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Proceedings of the National Academy of Sciences of the United States of America|September 28, 2011
Sir-two-homolog 2 (Sirt2) modulates peripheral myelination through polarity protein Par-3/atypical protein kinase C (aPKC) signalingBogdan Beirowski, Jason Gustin, Sean M Armour, et al.
Scientific Reports|April 19, 2024
Deep learning prediction of renal anomalies for prenatal ultrasound diagnosisOlivier X Miguel, Emily Kaczmarek, Inok Lee, et al.
Molecular Therapy. Nucleic Acids|April 10, 2025
Inhibition of IFNAR-JAK signaling enhances tolerability and transgene expression of systemic non-viral DNA deliverySujata Senapati, Thais B Bertolini, Michael A Minnier, et al.
The EMBO Journal|June 22, 2007
SIRT1 deacetylase protects against neurodegeneration in models for Alzheimer's disease and amyotrophic lateral sclerosisDohoon Kim, Minh Dang Nguyen, Matthew M Dobbin, et al.
Journal of Medical Genetics|March 3, 2018
Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in CanadaChristine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, et al.
The Journal of Biological Chemistry|April 7, 2011
Negative regulation of STAT3 protein-mediated cellular respiration by SIRT1 proteinMichel Bernier, Rajib K Paul, Alejandro Martin-Montalvo, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD)Christine M Armour, Dennis E Bulman, Olga Jarinova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2024
The Clinician-reported Genetic Testing Utility Index (C-GUIDE) for Prenatal Care: Initial evidence of content and construct validityRobin Z Hayeems, Stephanie Luca, Bowen Xiao, et al.
Molecular Therapy. Methods & Clinical Development|January 3, 2022
Preclinical assessment of an optimized AAV-FVIII vector in mice and non-human primates for the treatment of hemophilia ALiron Elkouby, Sean M Armour, Raffaella Toso, et al.
Journal of Medical Genetics|September 18, 2015
Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delayHussein Daoud, Dong Zhang, Fiona McMurray, et al.
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