Search Results - Denise Malicki

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  1. 1
    Novel PPP1CB-ALK fusion protein in a high-grade glioma of infancy

    Novel PPP1CB-ALK fusion protein in a high-grade glioma of infancy by Yasmin Aghajan, Michael L. Levy, Denise Malicki, John R. Crawford

    Published 2016
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  2. 2
    Homozygous deletions of methylthioadenosine phosphorylase (MTAP) are more frequent than p16INK4A (CDKN2) homozygous deletions in primary non-small cell lung cancers (NSCLC)

    Homozygous deletions of methylthioadenosine phosphorylase (MTAP) are more frequent than p16INK4A (CDKN2) homozygous deletions in primary non-small cell lung cancers (NSCLC) by Mathias Schmid, Denise Malicki, Tsutomu Nobori, Michael Rosenbach, Katari Campbell, Dennis A. Carson, Carlos J. Carrera

    Published 1998
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  3. 3
    Nivolumab in the Treatment of Recurrent or Refractory Pediatric Brain Tumors: A Single Institutional Experience

    Nivolumab in the Treatment of Recurrent or Refractory Pediatric Brain Tumors: A Single Institutional Experience by Hamza Gorsi, Denise Malicki, Valentin Barsan, Mark Tumblin, Lanipua Yeh‐Nayre, Mehrzad Milburn, Jennifer Elster, John R. Crawford

    Published 2018
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  4. 4
    Evaluation of a Congenital Infantile Fibrosarcoma by Comprehensive Genomic Profiling Reveals an LMNA-NTRK1 Gene Fusion Responsive to Crizotinib

    Evaluation of a Congenital Infantile Fibrosarcoma by Comprehensive Genomic Profiling Reveals an LMNA-NTRK1 Gene Fusion Responsive to Crizotinib by Victor Wong, Dean C. Pavlick, Timothy J. Brennan, Roman Yelensky, John R. Crawford, Jeffrey S. Ross, Vincent A. Miller, Denise Malicki, Philip J. Stephens, Siraj M. Ali, Hyunah Ahn

    Published 2015
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  5. 5
    Clinical characterization of Collagen <scp>XII</scp>‐related disease caused by biallelic <i>COL12A1</i> variants

    Clinical characterization of Collagen <scp>XII</scp>‐related disease caused by biallelic <i>COL12A1</i> variants by Riley M. McCarty, Dimah Saade, Pinki Munot, Chamindra G. Laverty, Hailey Pinz, Yaqun Zou, Meghan McAnally, Pomi Yun, Cuixia Tian, Ying Hu, Lucy Feng, Rahul Phadke, Sophia Ceulemans, Pilar Magoulas, Andrew J. Skalsky, Jennifer Friedman, Stephen R. Braddock, Sarah Neuhaus, Denise Malicki, Matthew N. Bainbridge, Shareef Nahas, David Dimmock, Stephen F. Kingsmore, Timothy Lotze, A. Reghan Foley, Francesco Muntoni, Volker Straub, Sandra Donkervoort, Carsten G. Bönnemann

    Published 2025
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  6. 6
    Recurrent <i>TTN</i> metatranscript‐only c.39974–11T&gt;G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy

    Recurrent <i>TTN</i> metatranscript‐only c.39974–11T&gt;G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy by Samantha J. Bryen, Lisa Ewans, Jason Pinner, Suzanna C. MacLennan, Sandra Donkervoort, Diana Castro, Ana Töpf, Gina O’Grady, Beryl B. Cummings, Katherine R. Chao, Ben Weisburd, Laurent C. Francioli, Fathimath Faiz, Adam Bournazos, Ying Hu, Carla Grosmann, Denise Malicki, Helen Doyle, Nanna Witting, John Vissing, Kristl G. Claeys, Kathryn Urankar, Ana Beleza‐Meireles, Júlia Baptista, Sian Ellard, Marco Savarese, Mridul Johari, Anna Vihola, Bjarne Udd, Anirban Majumdar, Volker Straub, Carsten G. Bönnemann, Daniel G. MacArthur, Mark R. Davis, Sandra T. Cooper

