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Stem Cell Research|July 2, 2021
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 geneDi Huang, Dan Zhang, Shang-Chih Chen, et al.Current Oncology (Toronto, Ont.)|December 21, 2011
Survivorship services for adult cancer populations: a pan-Canadian guideline, D Howell, T F Hack, et al.Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 1, 2000
Preoperative mobilization of circulating dendritic cells by Flt3 ligand administration to patients with metastatic colon cancerM A Morse, S Nair, M Fernandez-Casal, et al.Environmental Science & Technology|June 24, 2009
Environmental health impacts of equine estrogens derived from hormone replacement therapyCharles R Tyler, Amy L Filby, Lisa K Bickley, et al.Frontiers in Genetics|April 25, 2022
Single Stranded Fully Modified-Phosphorothioate Oligonucleotides can Induce Structured Nuclear Inclusions, Alter Nuclear Protein Localization and Disturb the Transcriptome In VitroLoren L Flynn, Ruohan Li, Ianthe L Pitout, et al.Cancer Research|July 28, 2012
MicroRNAs regulate tumor angiogenesis modulated by endothelial progenitor cellsPrue N Plummer, Ruth Freeman, Ryan J Taft, et al.Ophthalmic Genetics|September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathyDanial Roshandel, Jennifer A Thompson, Jason Charng, et al.Stem Cell Research|December 28, 2020
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A geneKhine Zaw, Elaine Y M Wong, Xiao Zhang, et al.Molecular Genetics & Genomic Medicine|July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defectDi Huang, Jennifer A Thompson, Jason Charng, et al.Pageof 24