Výsledky vyhledávání - Mark Curran

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  1. 1
    A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel

    A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel Autor Michael C. Sanguinetti, Changan Jiang, Mark Curran, Mark T. Keating

    Vydáno 1995
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  2. 2
    Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.

    Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia. Autor Michael C. Sanguinetti, Mark Curran, Peter Spector, Mark T. Keating

    Vydáno 1996
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  3. 3
    Fast inactivation causes rectification of the IKr channel.

    Fast inactivation causes rectification of the IKr channel. Autor Peter Spector, Mark Curran, Anruo Zou, Mark T. Keating, Michael C. Sanguinetti

    Vydáno 1996
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  4. 4
    A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

    A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome Autor Mark Curran, Igor Splawski, Katherine W. Timothy, G.Michael Vincen, Eric D. Green, Mark T. Keating

    Vydáno 1995
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  5. 5
    HLA-C*06:02 Allele and Response to IL-12/23 Inhibition: Results from the Ustekinumab Phase 3 Psoriasis Program

    HLA-C*06:02 Allele and Response to IL-12/23 Inhibition: Results from the Ustekinumab Phase 3 Psoriasis Program Autor Katherine Li, Chaohua Huang, B. Randazzo, Shu Li, Philippe Szapary, Mark Curran, Kim Campbell, Carrie Brodmerkel

    Vydáno 2016
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  6. 6
    Integrative genomic deconvolution of rheumatoid arthritis GWAS loci into gene and cell type associations

    Integrative genomic deconvolution of rheumatoid arthritis GWAS loci into gene and cell type associations Autor Alice M. Walsh, John W. Whitaker, Chaohua Huang, Yauheniya Cherkas, Sarah Lamberth, Carrie Brodmerkel, Mark Curran, Radu Dobrin

    Vydáno 2016
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  7. 7
    Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic Development

    Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic Development Autor Debra E. Weese‐Mayer, Elizabeth Berry‐Kravis, Lili Zhou, Brion S. Maher, Mark Curran, Jean M. Silvestri, Mary L. Marazita

    Vydáno 2004
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  8. 8
    Assessment of Belatacept-Mediated Costimulation Blockade Through Evaluation of CD80/86-Receptor Saturation

    Assessment of Belatacept-Mediated Costimulation Blockade Through Evaluation of CD80/86-Receptor Saturation Autor Robert Latek, Catherine Fleener, Vahideh Lamian, Edward J. Kulbokas, Patricia M. Davis, Suzanne J. Suchard, Mark Curran, Flavio Vincenti, Robert Townsend

    Vydáno 2009
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  9. 9
    Effects of immunomodulatory drugs on depressive symptoms: A mega-analysis of randomized, placebo-controlled clinical trials in inflammatory disorders

    Effects of immunomodulatory drugs on depressive symptoms: A mega-analysis of randomized, placebo-controlled clinical trials in inflammatory disorders Autor Gayle Wittenberg, Annie Stylianou, Yun Zhang, Yu Sun, Ashutosh Gupta, P. S. Jagannatha, Dai Wang, Benjamin Hsu, Mark Curran, Shahid A. Khan, Guang Chen, Edward T. Bullmore, Wayne C. Drevets

    Vydáno 2019
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  10. 10
    Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders

    Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders Autor Michaela Oswald, Mark Curran, Sarah Lamberth, Robert M. Townsend, Jennifer D. Hamilton, David Chernoff, John P. Carulli, Michael J. Townsend, Michael E. Weinblatt, Marlena Kern, Cassandra Pond, Annette Lee, Peter K. Gregersen

    Vydáno 2014
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  11. 11
    Genome Screen for QTLs Contributing to Normal Variation in Bone Mineral Density and Osteoporosis*

    Genome Screen for QTLs Contributing to Normal Variation in Bone Mineral Density and Osteoporosis* Autor Daphne Koller, Michael J. Econs, Phillip A. Morin, J.C. Christian, Siu L. Hui, P. Parry, Mark Curran, L. A. Rodríguez, P.M. Conneally, Geoff Joslyn, Munro Peacock, C. Conrad Johnston, Tatiana Foroud

    Vydáno 2000
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  12. 12
    Linkage of a QTL Contributing to Normal Variation in Bone Mineral Density to Chromosome 11q12–13

    Linkage of a QTL Contributing to Normal Variation in Bone Mineral Density to Chromosome 11q12–13 Autor Daphne Koller, L. A. Rodríguez, J. C. Christian, Charles W. Slemenda, Michael J. Econs, Siu L. Hui, Phillip A. Morin, P.M. Conneally, Geoff Joslyn, Mark Curran, Munro Peacock, C. Conrad Johnston, Tatiana Foroud

    Vydáno 1998
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  13. 13
    Evidence for a <i>NOD2</i> -independent susceptibility locus for inflammatory bowel disease on chromosome 16p

    Evidence for a <i>NOD2</i> -independent susceptibility locus for inflammatory bowel disease on chromosome 16p Autor Jochen Hampe, H Frenzel, Muddassar M. Mirza, Peter J.P. Croucher, Andrew Cuthbert, Silvia Mascheretti, Klaus Huse, Matthias Platzer, Stephen Bridger, Birgit Meyer, Peter Nürnberg, Pieter Stokkers, Michael Krawczak, Christopher G. Mathew, Mark Curran, Stefan Schreiber

    Vydáno 2001
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  14. 14
    Blood and Intestine eQTLs from an Anti-TNF-Resistant Crohn's Disease Cohort Inform IBD Genetic Association Loci

