Ohcanbohtosat - Steven A. Moore
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What Every Neuropathologist Needs to Know: The Muscle Biopsy Dahkki J. Stephen Nix, Steven A. Moore
Almmustuhtton 2020Revisão -
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Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast Dahkki Jakob S. Satz, Rita Barresi, Madeleine Durbeej, Tobias Willer, Amy Turner, Steven A. Moore, Kevin P. Campbell
Almmustuhtton 2008Artigo -
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LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle Dahkki George Dialynas, Kaitlin M. Flannery, Luka N. Zirbel, Péter L. Nagy, Katherine D. Mathews, Steven A. Moore, Lori L. Wallrath
Almmustuhtton 2011Artigo -
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Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy Dahkki Aaron A. Stence, Jon Thomason, Jonathan A. Pruessner, Ramakrishna Sompallae, Anthony N. Snow, Deqin Ma, Steven A. Moore, Aaron Bossler
Almmustuhtton 2021Artigo -
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Docosahexaenoic acid synthesis from n-3 polyunsaturated fatty acids in differentiated rat brain astrocytes Dahkki Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith A. Preuss, Steven A. Moore, Michael E. Robbins, Arthur A. Spector
Almmustuhtton 2001Artigo -
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Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E Dahkki Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell
Almmustuhtton 2000Artigo -
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Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells Dahkki Ashley Earle, Tyler J. Kirby, Gregory Fedorchak, Philipp Isermann, Jineet Patel, Sushruta Iruvanti, Steven A. Moore, Gisèle Bonne, Lori L. Wallrath, Jan Lammerding
Almmustuhtton 2019Artigo -
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Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy Dahkki 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
Almmustuhtton 2013Artigo -
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Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway Dahkki 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
Almmustuhtton 2015Artigo -
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<i>GMPPB</i>-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation Dahkki 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
Almmustuhtton 2015Artigo -
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Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification Dahkki 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
Almmustuhtton 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 Dahkki 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
Almmustuhtton 2012Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
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