Kết quả tìm kiếm - Waibhav Tembe
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Comparison of Analysis Tools for miRNA High Throughput Sequencing Using Nerve Crush as a Model Bằng Raghu Metpally, Sara Nasser, Ivana Malenica, Amanda Courtright, Elizabeth Carlson, Layla T. Ghaffari, Stephen Villa, Waibhav Tembe, Kendall Van Keuren‐Jensen
Được phát hành 2013Artigo -
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Identification of extracellular miRNA in human cerebrospinal fluid by next-generation sequencing Bằng Kasandra Burgos, Ashkan Javaherian, Roberto Bomprezzi, Layla T. Ghaffari, Susan N. Rhodes, Amanda Courtright, Waibhav Tembe, Seungchan Kim, Raghu Metpally, Kendall Van Keuren‐Jensen
Được phát hành 2013Artigo -
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Pathway Implications of Aberrant Global Methylation in Adrenocortical Cancer Bằng Legendre, Christophe R., Demeure, Michael J., Whitsett, Timothy G., Gooden, Gerald C., Bussey, Kimberly J., Jung, Sungwon, Waibhav, Tembe, Kim, Seungchan, Salhia, Bodour
Được phát hành 2016Text -
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Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays Bằng Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V. Pearson, Dietrich A. Stephan, Stanley F. Nelson, David W. Craig
Được phát hành 2008Artigo -
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Profiles of Extracellular miRNA in Cerebrospinal Fluid and Serum from Patients with Alzheimer's and Parkinson's Diseases Correlate with Disease Status and Features of Pathology Bằng Kasandra Burgos, Ivana Malenica, Raghu Metpally, Amanda Courtright, Benjamin Rakela, Thomas G. Beach, Holly A. Shill, Charles H. Adler, Marwan N. Sabbagh, Stephen Villa, Waibhav Tembe, David W. Craig, Kendall Van Keuren‐Jensen
Được phát hành 2014Artigo -
8
Comparative RNA-Seq and Microarray Analysis of Gene Expression Changes in B-Cell Lymphomas of Canis familiaris Bằng Marie R. Mooney, Jeffrey P. Bond, Noel R. Monks, Emily Eugster, David Cherba, Pamela J. Berlinski, Steve Kamerling, Keith R. Marotti, Heather Simpson, Tony Rusk, Waibhav Tembe, Christophe Legendre, Hollie Benson, Winnie S. Liang, Craig P. Webb
Được phát hành 2013Artigo -
9
Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides Bằng Jan B. Egan, Chang-Xin Shi, Waibhav Tembe, Alexis Christoforides, Ahmet Kurdoglu, Shripad Sinari, Sumit Middha, Yan W. Asmann, Jessica Schmidt, Esteban Braggio, Jonathan J. Keats, Rafaël Fonseca, P. Leif Bergsagel, David W. Craig, John D. Carpten, A. Keith Stewart
Được phát hành 2012Artigo -
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Personalized treatment of Sézary syndrome by targeting a novel <i><scp>CTLA</scp>4</i>:<i><scp>CD</scp>28</i> fusion Bằng Aleksandar Sekulić, Winnie S. Liang, Waibhav Tembe, Tyler Izatt, Semyon Kruglyak, Jeffrey Kiefer, Lori Cuyugan, Victoria Zismann, Christophe Legendre, Mark R. Pittelkow, John J. Gohmann, Fernando R. De Castro, Jeffrey M. Trent, John D. Carpten, David W. Craig, Timothy K. McDaniel
Được phát hành 2014Artigo -
11
Next-Generation Sequencing of<i>Coccidioides immitis</i>Isolated during Cluster Investigation Bằng David M. Engelthaler, Tom Chiller, James Schupp, Joshua Colvin, Stephen M. Beckstrom‐Sternberg, Elizabeth M. Driebe, Tracy Moses, Waibhav Tembe, Shripad Sinari, James S. Beckstrom‐Sternberg, Alexis Christoforides, John V. Pearson, John D. Carpten, Paul Keim, Ashley Peterson, Dawn Terashita, S. Arunmozhi Balajee
Được phát hành 2011Artigo -
12
Loss of the tumor suppressor SMARCA4 in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) Bằng Pilar Ramos, Anthony N. Karnezis, William P.D. Hendricks, Yemin Wang, Waibhav Tembe, Victoria Zismann, Christophe Legendre, Winnie S. Liang, Megan Russell, David W. Craig, John Farley, Bradley J. Monk, Stephen P. Anthony, Aleksandar Sekulić, Heather E. Cunliffe, David G. Huntsman, Jeffrey M. Trent
Được phát hành 2014Artigo -
13
Deep Clonal Profiling of Formalin Fixed Paraffin Embedded Clinical Samples Bằng Tara Holley, Elizabeth Lenkiewicz, Lisa Evers, Waibhav Tembe, Christian Ruiz, Joël Gsponer, Cyrill A. Rentsch, Lukas Bubendorf, Mark Stapleton, Doug Amorese, Christophe Legendre, Heather E. Cunliffe, Ann E. McCullough, Barbara A. Pockaj, David W. Craig, John D. Carpten, Daniel D. Von Hoff, Christine A. Iacobuzio‐Donahue, Michael T. Barrett
Được phát hành 2012Artigo -
