অনুসন্ধান ফলাফলগুলি - Steven A. Moore
- প্রদর্শন 1 - 20 ফলাফল এর 54
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What Every Neuropathologist Needs to Know: The Muscle Biopsy অনুযায়ী J. Stephen Nix, Steven A. Moore
প্রকাশিত 2020Revisão -
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Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast অনুযায়ী Jakob S. Satz, Rita Barresi, Madeleine Durbeej, Tobias Willer, Amy Turner, Steven A. Moore, Kevin P. Campbell
প্রকাশিত 2008Artigo -
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LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle অনুযায়ী George Dialynas, Kaitlin M. Flannery, Luka N. Zirbel, Péter L. Nagy, Katherine D. Mathews, Steven A. Moore, Lori L. Wallrath
প্রকাশিত 2011Artigo -
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Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy অনুযায়ী Aaron A. Stence, Jon Thomason, Jonathan A. Pruessner, Ramakrishna Sompallae, Anthony N. Snow, Deqin Ma, Steven A. Moore, Aaron Bossler
প্রকাশিত 2021Artigo -
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Docosahexaenoic acid synthesis from n-3 polyunsaturated fatty acids in differentiated rat brain astrocytes অনুযায়ী Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith A. Preuss, Steven A. Moore, Michael E. Robbins, Arthur A. Spector
প্রকাশিত 2001Artigo -
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Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E অনুযায়ী Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell
প্রকাশিত 2000Artigo -
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Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells অনুযায়ী Ashley Earle, Tyler J. Kirby, Gregory Fedorchak, Philipp Isermann, Jineet Patel, Sushruta Iruvanti, Steven A. Moore, Gisèle Bonne, Lori L. Wallrath, Jan Lammerding
প্রকাশিত 2019Artigo -
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Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy অনুযায়ী 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
প্রকাশিত 2013Artigo -
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Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway অনুযায়ী 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
প্রকাশিত 2015Artigo -
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<i>GMPPB</i>-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation অনুযায়ী 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
প্রকাশিত 2015Artigo -
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Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification অনুযায়ী 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
প্রকাশিত 2017Revisão -
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Dystroglycan on Radial Glia End Feet Is Required for Pial Basement Membrane Integrity and Columnar Organization of the Developing Cerebral Cortex অনুযায়ী 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
প্রকাশিত 2012Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Biology
Genetics
Gene
Medicine
Muscular dystrophy
Cell biology
Mutation
Pathology
Biochemistry
Dystroglycan
Internal medicine
Laminin
Extracellular matrix
Anatomy
Chemistry
Congenital muscular dystrophy
Endocrinology
Neuroscience
Phenotype
Dystrophin
Myopathy
Biopsy
Immunology
Limb-girdle muscular dystrophy
Muscle biopsy
Skeletal muscle
Central nervous system
Computational biology
Disease
Enzyme