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There are 13069 results for: content related to: Crystal structure of methenyltetrahydrofolate synthetase from Mycoplasma pneumoniae (GI: 13508087) at 2.2 Å resolution

  1. Structural and functional characterization of a 5,10-methenyltetrahydrofolate synthetase from Mycoplasma pneumoniae (GI: 13508087)

    Proteins: Structure, Function, and Bioinformatics

    Volume 61, Issue 2, 1 November 2005, Pages: 433–443, Shengfeng Chen, Alexander F. Yakunin, Michael Proudfoot, Rosalind Kim and Sung-Hou Kim

    Version of Record online : 15 AUG 2005, DOI: 10.1002/prot.20591

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    Biochemical and Molecular Studies of Human Methenyltetrahydrofolate Synthetase

    STEM CELLS

    Volume 14, Issue 1, January 1996, Pages: 33–40, Dr. Jacques Jolivet, Alain Dayan, Myriam Beauchemin, Dounia Chahla, Aline Mamo and Richard Bertrand

    Version of Record online : 1 JAN 2009, DOI: 10.1002/stem.140033

  3. Modeling cellular compartmentation in one-carbon metabolism

    Wiley Interdisciplinary Reviews: Systems Biology and Medicine

    Volume 5, Issue 3, May/June 2013, Pages: 343–365, Marco Scotti, Lorenzo Stella, Emily J. Shearer and Patrick J. Stover

    Version of Record online : 13 FEB 2013, DOI: 10.1002/wsbm.1209

  4. A Computational Kinetics Study on the Intramolecular Hydrogen Shift Reactions of Alkylperoxy Radicals in 2-Methyltetrahydrofuran Oxidation

    International Journal of Chemical Kinetics

    Volume 49, Issue 6, June 2017, Pages: 419–437, Prajakta R. Parab, Naoki Sakade, Yasuyuki Sakai, Ravi Fernandes and K. Alexander Heufer

    Version of Record online : 29 MAR 2017, DOI: 10.1002/kin.21087

  5. High intake of folic acid disrupts embryonic development in mice

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 91, Issue 1, January 2011, Pages: 8–19, Laura Pickell, Katharine Brown, Deqiang Li, Xiao-Ling Wang, Liyuan Deng, Qing Wu, Jacob Selhub, Li Luo, Loydie Jerome-Majewska and Rima Rozen

    Version of Record online : 22 DEC 2010, DOI: 10.1002/bdra.20754

  6. Quantification of key red blood cell folates from subjects with defined MTHFR 677C>T genotypes using stable isotope dilution liquid chromatography/mass spectrometry

    Rapid Communications in Mass Spectrometry

    Volume 22, Issue 16, 30 August 2008, Pages: 2403–2412, Yuehua Huang, Stefanie Khartulyari, Megan E. Morales, Anna Stanislawska-Sachadyn, Joan M. Von Feldt, Alexander S. Whitehead and Ian A. Blair

    Version of Record online : 15 JUL 2008, DOI: 10.1002/rcm.3624

  7. Insights into metabolic mechanisms underlying folate-responsive neural tube defects: A minireview

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 85, Issue 4, April 2009, Pages: 274–284, Anna E. Beaudin and Patrick J. Stover

    Version of Record online : 29 JAN 2009, DOI: 10.1002/bdra.20553

  8. Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 85, Issue 6, June 2009, Pages: 531–541, Laura Pickell, Deqiang Li, Katharine Brown, Leonie G. Mikael, Xiao-Ling Wang, Qing Wu, Li Luo, Loydie Jerome-Majewska and Rima Rozen

    Version of Record online : 12 FEB 2009, DOI: 10.1002/bdra.20575

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    [6S]-5-methyltetrahydrofolate increases plasma folate more effectively than folic acid in women with the homozygous or wild-type 677C[RIGHTWARDS ARROW]T polymorphism of methylenetetrahydrofolate reductase

    British Journal of Pharmacology

    Volume 158, Issue 8, December 2009, Pages: 2014–2021, R Prinz-Langenohl, S Brämswig, O Tobolski, YM Smulders, DEC Smith, PM Finglas and K Pietrzik

    Version of Record online : 16 NOV 2009, DOI: 10.1111/j.1476-5381.2009.00492.x

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    Pharmacokinetic study on the utilisation of 5-methyltetrahydrofolate and folic acid in patients with coronary artery disease

    British Journal of Pharmacology

    Volume 141, Issue 5, March 2004, Pages: 825–830, Frank F Willems, Godfried H J Boers, Henk J Blom, Wim R M Aengevaeren and Freek W A Verheugt

