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Patrick F Chinnery

Showing results (261-270 of 473) with videos related to

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Journal of Neuropathology and Experimental Neurology|August 22, 2008
Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gammaGábor Zsurka, Miriam Baron, Joanna D Stewart, et al.
Archives of Neurology|April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Molecular Neurodegeneration|April 17, 2015
Selective loss of glucocerebrosidase activity in sporadic Parkinson's disease and dementia with Lewy bodiesDavide Chiasserini, Silvia Paciotti, Paolo Eusebi, et al.
Nature Communications|May 2, 2026
Genetic landscape of adult executive function reveals a cell-type-specific developmental originMd Shafiqur Rahman, Azra Frkatović-Hodžić, Jelle van den Ameele, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?Kate Craig, Yoshihisa Takiyama, Bing-Wen Soong, et al.
Nature Genetics|January 29, 2008
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypesLynsey M Cree, David C Samuels, Susana Chuva de Sousa Lopes, et al.
Archives of Neurology|January 16, 2008
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth diseaseTimothy Harrower, Joanna D Stewart, Gavin Hudson, et al.
Mutation Research|March 26, 2003
Changes in the human mitochondrial genome after treatment of malignant diseaseTheresa M Wardell, Elaine Ferguson, Patrick F Chinnery, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Pageof 48

Showing results (261-270 of 473) with videos related to

Sort By:
Pageof 48
Journal of Neuropathology and Experimental Neurology|August 22, 2008
Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gammaGábor Zsurka, Miriam Baron, Joanna D Stewart, et al.
Archives of Neurology|April 11, 2007
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and ParkinsonismGavin Hudson, Andrew M Schaefer, Robert W Taylor, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
Molecular Neurodegeneration|April 17, 2015
Selective loss of glucocerebrosidase activity in sporadic Parkinson's disease and dementia with Lewy bodiesDavide Chiasserini, Silvia Paciotti, Paolo Eusebi, et al.
Nature Communications|May 2, 2026
Genetic landscape of adult executive function reveals a cell-type-specific developmental originMd Shafiqur Rahman, Azra Frkatović-Hodžić, Jelle van den Ameele, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?Kate Craig, Yoshihisa Takiyama, Bing-Wen Soong, et al.
Nature Genetics|January 29, 2008
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypesLynsey M Cree, David C Samuels, Susana Chuva de Sousa Lopes, et al.
Archives of Neurology|January 16, 2008
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth diseaseTimothy Harrower, Joanna D Stewart, Gavin Hudson, et al.
Mutation Research|March 26, 2003
Changes in the human mitochondrial genome after treatment of malignant diseaseTheresa M Wardell, Elaine Ferguson, Patrick F Chinnery, et al.
Mitochondrion|October 5, 2010
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver diseaseNimantha de Alwis, Guruprasad Aithal, Elizabetta Bugianesi, et al.
Pageof 48