with fetal growth restriction. Genet Mol Res. 2016;15(4). https://doi.org/10.4238/gmr15048890Test.; Liu C., Luo D., Wang Q. et al. Serum homocysteine and folate concentrations in early pregnancy and subsequent events of adverse pregnancy outcome: The Sichuan Homocysteine study. BMC Pregnancy Childbirth. 2020;20(1):176. https://doi.org/10.1186/s12884-020-02860-9Test.; Gaiday A., Balash L., Tussupkaliyev A. The role of high concentrations of homocysteine for the development of fetal growth restriction. Rev Bras Ginecol Obstet. 2022;44(4):352–9. https://doi.org/10.1055/s-0042-1743093Test.; Yila T.A., Sasaki S., Miyashita C. et al. Effects of maternal 5,10-methylenetetrahydrofolate reductase C677T and A1298C Polymorphisms and tobacco smoking on infant birth weight in a Japanese population. J Epidemiol. 2012;22(2):91–102. https://doi.org/10.2188/jea.JE20110039Test.; Sukla K.K., Tiwari P.K., Kumar A., Raman R. Low birthweight (LBW) and neonatal hyperbilirubinemia (NNH) in an Indian cohort: Association of homocysteine, its metabolic pathway genes and micronutrients as risk factors. PLoS ONE. 2013;8(8):e71587. https://doi.org/10.1371/journal.pone.0071587Test.; Liew S.C., Gupta E.D. Methylenetetrahydrofolatereductase (MTHFR) C677T polymorphism: epidemiology, metabolism and the associated diseases. Eur J Med Genet. 2015;58(1):1–10. https://doi.org/10.1016/j.ejmg.2014.10.004Test.; Tiwari D., Bose P.D., Das S. et al. MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: A Northeast Indian population based study. Meta Gene. 2015;3:31–42. https://doi.org/10.1016/j.mgene.2014.12.002Test.; Wu H., Zhu P., Geng X. et al. Genetic polymorphism of MTHFR C677T with preterm birth and low birth weight susceptibility: a meta-analysis. Arch Gynecol Obstet. 2017;295(5):1105–18. https://doi.org/10.1007/s00404-017-4322-zTest.; Wang S., Duan Y., Jiang S. et al. Relationships between maternal gene polymorphisms in one carbon metabolism and adverse pregnancy outcomes: a prospective mother and child cohort study in China. Nutrients. 2022;14(10):2108. https://doi.org/10.3390/nu14102108Test.; Медведев М.В. Пренатальнаяэхография: дифференциальный диагноз и прогноз. М.: Реал Тайм, 2012. 448 с.; Пономаренко И.В., Решетников Е.А., Полоников А.В., Чурносов М.И. Полиморфный локус rs314276 гена LIN28B ассоциирован с возрастом менархе у женщин Центрального Черноземья России. Акушерство и гинекология. 2019;(2):98–104. https://doi.org/10.18565/aig.2019.2.98-104Test.; Wu P.P., Tang R.N., An L. A meta-analysis of MTRR A66G polymorphism and colorectal cancer susceptibility. J BUON. 2015;20(3):918–22.; Bergen N.E., Schalekamp-Timmermans S., Jaddoe V.W. et al. Maternal and neonatal markers of the homocysteine pathway and fetal growth: The Generation R Study. Paediatr Perinat Epidemiol. 2016;30(4):386–96. https://doi.org/10.1111/ppe.12297Test.; Laskowska M., Laskowska K., Oleszczuk J. Differences in the association between maternal serum homocysteine and ADMA levels in women with pregnancies complicated by preeclampsia and/or intrauterine growth restriction. Hypertens Pregnancy. 2013;32(1):83–93. https://doi.org/10.3109/10641955.2012.751993Test.; Cawley S., O'Malley E.G., Kennedy R.A.K. et al. The relationship between maternal plasma homocysteine in early pregnancy and birth weight. J Matern Fetal Neonatal Med. 2020;33(18):3045–9. https://doi.org/10.1080/14767058.2019.1567705Test.; Gaughan D.J., Kluijtmans L.A., Barbaux S. et al The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations. Atherosclerosis. 2001;157(2):451–6. https://doi.org/10.1016/s0021-9150Test(00)00739-5.; Wu X., Zou T., Cao N. Plasma homocysteine levels and genetic polymorphisms in folatemetablism are associated with breast cancer risk in chinese women. Hered Cancer Clin Pract. 2014;12(1):2. https://doi.org/10.1186/1897-4287-12-2Test.; Ni J., Liu Y., Zhou T., Wu X., Wang X. Single nucleotide polymorphisms in key one-carbon metabolism genes and their association with blood folate and homocysteine levels in a Chinese population in Yunnan. Genet Test Mol Biomarkers. 