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John Burn

Showing results (41-50 of 162) with videos related to

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Journal of Neurology|November 17, 2011
Understanding the impact of deep brain stimulation on ambulatory activity in advanced Parkinson's diseaseLynn Rochester, Sebastien Francois Martin Chastin, Sue Lord, et al.
Plos Genetics|April 14, 2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL ExpressionMichael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, et al.
European Journal of Cancer (Oxford, England : 1990)|March 26, 2008
Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers: a cost-effectiveness analysisJan Norum, Anne Irene Hagen, Lovise Maehle, et al.
The Journal of Pathology|May 21, 2011
Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expressionNeil Rajan, John Burn, James Langtry, et al.
American Journal of Human Genetics|March 9, 2002
A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndromeSabine M Klauck, Susan Lindsay, Kim S Beyer, et al.
Biochimica Et Biophysica Acta|November 14, 2006
Preliminary observation of elevated levels of nanocrystalline iron oxide in the basal ganglia of neuroferritinopathy patientsDimitri Hautot, Quentin A Pankhurst, Chris M Morris, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 3, 2006
Therapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanismGillian M Borthwick, A Sarah Johnson, Matthew Partington, et al.
Circulation|April 2, 2003
Mouse model for hereditary hemorrhagic telangiectasia has a generalized vascular abnormalityEvelyn Torsney, Richard Charlton, Austin G Diamond, et al.
Mutation Research|May 9, 2002
Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newbornsCaroline L Relton, C Paul Daniel, Ann Fisher, et al.
Mutation Research|December 31, 2003
DNA repair gene polymorphisms, pre-natal factors and the frequency of somatic mutations in the glycophorin-A gene among healthy newbornsCaroline L Relton, C Paul Daniel, Donna M Hammal, et al.
Pageof 17

Showing results (41-50 of 162) with videos related to

Sort By:
Pageof 17
Journal of Neurology|November 17, 2011
Understanding the impact of deep brain stimulation on ambulatory activity in advanced Parkinson's diseaseLynn Rochester, Sebastien Francois Martin Chastin, Sue Lord, et al.
Plos Genetics|April 14, 2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL ExpressionMichael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, et al.
European Journal of Cancer (Oxford, England : 1990)|March 26, 2008
Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers: a cost-effectiveness analysisJan Norum, Anne Irene Hagen, Lovise Maehle, et al.
The Journal of Pathology|May 21, 2011
Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expressionNeil Rajan, John Burn, James Langtry, et al.
American Journal of Human Genetics|March 9, 2002
A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndromeSabine M Klauck, Susan Lindsay, Kim S Beyer, et al.
Biochimica Et Biophysica Acta|November 14, 2006
Preliminary observation of elevated levels of nanocrystalline iron oxide in the basal ganglia of neuroferritinopathy patientsDimitri Hautot, Quentin A Pankhurst, Chris M Morris, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 3, 2006
Therapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanismGillian M Borthwick, A Sarah Johnson, Matthew Partington, et al.
Circulation|April 2, 2003
Mouse model for hereditary hemorrhagic telangiectasia has a generalized vascular abnormalityEvelyn Torsney, Richard Charlton, Austin G Diamond, et al.
Mutation Research|May 9, 2002
Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newbornsCaroline L Relton, C Paul Daniel, Ann Fisher, et al.
Mutation Research|December 31, 2003
DNA repair gene polymorphisms, pre-natal factors and the frequency of somatic mutations in the glycophorin-A gene among healthy newbornsCaroline L Relton, C Paul Daniel, Donna M Hammal, et al.
Pageof 17