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Steven J Collins

Showing results (21-30 of 121) with videos related to

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Mitochondrion|August 31, 2020
Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical featuresRosetta Marotta, Judy Chin, Maria Chiotis, et al.
Advances in Neurobiology|July 5, 2017
Prion DiseasesBenjamin C Whitechurch, Jeremy M Welton, Steven J Collins, et al.
Therapeutic Delivery|May 8, 2013
Immunotherapeutic approaches in prion disease: progress, challenges and potential directionsMarcus W Brazier, Alexandra I Mot, Anthony R White, et al.
Journal of Neurochemistry|April 29, 2005
Prion protein glycosylationVictoria A Lawson, Steven J Collins, Colin L Masters, et al.
Free Radical Biology & Medicine|May 6, 2008
A manganese-superoxide dismutase/catalase mimetic extends survival in a mouse model of human prion diseaseMarcus W Brazier, Susan R Doctrow, Colin L Masters, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 4, 2004
Retinoid-modulated MAT1 ubiquitination and CAK activityQiaojun He, Hui Peng, Steven J Collins, et al.
Leukemia Research|September 12, 2006
KN-62 analogues as potent differentiating agents of HL-60 cellsAaron D Schuler, Jutong Si, LeMoyne Mueller, et al.
BMJ Neurology Open|May 6, 2022
Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJDSarah Holper, Victoria Lewis, Robb Wesselingh, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 18, 2010
Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysisRosetta Marotta, Judy Chin, Denise M Kirby, et al.
The Medical Journal of Australia|February 13, 2004
Lyodura use and the risk of iatrogenic Creutzfeldt-Jakob disease in AustraliaFiona J Brooke, Alison Boyd, Genevieve M Klug, et al.
Pageof 13

Showing results (21-30 of 121) with videos related to

Sort By:
Pageof 13
Mitochondrion|August 31, 2020
Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical featuresRosetta Marotta, Judy Chin, Maria Chiotis, et al.
Advances in Neurobiology|July 5, 2017
Prion DiseasesBenjamin C Whitechurch, Jeremy M Welton, Steven J Collins, et al.
Therapeutic Delivery|May 8, 2013
Immunotherapeutic approaches in prion disease: progress, challenges and potential directionsMarcus W Brazier, Alexandra I Mot, Anthony R White, et al.
Journal of Neurochemistry|April 29, 2005
Prion protein glycosylationVictoria A Lawson, Steven J Collins, Colin L Masters, et al.
Free Radical Biology & Medicine|May 6, 2008
A manganese-superoxide dismutase/catalase mimetic extends survival in a mouse model of human prion diseaseMarcus W Brazier, Susan R Doctrow, Colin L Masters, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 4, 2004
Retinoid-modulated MAT1 ubiquitination and CAK activityQiaojun He, Hui Peng, Steven J Collins, et al.
Leukemia Research|September 12, 2006
KN-62 analogues as potent differentiating agents of HL-60 cellsAaron D Schuler, Jutong Si, LeMoyne Mueller, et al.
BMJ Neurology Open|May 6, 2022
Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJDSarah Holper, Victoria Lewis, Robb Wesselingh, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 18, 2010
Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysisRosetta Marotta, Judy Chin, Denise M Kirby, et al.
The Medical Journal of Australia|February 13, 2004
Lyodura use and the risk of iatrogenic Creutzfeldt-Jakob disease in AustraliaFiona J Brooke, Alison Boyd, Genevieve M Klug, et al.
Pageof 13