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Nature Medicine|January 31, 2006
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathologyJulia Alter, Fang Lou, Adam Rabinowitz, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|August 30, 2022
Pathogenesis and Treatment of Usher Syndrome Type IIAKhine Zaw, Livia S Carvalho, May T Aung-Htut, et al.
Pathology|October 1, 1979
An enzyme-immunoassay for myoglobin in human serum and urine. Method development, normal values and application to acute myocardial infarctionM J Cloonan, G A Bishop, P D Wilton-Smith, et al.
Plos One|May 1, 2013
Improved antisense oligonucleotide design to suppress aberrant SMN2 gene transcript processing: towards a treatment for spinal muscular atrophyChalermchai Mitrpant, Paul Porensky, Haiyan Zhou, et al.
Bio-Protocol|January 10, 2022
A Phenotypic Screen for the Liver Stages of Plasmodium vivaxSteven P Maher, Amélie Vantaux, Caitlin A Cooper, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathyP Tan, J Briner, E Boltshauser, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridizationS D Wilton, L Lim, S D Dorosz, et al.
The Medical Journal of Australia|July 15, 1996
Alzheimer's disease and apolipoprotein E genotype in Western Australia: an autopsy-verified seriesV A Fabian, T M Jones, S D Wilton, et al.
Plos One|September 10, 2013
Revertant fibers in the mdx murine model of Duchenne muscular dystrophy: an age- and muscle-related reappraisalSarah R Pigozzo, Lorena Da Re, Chiara Romualdi, et al.
Ophthalmic Genetics|August 30, 2021
Stargardt disease and progress in therapeutic strategiesDi Huang, Rachael C Heath Jeffery, May Thandar Aung-Htut, et al.
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