Works matching DE "METHIONINE synthase reductase"

Results: 51

Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.

Published in:

Free Radical Research, 2013, v. 47, n. 6/7, p. 498, doi. 10.3109/10715762.2013.793319

By:

Teranishi, Masaaki;
Uchida, Yasue;
Nishio, Naoki;
Kato, Ken;
Otake, Hironao;
Yoshida, Tadao;
Suzuki, Hirokazu;
Sone, Michihiko;
Sugiura, Saiko;
Ando, Fujiko;
Shimokata, Hiroshi;
Nakashima, Tsutomu

Publication type:

Article

A study of MTRR 66A>G gene polymorphism in patients with autism from northern Iran.

Published in:

Neurology Asia, 2017, v. 22, n. 1, p. 59

By:

Ajabi, Samereh;
Mashayekhi, Farhad;
Bidabadi, Elham

Publication type:

Article

5,10-Methylenetetrahydrofolate reductase ( MTHFR), methionine synthase ( MTRR), and methionine synthase reductase ( MTR) gene polymorphisms and adult meningioma risk.

Published in:

Journal of Neuro-Oncology, 2013, v. 115, n. 2, p. 233, doi. 10.1007/s11060-013-1218-z

By:

Zhang, Jun;
Zhou, Yan-Wen;
Shi, Hua-Ping;
Wang, Yan-Zhong;
Li, Gui-Ling;
Yu, Hai-Tao;
Xie, Xin-You

Publication type:

Article

Update analysis on the association between Methionine synthase rs1805087 A/G variant and risk of prostate cancer.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70223-7

By:

Zhang, Wei;
Zhang, Ze;
Wu, Hao;
Xu, Kai;
Yuan, Wei;
Mi, Yuan-Yuan;
Shi, Li;
Zuo, Li;
Shi, Yun-Feng

Publication type:

Article

Methionine synthase reductase A66G polymorphism and leukemia risk: evidence from published studies.

Published in:

Leukemia & Lymphoma, 2014, v. 55, n. 8, p. 1910, doi. 10.3109/10428194.2013.867492

By:

Fang, Dai-Hua;
Ji, Qiang;
Fan, Cong-Hai;
An, Qi;
Li, Juan

Publication type:

Article

Gender-specific interactions of MTHFR C677T and MTRR A66G polymorphisms with overweight/obesity on serum lipid levels in a Chinese Han population.

Published in:

Lipids in Health & Disease, 2016, v. 15, p. 1, doi. 10.1186/s12944-016-0354-9

By:

Xueyuan Zhi;
Boyi Yang;
Shujun Fan;
Yanxun Wang;
Jian Wei;
Quanmei Zheng;
Guifan Sun

Publication type:

Article

Joint associations of folate, homocysteine and MTHFR, MTR and MTRR gene polymorphisms with dyslipidemia in a Chinese hypertensive population: a cross-sectional study.

Published in:

Lipids in Health & Disease, 2015, v. 14, n. 1, p. 1, doi. 10.1186/s12944-015-0099-x

By:

Wen-Xing Li;
Wen-Wen Lv;
Shao-Xing Dai;
Ming-Luo Pan;
Jing-Fei Huang

Publication type:

Article

NaCl stress induces CsSAMs gene expression in Cucumis sativus by mediating the binding of CsGT-3b to the GT-1 element within the CsSAMs promoter.

Published in:

Planta: An International Journal of Plant Biology, 2017, v. 245, n. 5, p. 889, doi. 10.1007/s00425-017-2650-7

By:

Wang, Li-Wei;
He, Mei-Wen;
Guo, Shi-Rong;
Zhong, Min;
Shu, Sheng;
Sun, Jin

Publication type:

Article

Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.

Published in:

Cephalalgia, 2013, v. 33, n. 7, p. 469, doi. 10.1177/0333102413477738

By:

Roecklein, Kathryn A;
Scher, Ann I;
Smith, Albert;
Harris, Tamara;
Eiriksdottir, Gudny;
Garcia, Melissa;
Gudnason, Villi;
Launer, Lenore J

Publication type:

Article

Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia.

Published in:

Systems Biology in Reproductive Medicine, 2015, v. 61, n. 5, p. 286, doi. 10.3109/19396368.2015.1049752

By:

Kim, Shin Young;
Lim, Jung Wook;
Kim, Jin Woo;
Park, So Yeon;
Seo, Ju Tae

Publication type:

Article

Geographical and Ethnic Distributions of the MTHFR C677T, A1298C and MTRR A66G Gene Polymorphisms in Chinese Populations: A Meta-Analysis.

