Search Results - Peter B. Kang

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  1. 1
    PLIN2 inhibits insulin-induced glucose uptake in myoblasts through the activation of the NLRP3 inflammasome

    PLIN2 inhibits insulin-induced glucose uptake in myoblasts through the activation of the NLRP3 inflammasome by KYUNG-AH CHO, Peter B. Kang

    Published 2015
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  2. 2
    Emery‐Dreifuss muscular dystrophy

    Emery‐Dreifuss muscular dystrophy by Scott Heller, Renata Shih, Raghav Kalra, Peter B. Kang

    Published 2019
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  3. 3
    The Notch signaling pathway in skeletal muscle health and disease

    The Notch signaling pathway in skeletal muscle health and disease by Dorianmarie Vargas‐Franco, Raghav Kalra, Isabelle Draper, Christina A. Pacak, Atsushi Asakura, Peter B. Kang

    Published 2022
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  4. 4
    The human macrophage mannose receptor directs <i>Mycobacterium tuberculosis</i> lipoarabinomannan-mediated phagosome biogenesis

    The human macrophage mannose receptor directs <i>Mycobacterium tuberculosis</i> lipoarabinomannan-mediated phagosome biogenesis by Peter B. Kang, Abul Azad, Jordi B. Torrelles, Thomas M. Kaufman, A.A. Beharka, Eric Tibesar, Lucy E. DesJardin, Larry S. Schlesinger

    Published 2005
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  5. 5
    Surfactant Protein D Increases Fusion of<i>Mycobacterium tuberculosis</i>- Containing Phagosomes with Lysosomes in Human Macrophages

    Surfactant Protein D Increases Fusion of<i>Mycobacterium tuberculosis</i>- Containing Phagosomes with Lysosomes in Human Macrophages by J. Scott Ferguson, Jennifer L. Martin, Abul Azad, Travis R. McCarthy, Peter B. Kang, Dennis R. Voelker, Erika C. Crouch, Larry S. Schlesinger

    Published 2006
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  6. 6
    Regulation of DMD pathology by an ankyrin-encoded miRNA

    Regulation of DMD pathology by an ankyrin-encoded miRNA by Matthew S. Alexander, Juan Carlos Casar, Norio Motohashi, Jennifer A. Myers, Iris Eisenberg, Robert T Gonzalez, Elicia Estrella, Peter B. Kang, Genri Kawahara, Louis M. Kunkel

    Published 2011
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  7. 7
    Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

    Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing by Takako I. Jones, Chi Yan, Peter C. Sapp, Diane McKenna‐Yasek, Peter B. Kang, Colin Quinn, Johnny Salameh, Oliver D. King, Peter L. Jones

    Published 2014
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  8. 8
    Mitochondrial fusion and function in Charcot–Marie–Tooth type 2A patient fibroblasts with mitofusin 2 mutations

    Mitochondrial fusion and function in Charcot–Marie–Tooth type 2A patient fibroblasts with mitofusin 2 mutations by Elizabeth Amiott, Paul C. Lott, Jamie Soto, Peter B. Kang, J. Michael McCaffery, Salvatore DiMauro, E. Dale Abel, Kevin M. Flanigan, Victoria H. Lawson, Janet M. Shaw

    Published 2008
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  9. 9
    Identification of Mycobacterium tuberculosis Clinical Isolates with Altered Phagocytosis by Human Macrophages Due to a Truncated Lipoarabinomannan

    Identification of Mycobacterium tuberculosis Clinical Isolates with Altered Phagocytosis by Human Macrophages Due to a Truncated Lipoarabinomannan by Jordi B. Torrelles, Rose Knaup, Avina Kolareth, Tatiana Slepushkina, Thomas M. Kaufman, Peter B. Kang, Preston J. Hill, Patrick J. Brennan, Delphi Chatterjee, John T. Belisle, James M. Musser, Larry S. Schlesinger

    Published 2008
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  10. 10
    MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation

    MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation by Matthew S. Alexander, Genri Kawahara, Norio Motohashi, Juan Carlos Casar, Iris Eisenberg, Jennifer A. Myers, Molly Gasperini, Elicia Estrella, Alvin T. Kho, Satomi Mitsuhashi, Frederic Shapiro, Peter B. Kang, Louis M. Kunkel

    Published 2013
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  11. 11
    AAV-Mediated<i>TAZ</i>Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome

    AAV-Mediated<i>TAZ</i>Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome by Silveli Suzuki‐Hatano, Madhurima Saha, Skylar A. Rizzo, Rachael L. Witko, Bennett J. Gosiker, Manashwi Ramanathan, Meghan S. Soustek, Michael D. Jones, Peter B. Kang, Barry J. Byrne, W. Todd Cade, Christina A. Pacak

    Published 2018
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  12. 12
    POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations

    POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations by Stefania Di Costanzo, Anuradha Balasubramanian, Heather L. Pond, Anete Rozkalne, Chiara Pantaleoni, S. Saredi, Vandana Gupta, Christine Sunu, Timothy W. Yu, Peter B. Kang, Mustafa A. Salih, Marina Mora, Emanuela Gussoni, Christopher A. Walsh, M. Chiara Manzini

    Published 2014
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  13. 13
    MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms

    MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms by Matthew S. Alexander, Juan Carlos Casar, Norio Motohashi, Natássia M. Vieira, Iris Eisenberg, Jamie L. Marshall, Molly Gasperini, Angela Lek, Jennifer A. Myers, Elicia Estrella, Peter B. Kang, Frederic Shapiro, Fedik Rahimov, Genri Kawahara, Jeffrey J. Widrick, Louis M. Kunkel

    Published 2014
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  14. 14
    Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy

    Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy by Peter B. Kang, Leslie Morrison, Susan T. Iannaccone, Robert J. Graham, Carsten G. Bönnemann, Anne Rutkowski, Joseph E. Hornyak, Ching H. Wang, Kathryn N. North, Maryam Oskoui, Thomas S.D. Getchius, Julie A. Cox, Erin E. Hagen, Gary Gronseth, Robert C. Griggs

    Published 2015
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  15. 15
    Distinctive patterns of microRNA expression in primary muscular disorders

    Distinctive patterns of microRNA expression in primary muscular disorders by Iris Eisenberg, Alal Eran, Ichizo Nishino, Maurizio Moggio, C. Lamperti, Anthony A. Amato, Hart G.W. Lidov, Peter B. Kang, Kathryn N. North, Stella Mitrani‐Rosenbaum, Kevin M. Flanigan, Lori A. Neely, Duncan Whitney, Alan H. Beggs, Isaac S. Kohane, Louis M. Kunkel

    Published 2007
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  16. 16
    A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

    A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 by Sheena Chew, Ravikumar Balasubramanian, Wai‐Man Chan, Peter B. Kang, Caroline Andrews, Bryn D. Webb, Sarah MacKinnon, Darren T. Oystreck, Jessica K. Rankin, Thomas O. Crawford, Michael T. Geraghty, Scott L. Pomeroy, William F. Crowley, Ethylin Wang Jabs, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle

    Published 2013
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  17. 17
    The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States

    The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States by Hemakumar M. Reddy, Kyung‐Ah Cho, Monkol Lek, Elicia Estrella, Elise Valkanas, Michael D. Jones, Satomi Mitsuhashi, Basil T. Darras, Anthony A. Amato, Hart G.W. Lidov, Catherine A. Brownstein, David Margulies, Timothy W. Yu, Mustafa A. Salih, Louis M. Kunkel, Daniel G. MacArthur, Peter B. Kang

    Published 2016
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  18. 18
    Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

    Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores by Steven E. Boyden, Lane J. Mahoney, Genri Kawahara, Jennifer A. Myers, Satomi Mitsuhashi, Elicia Estrella, Anna R. Duncan, Friederike Dey, Elizabeth T. DeChene, Jessica M. Blasko-Goehringer, Carsten G. Bönnemann, Basil T. Darras, Jerry R. Mendell, Hart G.W. Lidov, Ichizo Nishino, Alan H. Beggs, Louis M. Kunkel, Peter B. Kang

    Published 2012
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  19. 19
    Outcome reliability in non‐Ambulatory Boys/Men with duchenne muscular dystrophy

    Outcome reliability in non‐Ambulatory Boys/Men with duchenne muscular dystrophy by Anne M. Connolly, Elizabeth C. Malkus, Jerry R. Mendell, Kevin M. Flanigan, J. Philip Miller, Jeanine Schierbecker, Catherine Siener, Paul T. Golumbek, Craig M. Zaidman, Craig M. McDonald, Linda B. Johnson, Alina Nicorici, Peter Karachunski, John Day, Jason M. Kelecic, Linda Lowes, Lindsay N. Alfano, Basil T. Darras, Peter B. Kang, Janet Quigley, Amy Pasternak, Julaine Florence

    Published 2014
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  20. 20
    Observational study of spinal muscular atrophy type I and implications for clinical trials

    Observational study of spinal muscular atrophy type I and implications for clinical trials by Richard S. Finkel, Michael McDermott, Petra Kaufmann, Basil T. Darras, Wendy K. Chung, Douglas M. Sproule, Peter B. Kang, A. Reghan Foley, Michelle Yang, William B. Martens, Maryam Oskoui, Allan M. Glanzman, Jean Flickinger, Jacqueline Montes, Sally Dunaway Young, Jessica O’Hagen, Janet Quigley, Susan Riley, Maryjane Benton, Patricia Ryan, Megan Montgomery, Jonathan Marra, Clifton L. Gooch, Darryl C. De Vivo

    Published 2014
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