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There are 5224 results for: content related to: Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

  1. Analysis of complement receptor Type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms


    Volume 50, Issue 7, July 2010, Pages: 1435–1443, Bach-Nga Pham, Aymric Kisserli, Béatrice Donvito, Valérie Duret, Brigitte Reveil, Thierry Tabary, Pierre-Yves Le Pennec, Thierry Peyrard, Philippe Rouger and Jacques H.M. Cohen

    Version of Record online : 19 FEB 2010, DOI: 10.1111/j.1537-2995.2010.02599.x

  2. You have full text access to this OnlineOpen article
    Whole genome sequencing shows sleeping sickness relapse is due to parasite regrowth and not reinfection

    Evolutionary Applications

    Volume 9, Issue 2, February 2016, Pages: 381–393, Joshua B. Richardson, Benjamin Evans, Patient P. Pyana, Nick Van Reet, Mark Sistrom, Philippe Büscher, Serap Aksoy and Adalgisa Caccone

    Version of Record online : 9 JAN 2016, DOI: 10.1111/eva.12338

  3. You have full text access to this OnlineOpen article
    Who's behind that mask and cape? The Asian leopard cat's Agouti (ASIP) allele likely affects coat colour phenotype in the Bengal cat breed

    Animal Genetics

    Volume 45, Issue 6, December 2014, Pages: 893–897, L. C. Gershony, M. C. T. Penedo, B. W. Davis, W. J. Murphy, C. R. Helps and L. A. Lyons

    Version of Record online : 20 AUG 2014, DOI: 10.1111/age.12206

  4. Effects of polymorphisms of the SLCO2B1 transporter gene on the pharmacokinetics of montelukast in humans

    The Journal of Clinical Pharmacology

    Volume 53, Issue 11, November 2013, Pages: 1186–1193, Kyoung-Ah Kim, Hye-Mi Lee, Hyun-Jin Joo, In-Bae Park and Ji-Young Park

    Version of Record online : 23 AUG 2013, DOI: 10.1002/jcph.144

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    Homozygosity at the MTL locus in clinical strains of Candida albicans: karyotypic rearrangements and tetraploid formation

    Molecular Microbiology

    Volume 52, Issue 5, June 2004, Pages: 1451–1462, Melanie Legrand, Paul Lephart, Anja Forche, Frank-Michael C. Mueller, T. Walsh, P.T. Magee and Beatrice B. Magee

    Version of Record online : 22 APR 2004, DOI: 10.1111/j.1365-2958.2004.04068.x

  6. Low SPINK5 expression in chronic rhinosinusitis

    The Laryngoscope

    Volume 122, Issue 6, June 2012, Pages: 1198–1204, Kai Fruth, Gyula Goebel, Dimitrios Koutsimpelas, Jan Gosepath, Irene Schmidtmann, Wolf J. Mann and Juergen Brieger

    Version of Record online : 8 MAY 2012, DOI: 10.1002/lary.23300

  7. A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

    Clinical Genetics

    Volume 62, Issue 4, October 2002, Pages: 334–339, A Belmouden, R Melki, M Hamdani, K Zaghloul, A Amraoui, S Nadifi, O Akhayat and H-J Garchon

    Version of Record online : 8 OCT 2002, DOI: 10.1034/j.1399-0004.2002.620415.x

  8. Variation in genes involved in the immune response and prostate cancer risk in the placebo arm of the Prostate Cancer Prevention Trial

    The Prostate

    Volume 75, Issue 13, September 15, 2015, Pages: 1403–1418, Danyelle A. Winchester, Cathee Till, Phyllis J. Goodman, Catherine M. Tangen, Regina M. Santella, Teresa L. Johnson-Pais, Robin J. Leach, Jianfeng Xu, S. Lilly Zheng, Ian M. Thompson, M. Scott Lucia, Scott M. Lippmann, Howard L. Parnes, Paul J. Dluzniewski, William B. Isaacs, Angelo M. De Marzo, Charles G. Drake and Elizabeth A. Platz

