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There are 6232 results for: content related to: Oxidative stress and apoptosis in homocystinuria patients with genetic remethylation defects

  1. You have free access to this content
    Response of the methionine synthase system to short-term culture with homocysteine and nitrous oxide and its relation to methionine dependence

    International Journal of Cancer

    Volume 72, Issue 2, 17 July 1997, Pages: 301–306, Torunn Fiskerstrand, Per M. Ueland and Helga Refsum

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1097-0215(19970717)72:2<301::AID-IJC17>3.0.CO;2-I

  2. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in Brazilian children

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 3, 30 July 2004, Pages: 256–260, Ana Claudia M. Aléssio, Joyce M. Annichino-Bizzacchi, Sergio P. Bydlowski, Marcos N. Eberlin, Adriana P. Vellasco and Nelci Fenalti Höehr

    Version of Record online : 18 MAY 2004, DOI: 10.1002/ajmg.a.30108

  3. You have free access to this content
    Acquired and inherited disorders of cobalamin and folate in children

    British Journal of Haematology

    Volume 134, Issue 2, July 2006, Pages: 125–136, V. Michael Whitehead

    Version of Record online : 23 MAY 2006, DOI: 10.1111/j.1365-2141.2006.06133.x

  4. Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for down syndrome among Turkish women

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 1, 15 May 2004, Pages: 5–10, Koray Boduroğlu, Yasemin Alanay, Berrin Koldan and Ergül Tunçbilek

    Version of Record online : 29 MAR 2004, DOI: 10.1002/ajmg.a.20432

  5. Inborn errors of cobalamin absorption and metabolism

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 157, Issue 1, 15 February 2011, Pages: 33–44, David Watkins and David S. Rosenblatt

    Version of Record online : 10 FEB 2011, DOI: 10.1002/ajmg.c.30288

  6. cblE Type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression

    Human Mutation

    Volume 25, Issue 3, March 2005, Pages: 239–247, Petra Zavadáková, Brian Fowler, Terttu Suormala, Zorka Novotna, Peter Mueller, Julia B. Hennermann, Jiří Zeman, M. Antonia Vilaseca, Laura Vilarinho, Sven Gutsche, Ekkehard Wilichowski, Gerd Horneff and Viktor Kožich

    Version of Record online : 15 FEB 2005, DOI: 10.1002/humu.20131

  7. Genetic and non-genetic factors that increase the risk of non-syndromic cleft lip and/or palate development

    Oral Diseases

    Volume 21, Issue 3, April 2015, Pages: 393–399, JF Bezerra, GHM Oliveira, CD Soares, ML Cardoso, MAG Ururahy, FPF Neto, LG Lima-Neto, AD Luchessi, VN Silbiger, CM Fajardo, SR de Oliveira, M das G Almeida, RDC Hirata, AA de Rezende and MH Hirata

    Version of Record online : 8 OCT 2014, DOI: 10.1111/odi.12292

  8. Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms and protection from microvascular complications in adolescents with type 1 diabetes

    Pediatric Diabetes

    Volume 9, Issue 4pt2, August 2008, Pages: 348–353, Esko J Wiltshire, Fauzia Mohsin, Albert Chan and Kim C Donaghue

    Version of Record online : 29 JUL 2008, DOI: 10.1111/j.1399-5448.2008.00374.x

  9. 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

  10. You have full text access to this OnlineOpen article
    The deep intronic c.903+469T>C mutation in the MTRR gene creates an SF2/ASF binding exonic splicing enhancer, which leads to pseudoexon activation and causes the cblE type of homocystinuria

    Human Mutation

    Volume 31, Issue 4, April 2010, Pages: 437–444, Katerina Homolova, Petra Zavadakova, Thomas Koed Doktor, Lisbeth Dahl Schroeder, Viktor Kozich and Brage S. Andresen

    Version of Record online : 29 JAN 2010, DOI: 10.1002/humu.21206

  11. Genetic variants in one-carbon metabolism genes and breast cancer risk in European American and African American women

