Works matching DE "METHYLENETETRAHYDROFOLATE reductase"

Results: 1002

Association of prothrombin, FV Leiden and MTHFR gene polymorphisms in the Montenegrin patients with venous thromboembolism.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2021, v. 78, n. 4, p. 415, doi. 10.2298/VSP190402086T

By:

Teofilov, Sladjana;
Magić, Zvonko;
Miljanović, Olivera;
Ostojić, Tatjana;
Bulatović, Milena

Publication type:

Article

Association of factor II G20210A, factor V G1691A and methylenetetrahydrofolate reductase C677T gene polymorphism with different forms of myocardial infarction: ST segment elevation and non-ST segment elevation.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 10, p. 1041, doi. 10.2298/VSP180621170C

By:

Jokić, Milica Ćućuz;
Ilić, Vesna;
Aleksić, Bojana Cikota;
Obradović, Slobodan;
Magić, Zvonko

Publication type:

Article

Angiotensin-converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgia syndrome.

Published in:

Klinik Psikofarmakoloji Bulteni, 2015, v. 25, p. S94

By:

Inanir, Ahmet;
Inanir, Sema;
Yigit, Serbulent;
Tekcan, Akin;
Pinarli, Ferda Alpaslan;
Karakus, Pinarli

Publication type:

Article

Adolescent/Adult‑Onset Leukodystrophy with MTHFR Deficiency – A Treatable Cause.

Published in:

Neurology India, 2023, v. 71, n. 2, p. 326, doi. 10.4103/0028-3886.375409

By:

Kumar, N. Hemanth;
Mounika, K. Joy;
Sundarachary, N. V.

Publication type:

Article

Effect of polymorphisms of MTHFR in controlled ovarian stimulation: a systematic review and meta-analysis.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 9, p. 2237, doi. 10.1007/s10815-021-02236-8

By:

Wang, Xinrui;
Sun, Ximu;
Tang, Borui;
Liu, Lihong;
Feng, Xin

Publication type:

Article

MTHFR (methylenetetrahydrofolate reductase: EC 1.5.1.20) SNPs (single-nucleotide polymorphisms) and homocysteine in patients referred for investigation of fertility.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 9, p. 2383, doi. 10.1007/s10815-021-02200-6

By:

Ménézo, Yves;
Patrizio, Pasquale;
Alvarez, Silvia;
Amar, Edouard;
Brack, Michel;
Brami, Charles;
Chouteau, Jacques;
Clement, Arthur;
Clement, Patrice;
Cohen, Marc;
Cornet, Dominique;
Dale, Brian;
D' Amato, Guiseppe;
Jacquesson-Fournols, Laetitia;
Mares, Pierre;
Neveux, Paul;
Sage, Jean Clement;
Servy, Edouard;
Huong, To Minh;
Viot, Geraldine

Publication type:

Article

Embryonic MTHFR contributes to blastocyst development.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 8, p. 1807, doi. 10.1007/s10815-020-01898-0

By:

Ishitani, Hiroki;
Ikeda, Shuntaro;
Egashira, Kai;
Sugimoto, Miki;
Kume, Shinichi;
Minami, Naojiro;
Ohta, Takeshi

Publication type:

Article

C677T polymorphism increases the risk of early spontaneous abortion.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 8, p. 1737, doi. 10.1007/s10815-019-01500-2

By:

Liu, Yongjie;
Zhang, Fan;
Dai, Liang

Publication type:

Article

Comparison of different types of twin pregnancies in terms of obstetric and perinatal outcomes: association of vanished twins with methylenetetrahydrofolate reductase (MTHFR) polymorphism(s).

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 12, p. 2149, doi. 10.1007/s10815-018-1346-7

By:

Ozek, Murat Aykut;
Karaagaoglu, Ergun;
Orgul, Gokcen;
Gumruk, Fatma;
Yurdakök, Murat;
Beksac, M. Sinan

Publication type:

Article

MTHFR isoform carriers. 5-MTHF (5-methyl tetrahydrofolate) vs folic acid: a key to pregnancy outcome: a case series.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 8, p. 1431, doi. 10.1007/s10815-018-1225-2

By:

Servy, Edouard J.;
Jacquesson-Fournols, Laetitia;
Cohen, Marc;
Menezo, Yves J. R.