    Version of Record online : 30 JAN 2009, DOI: 10.1038/sj.bjp.0705446

  11. MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 12, December 2015, Pages: 1031–1038, Karen E. Christensen, Liyuan Deng, Renata H. Bahous, Loydie A. Jerome-Majewska and Rima Rozen

    Version of Record online : 26 SEP 2015, DOI: 10.1002/bdra.23451

  12. Genetic variants in 3′-UTRs of MTHFR in the pregnancies complicated with preeclampsia and bioinformatics analysis

    Journal of Cellular Biochemistry

    Abbas Mohammadpour-Gharehbagh, Saeedeh Salimi, Farshid Keshavarzi, Foozieh Saeidian, Mahdieh Mousavi, Batool Teimoori, Maryam Esmaeilipour and Mojgan Mokhtari

    Version of Record online : 17 AUG 2017, DOI: 10.1002/jcb.26240

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    Women with polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase (MS) are less likely to have cervical intraepithelial neoplasia (CIN) 2 or 3

    International Journal of Cancer

    Volume 113, Issue 6, 1 March 2005, Pages: 991–997, Olga L. Henao, Chandrika J Piyathilake, John W. Waterbor, Ellen Funkhouser, Gary L. Johanning, Douglas C. Heimburger and Edward E. Partridge

    Version of Record online : 28 OCT 2004, DOI: 10.1002/ijc.20695

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    The methylenetetrahydrofolate reductase C677T mutation induces cell-specific changes in genomic DNA methylation and uracil misincorporation: A possible molecular basis for the site-specific cancer risk modification

    International Journal of Cancer

    Volume 124, Issue 9, 1 May 2009, Pages: 1999–2005, Kyoung-Jin Sohn, Hyeran Jang, Mihaela Campan, Daniel J. Weisenberger, Jeffrey Dickhout, Yi-Cheng Wang, Robert C. Cho, Zoe Yates, Mark Lucock, En-Pei Chiang, Richard C. Austin, Sang-Woon Choi, Peter W. Laird and Young-In Kim

    Version of Record online : 16 SEP 2008, DOI: 10.1002/ijc.24003

  15. An NTD-Associated Polymorphism in the 3′ UTR of MTHFD1L can Affect Disease Risk by Altering miRNA Binding

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 96–104, Stefano Minguzzi, S. Duygu Selcuklu, Charles Spillane and Anne Parle-McDermott

    Version of Record online : 18 DEC 2013, DOI: 10.1002/humu.22459

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    MTHFR polymorphisms and cognitive ageing in the ninth decade: the Lothian Birth Cohort 1921

    Genes, Brain and Behavior

    Volume 10, Issue 3, April 2011, Pages: 354–364, O. J. G. Schiepers, M. P. J. van Boxtel, S. E. Harris, A. J. Gow, A. Pattie, C. E. Brett, R. H. M. de Groot, J. Jolles, J. M. Starr and I. J. Deary

    Version of Record online : 24 JAN 2011, DOI: 10.1111/j.1601-183X.2010.00675.x

  17. Relationship between three polymorphisms of methylenetetrahydrofolate reductase (MTHFR C677T, A1298C, and G1793A) gene and risk of prostate cancer: A case–control study

    The Prostate

    Volume 70, Issue 15, 1 November 2010, Pages: 1645–1657, Mohammad Reza Safarinejad, Nayyer Shafiei and Shiva Safarinejad

    Version of Record online : 16 JUN 2010, DOI: 10.1002/pros.21200

  18. Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 88, Issue 8, August 2010, Pages: 679–688, Carolyn M. Summers, Laura E. Mitchell, Anna Stanislawska-Sachadyn, Shirley F. Baido, Ian A. Blair, Joan M. Von Feldt and Alexander S. Whitehead

    Version of Record online : 11 JUN 2010, DOI: 10.1002/bdra.20683

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    Methylenetetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia in Budd–Chiari syndrome and portal vein thrombosis: A systematic review and meta-analysis of observational studies

    Hepatology Research

    Volume 44, Issue 14, December 2014, Pages: E480–E498, Xingshun Qi, Zhiping Yang, Valerio De Stefano and Daiming Fan

    Version of Record online : 20 MAY 2014, DOI: 10.1111/hepr.12348

  20. Patterns of co-occurrence of three single nucleotide polymorphisms of the 5,10-methylenetetrahydrofolate reductase gene in kidney transplant recipients

    European Journal of Clinical Investigation

    Volume 34, Issue 9, September 2004, Pages: 613–618, W. C. Winkelmayer, G. Sunder-Plassmann, A. Huber and M. Födinger

    Version of Record online : 17 SEP 2004, DOI: 10.1111/j.1365-2362.2004.01394.x