    Blood and Intestine eQTLs from an Anti-TNF-Resistant Crohn's Disease Cohort Inform IBD Genetic Association Loci Autor Antonio Fabio Di Narzo, Lauren Peters, Carmen Argmann, Aleksandar Stojmirović, Jacqueline Perrigoue, Katherine Li, Shannon Telesco, Brian Kidd, Jennifer S. Walker, Joel T. Dudley, Judy H. Cho, Eric E. Schadt, Andrew Kasarskis, Mark Curran, Radu Dobrin, Ke Hao

    Vydáno 2016
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  15. 15
    Linkage of Inflammatory Bowel Disease to Human Chromosome 6p

    Linkage of Inflammatory Bowel Disease to Human Chromosome 6p Autor Jochen Hampe, Sarah H. Shaw, Robert Saiz, Nancy J. Leysens, Annette Lantermann, Silvia Mascheretti, Nicholas J. Lynch, Andrew J. Macpherson, Stephen Bridger, Sander van Deventer, Pieter Stokkers, Phil Morin, Mudassar M. Mirza, Alastair Forbes, John Edward Lennard-Jones, Christopher G. Mathew, Mark Curran, Stefan Schreiber

    Vydáno 1999
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  16. 16
    Gene Expression Signature for Prediction of Golimumab Response in a Phase 2a Open-Label Trial of Patients With Ulcerative Colitis

    Gene Expression Signature for Prediction of Golimumab Response in a Phase 2a Open-Label Trial of Patients With Ulcerative Colitis Autor Shannon Telesco, Carrie Brodmerkel, Hongyan Zhang, Lilianne Kim, Jewel Johanns, Abhijit Mazumder, Katherine Li, Frédéric Baribaud, Mark Curran, Richard Strauß, Bethany Paxson, Scott E. Plevy, Timothy S. Davison, Laura A. Knight, Siân Dibben, Stefan Schreiber, William J. Sandborn, Paul Rutgeerts, Corey A. Siegel, Walter Reinisch, Linda E. Greenbaum

    Vydáno 2018
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  17. 17
    Challenges in IBD Research: Precision Medicine

    Challenges in IBD Research: Precision Medicine Autor Lee A. Denson, Mark Curran, Dermot McGovern, Walter A. Koltun, Richard H. Duerr, Sandra C. Kim, R. Balfour Sartor, Francisco Sylvester, Clara Abraham, Edwin F. de Zoeten, Corey A. Siegel, Richéal Burns, Angela Dobes, Nataly Shtraizent, Gerard Honig, Caren Heller, Andres Hurtado‐Lorenzo, Judy H. Cho

    Vydáno 2019
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  18. 18
    A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort

    A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort Autor Jochen Hampe, Stefan Schreiber, Sarah H. Shaw, Kit Lau, Stephen Bridger, Andrew J. Macpherson, Lon R. Cardon, H. Sakul, Timothy Harris, Alan Buckler, Jeff Hall, Pieter Stokkers, Sander J. H. van Deventer, Peter Nürnberg, Mudassar M. Mirza, John C.W. Lee, John Edward Lennard-Jones, Christopher G. Mathew, Mark Curran

    Vydáno 1999
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  19. 19
    Integrative Analysis of the Inflammatory Bowel Disease Serum Metabolome Improves Our Understanding of Genetic Etiology and Points to Novel Putative Therapeutic Targets

    Integrative Analysis of the Inflammatory Bowel Disease Serum Metabolome Improves Our Understanding of Genetic Etiology and Points to Novel Putative Therapeutic Targets Autor Antonio Di Narzo, Sander M. Houten, Roman Kosoy, Ruiqi Huang, Frédéric M. Vaz, Ruixue Hou, Gabrielle Wei, Wenhui Wang, Phillip Comella, Tetyana Dodatko, Eduard Rogatsky, Aleksandar Stojmirović, Carrie Brodmerkel, Jacqueline Perrigoue, Amy Hart, Mark Curran, Joshua R. Friedman, Jun Zhu, Manasi Agrawal, Judy H. Cho, Ryan C. Ungaro, Marla C. Dubinsky, Bruce E. Sands, Mayte Suárez‐Fariñas, Eric E. Schadt, Jean‐Frédéric Colombel, Andrew Kasarskis, Ke Hao, Carmen Argmann

    Vydáno 2021
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  20. 20
    Biopsy and blood-based molecular biomarker of inflammation in IBD

    Biopsy and blood-based molecular biomarker of inflammation in IBD Autor Carmen Argmann, Ruixue Hou, Ryan C. Ungaro, Haritz Irizar, Zainab Al-Taie, Ruiqi Huang, Roman Kosoy, Swati Venkat, Won‐Min Song, Antonio Di Narzo, Bojan Losic, Ke Hao, Lauren Peters, Phillip Comella, Gabrielle Wei, Ashish Atreja, Milind Mahajan, Alina C. Iuga, Prerak Desai, Patrick Branigan, Aleksandar Stojmirović, Jacqueline Perrigoue, Carrie Brodmerkel, Mark Curran, Joshua R. Friedman, Amy Hart, Esi Lamousé‐Smith, Jan Wehkamp, Saurabh Mehandru, Eric E. Schadt, Bruce E. Sands, Marla C. Dubinsky, Jean‐Frédéric Colombel, Andrew Kasarskis, Mayte Suárez‐Fariñas

    Vydáno 2022
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