Search Results - "McCallion, Eve"

Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice by Meijboom, Katharina E., Sutton, Emma R., McCallion, Eve, McFall, Emily, Anthony, Daniel, Edwards, Benjamin, Kubinski, Sabrina, Tapken, Ines, Bünermann, Ines, Hazell, Gareth, Ahlskog, Nina, Claus, Peter, Davies, Kay E., Kothary, Rashmi, Wood, Matthew J. A., Bowerman, Melissa

“…Abstract Background Spinal muscular atrophy (SMA) is a childhood neuromuscular disorder caused by depletion of the survival motor neuron (SMN) protein. SMA is…”
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A transcriptomics-based drug repositioning approach to identify drugs with similar activities for the treatment of muscle pathologies in spinal muscular atrophy (SMA) models by Hoolachan, Joseph M, McCallion, Eve, Sutton, Emma R, Çetin, Özge, Pacheco-Torres, Paloma, Dimitriadi, Maria, Sari, Suat, Miller, Gavin J, Okoh, Magnus, Walter, Lisa M, Claus, Peter, Wood, Matthew J A, Tonge, Daniel P, Bowerman, Melissa

“…Abstract Spinal muscular atrophy (SMA) is a genetic neuromuscular disorder caused by the reduction of survival of motor neuron (SMN) protein levels. Although…”
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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis by Hazell, Gareth, McCallion, Eve, Ahlskog, Nina, Sutton, Emma R, Okoh, Magnus, Shaqoura, Emad I. H, Hoolachan, Joseph M, Scaife, Taylor, Iqbal, Sara, Bhomra, Amarjit, Kordala, Anna J, Scamps, Frederique, Raoul, Cedric, Wood, Matthew J. A, Bowerman, Melissa

“…Amyotrophic lateral sclerosis (ALS) is a devastating and incurable neurodegenerative disease. Accumulating evidence strongly suggests that intrinsic muscle…”
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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1G93A amyotrophic lateral sclerosis (ALS) mouse model by Hazell, Gareth, McCallion, Eve, Ahlskog, Nina, Sutton, Emma R, Okoh, Magnus, Shaqoura, Emad I. H, Hoolachan, Joseph M, Scaife, Taylor, Iqbal, Sara, Bhomra, Amarjit, Kordala, Anna J, Scamps, Frederique, Raoul, Cedric, Wood, Matthew J. A, Bowerman, Melissa

“…Abstract Background Amyotrophic lateral sclerosis (ALS) is a devastating and incurable neurodegenerative disease. Accumulating evidence strongly suggests that…”
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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model by Hazell, Gareth, McCallion, Eve, Ahlskog, Nina, Sutton, Emma R, Okoh, Magnus, Shaqoura, Emad I H, Hoolachan, Joseph M, Scaife, Taylor, Iqbal, Sara, Bhomra, Amarjit, Kordala, Anna J, Scamps, Frederique, Raoul, Cedric, Wood, Matthew J A, Bowerman, Melissa

“…Amyotrophic lateral sclerosis (ALS) is a devastating and incurable neurodegenerative disease. Accumulating evidence strongly suggests that intrinsic muscle…”
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Exercise, disease state and sex influence the beneficial effects of Fn14-depletion on survival and muscle pathology in the SOD1 G93A amyotrophic lateral sclerosis (ALS) mouse model by Gareth Hazell, Eve McCallion, Nina Ahlskog, Emma R. Sutton, Magnus Okoh, Emad I. H. Shaqoura, Joseph M. Hoolachan, Taylor Scaife, Sara Iqbal, Amarjit Bhomra, Anna J. Kordala, Frederique Scamps, Cedric Raoul, Matthew J. A. Wood, Melissa Bowerman

“…Abstract Background Amyotrophic lateral sclerosis (ALS) is a devastating and incurable neurodegenerative disease. Accumulating evidence strongly suggests that…”
Get full text