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Ian J Wilson

Showing results (11-20 of 33) with videos related to

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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|January 4, 2014
Titinopathy in a Canadian family sharing the British founder haplotypeGerald Pfeffer, Jeffrey T Joseph, A Micheil Innes, et al.
The New England Journal of Medicine|May 16, 2019
Mitochondrial Donation - Which Women Could Benefit?Sarah J Pickett, Alasdair Blain, Yi Shiau Ng, et al.
Orphanet Journal of Rare Diseases|July 6, 2017
Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature reviewIngrid E C Verhaart, Agata Robertson, Ian J Wilson, et al.
Nature Genetics|June 28, 2011
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutationsBrendan A I Payne, Ian J Wilson, Charlotte A Hateley, et al.
Journal of Theoretical Biology|August 6, 2013
Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumoursNicolas Bonello, James Sampson, John Burn, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2008
Filaggrin null mutations and childhood atopic eczema: a population-based case-control studySara J Brown, Caroline L Relton, Haihui Liao, et al.
Kidney International Reports|December 19, 2024
<i>UMOD</i> Genotype and Determinants of Urinary Uromodulin in African PopulationsMichél Strauss-Kruger, Eric Olinger, Patrick Hofmann, et al.
Journal of Vascular and Interventional Radiology : JVIR|September 23, 2006
Inadvertent discontinuation of percutaneous nephrostomy catheters in adult native kidneys: incidence and percutaneous managementWael E A Saad, Sanjiv Virdee, Mark G Davies, et al.
Annals of Clinical and Translational Neurology|March 22, 2018
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factorsSarah J Pickett, John P Grady, Yi Shiau Ng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|January 4, 2014
Titinopathy in a Canadian family sharing the British founder haplotypeGerald Pfeffer, Jeffrey T Joseph, A Micheil Innes, et al.
The New England Journal of Medicine|May 16, 2019
Mitochondrial Donation - Which Women Could Benefit?Sarah J Pickett, Alasdair Blain, Yi Shiau Ng, et al.
Orphanet Journal of Rare Diseases|July 6, 2017
Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature reviewIngrid E C Verhaart, Agata Robertson, Ian J Wilson, et al.
Nature Genetics|June 28, 2011
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutationsBrendan A I Payne, Ian J Wilson, Charlotte A Hateley, et al.
Journal of Theoretical Biology|August 6, 2013
Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumoursNicolas Bonello, James Sampson, John Burn, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2008
Filaggrin null mutations and childhood atopic eczema: a population-based case-control studySara J Brown, Caroline L Relton, Haihui Liao, et al.
Kidney International Reports|December 19, 2024
<i>UMOD</i> Genotype and Determinants of Urinary Uromodulin in African PopulationsMichél Strauss-Kruger, Eric Olinger, Patrick Hofmann, et al.
Journal of Vascular and Interventional Radiology : JVIR|September 23, 2006
Inadvertent discontinuation of percutaneous nephrostomy catheters in adult native kidneys: incidence and percutaneous managementWael E A Saad, Sanjiv Virdee, Mark G Davies, et al.
Annals of Clinical and Translational Neurology|March 22, 2018
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factorsSarah J Pickett, John P Grady, Yi Shiau Ng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
Pageof 4