    Version of Record online : 5 JUN 2015, DOI: 10.1002/pros.23021

  9. Sudden Infant Death Syndrome: The Role of Cardiac Ion Channel Mutations

    Standard Article


    Ronald Wilders

    Published Online : 15 OCT 2012, DOI: 10.1002/9780470015902.a0024378

  10. Potassium Channels

    Standard Article


    William A Coetzee and Bernardo Rudy

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0005670

  11. Functional and Molecular Diversity of Native Neuronal K+ Channels

    Standard Article


    Jeanne M Nerbonne

    Published Online : 16 MAY 2016, DOI: 10.1002/9780470015902.a0000049

  12. You have free access to this content
    Long QT syndrome: beyond the causal mutation

    The Journal of Physiology

    Volume 591, Issue 17, September 2013, Pages: 4125–4139, Ahmad S. Amin, Yigal M. Pinto and Arthur A. M. Wilde

    Version of Record online : 19 JUL 2013, DOI: 10.1113/jphysiol.2013.254920

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    Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

    Journal of Thrombosis and Haemostasis

    Volume 2, Issue 1, January 2004, Pages: 71–76, F. Quélin, M. Trossaërt, M. Sigaud, P. D. E. Mazancourt and E. Fressinaud

    Version of Record online : 9 JAN 2004, DOI: 10.1111/j.1538-7836.2004.00554.x

  14. Association of RBP4 genetic variants with childhood obesity and cardiovascular risk factors

    Pediatric Diabetes

    Pilar Codoñer-Franch, Joaquín Carrasco-Luna, Paula Allepuz, Alan Codoñer-Alejos and Vicent Guillem

    Version of Record online : 26 NOV 2015, DOI: 10.1111/pedi.12339

  15. The biallelic expression pattern of X-linked genes in Klinefelter syndrome by pyrosequencing

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 5, 1 March 2006, Pages: 527–532, In Hyuk Chung, Han Chul Lee, Jung Hoon Park, Jung Jae Ko, Sook Hwan Lee, Tae-Gyu Chung, Hyun-Joo Kim, Kwang-Yul Cha and Suman Lee

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31102

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    Association Study of Single-Nucleotide Polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 Genes With Male Infertility

    Journal of Andrology

    Volume 33, Issue 4, July-August 2012, Pages: 675–683, Toso Plaseski, Predrag Noveski, Zaneta Popeska, Georgi D. Efremov and Dijana Plaseska-Karanfilska

    Version of Record online : 2 JAN 2013, DOI: 10.2164/jandrol.111.013995

  17. Incidence and dynamics of active cytomegalovirus infection in allogeneic stem cell transplant patients according to single nucleotide polymorphisms in donor and recipient CCR5, MCP-1, IL-10, and TLR9 genes

    Journal of Medical Virology

    Volume 87, Issue 2, February 2015, Pages: 248–255, Isabel Corrales, Estela Giménez, Carlos Solano, Paula Amat, Rafael de la Cámara, José Nieto, Ana Garcia-Noblejas and David Navarro

    Version of Record online : 17 AUG 2014, DOI: 10.1002/jmv.24050

  18. Polymorphism of OAS-1 determines liver fibrosis progression in hepatitis C by reduced ability to inhibit viral replication

    Liver International

    Volume 29, Issue 9, October 2009, Pages: 1413–1421, Chang-Zheng Li, Naoya Kato, Jin-Hai Chang, Ryosuke Muroyama, Run-Xuan Shao, Narayan Dharel, Radsamee Sermsathanasawadi, Takao Kawabe and Masao Omata

    Version of Record online : 9 JUN 2009, DOI: 10.1111/j.1478-3231.2009.02061.x

  19. Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

    British Journal of Dermatology

    Volume 172, Issue 2, February 2015, Pages: 527–531, T. Takeichi, A. Nanda, L. Liu, S. Aristodemou, J.R. McMillan, K. Sugiura, M. Akiyama, H. Al-Ajmi, M.A. Simpson and J.A. McGrath

    Version of Record online : 30 DEC 2014, DOI: 10.1111/bjd.13294

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    Cytotoxic T-lymphocyte antigen 4 gene +49A/G polymorphism significantly associated with susceptibility to primary biliary cirrhosis: A meta-analysis

    Journal of Digestive Diseases

    Volume 12, Issue 6, December 2011, Pages: 428–435, Rui Rui CHEN, Zhe Yi HAN, Jin Ge LI, Yong Quan SHI, Xin Min ZHOU, Jing Bo WANG, Xi Qiang CAI, Xue Chang WANG, Ying HAN and Dai Ming FAN

    Version of Record online : 24 NOV 2011, DOI: 10.1111/j.1751-2980.2011.00537.x