Výsledky vyhledávání - Mehdi Keddache

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  1. 1
    Serotonin 2c receptor RNA editing in major depression and suicide

    Serotonin 2c receptor RNA editing in major depression and suicide Autor Rebecca Lyddon, Andrew J. Dwork, Mehdi Keddache, Larry J. Siever, Stella Dracheva

    Vydáno 2012
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    Artigo
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  2. 2
    Mapping of a Major Susceptibility Locus for Graves’ Disease (GD-1) to Chromosome 14q31

    Mapping of a Major Susceptibility Locus for Graves’ Disease (GD-1) to Chromosome 14q31 Autor Yaron Tomer, Giuseppe Barbesino, Mehdi Keddache, David A. Greenberg, Terry F. Davies

    Vydáno 1997
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  3. 3
    IFN-α Mediates the Development of Autoimmunity both by Direct Tissue Toxicity and through Immune Cell Recruitment Mechanisms

    IFN-α Mediates the Development of Autoimmunity both by Direct Tissue Toxicity and through Immune Cell Recruitment Mechanisms Autor Nagako Akeno, Eric P. Smith, Mihaela Stefan, Amanda K. Huber, Weijia Zhang, Mehdi Keddache, Yaron Tomer

    Vydáno 2011
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  4. 4
    Fine Mapping of Loci Linked to Autoimmune Thyroid Disease Identifies Novel Susceptibility Genes

    Fine Mapping of Loci Linked to Autoimmune Thyroid Disease Identifies Novel Susceptibility Genes Autor Yaron Tomer, Alia Hasham, Terry F. Davies, Mihaela Stefan, Erlinda Concepcion, Mehdi Keddache, David A. Greenberg

    Vydáno 2012
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  5. 5
    Linkage analysis for autism in a subset families with obsessive–compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

    Linkage analysis for autism in a subset families with obsessive–compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibil... Autor Joseph D. Buxbaum, Jeremy M. Silverman, Mehdi Keddache, Caroline J. Smith, Eric Hollander, Nicolás Ramoz, Jennifer Reichert

    Vydáno 2003
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  6. 6
    Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

    Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy Autor Katherine D. Holland, Jennifer A. Kearney, Tracy A. Glauser, Gerri Buck, Mehdi Keddache, John R. Blankston, Ian W. Glaaser, Robert S. Kass, Miriam H. Meisler

    Vydáno 2008
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  7. 7
    Genetically Driven Target Tissue Overexpression of CD40: A Novel Mechanism in Autoimmune Disease

    Genetically Driven Target Tissue Overexpression of CD40: A Novel Mechanism in Autoimmune Disease Autor Amanda K. Huber, Fred D. Finkelman, Cheuk Wun Li, Erlinda Concepcion, Eric P. Smith, Eric S. Jacobson, Rauf Latif, Mehdi Keddache, Weijia Zhang, Yaron Tomer

    Vydáno 2012
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  8. 8
    Fucosyltransferase 2 Non-Secretor and Low Secretor Status Predicts Severe Outcomes in Premature Infants

    Fucosyltransferase 2 Non-Secretor and Low Secretor Status Predicts Severe Outcomes in Premature Infants Autor Ardythe L. Morrow, Jareen Meinzen‐Derr, Pengwei Huang, Kurt Schibler, Tanya Cahill, Mehdi Keddache, Suhas G. Kallapur, David S. Newburg, Meredith E. Tabangin, Barbara Warner, Xi Jiang

    Vydáno 2011
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  9. 9
    Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy

    Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy Autor Tracy A. Glauser, Katherine Holland, Valerie P. O’Brien, Mehdi Keddache, Lisa J. Martin, Peggy O. Clark, Avital Cnaan, Dennis Dlugos, Deborah G. Hirtz, Shlomo Shinnar, Gregory A. Grabowski

    Vydáno 2017
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  10. 10
    Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model

    Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model Autor Nupur Dasgupta, Yongping Xu, Ronghua Li, Yanyan Peng, Manoj K. Pandey, Stuart L. Tinch, Benjamin Liou, Venette Inskeep, Wujuan Zhang, Kenneth D.R. Setchell, Mehdi Keddache, Gregory A. Grabowski, Ying Sun

    Vydáno 2015
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  11. 11
    EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children

    EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children Autor Bahram Namjou, Mehdi Keddache, Keith Marsolo, Michael Wagner, Todd Lingren, Beth L. Cobb, Cassandra Perry, Stephanie Kennebeck, Ingrid A. Holm, Rongling Li, Nancy A. Crimmins, Lisa J. Martin, Imre Solti, Isaac S. Kohane, John B. Harley

    Vydáno 2013
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  12. 12
    Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy

    Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy Autor David A. Greenberg, Martina Durner, Mehdi Keddache, Shlomo Shinnar, Stanley R. Resor, Solomon L. Moshé, David Rosenbaum, Jeffrey Cohen, Cynthia L. Harden, Harriet Kang, Sibylle Wallace, D Luciano, Karen Ballaban‐Gil, Livia Tomasini, Guilian Zhou, Irene Klotz, Elisa Dicker

