Thornton, Charles A.

A Muscleblind Knockout Model for Myotonic Dystrophy

Kanadia, R. N., Johnstone, K. A., Mankodi, A., Lungu, C., Thornton, C. A., Esson, D., Timmers, A. M., Hauswirth, W. W., & Swanson, M. S. (2003) · Science

Genetic Neurodegenerative DiseasesRNA Research and Splicing

Cited by 743

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

Lin, X., Miller, J. W., Mankodi, A., Kanadia, R. N., Yuan, Y., Moxley, R. T., Swanson, M. S., & Thornton, C. A. (2006) · Human Molecular Genetics

RNA Research and SplicingGenetic Neurodegenerative Diseases

Cited by 510

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

Du, H., Cline, M. S., Osborne, R. J., Tuttle, D. L., Clark, T. A., Donohue, J. P., Hall, M. P., Shiue, L., Swanson, M. S., Thornton, C. A., et al. (2010) · Nature Structural & Molecular Biology

Genetic Neurodegenerative DiseasesRNA Research and Splicing

Cited by 332

Loss of MBNL Leads to Disruption of Developmentally Regulated Alternative Polyadenylation in RNA-Mediated Disease

Batra, R., Charizanis, K., Manchanda, M., Mohan, A., Li, M., Finn, D. J., Goodwin, M., Zhang, C., Sobczak, K., Thornton, C. A., et al. (2014) · Molecular Cell

RNA Research and SplicingGenetic Neurodegenerative Diseases

Cited by 292

Sex-Related Differences in Gene Expression in Human Skeletal Muscle

Welle, S., Tawil, R., & Thornton, C. A. (2008) · PLoS ONE

Muscle Physiology and DisordersGenetics and Physical Performance

Cited by 224

Skeletal muscle gene expression profiles in 20–29 year old and 65–71 year old women

Welle, S., Brooks, A. I., Delehanty, J. M., Needler, N., Bhatt, K., Shah, B., & Thornton, C. A. (2004) · Experimental Gerontology

Muscle Physiology and DisordersNutrition and Health in Aging

Cited by 210

Reduced amount of mitochondrial DNA in aged human muscle

Welle, S., Bhatt, K., Shah, B., Needler, N., Delehanty, J. M., & Thornton, C. A. (2003) · Journal of Applied Physiology

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 86

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2

Hilbert, J. E., Barohn, R. J., Clemens, P. R., Luebbe, E. A., Martens, W. B., McDermott, M. P., Parkhill, A. L., Tawil, R., Thornton, C. A., Moxley, R. T., et al. (2017) · Neurology

Genetic Neurodegenerative DiseasesGastrointestinal motility and disorders

Cited by 70