Published in:

PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0152414

By:

Wang, Xingmin;
Fu, Jinjian;
Li, Qianxi;
Zeng, Dingyuan

Publication type:

Article

The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case-control study and a meta-analysis.

Published in:

Molecular Biology Reports, 2014, v. 41, n. 9, p. 5571, doi. 10.1007/s11033-014-3462-5

By:

Coppedè, Fabio;
Bosco, Paolo;
Lorenzoni, Valentina;
Denaro, Maria;
Anello, Guido;
Antonucci, Ivana;
Barone, Concetta;
Stuppia, Liborio;
Romano, Corrado;
Migliore, Lucia

Publication type:

Article

Biochemical profile of children with autism spectrum disorders associated with genetic deficiency of the folate cycle.

Published in:

Biochimica Clinica, 2023, v. 47, n. 2, p. 132, doi. 10.19186/BC_2022.082

By:

Maltsev, Dmitry;
Kurchenko, Andrii;
Marushko, Yurii;
Yuriev, Serhii

Publication type:

Article

Association of polymorphisms in DNMT1, DNMT3A, DNMT3B, MTHFR and MTRR genes with global DNA methylation levels and prognosis of autoimmune thyroid disease.

Published in:

Clinical & Experimental Immunology, 2012, v. 170, n. 2, p. 194, doi. 10.1111/j.1365-2249.2012.04646.x

By:

Arakawa, Y.;
Watanabe, M.;
Inoue, N.;
Sarumaru, M.;
Hidaka, Y.;
Iwatani, Y.

Publication type:

Article

Folate metabolism-related gene polymorphisms and susceptibility to primary liver cancer in North China.

Published in:

Medical Oncology, 2012, v. 29, n. 3, p. 1837, doi. 10.1007/s12032-011-0066-y

By:

Cui, Lian-Hua;
Song, Yang;
Si, Hongzong;
Shen, Fangzhen;
Shin, Min-Ho;
Kim, Hee;
Choi, Jin-Su

Publication type:

Article

A Polymorphism in the MTRR Gene Is Associated with Early Childhood Caries and Underweight.

Published in:

Caries Research, 2017, v. 51, n. 2, p. 102, doi. 10.1159/000451037

By:

Cunha de Sena, Fernanda;
Volpe Abreu, Fernanda;
Alves Antunes, Lívia Azeredo;
Silva Fraga, Renato;
Santos Antunes, Leonardo;
Cabral Machado, Claudio Manoel;
Kuntz Couto, Ana Carolina;
Barbosa Lopes, Ludiana;
Küchler, Erika Calvano

Publication type:

Article

A Polymorphism in the MTRR Gene Is Associated with Early Childhood Caries and Underweight.

Published in:

2017

By:

Alves Antunes, Lívia Azeredo;
Cabral Machado, Claudio Manoel;
Kuntz Couto, Ana Carolina;
Lopes, Ludiana Barbosa;
de Sena, Fernanda Cunha;
Abreu, Fernanda Volpe;
Fraga, Renato Silva;
Küchler, Erika Calvano;
Antunes, Leonardo Santos;
Antunes, Lívia Azeredo Alves;
Machado, Claudio Manoel Cabral;
Couto, Ana Carolina Kuntz;
Sena, Fernanda Cunha

Publication type:

journal article

Methionine synthase 2756AA polymorphism is associated with the risk of cognitive impairment in patients with late-life depression.

Published in:

Asia-Pacific Psychiatry, 2017, v. 9, n. 1, p. n/a, doi. 10.1111/appy.12242

By:

Yang, Ya‐Hsu;
Chiu, Chih‐Chiang;
Teng, Hao‐Wei;
Chu, Chih‐Pang;
Chang, Ching‐Jui;
Chiu, Wei‐Che;
Chen, Chin‐Hsin;
Lu, Mong‐Liang;
Liu, Shen‐Ing;
Huang, Shih‐Yi;
Liu, Hsing‐Cheng;
Sun, I‐Wen

Publication type:

Article

Mouse model for deficiency of methionine synthase reductase exhibits short-term memory impairment and disturbances in brain choline metabolism.

