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Angela Pyle

Showing results (21-30 of 119) with videos related to

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The British Journal of Ophthalmology|January 25, 2014
Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypesPatrick Yu-Wai-Man, Angela Pyle, Helen Griffin, et al.
The Journal of Pediatrics|August 5, 2006
The mitochondrial DNA A3243A>G mutation must be an infrequent cause of Asperger syndromeLindsey Kent, Claire Lambert, Angela Pyle, et al.
JAMA Neurology|October 25, 2016
A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance ProblemsAlastair J C Hughes, Hannah E Steele, Angela Pyle, et al.
Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Analytical and Bioanalytical Chemistry|March 2, 2022
A subcellular cookie cutter for spatial genomics in human tissueAlexander G Bury, Angela Pyle, Fabio Marcuccio, et al.
Annals of Neurology|November 18, 2017
Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson diseaseAlexander G Bury, Angela Pyle, Joanna L Elson, et al.
Neurology|October 27, 2015
SCP2 mutations and neurodegeneration with brain iron accumulationRita Horvath, David Lewis-Smith, Konstantinos Douroudis, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Pageof 12

Showing results (21-30 of 119) with videos related to

Sort By:
Pageof 12
The British Journal of Ophthalmology|January 25, 2014
Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypesPatrick Yu-Wai-Man, Angela Pyle, Helen Griffin, et al.
The Journal of Pediatrics|August 5, 2006
The mitochondrial DNA A3243A>G mutation must be an infrequent cause of Asperger syndromeLindsey Kent, Claire Lambert, Angela Pyle, et al.
JAMA Neurology|October 25, 2016
A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance ProblemsAlastair J C Hughes, Hannah E Steele, Angela Pyle, et al.
Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Analytical and Bioanalytical Chemistry|March 2, 2022
A subcellular cookie cutter for spatial genomics in human tissueAlexander G Bury, Angela Pyle, Fabio Marcuccio, et al.
Annals of Neurology|November 18, 2017
Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson diseaseAlexander G Bury, Angela Pyle, Joanna L Elson, et al.
Neurology|October 27, 2015
SCP2 mutations and neurodegeneration with brain iron accumulationRita Horvath, David Lewis-Smith, Konstantinos Douroudis, et al.
Journal of Medical Genetics|September 5, 2006
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutationAngela Pyle, Robert W Taylor, Steve E Durham, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Pageof 12