2018;22(3):193–8. https://doi.org/10.1089/gtmb.2017.0195Test.; Dewelle W.K., Melka D.S., Aklilu A.T. et al. Polymorphisms in maternal selected folate metabolism-related genes in neural tube defect-affected pregnancy. Adv Biomed Res. 2023;12:160. https://doi.org/10.4103/abr.abr_103_22Test.; Su J., Li Z. Analysis of MTR and MTRR gene polymorphisms in Chinese patients with ventricular septal defect. Appl Immunohistochem Mol Morphol. 2018;26(10):769–74. https://doi.org/10.1097/PAI.0000000000000512Test.; Yadav U., Kumar P., Rai V. Distribution of methionine synthase reductase (MTRR) gene A66G polymorphism in Indian Population. Indian J Clin Biochem. 2021;36(1):23–32. https://doi.org/10.1007/s12291-019-00862-9Test.; https://www.gynecology.su/jour/article/view/1878Test
الإتاحة: https://doi.org/10.17749/2313-7347/ob.gyn.rep.2024.466Test
https://doi.org/10.1016/j.ajog.2020.05.010Test
https://doi.org/10.18413/2658-6533-2019-5-4-0-11Test
https://doi.org/10.18413/2658-6533-2020-6-3-0-5Test
https://doi.org/10.18413/2658-6533-2023-9-1-0-8Test
https://doi.org/10.1111/aogs.13702Test
https://doi.org/10.12998/wjcc.v11.i13.2855Test
https://doi.org/10.1371/journal.pone.0234907Test
https://doi.org/10.3389/fphys.2016.00040Test
https://doi.org/10.1016/j.cmet.2016.08.009Test -
5دورية أكاديمية
المؤلفون: Evgeny Pokushalov, Andrey Ponomarenko, Sevda Bayramova, Claire Garcia, Inessa Pak, Evgenya Shrainer, Marina Ermolaeva, Dmitry Kudlay, Michael Johnson, Richard Miller
المصدر: Nutrients, Vol 16, Iss 11, p 1550 (2024)
مصطلحات موضوعية: MTHFR, MTR, MTRR polymorphisms, methylfolate, pyridoxal-5′-phosphate, methylcobalamin, Nutrition. Foods and food supply, TX341-641
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Strelkova, Yuliya, Boiko, Oksana, Kim, Vladimir, Mukhamedzyanova, Rushaniya, Shiryaeva, Nina, Tabolina, Anna, Abramova, Anna, Selezneva, Tatyana
مصطلحات موضوعية: folate cycle genes, MTHFR 1298 A>C, MTHFR 677 C>T, MTR 2756 A>G, MTRR 66 A>G, гены фолатного цикла
وصف الملف: text/html
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7دورية أكاديمية
المؤلفون: Yongxin Liu, Chunping Xu, Yuqing Wang, Caiting Yang, Genyuan Pu, Le Zhang, Zhuang Wang, Pengyan Tao, Shenghe Hu, Mingming Lai
المصدر: Clinical and Experimental Hypertension, Vol 45, Iss 1 (2023)
مصطلحات موضوعية: mthfr, mtrr, gene polymorphisms, hypertension, bai nationality population, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
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8دورية أكاديمية
المؤلفون: Mashaer Taha Edris, Maye Mohammad Merghani, Shaza Salih Gafar, Ahmed Mohamed Asmali, Elrashed B. Yasin, Raed Alserihi, Heba Alkhatabi, Haitham MH. Qutob, Rowaid Qahwaji, Elshazali Widaa Ali
المصدر: Italian Journal of Medicine, Vol 17, Iss 2 (2023)
مصطلحات موضوعية: Acute lymphoblastic leukemia, methionine synthase reductase, MTRR A66G polymorphism, Medicine
وصف الملف: electronic resource
العلاقة: https://www.italjmed.org/index.php/ijm/article/view/1644Test; https://doaj.org/toc/1877-9344Test; https://doaj.org/toc/1877-9352Test
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9دورية أكاديمية
المؤلفون: Claire E. Senner, Ziqi Dong, Malwina Prater, Miguel R. Branco, Erica D. Watson
المصدر: Frontiers in Cell and Developmental Biology, Vol 11 (2023)
مصطلحات موضوعية: DNA methylation, folate, histone methylation, MTRR, sperm, transposable elements, Biology (General), QH301-705.5
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fcell.2023.1209928/fullTest; https://doaj.org/toc/2296-634XTest
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10دورية أكاديمية
المؤلفون: Shunhua Qiu, Lifen Jin, Dan Yang, Dewen Zhang
المصدر: Annals of Human Biology, Vol 51, Iss 1 (2024)
مصطلحات موضوعية: Chronic hepatitis B virus infection, MTHFR C677T, MTHFR A1298C, MTRR A66G, Biology (General), QH301-705.5, Human anatomy, QM1-695, Physiology, QP1-981
وصف الملف: electronic resource