Výsledky vyhledávání - Joshua D. Smith
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High Rates of<i>Rickettsia parkeri</i>Infection in Gulf Coast Ticks (<i>Amblyomma maculatum</i>) and Identification of “<i>Candidatus</i>Rickettsia Andeanae” from Fairfax County, V... Autor Christen Fornadel, Xing Zhang, Joshua D. Smith, Christopher D. Paddock, Jorge R. Arias, Douglas E. Norris
Vydáno 2011Artigo -
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Soluble Transforming Growth Factor-β Type II Receptor Inhibits Negative Remodeling, Fibroblast Transdifferentiation, and Intimal Lesion Formation But Not Endothelial Growth Autor Joshua D. Smith, Shane R. Bryant, Leslie L. Couper, Calvin Vary, Philip J. Gotwals, Victor Koteliansky, Volkhard Lindner
Vydáno 1999Artigo -
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A Multivariate Genome-Wide Association Analysis of 10 LDL Subfractions, and Their Response to Statin Treatment, in 1868 Caucasians Autor Heejung Shim, Daniel I. Chasman, Joshua D. Smith, Samia Mora, Paul M. Ridker, Deborah A. Nickerson, Ronald M. Krauss, Matthew Stephens
Vydáno 2015Artigo -
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Genetic Variation Is Associated With C-Reactive Protein Levels in the Third National Health and Nutrition Examination Survey Autor Dana C. Crawford, Christopher Sanders, Xiaoting Qin, Joshua D. Smith, Cynthia Shephard, Michelle Wong, Laura Witrak, Mark J. Rieder, Deborah A. Nickerson
Vydáno 2006Artigo -
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Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations Autor Dana C. Crawford, Christopher S. Carlson, Mark J. Rieder, Dana P. Carrington, Yi Qian, Joshua D. Smith, Michael A. Eberle, Leonid Kruglyak, Deborah A. Nickerson
Vydáno 2004Artigo -
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Tracing Sub-Structure in the European American Population with PCA-Informative Markers Autor Peristera Paschou, Petros Drineas, Jamey Lewis, Caroline M. Nievergelt, Deborah A. Nickerson, Joshua D. Smith, Paul M. Ridker, Daniel I. Chasman, Ronald M. Krauss, Elad Ziv
Vydáno 2008Artigo -
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Combined Influence of <i>LDLR</i> and <i>HMGCR</i> Sequence Variation on Lipid-Lowering Response to Simvastatin Autor Lara M. Mangravite, Marisa W. Medina, Jinrui Cui, Sheila Pressman, Joshua D. Smith, Mark J. Rieder, Xiuqing Guo, Deborah A. Nickerson, Jerome I. Rotter, Ronald M. Krauss
Vydáno 2010Artigo -
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Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis Autor Tassos Grammatikopoulos, Melissa Sambrotta, Sandra Strautnieks, Pierre Foskett, A. S. Knisely, Bart Wagner, Maesha Deheragoda, Chris Starling, Giorgina Mieli‐Vergani, Joshua D. Smith, Laura N. Bull, Richard J. Thompson
Vydáno 2016Artigo -
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Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis Autor Joshua D. Smith, Anne Hing, Christine M. Clarke, Nathan M. Johnson, Francisco A. Perez, Sarah S. Park, Jeremy A. Horst, Brig Mecham, Lisa Maves, Deborah A. Nickerson, Michael L. Cunningham
Vydáno 2014Artigo -
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A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease Autor Heather C Mefford, Gregory M. Cooper, Troy Zerr, Joshua D. Smith, Carl Baker, Neil Shafer, Erik C. Thorland, Cindy Skinner, Charles E. Schwartz, Deborah A. Nickerson, Evan E. Eichler
Vydáno 2009Artigo -
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A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex Autor Marie‐Estelle Losfeld, Bobby G. Ng, Martin Kircher, Kati J. Buckingham, Emily H. Turner, Alexey M. Eroshkin, Joshua D. Smith, Jay Shendure, D. A. Nickerson, Michael J. Bamshad, Hudson H. Freeze
Vydáno 2013Artigo -
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De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism Autor Ash Zawerton, Baojin Yao, J. Paige Yeager, Tommaso Pippucci, Abdul Haseeb, Joshua D. Smith, Lisa Wischmann, Susanne J. Kühl, John Dean, Daniela T. Pilz, Susan Holder, Alisdair McNeill, Claudio Graziano, Véronique Lefebvre
Vydáno 2019Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Mutation
Genotype
Internal medicine
Single-nucleotide polymorphism
Exome sequencing
Computational biology
Endocrinology
Exome
Phenotype
Population
Bioinformatics
Genetic association
Genome-wide association study
Missense mutation
Biochemistry
Genome
Allele
Environmental health
Pathology
Autism
Cholesterol
Computer science
Demography
Evolutionary biology
Haplotype
Psychiatry