Výsledky vyhledávání - Arun Ramani
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A Pair of RNA-Binding Proteins Controls Networks of Splicing Events Contributing to Specialization of Neural Cell Types Autor Adam Norris, Shangbang Gao, Megan L. Norris, Debashish Ray, Arun Ramani, Andrew Fraser, Quaid Morris, Timothy Hughes, Mei Zhen, John A. Calarco
Vydáno 2014Artigo -
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Tamoxifen therapy in a murine model of myotubular myopathy Autor Nika Maani, Nesrin Sabha, Kamran Rezai, Arun Ramani, Linda Groom, Nadine Eltayeb, Faranak Mavandadnejad, Andrea Pang, Giulia Russo, Michael Brudno, Volker Haucke, Robert T. Dirksen, James J. Dowling
Vydáno 2018Artigo -
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Conserved transcriptional programming across sex and species after peripheral nerve injury predicts treatments for neuropathic pain Autor Shahrzad Ghazisaeidi, Milind M. Muley, YuShan Tu, David P. Finn, Mahshad Kolahdouzan, Graham M. Pitcher, Doyeon Kim, Ameet S. Sengar, Arun Ramani, Michael Brudno, Michael W. Salter
Vydáno 2023Artigo -
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Splicing is an alternate oncogenic pathway activation mechanism in glioma Autor Robert Siddaway, Scott Milos, Arun Kumaran Anguraj Vadivel, Tara Dobson, Jyothishmathi Swaminathan, Scott Ryall, Sanja Pajovic, Palak Patel, Javad Nazarian, Oren J. Becher, Michael Brudno, Arun Ramani, Vidya Gopalakrishnan, Cynthia Hawkins
Vydáno 2022Artigo -
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Control of Long-Term Synaptic Potentiation and Learning by Alternative Splicing of the NMDA Receptor Subunit GluN1 Autor Ameet S. Sengar, Hongbin Li, Wenbo Zhang, Celeste Leung, Arun Ramani, Ner Mu Nar Saw, Yongqian Wang, YuShan Tu, P. Joel Ross, Stephen W. Scherer, James Ellis, Michael Brudno, Zhengping Jia, Michael W. Salter
Vydáno 2019Artigo -
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Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease Autor Hernán Gonorazky, Sergey Naumenko, Arun Ramani, Viswateja Nelakuditi, Pouria Mashouri, Peiqui Wang, Dennis Kao, Krish Ohri, Senthuri Viththiyapaskaran, Mark A. Tarnopolsky, Katherine D. Mathews, Steven A. Moore, Andres Nascimiento Osorio, David Villanova, Dwi U. Kemaladewi, Ronald D. Cohn, Michael Brudno, James J. Dowling
Vydáno 2019Errata/Corrigenda -
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Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease Autor Hernán Gonorazky, Sergey Naumenko, Arun Ramani, Viswateja Nelakuditi, Pouria Mashouri, Peiqui Wang, Dennis Kao, Krish Ohri, Senthuri Viththiyapaskaran, Mark A. Tarnopolsky, Katherine D. Mathews, Steven A. Moore, Andres Nascimiento Osorio, David Villanova, Dwi U. Kemaladewi, Ronald D. Cohn, Michael Brudno, James J. Dowling
Vydáno 2019Artigo -
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Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity Autor Kevin A. Peterson, Sam Khalouei, Nour Hanafi, Joshua A. Wood, Denise G. Lanza, Lauri G. Lintott, Brandon Willis, John R. Seavitt, Robert E. Braun, Mary E. Dickinson, Jacqueline K. White, K. C. Kent Lloyd, Jason D. Heaney, Stephen A. Murray, Arun Ramani, Lauryl M. J. Nutter
Vydáno 2023Artigo -
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Trio RNA sequencing in a cohort of medically complex children Autor Ashish R. Deshwar, Kyoko E. Yuki, Huayun Hou, Yijing Liang, Tayyaba Khan, Alper Celik, Arun Ramani, Roberto Mendoza‐Londono, Christian R. Marshall, Michael Brudno, Adam Shlien, M. Stephen Meyn, Robin Z. Hayeems, Brandon J. McKinlay, Panagiota Klentrou, Michael D. Wilson, Lianna Kyriakopoulou, Gregory Costain, James J. Dowling
Vydáno 2023Artigo -
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Spatial genomic heterogeneity in diffuse intrinsic pontine and midline high-grade glioma: implications for diagnostic biopsy and targeted therapeutics Autor Lindsey M. Hoffman, Mariko DeWire, Scott Ryall, Pawel Buczkowicz, James Leach, Lili Miles, Arun Ramani, Michael Brudno, Shiva Senthil Kumar, Rachid Drissi, Phillip J. Dexheimer, Ralph Salloum, Lionel M.L. Chow, Trent R. Hummel, Charles B. Stevenson, Q. Richard Lu, Blaise V. Jones, David P. Witte, Bruce J. Aronow, Cynthia Hawkins, Maryam Fouladi
Vydáno 2016Artigo -
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Basophil activation test shows high accuracy in the diagnosis of peanut and tree nut allergy: The Markers of Nut Allergy Study Autor Lucy Duan, Alper Çelik, Jennifer A. Hoang, Klara Schmidthaler, Delvin So, Xiaojun Yin, Christina Ditlof, Marta Ponce, Julia Upton, Jean‐Soo Lee, Lisa Hung, Heimo Breiteneder, Chiara Palladino, Adelle Atkinson, Vy H.D. Kim, Alireza Berenjy, Maria Asper, David Hummel, Samantha Wong, Mara Alexanian‐Farr, Ahuva Magder, R. Sharon Chinthrajah, Kaori Mukai, Mindy Tsai, Kari C. Nadeau, Stephen J. Galli, Arun Ramani, Zsolt Szépfalusi, Thomas Eiwegger
Vydáno 2020Artigo -
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Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center Autor Eileen Crowley, Neil Warner, Jie Pan, Sam Khalouei, Abdul Elkadri, Karoline Fiedler, Justin Foong, Andrei L. Turinsky, Dana M. Bronte-Tinkew, Shiqi Zhang, Jamie Hu, David Tian, Dalin Li, Julie Horowitz, Iram Siddiqui, Julia Upton, Chaim M. Roifman, Peter Church, Donna A. Wall, Arun Ramani, Daniel Kotlarz, Christoph Klein, Holm H. Uhlig, Scott B. Snapper, Claudia Gonzaga‐Jauregui, Andrew D. Paterson, Dermot McGovern, Michael Brudno, Thomas D. Walters, Anne M. Griffiths, Aleixo M. Muise
Vydáno 2020Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Computational biology
Medicine
Mutation
RNA
Genome
Alternative splicing
Internal medicine
Bioinformatics
Cancer
Exon
RNA splicing
Caenorhabditis elegans
Cancer research
Exome sequencing
Gene expression
Phenotype
Receptor
Computer science
DNA sequencing
Exome
Genomics
Glioma
Oncology
Transcriptome
Artificial intelligence
Cell biology
Evolutionary biology