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Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies Bằng John V. Pearson, Matthew J. Huentelman, Rebecca F. Halperin, Waibhav Tembe, Stacey Melquist, Nils Homer, Marcel Brun, Szabolcs Szelinger, Keith D. Coon, Victoria Zismann, Jennifer Webster, Thomas G. Beach, Sigrid Botne Sando, Jan Aasly, Reinhard Heun, Frank Jessen, Heike Kölsch, Magda Tsolaki, Makrina Daniilidou, Eric M. Reiman, Andreas Papassotiropoulos, Michael Hutton, Dietrich A. Stephan, David W. Craig
Được phát hành 2006Artigo -
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Integrated Genomic and Epigenomic Analysis of Breast Cancer Brain Metastasis Bằng Bodour Salhia, Jeffrey Kiefer, Julianna T.D. Ross, Raghu Metapally, Rae Anne Martinez, Kyle N. Johnson, Danielle M. DiPerna, Kimberly Paquette, Sungwon Jung, Sara Nasser, Garrick Wallstrom, Waibhav Tembe, Angela Baker, John D. Carpten, Jim Resau, Timothy C. Ryken, Zita A. Sibenaller, Emanuel F. Petricoin, Lance A. Liotta, Ramesh K. Ramanathan, Michael E. Berens, Nhan L. Tran
Được phát hành 2014Artigo -
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Toward precision medicine in glioblastoma: the promise and the challenges Bằng Michael D. Prados, Sara A. Byron, Nhan L. Tran, Joanna J. Phillips, Annette M. Molinaro, Keith L. Ligon, Patrick Y. Wen, John G. Kuhn, Ingo K. Mellinghoff, John de Groot, Howard Colman, Timothy F. Cloughesy, Susan M. Chang, Timothy C. Ryken, Waibhav Tembe, Jeffrey Kiefer, Michael E. Berens, David W. Craig, John D. Carpten, Jeffrey M. Trent
Được phát hành 2015Revisão -
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A somatic reference standard for cancer genome sequencing Bằng David W. Craig, Sara Nasser, Richard Corbett, Simon K. Chan, Lisa Murray, Christophe Legendre, Waibhav Tembe, Jonathan Adkins, Nancy Kim, Shukmei Wong, Angela Baker, Daniel Enríquez, Stephanie J. K. Pond, Erin Pleasance, Andrew J. Mungall, Richard A. Moore, Timothy K. McDaniel, Yussanne Ma, Steven J.M. Jones, Marco A. Marra, John D. Carpten, Winnie S. Liang
Được phát hành 2016Artigo -
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Germline Mutations in<i>HOXB13</i>and Prostate-Cancer Risk Bằng Charles M. Ewing, Anna M. Ray, Ethan M. Lange, Kimberly A. Zuhlke, Christiane M. Robbins, Waibhav Tembe, Kathleen E. Wiley, Sarah D. Isaacs, Dorhyun Johng, Yunfei Wang, Chris Bizon, Guifang Yan, Marta Gielzak, Alan W. Partin, Vijayalakshmi Shanmugam, Tyler Izatt, Shripad Sinari, David W. Craig, S. Lilly Zheng, Patrick C. Walsh, James E. Montie, Jianfeng Xu, John D. Carpten, William B. Isaacs, Kathleen A. Cooney
Được phát hành 2012Artigo -
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Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing Bằng Winnie S. Liang, David W. Craig, John D. Carpten, Mitesh J. Borad, Michael J. Demeure, Glen J. Weiss, Tyler Izatt, Shripad Sinari, Alexis Christoforides, Jessica Aldrich, Ahmet Kurdoglu, Michael T. Barrett, L Taylor Phillips, Hollie Benson, Waibhav Tembe, Esteban Braggio, Jeffrey Kiefer, Christophe Legendre, Richard G. Posner, Galen Hostetter, Angela Baker, Jan B. Egan, Haiyong Han, Douglas F. Lake, Edward C. Stites, Ramesh K. Ramanathan, Rafaël Fonseca, A. Keith Stewart, Daniel D. Von Hoff
Được phát hành 2012Artigo -
20
GRM7 variants confer susceptibility to age-related hearing impairment Bằng Rick A. Friedman, Lut Van Laer, Matthew J. Huentelman, Sonal S. Sheth, Els Van Eyken, Jason J. Corneveaux, Waibhav Tembe, Rebecca F. Halperin, Ashley Q. Thorburn, Sofie Thys, Sarah Bonneux, Erik Fransén, Jeroen R. Huyghe, Ilmari Pyykkö, Cor W. R. J. Cremers, Hannie Kremer, Ingeborg Dhooge, Dafydd Stephens, Eva Orzan, Markus Pfister, Michael Bille, Agnete Parving, Martti Sorri, Paul Van de Heyning, Linna Makmura, Jeffrey D. Ohmen, F. H. Linthicum, José N. Fayad, John V. Pearson, David W. Craig, Dietrich Stephan, Guy Van Camp
Được phát hành 2008Artigo
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Các môn học liên quan
Biology
Gene
Genetics
Computational biology
Genome
Cancer
Medicine
Cancer research
DNA sequencing
Gene expression
Genotype
Bioinformatics
Genotyping
Immunology
Internal medicine
Mutation
Single-nucleotide polymorphism
Whole genome sequencing
DNA microarray
Deep sequencing
Pathology
RNA
microRNA
Computer science
DNA
DNA methylation
Epigenetics
Genome-wide association study
Germline mutation
Lymphoma