Publication type:

Article

Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR) in recurrent miscarriage and recurrent implantation failure.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 8, p. 1437, doi. 10.1007/s10815-018-1205-6

By:

Zhu, Yuanchang;
Wu, Tonghua;
Ye, Lijun;
Li, Guangui;
Zeng, Yong;
Zhang, Yaou

Publication type:

Article

Association between the MTHFR-C677T isoform and structure of sperm DNA.

Published in:

Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 10, p. 1283, doi. 10.1007/s10815-017-1015-2

By:

Cornet, Dominique;
Cohen, Marc;
Clement, Arthur;
Amar, Edouard;
Fournols, Laetitia;
Clement, Patrice;
Neveux, Paul;
Ménézo, Yves

Publication type:

Article

Folate metabolism gene polymorphisms MTHFR C677T and A1298C and risk for preeclampsia: a meta-analysis.

Published in:

Journal of Assisted Reproduction & Genetics, 2015, v. 32, n. 5, p. 797, doi. 10.1007/s10815-014-0408-8

By:

Wu, Xiaoming;
Yang, Kunxian;
Tang, Xiaodan;
Sa, Yalian;
Zhou, Ruoyu;
Liu, Jing;
Luo, Ying;
Tang, Wenru

Publication type:

Article

Lack of association of MTHFR rs1801133 polymorphism and CTCFL mutations with sperm methylation errors in infertile patients.

Published in:

Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 9, p. 1125, doi. 10.1007/s10815-013-0013-2

By:

Camprubí, Cristina;
Pladevall, Marta;
Grossmann, Mark;
Garrido, Nicolás;
Pons, Maria;
Blanco, Joan

Publication type:

Article

Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and five related serum molecular levels in 2587 patients: Associated differentially with adverse pregnancy.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09948-x

By:

Feng, Zhanqi;
Gao, Yue;
Zhang, Mengting;
Wang, Yaoping;
Liu, Xiuming;
Zhang, Bo;
Su, Junxiang;
Wang, Hongdan

Publication type:

Article

Cerebral venous sinus thrombosis and SCN1A, a novel association?

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09820-y

By:

Prasun, Pankaj;
Vermeire, Kylie;
Alali, Abdulrazak

Publication type:

Article

Assessing the possible association between MTHFR (rs1801133) and GPx-1 (rs1050450) polymorphisms with the risk of type 2 diabetes, diabetic neuropathy, and diabetic retinopathy.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09519-0

By:

Asadi, Soheila;
Rahimi, Zohreh;
Kohsari, Maryam;
Babajani, Fatemeh;
Amiri, Mohammad;
Jalilian, Nazanin;
Naseri, Rozita;
Haghnazari, Lida

Publication type:

Article

Study on Maternal SNPs of MTHFR Gene and HCY Level Related to Congenital Heart Diseases.

Published in:

Pediatric Cardiology, 2021, v. 42, n. 1, p. 42, doi. 10.1007/s00246-020-02449-1

By:

Shi, Hui;
Yang, Shiwei;
Lin, Ning;
Huang, Peng;
Yu, Rongbin;
Chen, Mei;
Wang, Lijuan;
Jiang, Zhixin;
Sun, Xiaoru

Publication type:

Article

Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation (Communicated by Jan P. Kraus).

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 509, doi. 10.1002/humu.10193

By:

Sahar Sibani;
Daniel Leclerc;
Ilan S. Weisberg;
Erin O'Ferrall;
David Watkins;
Carmen Artigas

Publication type:

Article

Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD‐responsive mutationCommunicated by Jan P. Kraus.

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 509, doi. 10.1002/humu.10193

By:

Sahar Sibani;
Daniel Leclerc;
Ilan S. Weisberg;
Erin O'Ferrall;
David Watkins;
Carmen Artigas;
David S. Rosenblatt;
Rima Rozen

Publication type:

Article

Rehydration during exercise prevents the increase of homocysteine concentrations.

