Recherche
Enseignement
S'identifier
FR
EN - English
CN - 中文
DE - Deutsch
ES - Español
KR - 한국어
IT - Italiano
FR - Français
PT - Português
TR - Turkish
JA - Japanese
Alex MacKenzie has not added Biography.
If you are Alex MacKenzie and would like to personalize this page please email our Author Liaison for assistance.
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
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
Distinct expression of neuronal apoptosis inhibitory protein (NAIP) during murine development.
Neuroreport Mar, 2002 | Pubmed ID: 11930148
Estrogen suppresses uterine epithelial apoptosis by inducing birc1 expression.
Molecular endocrinology (Baltimore, Md.) Jan, 2008 | Pubmed ID: 17901126
CHRIMCY: A proposed institute for research on reproduction, development, and mother, child and youth health.
Paediatrics & child health Jan, 2000 | Pubmed ID: 20107590
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
A generalizable pre-clinical research approach for orphan disease therapy.
Orphanet journal of rare diseases Jun, 2012 | Pubmed ID: 22704758
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
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
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
Neuronal apoptosis inhibitory protein (NAIP) localizes to the cytokinetic machinery during cell division.
Scientific reports 01, 2017 | Pubmed ID: 28059125
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency.
Genetics Dec, 2017 | Pubmed ID: 29061647
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
Inhibitor of apoptosis proteins, NAIP, cIAP1 and cIAP2 expression during macrophage differentiation and M1/M2 polarization.
PloS one , 2018 | Pubmed ID: 29518103
Transcriptomic RNAseq drug screen in cerebrocortical cultures; towards novel neurogenetic disease therapies.
Human molecular genetics Jun, 2018 | Pubmed ID: 29901742
Children's Hospital of Eastern Ontario Research Institute
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
1, Children's Hospital of Eastern Ontario Research Institute,
2Department of Biology, University of Ottawa
Confidentialité
Conditions d'utilisation
Politiques
Contactez-nous
RECOMMANDER À LA BIBLIOTHÈQUE
NEWSLETTERS JoVE
JoVE Journal
Collections de méthodes
JoVE Encyclopedia of Experiments
Archives
JoVE Core
JoVE Business
JoVE Science Education
JoVE Lab Manual
Centre de ressources universitaires
Auteurs
Bibliothécaires
Accès
À PROPOS DE JoVE
Copyright © 2024 MyJoVE Corporation. Tous droits réservés.