Published in:

Biochemical Journal, 2014, v. 461, n. 2, p. 205, doi. 10.1042/BJ20131568

By:

JADAVJI, Nafisa M.;
BAHOUS, Renata H.;
DENG, Liyuan;
MALYSHEVA, Olga;
GRAND'MAISON, Marilyn;
BEDELL, Barry J.;
CAUDILL, Marie A.;
ROZEN, Rima

Publication type:

Article

Effects of increased temperature on dimethylsulfoniopropionate (DMSP) concentration and methionine synthase activity in Symbiodinium microadriaticum.

Published in:

Biogeochemistry, 2012, v. 110, n. 1-3, p. 17, doi. 10.1007/s10533-012-9733-0

By:

McLenon, Amanda;
DiTullio, Giacomo

Publication type:

Article

Identification and characterization of a bacterial core methionine synthase.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-58873-z

By:

Deobald, Darja;
Hanna, Rafael;
Shahryari, Shahab;
Layer, Gunhild;
Adrian, Lorenz

Publication type:

Article

MTRR gene variants may predispose to the risk of Congenital Heart Disease in Down syndrome patients of Indian origin.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 61, doi. 10.1016/j.ejmhg.2016.02.006

By:

Asim, Ambreen;
Agarwal, Sarita;
Panigrahi, Inusha

Publication type:

Article

Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt.

Published in:

Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 2, p. 217, doi. 10.1016/j.ejmhg.2015.09.003

By:

Moustafa, Maha;
Gaber, Elham;
El Fath, Gamal Abo

Publication type:

Article

Individualized Supplementation of Folic Acid According to Polymorphisms of Methylenetetrahydrofolate Reductase (MTHFR), Methionine Synthase Reductase (MTRR) Reduced Pregnant Complications.

Published in:

Gynecologic & Obstetric Investigation, 2015, v. 79, n. 2, p. 107, doi. 10.1159/000367656

By:

Li, Xiujuan;
Jiang, Jing;
Xu, Min;
Xu, Mei;
Yang, Yan;
Lu, Wei;
Yu, Xuemei;
Ma, Jianlin;
Pan, Jiakui

Publication type:

Article

Massive hyperhomocysteinaemia as a complication of nitrous oxide inhalation.

Published in:

British Journal of Clinical Pharmacology, 2016, v. 81, n. 2, p. 391, doi. 10.1111/bcp.12813

By:

Faguer, Stanislas;
Ruiz, Jean;
Mari, Arnaud

Publication type:

Article

Are MTHFR C677T and MTRR A66G Polymorphisms Associated with Overweight/Obesity Risk? From a Case-Control to a Meta-Analysis of 30,327 Subjects.

Published in:

International Journal of Molecular Sciences, 2015, v. 16, n. 6, p. 11849, doi. 10.3390/ijms160611849

By:

Shu-Jun Fan;
Bo-Yi Yang;
Xue-Yuan Zhi;
Miao He;
Da Wang;
Yan-Xun Wang;
Yi-Nuo Wang;
Jian Wei;
Quan-Mei Zheng;
Gui-Fan Sun

Publication type:

Article

Associations of MTHFR C677T and MTRR A66G Gene Polymorphisms with Metabolic Syndrome: A Case-Control Study in Northern China.

Published in:

International Journal of Molecular Sciences, 2014, v. 15, n. 12, p. 21687, doi. 10.3390/ijms151221687

By:

Boyi Yang;
Shujun Fan;
Xueyuan Zhi;
Da Wang;
Yongfang Li;
Yinuo Wang;
Yanxun Wang;
Jian Wei;
Quanmei Zheng;
Guifan Sun

Publication type:

Article

The polymorphisms of methionine synthase (MTR) and methionine synthase reductase (MTRR) genes in pathogenesis of preeclampsia.

Published in:

2017

By:

Seremak-Mrozikiewicz, Agnieszka;
Bogacz, Anna;
Deka-Pawlik, Donata;
Klejewski, Andrzej;
Wolski, Hubert;
Drews, Krzysztof;
Karasiewicz, Monika;
Czerny, Boguslaw

Publication type:

journal article

Meta-analyses on the association of MTR A2756G and MTRR A66G polymorphisms with neural tube defect risks in Caucasian children.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2013, v. 26, n. 12, p. 1166, doi. 10.3109/14767058.2013.777699

By:

Ouyang, Shengrong;
Liu, Zhuo;
Li, Yuanyuan;
Wu, Jianxin

Publication type:

Article

Methylcobalamin in Vitamin B12 Deficiency: To Give or not to Give?

