Suchergebnisse - 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 von J. Stephen Nix, Steven A. Moore

    Veröffentlicht 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 von Rajan Radhakrishnan, Steven A. Moore, Kathleen A. Sluka

    Veröffentlicht 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 von Daniel Berg, Juan Zhang, Dina M. Lauricella, Steven A. Moore

    Veröffentlicht 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 von Geoffrey D. Girnun, Frederick E. Domann, Steven A. Moore, Mike E. Robbins

    Veröffentlicht 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 von Jason Netland, David K. Meyerholz, Steven A. Moore, Martin D. Cassell, Stanley Perlman

    Veröffentlicht 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 von Steven A. Moore, Eduard C. Hurt, Elizabeth Yoder, Howard Sprecher, Arthur A. Spector

    Veröffentlicht 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 von Jakob S. Satz, Rita Barresi, Madeleine Durbeej, Tobias Willer, Amy Turner, Steven A. Moore, Kevin P. Campbell

    Veröffentlicht 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 von Nicholas K.H. Khoo, Sachin Hebbar, Weiling Zhao, Steven A. Moore, Frederick E. Domann, Mike E. Robbins

    Veröffentlicht 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 von Ronald D. Cohn, Madeleine Durbeej, Steven A. Moore, Ramón Mauricio Coral‐Vázquez, Sally Prouty, Kevin P. Campbell

    Veröffentlicht 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 von Matthew M. Goddeeris, Biming Wu, David Venzke, Takako Yoshida‐Moriguchi, Fumiaki Saito, Kiichiro Matsumura, Steven A. Moore, Kevin P. Campbell

    Veröffentlicht 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 von George Dialynas, Kaitlin M. Flannery, Luka N. Zirbel, Péter L. Nagy, Katherine D. Mathews, Steven A. Moore, Lori L. Wallrath

    Veröffentlicht 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 von Aaron A. Stence, Jon Thomason, Jonathan A. Pruessner, Ramakrishna Sompallae, Anthony N. Snow, Deqin Ma, Steven A. Moore, Aaron Bossler

    Veröffentlicht 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 von Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith A. Preuss, Steven A. Moore, Michael E. Robbins, Arthur A. Spector

    Veröffentlicht 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 von Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell

    Veröffentlicht 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 von Ashley Earle, Tyler J. Kirby, Gregory Fedorchak, Philipp Isermann, Jineet Patel, Sushruta Iruvanti, Steven A. Moore, Gisèle Bonne, Lori L. Wallrath, Jan Lammerding

    Veröffentlicht 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 von 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

    Veröffentlicht 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 von 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

    Veröffentlicht 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 von 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

    Veröffentlicht 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 von 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

    Veröffentlicht 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 von 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

    Veröffentlicht 2012
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