Ngā hua rapu - 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 mā J. Stephen Nix, Steven A. Moore

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā Rajan Radhakrishnan, Steven A. Moore, Kathleen A. Sluka

    I whakaputaina 2003
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Daniel Berg, Juan Zhang, Dina M. Lauricella, Steven A. Moore

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Geoffrey D. Girnun, Frederick E. Domann, Steven A. Moore, Mike E. Robbins

    I whakaputaina 2002
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Jason Netland, David K. Meyerholz, Steven A. Moore, Martin D. Cassell, Stanley Perlman

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Steven A. Moore, Eduard C. Hurt, Elizabeth Yoder, Howard Sprecher, Arthur A. Spector

    I whakaputaina 1995
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Jakob S. Satz, Rita Barresi, Madeleine Durbeej, Tobias Willer, Amy Turner, Steven A. Moore, Kevin P. Campbell

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Nicholas K.H. Khoo, Sachin Hebbar, Weiling Zhao, Steven A. Moore, Frederick E. Domann, Mike E. Robbins

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Ronald D. Cohn, Madeleine Durbeej, Steven A. Moore, Ramón Mauricio Coral‐Vázquez, Sally Prouty, Kevin P. Campbell

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Matthew M. Goddeeris, Biming Wu, David Venzke, Takako Yoshida‐Moriguchi, Fumiaki Saito, Kiichiro Matsumura, Steven A. Moore, Kevin P. Campbell

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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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 mā George Dialynas, Kaitlin M. Flannery, Luka N. Zirbel, Péter L. Nagy, Katherine D. Mathews, Steven A. Moore, Lori L. Wallrath

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Aaron A. Stence, Jon Thomason, Jonathan A. Pruessner, Ramakrishna Sompallae, Anthony N. Snow, Deqin Ma, Steven A. Moore, Aaron Bossler

    I whakaputaina 2021
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith A. Preuss, Steven A. Moore, Michael E. Robbins, Arthur A. Spector

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell

    I whakaputaina 2000
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Ashley Earle, Tyler J. Kirby, Gregory Fedorchak, Philipp Isermann, Jineet Patel, Sushruta Iruvanti, Steven A. Moore, Gisèle Bonne, Lori L. Wallrath, Jan Lammerding

    I whakaputaina 2019
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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 mā 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

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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