Vamorolone improves Becker muscular dystrophy and increases dystrophin protein in bmx model mice

por McCormack, Nikki M., Nguyen, Nhu Y., Tully, Christopher B., Oliver, Trinitee, Fiorillo, Alyson A., Heier, Christopher R.
Publicado 2023

Deletion of miR-146a enhances therapeutic protein restoration in model of dystrophin exon skipping

por McCormack, Nikki M., Calabrese, Kelsey A., Sun, Christina M., Tully, Christopher B., Heier, Christopher R., Fiorillo, Alyson A.
Publicado 2023

Survival motor neuron deficiency slows myoblast fusion through reduced myomaker and myomixer expression

por McCormack, Nikki M., Villalón, Eric, Viollet, Coralie, Soltis, Anthony R., Dalgard, Clifton L., Lorson, Christian L., Burnett, Barrington G.
Publicado 2021

The X‐linked Becker muscular dystrophy (bmx) mouse models Becker muscular dystrophy via deletion of murine dystrophin exons 45–47

por Heier, Christopher R., McCormack, Nikki M., Tully, Christopher B., Novak, James S., Newell‐Stamper, Breanne L., Russell, Alan J., Fiorillo, Alyson A.
Publicado 2023

The role of the immunoproteasome in interferon-γ-mediated microglial activation

por Moritz, Kasey E., McCormack, Nikki M., Abera, Mahlet B., Viollet, Coralie, Yauger, Young J., Sukumar, Gauthaman, Dalgard, Clifton L., Burnett, Barrington G.
Publicado 2017

A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein

por McCormack, Nikki M., Abera, Mahlet B., Arnold, Eveline S., Gibbs, Rebecca M., Martin, Scott E., Buehler, Eugen, Chen, Yu-Chi, Chen, Lu, Fischbeck, Kenneth H., Burnett, Barrington G.
Publicado 2021

SMN-deficiency disrupts SERCA2 expression and intracellular Ca(2+) signaling in cardiomyocytes from SMA mice and patient-derived iPSCs

por Khayrullina, Guzal, Moritz, Kasey E., Schooley, James F., Fatima, Naheed, Viollet, Coralie, McCormack, Nikki M., Smyth, Jeremy T., Doughty, Martin L., Dalgard, Clifton L., Flagg, Thomas P., Burnett, Barrington G.
Publicado 2020