Alex MacKenzie Children's Hospital of Eastern Ontario Research Institute Biography Publications Institution JoVE Articles Alex MacKenzie has not added a biography. If you are Alex MacKenzie and would like to personalize this page please email our Author Liaison for assistance. Publications Transcriptomic RNAseq Drug Screen in Cerebrocortical Cultures; Towards Novel Neurogenetic Disease Therapies Human Molecular Genetics. Jun, 2018 | Pubmed ID: 29901742 Inhibitor of Apoptosis Proteins, NAIP, CIAP1 and CIAP2 Expression During Macrophage Differentiation and M1/M2 Polarization PloS One. 2018 | Pubmed ID: 29518103 Establishing Core Outcome Sets for Phenylketonuria (PKU) and Medium-chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Children: Study Protocol for Systematic Reviews and Delphi Surveys Trials. Dec, 2017 | Pubmed ID: 29258568 Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency Genetics. Dec, 2017 | Pubmed ID: 29061647 Neuronal Apoptosis Inhibitory Protein (NAIP) Localizes to the Cytokinetic Machinery During Cell Division Scientific Reports. 01, 2017 | Pubmed ID: 28059125 DNM1L-related Mitochondrial Fission Defect Presenting As Refractory Epilepsy European Journal of Human Genetics : EJHG. 07, 2016 | Pubmed ID: 26604000 The Search for Pompe Patients in Canada: Assessing Feasibility of a National Disease Registry to Facilitate Research Journal of Neuromuscular Diseases. 2015 | Pubmed ID: 27858639 Human Growth Hormone Increases SMN Expression and Survival in Severe Spinal Muscular Atrophy Mouse Model Journal of Neuromuscular Diseases. 2014 | Pubmed ID: 27858661 VPAC2 Receptor Agonist BAY 55-9837 Increases SMN Protein Levels and Moderates Disease Phenotype in Severe Spinal Muscular Atrophy Mouse Models Orphanet Journal of Rare Diseases. 2014 | Pubmed ID: 24405637 Specific Combination of Compound Heterozygous Mutations in 17β-hydroxysteroid Dehydrogenase Type 4 (HSD17B4) Defines a New Subtype of D-bifunctional Protein Deficiency Orphanet Journal of Rare Diseases. Nov, 2012 | Pubmed ID: 23181892 A Generalizable Pre-clinical Research Approach for Orphan Disease Therapy Orphanet Journal of Rare Diseases. Jun, 2012 | Pubmed ID: 22704758 Prolactin Increases SMN Expression and Survival in a Mouse Model of Severe Spinal Muscular Atrophy Via the STAT5 Pathway The Journal of Clinical Investigation. Aug, 2011 | Pubmed ID: 21785216 Estrogen Suppresses Uterine Epithelial Apoptosis by Inducing Birc1 Expression Molecular Endocrinology (Baltimore, Md.). Jan, 2008 | Pubmed ID: 17901126 Distinct Expression of Neuronal Apoptosis Inhibitory Protein (NAIP) During Murine Development Neuroreport. Mar, 2002 | Pubmed ID: 11930148 The Neuronal Apoptosis Inhibitory Protein is a Direct Inhibitor of Caspases 3 and 7 The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Mar, 2002 | Pubmed ID: 11896143 CHRIMCY: A Proposed Institute for Research on Reproduction, Development, and Mother, Child and Youth Health Paediatrics & Child Health. Jan, 2000 | Pubmed ID: 20107590 The Hippocampal Neurons of Neuronal Apoptosis Inhibitory Protein 1 (NAIP1)-deleted Mice Display Increased Vulnerability to Kainic Acid-induced Injury Proceedings of the National Academy of Sciences of the United States of America. Feb, 2000 | Pubmed ID: 10681452 Extraction d’ADN de haut débit et le génotypage des larves de poisson zèbre 3dpf de découpage Fin Ceres Kosuta1,2, Kate Daniel1, Devon L. Johnstone1,2, Kevin Mongeon1,2, Kevin Ban1,2, Sophie LeBlanc1, Stuart MacLeod1, Karim Et-Tahiry2, Marc Ekker2, Alex MacKenzie1, Izabella Pena1,2 1Children's Hospital of Eastern Ontario Research Institute, 2Department of Biology, University of Ottawa JoVE 58024 Genetics
Extraction d’ADN de haut débit et le génotypage des larves de poisson zèbre 3dpf de découpage Fin Ceres Kosuta1,2, Kate Daniel1, Devon L. Johnstone1,2, Kevin Mongeon1,2, Kevin Ban1,2, Sophie LeBlanc1, Stuart MacLeod1, Karim Et-Tahiry2, Marc Ekker2, Alex MacKenzie1, Izabella Pena1,2 1Children's Hospital of Eastern Ontario Research Institute, 2Department of Biology, University of Ottawa JoVE 58024 Genetics