Machine learning algorithms reveal the secrets of mitochondrial dynamics

por Collier, Jack J, Taylor, Robert W
Publicado 2021

Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways

por Tang, Jia Xin, Thompson, Kyle, Taylor, Robert W., Oláhová, Monika
Publicado 2020

Interrogating Mitochondrial Biology and Disease Using CRISPR/Cas9 Gene Editing

por Tang, Jia-Xin, Pyle, Angela, Taylor, Robert W., Oláhová, Monika
Publicado 2021

Endocrine disorders in mitochondrial disease()

por Schaefer, Andrew M., Walker, Mark, Turnbull, Douglass M., Taylor, Robert W.
Publicado 2013

The genetic basis of isolated mitochondrial complex II deficiency

por Fullerton, Millie, McFarland, Robert, Taylor, Robert W., Alston, Charlotte L.
Publicado 2020

The molecular pathology of pathogenic mitochondrial tRNA variants

por Richter, Uwe, McFarland, Robert, Taylor, Robert W., Pickett, Sarah J.
Publicado 2021

Lower extremity amputation increases oscillatory flow in the infrarenal aorta: A new potential risk factor for abdominal aortic aneurysm development

por Smolensky, Alexander V, Clement-Guinaudeau, Stephanie, Taylor, Robert W, Oshinski, John N
Publicado 2012

A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations

por Yarham, John W., McFarland, Robert, Taylor, Robert W., Elson, Joanna L.
Publicado 2012

The m.15043G > A MT-CYB variant is not a pathogenic mtDNA variant

por Alston, Charlotte L., Blakely, Emma L., McFarland, Robert, Taylor, Robert W.
Publicado 2020

A genomic perspective on climate change

por Forzano, Francesca, Babb de Villiers, Chantal, Farley, Martin, Fowler, Hayley, Taylor, Robert W.
Publicado 2023

Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle

por Campbell, Georgia, Krishnan, Kim J., Deschauer, Marcus, Taylor, Robert W., Turnbull, Doug M.
Publicado 2014

The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines

por Alston, Charlotte L, Stenton, Sarah L, Hudson, Gavin, Prokisch, Holger, Taylor, Robert W
Publicado 2021

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

por Abu-Amero, Khaled K, Al-Dhalaan, Hesham, Bohlega, Saeed, Hellani, Ali, Taylor, Robert W
Publicado 2009

Activated protein C in septic shock: a propensity-matched analysis

por Sadaka, Farid, O'Brien, Jacklyn, Migneron, Matthew, Stortz, Julie, Vanston, Alexander, Taylor, Robert W
Publicado 2011

A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency

por Simard, Marie‐Lune, Mourier, Arnaud, Greaves, Laura C, Taylor, Robert W, Stewart, James B
Publicado 2018

Emerging roles of ATG7 in human health and disease

por Collier, Jack J, Suomi, Fumi, Oláhová, Monika, McWilliams, Thomas G, Taylor, Robert W
Publicado 2021

The effect of red blood cell transfusion on tissue oxygenation and microcirculation in severe septic patients

por Sadaka, Farid, Aggu-Sher, Ravi, Krause, Katie, O'Brien, Jacklyn, Armbrecht, Eric S, Taylor, Robert W
Publicado 2011

The genetics and pathology of mitochondrial disease

por Alston, Charlotte L, Rocha, Mariana C, Lax, Nichola Z, Turnbull, Doug M, Taylor, Robert W
Publicado 2016

Novel POLG variants associated with late-onset de novo status epilepticus and progressive ataxia

por Ng, Yi Shiau, Powell, Helen, Hoggard, Nigel, Turnbull, Doug M., Taylor, Robert W., Hadjivassiliou, Marios
Publicado 2017

Scientific and Ethical Issues in Mitochondrial Donation

por Craven, Lyndsey, Murphy, Julie, Turnbull, Doug M., Taylor, Robert W., Gorman, Grainne S., McFarland, Robert
Publicado 2018