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Mitochondrion
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August 31, 2020
Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features
Rosetta Marotta, Judy Chin, Maria Chiotis, et al.
Advances in Neurobiology
|
July 5, 2017
Prion Diseases
Benjamin C Whitechurch, Jeremy M Welton, Steven J Collins, et al.
Therapeutic Delivery
|
May 8, 2013
Immunotherapeutic approaches in prion disease: progress, challenges and potential directions
Marcus W Brazier, Alexandra I Mot, Anthony R White, et al.
Journal of Neurochemistry
|
April 29, 2005
Prion protein glycosylation
Victoria 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 disease
Marcus 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 activity
Qiaojun He, Hui Peng, Steven J Collins, et al.
Leukemia Research
|
September 12, 2006
KN-62 analogues as potent differentiating agents of HL-60 cells
Aaron 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 CJD
Sarah 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 rhabdomyolysis
Rosetta 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 Australia
Fiona J Brooke, Alison Boyd, Genevieve M Klug, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 121) with videos related to
Sort By:
Page
of 13
Mitochondrion
|
August 31, 2020
Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features
Rosetta Marotta, Judy Chin, Maria Chiotis, et al.
Advances in Neurobiology
|
July 5, 2017
Prion Diseases
Benjamin C Whitechurch, Jeremy M Welton, Steven J Collins, et al.
Therapeutic Delivery
|
May 8, 2013
Immunotherapeutic approaches in prion disease: progress, challenges and potential directions
Marcus W Brazier, Alexandra I Mot, Anthony R White, et al.
Journal of Neurochemistry
|
April 29, 2005
Prion protein glycosylation
Victoria 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 disease
Marcus 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 activity
Qiaojun He, Hui Peng, Steven J Collins, et al.
Leukemia Research
|
September 12, 2006
KN-62 analogues as potent differentiating agents of HL-60 cells
Aaron 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 CJD
Sarah 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 rhabdomyolysis
Rosetta 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 Australia
Fiona J Brooke, Alison Boyd, Genevieve M Klug, et al.
Page
of 13