    Published 2019
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  7. 7
    Functional Precision Medicine Identifies New Therapeutic Candidates for Medulloblastoma

    Functional Precision Medicine Identifies New Therapeutic Candidates for Medulloblastoma by Jessica M. Rusert, Edwin F. Juarez, Sebastian Brabetz, James Jensen, Alexandra Garancher, Lianne Q. Chau, Silvia K. Tacheva-Grigorova, Sameerah Wahab, Yoko T. Udaka, Darren Finlay, Huriye Seker‐Cin, Brendan Reardon, Susanne Gröbner, Jonathan Serrano, Jonas Ecker, Lin Qi, Mari Kogiso, Yuchen Du, Patricia Baxter, Jacob J. Henderson, Michael E. Berens, Kristiina Vuori, Till Milde, Yoon-Jae Cho, Xiao‐Nan Li, James M. Olson, Iris Reyes, Matija Snuderl, Terence C. Wong, David Dimmock, Shareef Nahas, Denise Malicki, John R. Crawford, Michael L. Levy, Eliezer M. Van Allen, Stefan M. Pfister, Pablo Tamayo, Marcel Kool, Jill P. Mesirov, Robert J. Wechsler‐Reya

    Published 2020
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  8. 8
    3D genome mapping identifies subgroup-specific chromosome conformations and tumor-dependency genes in ependymoma

    3D genome mapping identifies subgroup-specific chromosome conformations and tumor-dependency genes in ependymoma by Konstantin Okonechnikov, Aylin Camgöz, Owen Chapman, Sameena Wani, Donglim Esther Park, Jens-Martin Hübner, Abhijit Chakraborty, Meghana S. Pagadala, Rosalind Bump, Sahaana Chandran, Katerina Kraft, Rocío Acuña‐Hidalgo, Derek A. Reid, Kristin Sikkink, Monika Mauermann, Edwin F. Juarez, Anne Jenseit, James Robinson, Kristian W. Pajtler, Till Milde, Natalie Jäger, Petra Fiesel, Ling Morgan, Sunita Sridhar, Nicole G. Coufal, Michael L. Levy, Denise Malicki, Charlotte A. Hobbs, Stephen F. Kingsmore, Shareef Nahas, Matija Snuderl, John R. Crawford, Robert J. Wechsler‐Reya, Tom B. Davidson, Jennifer Cotter, George Michaiel, Gudrun Fleischhack, Stefan Mundlos, Anthony D. Schmitt, Hannah Carter, Kulandaimanuvel Antony Michealraj, Sachin Kumar, Michael D. Taylor, Jeremy N. Rich, Frank Buchholz, Jill P. Mesirov, Stefan M. Pfister, Ferhat Ay, Jesse R. Dixon, Marcel Kool, Lukas Chávez

    Published 2023
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  9. 9
    Circular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastoma

    Circular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastoma by Owen Chapman, Jens Luebeck, Sunita Sridhar, Ivy Tsz-Lo Wong, Deobrat Dixit, Shanqing Wang, Gino Prasad, Utkrisht Rajkumar, Meghana S. Pagadala, Jon D. Larson, Britney Jiayu He, King L. Hung, Joshua T. Lange, Siavash R. Dehkordi, Sahaana Chandran, Miriam Adam, Ling Morgan, Sameena Wani, Ashutosh Tiwari, Caitlin Guccione, Yingxi Lin, Aditi Dutta, Yan Yuen Lo, Edwin F. Juarez, James Robinson, Andrey Korshunov, John-Edward A. Michaels, Yoon‐Jae Cho, Denise Malicki, Nicole G. Coufal, Michael L. Levy, Charlotte A. Hobbs, Richard H. Scheuermann, John R. Crawford, Scott L. Pomeroy, Jeremy N. Rich, Xinlian Zhang, Howard Y. Chang, Jesse R. Dixon, Anindya Bagchi, Aniruddha J. Deshpande, Hannah Carter, Ernest Fraenkel, Paul S. Mischel, Robert J. Wechsler‐Reya, Vineet Bafna, Jill P. Mesirov, Lukas Chávez

    Published 2023
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