    International Journal of Cancer

    Volume 137, Issue 3, 1 August 2015, Pages: 666–677, Zhihong Gong, Song Yao, Gary Zirpoli, Ting-Yuan David Cheng, Michelle Roberts, Thaer Khoury, Gregory Ciupak, Warren Davis, Karen Pawlish, Lina Jandorf, Dana H. Bovbjerg, Elisa V. Bandera and Christine B. Ambrosone

    Version of Record online : 29 JAN 2015, DOI: 10.1002/ijc.29434

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    Modulation of the mtrCDE-encoded efflux pump gene complex of Neisseria meningitidis due to a Correia element insertion sequence

    Molecular Microbiology

    Volume 54, Issue 3, November 2004, Pages: 731–741, Corinne E. Rouquette-Loughlin, Jacqueline T. Balthazar, Stuart A. Hill and William M. Shafer

    Version of Record online : 28 SEP 2004, DOI: 10.1111/j.1365-2958.2004.04299.x

  13. Folate-mediated one-carbon metabolism and neural tube defects: Balancing genome synthesis and gene expression

    Birth Defects Research Part C: Embryo Today: Reviews

    Volume 81, Issue 3, September 2007, Pages: 183–203, Anna E. Beaudin and Patrick J. Stover

    Version of Record online : 26 OCT 2007, DOI: 10.1002/bdrc.20100

  14. You have free access to this content
    Asymmetry of Dam remethylation on the leading and lagging arms of plasmid replicative intermediates

    The EMBO Journal

    Volume 18, Issue 22, November 15, 1999, Pages: 6542–6551, Irina Stancheva, Theodor Koller and José M. Sogo

    Version of Record online : 15 NOV 1999, DOI: 10.1093/emboj/18.22.6542

  15. Fetal anticonvulsant syndromes and polymorphisms in MTHFR, MTR, and MTRR

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 19, 1 October 2007, Pages: 2303–2311, John Dean, Zoe Robertson, V. Reid, Q. Diana Wang, Hazel Hailey, Sue Moore, A. Dee Rasalam, Peter Turnpenny, David Lloyd, Amanda Cardy, Duncan Shaw and Julian Little

    Version of Record online : 12 SEP 2007, DOI: 10.1002/ajmg.a.31914

  16. You have full text access to this OnlineOpen article
    A dodecylamine derivative of cyanocobalamin potently inhibits the activities of cobalamin-dependent methylmalonyl-CoA mutase and methionine synthase of Caenorhabditis elegans

    FEBS Open Bio

    Volume 4, Issue 1, January 01, 2014, Pages: 722–729, Tomohiro Bito, Yukinori Yabuta, Tsuyoshi Ichiyanagi, Tsuyoshi Kawano and Fumio Watanabe

    Version of Record online : 1 AUG 2014, DOI: 10.1016/j.fob.2014.07.008

  17. Abstracts

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 76, Issue 3, March 2006, Pages: 145–169, NDE Greene, LPE Dunlevy, K Burren, LS Chitty and AJ Copp

    Version of Record online : 14 MAR 2006, DOI: 10.1002/bdra.20242

  18. You have free access to this content
    Hyperhomocysteinemia: Impact on Neurodegenerative Diseases

    Basic & Clinical Pharmacology & Toxicology

    Volume 117, Issue 5, November 2015, Pages: 287–296, Meenakshi Sharma, Manisha Tiwari and Rakesh Kumar Tiwari

    Version of Record online : 19 JUN 2015, DOI: 10.1111/bcpt.12424

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    Remethylation and transsulfuration of methionine in cirrhosis: Studies with L-[2H3-methyl-1-13C]methionine


    Volume 36, Issue 5, November 2002, Pages: 1190–1196, Stefan Russmann, Edith Junker and Bernhard H. Lauterburg

    Version of Record online : 30 DEC 2003, DOI: 10.1053/jhep.2002.36499

  20. Neural tube defects on the Texas-Mexico border: What we've learned in the 20 years since the Brownsville cluster

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 94, Issue 11, November 2012, Pages: 882–892, Lucina Suarez, Marilyn Felkner, Jean D. Brender, Mark Canfield, Huiping Zhu and Katherine A. Hendricks

    Version of Record online : 3 SEP 2012, DOI: 10.1002/bdra.23070