Published in:

Amino Acids, 2019, v. 51, n. 2, p. 193, doi. 10.1007/s00726-018-2655-y

By:

Maroto-Sánchez, Beatriz;
Lopez-Torres, Olga;
Valtueña, Jara;
Benito, Pedro J.;
Palacios, Gonzalo;
Díaz-Martínez, Ángel Enrique;
González-Lamuño, Domingo;
Zinellu, Angelo;
González-Gross, Marcela;
Carru, Ciriaco

Publication type:

Article

Dark Green Leafy Vegetable Intake, MTHFR Genotype, and Risk of Cutaneous Squamous Cell Carcinoma.

Published in:

Dermatology (10188665), 2022, v. 238, n. 4, p. 657, doi. 10.1159/000520941

By:

Hughes, Maria Celia B.;
Antonsson, Annika;
Rodriguez-Acevedo, Astrid J.;
Liyanage, Upekha E.;
Green, Adele C.;
van der Pols, Jolieke C.

Publication type:

Article

Role of Genetic and Acquired Prothrombotic Risk Factors in Genesis of Sudden Sensorineural Hearing Loss.

Published in:

Audiology & Neurotology, 2011, v. 16, n. 3, p. 185, doi. 10.1159/000319310

By:

Fusconi, Massimo;
Chistolini, Antonio;
Angelosanto, Noemi;
Pignoloni, Patrizia;
Tombolini, Mario;
de Virgilio, Armando;
Pagliarella, Martina;
de Vincentiis, Marco

Publication type:

Article

Impact of Methionine Synthase Gene and Methylenetetrahydrofolate Reductase Gene Polymorphisms on the Risk of Sudden Sensorineural Hearing Loss.

Published in:

Audiology & Neurotology, 2006, v. 11, n. 5, p. 287, doi. 10.1159/000093957

By:

Gross, Menachem;
Friedman, Gideon;
Eliashar, Ron;
Koren-Morag, Nira;
Goldschmidt, Neta;
Atta, Iman Abou;
Ben-Yehuda, Arie

Publication type:

Article

Structural and functional characterization of a mycobacterial methylenetetrahydrofolate reductase utilizing NADH as the exclusive cofactor.

Published in:

Biochemical Journal, 2023, v. 480, n. 14, p. 1129, doi. 10.1042/BCJ20230138

By:

Jiacong Li;
Mingxia Yang;
Weijia Li;
Chujie Lu;
Deyu Feng;
Zhuo Shang;
Chengyuan Wang;
Wei Lin

Publication type:

Article

diffloop: a computational framework for identifying and analyzing differential DNA loops from sequencing data.

Published in:

Bioinformatics, 2018, v. 34, n. 4, p. 672, doi. 10.1093/bioinformatics/btx623

By:

Lareau, Caleb A;
Aryee, Martin J

Publication type:

Article

Assessment of Methylenetetrahydrofolate Reductase Gene Polymorphism in Diabetic Peripheral Neuropathy.

Published in:

Zagazig University Medical Journal, 2022, v. 28, p. 272, doi. 10.21608/zumj.2020.10042.1072

By:

Abd El-Fatah, Azza Hassan;
Fawzy, Amal;
Abdulhamid, Abdullah Ali

Publication type:

Article

The combined effect of MTHFR C677T and A1298C polymorphisms on the risk of digestive system cancer among a hypertensive population.

Published in:

Discover Oncology, 2024, v. 15, n. 1, p. 1, doi. 10.1007/s12672-024-00960-y

By:

He, Qiangqiang;
Wei, Yaping;
Zhu, Hehao;
Liang, Qiongyue;
Chen, Ping;
Li, Shuqun;
Song, Yun;
Liu, Lishun;
Wang, Binyan;
Xu, Xiping;
Dong, Yuhan

Publication type:

Article

Association between maternal MTHFR C677T/A1298C combination polymorphisms and IVF/ICSI outcomes: a retrospective cohort study.

Published in:

Human Reproduction Open, 2023, v. 2023, n. 1, p. 1, doi. 10.1093/hropen/hoac055

By:

Lu, Yong-Jie;
Li, Qin;
Chen, Li-Xue;
Tian, Tian;
Kang, Jia;
Hao, Yong-Xiu;
Zhou, Jian-Suo;
Wang, Yuan-Yuan;
Yan, Li-Ying;
Li, Rong;
Chang, Liang;
Qiao, Jie

Publication type:

Article

H1299R in coagulation Factor V and Glu429Ala in MTHFR genes in recurrent pregnancy loss in Sari, Mazandaran.

