Hakutulokset - Steven A. Moore

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  1. 1
    What Every Neuropathologist Needs to Know: The Muscle Biopsy

    What Every Neuropathologist Needs to Know: The Muscle Biopsy Tekijä J. Stephen Nix, Steven A. Moore

    Julkaistu 2020
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  2. 2
    Unilateral carrageenan injection into muscle or joint induces chronic bilateral hyperalgesia in rats

    Unilateral carrageenan injection into muscle or joint induces chronic bilateral hyperalgesia in rats Tekijä Rajan Radhakrishnan, Steven A. Moore, Kathleen A. Sluka

    Julkaistu 2003
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  3. 3
    IL-10 Is a Central Regulator of Cyclooxygenase-2 Expression and Prostaglandin Production

    IL-10 Is a Central Regulator of Cyclooxygenase-2 Expression and Prostaglandin Production Tekijä Daniel Berg, Juan Zhang, Dina M. Lauricella, Steven A. Moore

    Julkaistu 2001
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  4. 4
    Identification of a Functional Peroxisome Proliferator-Activated Receptor Response Element in the Rat Catalase Promoter

    Identification of a Functional Peroxisome Proliferator-Activated Receptor Response Element in the Rat Catalase Promoter Tekijä Geoffrey D. Girnun, Frederick E. Domann, Steven A. Moore, Mike E. Robbins

    Julkaistu 2002
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  5. 5
    Severe Acute Respiratory Syndrome Coronavirus Infection Causes Neuronal Death in the Absence of Encephalitis in Mice Transgenic for Human ACE2

    Severe Acute Respiratory Syndrome Coronavirus Infection Causes Neuronal Death in the Absence of Encephalitis in Mice Transgenic for Human ACE2 Tekijä Jason Netland, David K. Meyerholz, Steven A. Moore, Martin D. Cassell, Stanley Perlman

    Julkaistu 2008
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  6. 6
    Docosahexaenoic acid synthesis in human skin fibroblasts involves peroxisomal retroconversion of tetracosahexaenoic acid

    Docosahexaenoic acid synthesis in human skin fibroblasts involves peroxisomal retroconversion of tetracosahexaenoic acid Tekijä Steven A. Moore, Eduard C. Hurt, Elizabeth Yoder, Howard Sprecher, Arthur A. Spector

    Julkaistu 1995
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  7. 7
    Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast

    Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast Tekijä Jakob S. Satz, Rita Barresi, Madeleine Durbeej, Tobias Willer, Amy Turner, Steven A. Moore, Kevin P. Campbell

    Julkaistu 2008
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  8. 8
    Differential activation of catalase expression and activity by PPAR agonists: Implications for astrocyte protection in anti-glioma therapy

    Differential activation of catalase expression and activity by PPAR agonists: Implications for astrocyte protection in anti-glioma therapy Tekijä Nicholas K.H. Khoo, Sachin Hebbar, Weiling Zhao, Steven A. Moore, Frederick E. Domann, Mike E. Robbins

    Julkaistu 2013
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  9. 9
    Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex

    Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex Tekijä Ronald D. Cohn, Madeleine Durbeej, Steven A. Moore, Ramón Mauricio Coral‐Vázquez, Sally Prouty, Kevin P. Campbell

    Julkaistu 2001
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  10. 10
    LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

    LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy Tekijä Matthew M. Goddeeris, Biming Wu, David Venzke, Takako Yoshida‐Moriguchi, Fumiaki Saito, Kiichiro Matsumura, Steven A. Moore, Kevin P. Campbell

    Julkaistu 2013
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  11. 11
    LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

    LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle Tekijä George Dialynas, Kaitlin M. Flannery, Luka N. Zirbel, Péter L. Nagy, Katherine D. Mathews, Steven A. Moore, Lori L. Wallrath

    Julkaistu 2011
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  12. 12
    Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy

    Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy Tekijä Aaron A. Stence, Jon Thomason, Jonathan A. Pruessner, Ramakrishna Sompallae, Anthony N. Snow, Deqin Ma, Steven A. Moore, Aaron Bossler

    Julkaistu 2021
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  13. 13
    Docosahexaenoic acid synthesis from n-3 polyunsaturated fatty acids in differentiated rat brain astrocytes

    Docosahexaenoic acid synthesis from n-3 polyunsaturated fatty acids in differentiated rat brain astrocytes Tekijä Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith A. Preuss, Steven A. Moore, Michael E. Robbins, Arthur A. Spector

    Julkaistu 2001
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  14. 14
    Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E

    Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E Tekijä Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell

    Julkaistu 2000
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  15. 15
    Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells

    Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells Tekijä Ashley Earle, Tyler J. Kirby, Gregory Fedorchak, Philipp Isermann, Jineet Patel, Sushruta Iruvanti, Steven A. Moore, Gisèle Bonne, Lori L. Wallrath, Jan Lammerding

    Julkaistu 2019
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  16. 16
    Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy

    Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy Tekijä Amy Yang, Bobby G. Ng, Steven A. Moore, Jeffrey S. Rush, Charles J. Waechter, Kimiyo Raymond, Tobias Willer, Kevin P. Campbell, Hudson H. Freeze, Lakshmi Mehta

    Julkaistu 2013
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  17. 17
    Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway

    Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway Tekijä George Dialynas, Om Kumar Shrestha, Jessica Ponce, Monika Zwerger, Dylan A. Thiemann, Grant H. Young, Steven A. Moore, Liping Yu, Jan Lammerding, Lori L. Wallrath

    Julkaistu 2015
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  18. 18
    <i>GMPPB</i>-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation

    <i>GMPPB</i>-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation Tekijä Braden S. Jensen, Tobias Willer, Dimah Saade, Mary O. Cox, Tahseen Mozaffar, Mena Scavina, Vikki Stefans, Thomas Winder, Kevin P. Campbell, Steven A. Moore, Katherine D. Mathews

    Julkaistu 2015
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  19. 19
    Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification

    Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification Tekijä Kristin Wilson, Crystal Faelan, Janet C. Patterson‐Kane, Daniel G. Rudmann, Steven A. Moore, Diane E. Frank, Jay S. Charleston, Jon Tinsley, Geoffrey D. Young, Anthony J. Milici

    Julkaistu 2017
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  20. 20
    Dystroglycan on Radial Glia End Feet Is Required for Pial Basement Membrane Integrity and Columnar Organization of the Developing Cerebral Cortex

    Dystroglycan on Radial Glia End Feet Is Required for Pial Basement Membrane Integrity and Columnar Organization of the Developing Cerebral Cortex Tekijä Timothy D. Myshrall, Steven A. Moore, Adam P. Ostendorf, Jakob S. Satz, Tom Kowalczyk, Huy Tien Nguyen, Ray A. M. Daza, Charmaine Lau, Kevin P. Campbell, Robert F. Hevner

    Julkaistu 2012
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