Urine mRNA to identify a novel pseudoexon causing dystrophinopathy

by Layal Antoury, Ningyan Hu, Basil Darras, Thurman M. Wheeler
Published 2019-06-01

Progressive myopathy in an inducible mouse model of oculopharyngeal muscular dystrophy

by Ami Mankodi, Thurman M. Wheeler, Reena Shetty, Kelly M. Salceies, Mark W. Becher, Charles A. Thornton
Published 2012-01-01

Antisense oligonucleotide and adjuvant exercise therapy reverse fatigue in old mice with myotonic dystrophy

by Ningyan Hu, Eunjoo Kim, Layal Antoury, Jia Li, Paloma González-Pérez, Seward B. Rutkove, Thurman M. Wheeler
Published 2021-03-01

Analysis of extracellular mRNA in human urine reveals splice variant biomarkers of muscular dystrophies

by Layal Antoury, Ningyan Hu, Leonora Balaj, Sudeshna Das, Sofia Georghiou, Basil Darras, Tim Clark, Xandra O. Breakefield, Thurman M. Wheeler
Published 2018-09-01

Non-invasive monitoring of alternative splicing outcomes to identify candidate therapies for myotonic dystrophy type 1

by Ningyan Hu, Layal Antoury, Timothy M. Baran, Soumya Mitra, C. Frank Bennett, Frank Rigo, Thomas H. Foster, Thurman M. Wheeler
Published 2018-12-01

Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice

by Dominic Jauvin, Jessina Chrétien, Sanjay K. Pandey, Laurie Martineau, Lucille Revillod, Guillaume Bassez, Aline Lachon, A. Robert McLeod, Geneviève Gourdon, Thurman M. Wheeler, Charles A. Thornton, C. Frank Bennett, Jack Puymirat
Published 2017-06-01