11. De novo mtDNA point mutations are common and have a low recurrence risk. Issue 2 (22nd July 2016) Authors: Sallevelt, Suzanne C E H; de Die-Smulders, Christine E M; Hendrickx, Alexandra T M; Hellebrekers, Debby M E I; de Coo, Irenaeus F M; Alston, Charlotte L; Knowles, Charlotte; Taylor, Robert W; McFarland, Robert; Smeets, Hubert J M Journal: Journal of medical genetics Issue: Volume 54:Issue 2(2017) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Defective mitochondrial protease LonP1 can cause classical mitochondrial disease. (6th March 2018) Authors: Peter, Bradley; Waddington, Christie L; Oláhová, Monika; Sommerville, Ewen W; Hopton, Sila; Pyle, Angela; Champion, Michael; Ohlson, Monica; Siibak, Triinu; Chrzanowska-Lightowlers, Zofia M A; Taylor, Robert W; Falkenberg, Maria; Lightowlers, Robert N Journal: Human molecular genetics Issue: Volume 27:Number 10(2018:May 15) Page Start: 1743 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Depletion of mitochondrial DNA in leucocytes harbouring the 3243A→G mtDNA mutation. Issue 1 (1st September 2006) Authors: Pyle, Angela; Taylor, Robert W; Durham, Steve E; Deschauer, Marcus; Schaefer, Andrew M; Samuels, David C; Chinnery, Patrick F Journal: Journal of medical genetics Issue: Volume 44:Issue 1(2007) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Development of stable, orally bioavailable small molecule positive modulators of HGF/MET signaling for the treatment of cognitive impairment. (20th December 2022) Authors: Taylor, Robert W; Boatman, Doug; Johnston, Jewel; Kneip, Maya; Church, Kevin Journal: Alzheimer's & dementia Issue: Volume 18(2022)Supplement 10 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Diagnostic investigations of patients with chronic progressive external ophthalmoplegia. Issue 12 (28th September 2012) Authors: Yu-Wai-Man, Patrick; Gorman, Grainne S; Taylor, Robert W; Turnbull, Douglass M Journal: British journal of ophthalmology Issue: Volume 96:Issue 12(2012) Page Start: 1536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Issue 4 (11th September 2021) Authors: Zheng, Wen-Qiang; Pedersen, Signe Vandal; Thompson, Kyle; Bellacchio, Emanuele; French, Courtney E; Munro, Benjamin; Pearson, Toni S; Vogt, Julie; Diodato, Daria; Diemer, Tue; Ernst, Anja; Horvath, Rita; Chitre, Manali; Ek, Jakob; Wibrand, Flemming; Grange, Dorothy K; Raymond, Lucy; Zhou, Xiao-Lo... Journal: Human molecular genetics Issue: Volume 31:Issue 4(2022) Page Start: 523 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Emerging roles of ATG7 in human health and disease. Issue 12 (2nd November 2021) Authors: Collier, Jack J; Suomi, Fumi; Oláhová, Monika; McWilliams, Thomas G; Taylor, Robert W Journal: EMBO molecular medicine Issue: Volume 13:Issue 12(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation. Issue 2 (11th November 2015) Authors: Spiegel, Ronen; Saada, Ann; Flannery, Padraig J; Burté, Florence; Soiferman, Devorah; Khayat, Morad; Eisner, Verónica; Vladovski, Eugene; Taylor, Robert W; Bindoff, Laurence A; Shaag, Avraham; Mandel, Hanna; Schuler-Furman, Ora; Shalev, Stavit A; Elpeleg, Orly; Yu-Wai-Man, Patrick Journal: Journal of medical genetics Issue: Volume 53:Issue 2(2016) Page Start: 127 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. FBXL4 deficiency increases mitochondrial removal by autophagy. Issue 7 (11th June 2020) Authors: Alsina, David; Lytovchenko, Oleksandr; Schab, Aleksandra; Atanassov, Ilian; Schober, Florian A; Jiang, Min; Koolmeister, Camilla; Wedell, Anna; Taylor, Robert W; Wredenberg, Anna; Larsson, Nils‐Göran Journal: EMBO molecular medicine Issue: Volume 12:Issue 7(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Fosgonimeton, a novel, small molecule positive modulator of the HGF/MET system is neuroprotective in primary neuron culture. (20th December 2022) Authors: Reda, Sherif; Johnston, Jewel; Taylor, Robert W; Church, Kevin Journal: Alzheimer's & dementia Issue: Volume 18(2022)Supplement 10 Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