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Molecular Genetics and Metabolism
|
November 9, 2020
The genetic basis of isolated mitochondrial complex II deficiency
Millie Fullerton, Robert McFarland, Robert W Taylor, et al.
Annual Review of Genomics and Human Genetics
|
April 19, 2017
Recent Advances in Mitochondrial Disease
Lyndsey Craven, Charlotte L Alston, Robert W Taylor, et al.
Journal of the Neurological Sciences
|
June 12, 2020
The m.15043G > A MT-CYB variant is not a pathogenic mtDNA variant
Charlotte L Alston, Emma L Blakely, Robert McFarland, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
February 22, 2023
Genomic Strategies in Mitochondrial Diagnostics
Dasha Deen, Charlotte L Alston, Gavin Hudson, et al.
The Journal of Pathology
|
February 15, 2021
The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines
Charlotte L Alston, Sarah L Stenton, Gavin Hudson, et al.
Journal of the Neurological Sciences
|
September 3, 2010
A novel mitochondrial tRNAGlu (MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscle
Charlotte L Alston, James Lowe, Douglass M Turnbull, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 22, 2014
SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions
Frank Hanisch, Malte Kornhuber, Charlotte L Alston, et al.
The Journal of Pathology
|
September 24, 2016
The genetics and pathology of mitochondrial disease
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, et al.
Biochemical and Biophysical Research Communications
|
February 23, 2010
The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells
John K Blackwood, Roger G Whittaker, Emma L Blakely, et al.
Neurology. Genetics
|
November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions
Diana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 103) with videos related to
Sort By:
Page
of 11
Molecular Genetics and Metabolism
|
November 9, 2020
The genetic basis of isolated mitochondrial complex II deficiency
Millie Fullerton, Robert McFarland, Robert W Taylor, et al.
Annual Review of Genomics and Human Genetics
|
April 19, 2017
Recent Advances in Mitochondrial Disease
Lyndsey Craven, Charlotte L Alston, Robert W Taylor, et al.
Journal of the Neurological Sciences
|
June 12, 2020
The m.15043G > A MT-CYB variant is not a pathogenic mtDNA variant
Charlotte L Alston, Emma L Blakely, Robert McFarland, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
February 22, 2023
Genomic Strategies in Mitochondrial Diagnostics
Dasha Deen, Charlotte L Alston, Gavin Hudson, et al.
The Journal of Pathology
|
February 15, 2021
The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines
Charlotte L Alston, Sarah L Stenton, Gavin Hudson, et al.
Journal of the Neurological Sciences
|
September 3, 2010
A novel mitochondrial tRNAGlu (MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscle
Charlotte L Alston, James Lowe, Douglass M Turnbull, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 22, 2014
SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions
Frank Hanisch, Malte Kornhuber, Charlotte L Alston, et al.
The Journal of Pathology
|
September 24, 2016
The genetics and pathology of mitochondrial disease
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, et al.
Biochemical and Biophysical Research Communications
|
February 23, 2010
The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells
John K Blackwood, Roger G Whittaker, Emma L Blakely, et al.
Neurology. Genetics
|
November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions
Diana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Page
of 11