Published in:

International Journal of Reproductive Biomedicine, 2016, v. 14, n. 5, p. 329

By:

Arabkhazaeli, Nadia;
Ghanaat, Kasra;
Hashemi-Soteh, Mohammad Bagher

Publication type:

Article

Methylenetetrahydrofolate reductase C677T polymorphism across acute leukemia.

Published in:

Egyptian Journal of Haematology, 2022, v. 47, n. 1, p. 1, doi. 10.4103/ejh.ejh_20_21

By:

Frikha, Rim

Publication type:

Article

Methylenetetrahydrofolate reductase (MTHFR) gene C677T (rs1801133) polymorphism and risk of alcohol dependence: a meta-analysis Running title: MTHFR and alcohol dependence.

Published in:

AIMS Neuroscience, 2021, v. 8, n. 2, p. 212, doi. 10.3934/Neuroscience.2021011

By:

Rai, Vandana;
Kumar, Pradeep

Publication type:

Article

Differentiated Thyroid Cancer Genetic Mechanisms - Focus on Vitamin D Receptor and Methylenetetrahydrofolate Reductase Gene Polymorphisms.

Published in:

Medicina Moderna, 2022, v. 29, n. 1, p. 7, doi. 10.31689/rmm.2021.29.1.7

By:

COCOLOS, Andra-Maria;
POIANA, Catalina

Publication type:

Article

MTHFR polymorphism and the risk of prostate cancer: a meta-analysis of case-control studies.

Published in:

Prostate Cancer & Prostatic Diseases, 2012, v. 15, n. 3, p. 244, doi. 10.1038/pcan.2012.5

By:

Li, X-L;
Xu, J-H

Publication type:

Article

Role of depth of response and MTHFR genotype as predictors of fluorouracil rechallenge therapy for refractory metastatic colorectal cancer.

Published in:

Oncology Letters, 2017, v. 14, n. 2, p. 2491, doi. 10.3892/ol.2017.6414

By:

KA-RHAM KIM;
JUNG-HWAN YOON;
HYUN-JEONG SHIM;
JUN-EUL HWANG;
WOO-KYUN BAE;
IK-JOO CHUNG;
HEE-NAM KIM;
MIN-HO SHIN;
SANG-HEE CHO

Publication type:

Article

Association between folate metabolism-related polymorphisms and colorectal cancer risk.

Published in:

Molecular & Clinical Oncology, 2015, v. 3, n. 3, p. 639, doi. 10.3892/mco.2015.520

By:

JONG WOO KIM;
YOUNG JOO JEON;
MOON JU JANG;
JUNG O KIM;
SO YOUNG CHONG;
KWANG HYUN KO;
SEONG GYU HWANG;
DOYEUN OH;
JISU OH;
NAM KEUN KIM

Publication type:

Article

Exploring the therapeutic efficacy of Bai-Shao in mitigating comorbid epileptic seizures and cognitive impairment via inflammatory signaling pathways: insights from in silico and in vivo studies.

Published in:

3 Biotech, 2025, v. 15, n. 6, p. 1, doi. 10.1007/s13205-025-04316-3

By:

Yu, Yanhong;
Lv, Hailing;
Liu, Xiaoyu;
Liu, Aiju

Publication type:

Article

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.

Published in:

Journal of Gastroenterology, 2005, v. 40, n. 10, p. 1002, doi. 10.1007/s00535-005-1664-2

By:

Barada, Kassem A.;
Azar, Cecilio R.;
Otrock, Zaher K.;
Taher, Ali T.

Publication type:

Article

Case Report: Homozygous C677T MTHFR Gene Mutation in Male with Hypogonadism.

Published in:

Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/6945124

By:

Salameh, Rami;
Miah, Mumtaheena;
Anastasopoulou, Catherine

Publication type:

Article

Case Report: Homozygous C677T MTHFR Gene Mutation in Male with Hypogonadism.