    Vydáno 2000
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  13. 13
    Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program

    Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program Autor Chirayu Goswami, Michael Sheldon, Christian Bixby, Mehdi Keddache, Alexander Bogdanowicz, Yihe Wang, Jonathan Schultz, Jessica McDevitt, James LaPorta, Elaine Kwon, Steven Buyske, Dana Garbolino, Glenys Biloholowski, Alex Pastuszak, Mary Storella, Amit Bhalla, Florence Charlier-Rodriguez, Russ Hager, Robin Grimwood, Shareef Nahas

    Vydáno 2022
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  14. 14
    The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1

    The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1 Autor Susan D. Thompson, Marc Sudman, Paula S. Ramos, Miranda C. Marion, Mary Ryan, Monica Tsoras, Tracey Weiler, Michael Wagner, Mehdi Keddache, Johannes‐Peter Haas, Cornelia Mueller, Sampath Prahalad, John F. Bohnsack, Carol A. Wise, Marilynn Punaro, Dongping Zhang, Carlos D. Rosé, Mary E. Comeau, Jasmin Divers, David N. Glass, Carl D. Langefeld

    Vydáno 2010
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  15. 15
    Genome‐wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13

    Genome‐wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13 Autor Susan D. Thompson, Miranda C. Marion, Marc Sudman, Mary Ryan, Monica Tsoras, Timothy D. Howard, Michael Barnes, Paula S. Ramos, Wendy Thomson, Anne Hinks, Johannes‐Peter Haas, Sampath Prahalad, John F. Bohnsack, Carol A. Wise, Marilynn Punaro, Carlos D. Rosé, Nicholas M. Pajewski, Michael G. Spigarelli, Mehdi Keddache, Michael Wagner, Carl D. Langefeld, David N. Glass

    Vydáno 2012
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    Revisão
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  16. 16
    Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience

    Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience Autor C. Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A. Johnson, Yaping Qian, Abhinav Mathur, Chao Wei, Subba Rao Indugula, Fanggeng Zou, Haiying Meng, Lijun Wang, Xia Li, Rachel S. Fisher, Tony Tan, Amber Begtrup, Kathleen Collins, Katie Wusik, Derek Neilson, Thomas Andrew Burrow, Elizabeth K. Schorry, Robert J. Hopkin, Mehdi Keddache, John B. Harley, Kenneth M. Kaufman, Kejian Zhang

    Vydáno 2015
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  17. 17
    Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium

    Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium Autor Nathan Salomonis, Phillip J. Dexheimer, Larsson Omberg, Robin Schroll, Stacy Bush, Jeffrey S. Huo, Lynn M. Schriml, Shannan Ho Sui, Mehdi Keddache, Christopher N. Mayhew, Shiva Kumar Shanmukhappa, James M. Wells, Kenneth Daily, Shane L. Hubler, Yuliang Wang, Elias T. Zambidis, Jake Lin, Yoshihide Hayashizaki, Antonis K. Hatzopoulos, Punam Malik, José A. Cancelas, Bruce J. Aronow, Carolyn Lutzko

    Vydáno 2016
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  18. 18
    Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives

    Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives Autor Kenneth Daily, Shannan J. Ho Sui, Lynn M. Schriml, Phillip J. Dexheimer, Nathan Salomonis, Robin Schroll, Stacy Bush, Mehdi Keddache, Christopher N. Mayhew, Samad Lotia, Thanneer M. Perumal, Kristen K. Dang, Lorena Pantano, Alexander R. Pico, Elke Grassman, Diana Nordling, Yoshihide Hayashizaki, Antonis K. Hatzopoulos, Punam Malik, José A. Cancelas, Carolyn Lutzko, Bruce J. Aronow, Larsson Omberg

    Vydáno 2017
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  19. 19
    Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis

    Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis Autor Anne Hinks, Joanna Cobb, Miranda C. Marion, Sampath Prahalad, Marc Sudman, John Bowes, Paul Martin, Mary E. Comeau, Satria P. Sajuthi, Robert Andrews, Milton R. Brown, Wei‐Min Chen, Patrick Concannon, Panos Deloukas, Sarah Edkins, Stephen Eyre, Patrick M. Gaffney, Stephen L. Guthery, Joel M. Guthridge, Sarah Hunt, Judith A. James, Mehdi Keddache, Kathy L. Moser, Peter A. Nigrović, Suna Önengüt-Gümüşcü, Mitchell Onslow, Carlos D. Rosé, Stephen S. Rich, Kathryn J. A. Steel, Edward K. Wakeland, Carol A. Wallace, Lucy R. Wedderburn, Patricia Woo, John F. Bohnsack, Johannes‐Peter Haas, David N. Glass, Carl D. Langefeld, Wendy Thomson, Susan D. Thompson

    Vydáno 2013
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