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L Alston

Showing results (111-120 of 174) with videos related to

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Genome Biology|September 18, 2020
Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and agingScott A Lujan, Matthew J Longley, Margaret H Humble, et al.
JAMA|July 2, 2025
HepB-CpG Vaccine in People With HIV and Prior Nonresponse to HBV Vaccine: The BEe-HIVe Trial End-of-Study ResultsKristen M Marks, Minhee Kang, Triin Umbleja, et al.
Nature Metabolism|May 8, 2024
Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial diseaseAndrew Y Sung, Rachel M Guerra, Laura H Steenberge, et al.
Annals of Neurology|July 26, 2016
Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combinationYi Shiau Ng, Catherine Feeney, Andrew M Schaefer, et al.
Clinical Genetics|April 10, 2025
Infantile Cerebellar-Retinal Degeneration Associated With Novel ACO2 Variants: Clinical Features and Insights From a Drosophila ModelEdgar Buhl, Suchika Garg, Marie Monaghan, et al.
Nucleic Acids Research|June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre levelDiana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Neurology|November 8, 2013
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletionsCharlotte L Alston, Andrew M Schaefer, Pravrutha Raman, et al.
Journal of Medical Genetics|July 25, 2016
De novo mtDNA point mutations are common and have a low recurrence riskSuzanne C E H Sallevelt, Christine E M de Die-Smulders, Alexandra T M Hendrickx, et al.
Journal of Neuropathology and Experimental Neurology|June 18, 2015
Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 MutationsNichola Z Lax, Charlotte L Alston, Katherine Schon, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
Pageof 18

Showing results (111-120 of 174) with videos related to

Sort By:
Pageof 18
Genome Biology|September 18, 2020
Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and agingScott A Lujan, Matthew J Longley, Margaret H Humble, et al.
JAMA|July 2, 2025
HepB-CpG Vaccine in People With HIV and Prior Nonresponse to HBV Vaccine: The BEe-HIVe Trial End-of-Study ResultsKristen M Marks, Minhee Kang, Triin Umbleja, et al.
Nature Metabolism|May 8, 2024
Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial diseaseAndrew Y Sung, Rachel M Guerra, Laura H Steenberge, et al.
Annals of Neurology|July 26, 2016
Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combinationYi Shiau Ng, Catherine Feeney, Andrew M Schaefer, et al.
Clinical Genetics|April 10, 2025
Infantile Cerebellar-Retinal Degeneration Associated With Novel ACO2 Variants: Clinical Features and Insights From a Drosophila ModelEdgar Buhl, Suchika Garg, Marie Monaghan, et al.
Nucleic Acids Research|June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre levelDiana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Neurology|November 8, 2013
Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletionsCharlotte L Alston, Andrew M Schaefer, Pravrutha Raman, et al.
Journal of Medical Genetics|July 25, 2016
De novo mtDNA point mutations are common and have a low recurrence riskSuzanne C E H Sallevelt, Christine E M de Die-Smulders, Alexandra T M Hendrickx, et al.
Journal of Neuropathology and Experimental Neurology|June 18, 2015
Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 MutationsNichola Z Lax, Charlotte L Alston, Katherine Schon, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
Pageof 18