Search Results - "Fallon, Katherine S."

High seroprevalence for SARS-CoV-2 among household members of essential workers detected using a dried blood spot assay by McDade, Thomas W, McNally, Elizabeth M, Zelikovich, Aaron S, D'Aquila, Richard, Mustanski, Brian, Miller, Aaron, Vaught, Lauren A, Reiser, Nina L, Bogdanovic, Elena, Fallon, Katherine S, Demonbreun, Alexis R

“…Serological testing is needed to investigate the extent of transmission of SARS-CoV-2 from front-line essential workers to their household members. However,…”
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A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping by Demonbreun, Alexis R, Wyatt, Eugene J, Fallon, Katherine S, Oosterbaan, Claire C, Page, Patrick G, Hadhazy, Michele, Quattrocelli, Mattia, Barefield, David Y, McNally, Elizabeth M

“…Limb-girdle muscular dystrophy type 2C is caused by autosomal recessive mutations in the γ-sarcoglycan ( ) gene. The most common mutation is a single…”
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A conserved annexin A6–mediated membrane repair mechanism in muscle, heart, and nerve by Demonbreun, Alexis R., Bogdanovic, Elena, Vaught, Lauren A., Reiser, Nina L., Fallon, Katherine S., Long, Ashlee M., Oosterbaan, Claire C., Hadhazy, Michele, Page, Patrick G.T., Joseph, Prem Raj B., Cowen, Gabrielle, Telenson, Alexander M., Khatri, Ammaarah, Sadleir, Katherine R., Vassar, Robert, McNally, Elizabeth M.

“…Membrane instability and disruption underlie myriad acute and chronic disorders. Anxa6 encodes the membrane-associated protein annexin A6 and was identified as…”
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Deletion of Sulfonylurea Receptor 2 in the Adult Myocardium Enhances Cardiac Glucose Uptake and Is Cardioprotective by Aubert, Gregory, MD, PhD, Barefield, David Y., PhD, Demonbreun, Alexis R., PhD, Ramratnam, Mohun, MD, Fallon, Katherine S., BS, Warner, James L., BA, Rossi, Ann E., PhD, Hadhazy, Michele, BS, Makielski, Jonathan C., MD, McNally, Elizabeth M., MD, PhD

“…Visual Abstract…”
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Recombinant annexin A6 promotes membrane repair and protects against muscle injury by Demonbreun, Alexis R, Fallon, Katherine S, Oosterbaan, Claire C, Bogdanovic, Elena, Warner, James L, Sell, Jordan J, Page, Patrick G, Quattrocelli, Mattia, Barefield, David Y, McNally, Elizabeth M

“…Membrane repair is essential to cell survival. In skeletal muscle, injury often associates with plasma membrane disruption. Additionally, muscular dystrophy is…”
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Anti-latent TGFβ binding protein 4 antibody improves muscle function and reduces muscle fibrosis in muscular dystrophy by Demonbreun, Alexis R, Fallon, Katherine S, Oosterbaan, Claire C, Vaught, Lauren A, Reiser, Nina L, Bogdanovic, Elena, Velez, Matthew P, Salamone, Isabella M, Page, Patrick G T, Hadhazy, Michele, Quattrocelli, Mattia, Barefield, David Y, Wood, Lauren D, Gonzalez, J Patrick, Morris, Carl, McNally, Elizabeth M

“…Duchenne muscular dystrophy, like other muscular dystrophies, is a progressive disorder hallmarked by muscle degeneration, inflammation, and fibrosis. Latent…”
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Dusp6 is a genetic modifier of growth through enhanced ERK activity by Vo, Andy H, Swaggart, Kayleigh A, Woo, Anna, Gao, Quan Q, Demonbreun, Alexis R, Fallon, Katherine S, Quattrocelli, Mattia, Hadhazy, Michele, Page, Patrick G T, Chen, Zugen, Eskin, Ascia, Squire, Kevin, Nelson, Stanley F, McNally, Elizabeth M

“…Abstract Like other single-gene disorders, muscular dystrophy displays a range of phenotypic heterogeneity even with the same primary mutation. Identifying…”
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