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Alex MacKenzie

Showing results (21-30 of 48) with videos related to

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Human Molecular Genetics|May 10, 2013
Celecoxib increases SMN and survival in a severe spinal muscular atrophy mouse model via p38 pathway activationFaraz Farooq, Francisco Abadía-Molina, Duncan MacKenzie, et al.
NPJ Genomic Medicine|December 22, 2017
Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screenA J Mears, S C Schock, J Hadwen, et al.
Orphanet Journal of Rare Diseases|August 14, 2025
A cost-utility analysis of newborn screening for spinal muscular atrophy in CanadaAlex Pace, Weston Roda, Corrina Poon, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 16, 2004
Motoneuron resistance to apoptotic cell death in vivo correlates with the ratio between X-linked inhibitor of apoptosis proteins (XIAPs) and its inhibitor, XIAP-associated factor 1Daniel Perrelet, Florence E Perrin, Peter Liston, et al.
Plos One|September 14, 2021
High-throughput kinome-RNAi screen identifies protein kinase R activator (PACT) as a novel genetic modifier of CUG foci integrity in myotonic dystrophy type 1 (DM1)Nafisa Neault, Sean O'Reilly, Aiman Tariq Baig, et al.
Cellular Oncology (Dordrecht, Netherlands)|April 26, 2021
Differential regulation of autophagy by STAU1 in alveolar rhabdomyosarcoma and non-transformed skeletal muscle cellsShekoufeh Almasi, Tara E Crawford Parks, Aymeric Ravel-Chapuis, et al.
American Journal of Physiology. Renal Physiology|June 1, 2006
Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2Alison Dziarmaga, Pierre-Alain Hueber, Diana Iglesias, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 13, 2016
Mouse lysine catabolism to aminoadipate occurs primarily through the saccharopine pathway; implications for pyridoxine dependent epilepsy (PDE)Izabella Agostinho Pena, Lygia Azevedo Marques, Ângelo B A Laranjeira, et al.
Journal of Visualized Experiments : Jove|July 17, 2018
High-throughput DNA Extraction and Genotyping of 3dpf Zebrafish Larvae by Fin ClippingCeres Kosuta, Kate Daniel, Devon L Johnstone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Direct health-care costs for children diagnosed with genetic diseases are significantly higher than for children with other chronic diseasesDeborah A Marshall, Eric I Benchimol, Alex MacKenzie, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|May 10, 2013
Celecoxib increases SMN and survival in a severe spinal muscular atrophy mouse model via p38 pathway activationFaraz Farooq, Francisco Abadía-Molina, Duncan MacKenzie, et al.
NPJ Genomic Medicine|December 22, 2017
Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screenA J Mears, S C Schock, J Hadwen, et al.
Orphanet Journal of Rare Diseases|August 14, 2025
A cost-utility analysis of newborn screening for spinal muscular atrophy in CanadaAlex Pace, Weston Roda, Corrina Poon, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 16, 2004
Motoneuron resistance to apoptotic cell death in vivo correlates with the ratio between X-linked inhibitor of apoptosis proteins (XIAPs) and its inhibitor, XIAP-associated factor 1Daniel Perrelet, Florence E Perrin, Peter Liston, et al.
Plos One|September 14, 2021
High-throughput kinome-RNAi screen identifies protein kinase R activator (PACT) as a novel genetic modifier of CUG foci integrity in myotonic dystrophy type 1 (DM1)Nafisa Neault, Sean O'Reilly, Aiman Tariq Baig, et al.
Cellular Oncology (Dordrecht, Netherlands)|April 26, 2021
Differential regulation of autophagy by STAU1 in alveolar rhabdomyosarcoma and non-transformed skeletal muscle cellsShekoufeh Almasi, Tara E Crawford Parks, Aymeric Ravel-Chapuis, et al.
American Journal of Physiology. Renal Physiology|June 1, 2006
Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2Alison Dziarmaga, Pierre-Alain Hueber, Diana Iglesias, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 13, 2016
Mouse lysine catabolism to aminoadipate occurs primarily through the saccharopine pathway; implications for pyridoxine dependent epilepsy (PDE)Izabella Agostinho Pena, Lygia Azevedo Marques, Ângelo B A Laranjeira, et al.
Journal of Visualized Experiments : Jove|July 17, 2018
High-throughput DNA Extraction and Genotyping of 3dpf Zebrafish Larvae by Fin ClippingCeres Kosuta, Kate Daniel, Devon L Johnstone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Direct health-care costs for children diagnosed with genetic diseases are significantly higher than for children with other chronic diseasesDeborah A Marshall, Eric I Benchimol, Alex MacKenzie, et al.
Pageof 5