Published in:

Journal of Pharmacology & Pharmacotherapeutics, 2017, v. 8, n. 1, p. 33, doi. 10.4103/jpp.JPP_173_16

By:

Kamath, Ashwin;
Pemminati, Sudhakar

Publication type:

Article

Unraveling Vitamin B12-Responsive Gene Regulation in Algae.

Published in:

Plant Physiology, 2014, v. 165, n. 1, p. 388, doi. 10.1104/pp.113.234369

By:

Helliwell, Katherine E.;
Scaife, Mark A.;
Sasso, Severin;
Ulian Araujo, Ana Paula;
Purton, Saul;
Smith, Alison G.

Publication type:

Article

Reductive elimination pathway for homocysteine to methionine conversion in cobalamin-dependent methionine synthase.

Published in:

Journal of Biological Inorganic Chemistry (JBIC), 2012, v. 17, n. 4, p. 611, doi. 10.1007/s00775-012-0881-4

By:

Kozlowski, Pawel;
Kamachi, Takashi;
Kumar, Manoj;
Yoshizawa, Kazunari

Publication type:

Article

Should we Still use Nitrous Oxide in our Clinical Practice? No!

Published in:

Turkish Journal of Anesthesia & Reanimation, 2017, v. 45, n. 1, p. 3, doi. 10.5152/TJAR.2017.24011

By:

Rossaint, Rolf;
Coburn, Mark;
Jantzen, Jan-Peter

Publication type:

Article

Nitrous Oxide is an Effective and Safe Anesthetic.

Published in:

Turkish Journal of Anesthesia & Reanimation, 2017, v. 45, n. 1, p. 1, doi. 10.5152/TJAR.2017.23011

By:

Sessler, Daniel I.

Publication type:

Article

Differentially expressed proteins in fluconazole-susceptible and fluconazole-resistant isolates of Candida glabrata.

Published in:

Drug Discoveries & Therapeutics, 2015, v. 9, n. 3, p. 191, doi. 10.5582/ddt.2015.01010

By:

Yinzhong Shen;
Lijun Zhang;
Xiaofang Jia;
Yongxin Zhang;
Hongzhou Lu

Publication type:

Article

Risk of congenital heart defects is influenced by genetic variation in folate metabolism.

Published in:

Cardiology in the Young, 2013, v. 23, n. 1, p. 89, doi. 10.1017/S1047951112000431

By:

Christensen, Karen E.;
Zada, Yassamin Feroz;
Rohlicek, Charles V.;
Andelfinger, Gregor U.;
Michaud, Jacques L.;
Bigras, Jean-Luc;
Richter, Andrea;
Dubé, Marie-Pierre;
Rozen, Rima

Publication type:

Article

Identification of metE as a Second Target of the sRNA scr5239 in Streptomyces coelicolor.

Published in:

PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120147

By:

Vockenhuber, Michael-Paul;
Heueis, Nona;
Suess, Beatrix

Publication type:

Article

Genetic Variant in MTRR, but Not MTR, Is Associated with Risk of Congenital Heart Disease: An Integrated Meta-Analysis.

Published in:

PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0089609

By:

Cai, Bingxi;
Zhang, Ti;
Zhong, Rong;
Zou, Li;
Zhu, Beibei;
Chen, Wei;
Shen, Na;
Ke, Juntao;
Lou, Jiao;
Wang, Zhenling;
Sun, Yu;
Liu, Lifeng;
Song, Ranran

Publication type:

Article

Methionine Synthase A2756G Polymorphism and Risk of Colorectal Adenoma and Cancer: Evidence Based on 27 Studies.

Published in:

PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060508

By:

Ding, Weixing;
Zhou, Dong-lei;
Jiang, Xun;
Lu, Lie-sheng

Publication type:

Article

Age-Dependent Decrease and Alternative Splicing of Methionine Synthase mRNA in Human Cerebral Cortex and an Accelerated Decrease in Autism.

Published in:

PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056927

By:

Muratore, Christina R.;
Hodgson, Nathaniel W.;
Trivedi, Malav S.;
Abdolmaleky, Hamid M.;
Persico, Antonio M.;
Lintas, Carla;
De La Monte, Suzanne;
Deth, Richard C.

Publication type:

Article

Maternal gene polymorphisms involved in folate metabolism and the risk of having a Down syndrome offspring: a meta-analysis.