Published in:

Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/6945124

By:

Salameh, Rami;
Miah, Mumtaheena;
Anastasopoulou, Catherine

Publication type:

Article

MTHFR C677T/A1298C genotype: a possible risk factor for liver sinusoidal obstruction syndrome.

Published in:

Bone Marrow Transplantation, 2014, v. 49, n. 5, p. 726, doi. 10.1038/bmt.2014.16

By:

Efrati, E;
Zuckerman, T;
Ben-Ami, E;
Krivoy, N

Publication type:

Article

Methylenetetrahydrofolate reductase and thymidylate synthase genotypes modify oral mucositis severity following hematopoietic stem cell transplantation.

Published in:

2006

By:

Robien, K.;
Schubert, M. M.;
Chay, T.;
Bigler, J.;
Storb, R.;
Yasui, Y.;
Potter, J. D.;
Ulrich, C. M.

Publication type:

Letter

SHOULD MTHFR 1298 A>C BE TESTED TOGETHER WITH MTHFR 677 C>T POLYMORPHISM IN WOMEN WITH REPRODUCTIVE CHALLENGES?

Published in:

Genetika (0534-0012), 2017, v. 49, n. 2, p. 377, doi. 10.2298/GENSR1702377D

By:

DJUROVIC, Jelena;
STOJKOVIC, Oliver;
TODOROVIC, elena;
SAVIC, Kristina;
STAMENKOVIC, Gorana

Publication type:

Article

THE IMPORTANCE OF MTHFR GENE MUTATION DETECTION IN PATIENT WITH RECURRENT MISCARRIAGES.

Published in:

Genetika (0534-0012), 2015, v. 47, n. 2, p. 609, doi. 10.2298/GENSR1502609D

By:

DAUGĖLAITĖ, Klaudija;
SERAPINAS, Danielius

Publication type:

Article

Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population.

Published in:

Clinical & Experimental Dermatology, 2017, v. 42, n. 1, p. 8, doi. 10.1111/ced.12909

By:

Kilic, S.;
Ozdemir, O.;
Silan, F.;
Isik, S.;
Yildiz, O.;
Karaagacli, D.;
Silan, C.;
Ogretmen, Z.

Publication type:

Article

Thrombus obstructing the right ventricle outflow tract in a neonate with methylenetetrahydrofolate reductase 677TT genotype.

Published in:

2011

By:

Kovacikova, Lubica;
Skrak, Peter;
Zahorec, Martin

Publication type:

journal article

Reply to the correspondence letter by G. Demirel et al.

Published in:

2011

By:

Kovacikova, Lubica

Publication type:

Letter

Titration of betaine therapy to optimize therapy in an infant with 5,10-methylenetetrahydrofolate reductase deficiency.

Published in:

2010

By:

Ucar, Sema Kalkan;
Koroglu, Özge Altun;
Berk, Ömer;
Yalaz, Mehmet;
Kültürsay, Nilgün;
Blom, Henk J.;
Coker, Mahmut;
Koroğlu, Ozge Altun;
Berk, Omer;
Kültürsay, Nilgün

Publication type:

journal article

SEVERE PURPURA FULMINANS DUE TO COEXISTENCE OF HOMOZYGOUS PROTEIN C DEFICIENCY AND HOMOZYGOUS METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION.

Published in:

Pediatric Hematology & Oncology, 2009, v. 26, n. 8, p. 597, doi. 10.3109/08880010903116413

By:

Demirel, Nihal;
Bas, Ahmet Yagmur;
Okumus, Nurullah;
Zenciroglu, Ayşegul;
Yarali, Nese

Publication type:

Article

PCR AMPLIFICATION ON WHOLE BLOOD SAMPLES TREATED WITH DIFFERENT COMMONLY USED ANTICOAGULANTS.

Published in:

Pediatric Hematology & Oncology, 2006, v. 23, n. 6, p. 517, doi. 10.1080/08880010600751900

By:

Djordjevic, V.;
Stankovic, M.;
Nikolic, A.;
Antonijevic, N.;
Rakicevic, L. J.;
Divac, A.;
Radojkovic, M.

Publication type:

Article