Published in:

Mutagenesis, 2013, v. 28, n. 6, p. 661, doi. 10.1093/mutage/get045

By:

Yang, Mei;
Gong, Tian;
Lin, Xiaofang;
Qi, Ling;
Guo, Yiyang;
Cao, Zhongqiang;
Shen, Min;
Du, Yukai

Publication type:

Article

Role of polymorphisms of folate-cycle enzymes in diabetic retinopathy progression in patients with type 2 diabetic mellitus.

Published in:

Journal of Ophthalmology (Ukraine) / Oftalʹmologičeskij Žurnal, 2022, n. 5, p. 3, doi. 10.31288/oftalmolzh20225311

By:

Rykov, S. O.;
Prokopenko, Iu. V.;
Natrus, L. V.;
Panchenko, Iu. O.

Publication type:

Article

Methionine synthase A2756G polymorphism and lymphoma risk: a meta-analysis.

Published in:

European Review for Medical & Pharmacological Sciences, 2017, v. 21, n. 13, p. 3075

By:

GUO, S.-J.;
LUO, S.-C.;
LIU, W.-Y.;
ZUO, Q.-N.;
LI, X.-H.

Publication type:

Article

Gating mechanisms for biological electron transfer: Integrating structure with biophysics reveals the nature of redox control in cytochrome P450 reductase and copper-dependent nitrite reductase

Published in:

FEBS Letters, 2012, v. 586, n. 5, p. 578, doi. 10.1016/j.febslet.2011.07.003

By:

Leferink, Nicole G.H.;
Pudney, Christopher R.;
Brenner, Sibylle;
Heyes, Derren J.;
Eady, Robert R.;
Samar Hasnain, S.;
Hay, Sam;
Rigby, Stephen E.J.;
Scrutton, Nigel S.

Publication type:

Article

Polymorphisms in Folate-Related Enzyme Genes in Idiopathic Infertile Brazilian Men.

Published in:

Reproductive Sciences, 2011, v. 18, n. 12, p. 1267, doi. 10.1177/1933719111411729

By:

Gava, Marcello M.;
Kayaki, Erika A.;
Bianco, Bianca;
Teles, Juliana S.;
Christofolini, Denise M.;
Pompeo, Antonio C. L.;
Glina, Sidney;
Barbosa, Caio P.

Publication type:

Article

Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations.

Published in:

Molecular & Cellular Biochemistry, 2015, v. 407, n. 1/2, p. 51, doi. 10.1007/s11010-015-2453-8

By:

Cheng, Haiqin;
Bu, Zhaoli;
Zhao, Hong;
Xie, Jun;
Li, Huili;
Zhang, Qin;
Bai, Baoling;
Zhang, Ting;
Li, Ren-Ke

Publication type:

Article

Association Between Methionine Synthase Reductase A66G Polymorphism and the Risk of Congenital Heart Defects: Evidence From Eight Case-Control Studies.

Published in:

Pediatric Cardiology, 2014, v. 35, n. 7, p. 1091, doi. 10.1007/s00246-014-0948-9

By:

Yu, Di;
Yang, Lei;
Shen, Shutong;
Fan, Changfeng;
Zhang, Weiyan;
Mo, Xuming

Publication type:

Article

Association of methionine synthase rs1801394 and methionine synthase reductase rs1805087 polymorphisms with meningioma in adults: A meta-analysis.

Published in:

Biomedical Reports, 2014, v. 2, n. 3, p. 432, doi. 10.3892/br.2014.248

By:

XIAN-TAO ZENG;
JUN-TI LU;
XIANG-JUN TANG;
HONG WENG;
JIE LUO

Publication type:

Article

Aberrant Expression of Folate Metabolism Enzymes and Its Diagnosis and Survival Prediction in Ovarian Carcinoma.

Published in:

Analytical Cellular Pathology: Cellular Oncology, 2019, p. 1, doi. 10.1155/2019/1438628

By:

Chen, Jia;
Li, Li

Publication type:

Article

Are Genes Connected with Homocysteine Metabolism Associated with Bipolar Disorder?

Published in:

Neuropsychobiology, 2014, v. 69, n. 2, p. 107, doi. 10.1159/000358091

By:

Permoda-Osip, agnieszka;
Dmitrzak-Weglarz, Monika;
Hauser, Joanna;
Rybakowski, Janusz K.

Publication type:

Article