21. INaturalist is useful at enhancing biodiversity studies as evident from southern African freshwater crabs (Decapoda: Brachyura: Potamonautidae). Issue 3 (30th August 2022) Authors: Daniels, Savel R; Barnes, Aaron; Peer, Nasreen; Egan, Vincent T; Taylor, Ricky; Taylor, Robert W; van der Colff, Dewidine Journal: Journal of crustacean biology Issue: Volume 42:Issue 3(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations. Issue 4 (5th November 2018) Authors: Su, Tianhong; Grady, John P; Afshar, Sorena; McDonald, Stuart AC; Taylor, Robert W; Turnbull, Doug M; Greaves, Laura C Journal: Journal of pathology Issue: Volume 246:Issue 4(2018) Page Start: 427 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy. (4th October 2018) Authors: Sommerville, Ewen W; Zhou, Xiao-Long; Oláhová, Monika; Jenkins, Janda; Euro, Liliya; Konovalova, Svetlana; Hilander, Taru; Pyle, Angela; He, Langping; Habeebu, Sultan; Saunders, Carol; Kelsey, Anna; Morris, Andrew A M; McFarland, Robert; Suomalainen, Anu; Gorman, Gráinne S; Wang, En-Duo; Thiffaul... Journal: Human molecular genetics Issue: Volume 28:Number 2(2019) Page Start: 258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. Machine learning algorithms reveal the secrets of mitochondrial dynamics. Issue 6 (27th May 2021) Authors: Collier, Jack J; Taylor, Robert W Journal: EMBO molecular medicine Issue: Volume 13:Issue 6(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. Metabolic effects of bezafibrate in mitochondrial disease. Issue 3 (28th February 2020) Authors: Steele, Hannah; Gomez‐Duran, Aurora; Pyle, Angela; Hopton, Sila; Newman, Jane; Stefanetti, Renae J; Charman, Sarah J; Parikh, Jehill D; He, Langping; Viscomi, Carlo; Jakovljevic, Djordje G; Hollingsworth, Kieren G; Robinson, Alan J; Taylor, Robert W; Bottolo, Leonardo; Horvath, Rita; Chinnery, Pa... Journal: EMBO molecular medicine Issue: Volume 12:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. Mitochondrial disease in adults: recent advances and future promise. Issue 7 (July 2021) Authors: Ng, Yi Shiau; Bindoff, Laurence A; Gorman, Gráinne S; Klopstock, Thomas; Kornblum, Cornelia; Mancuso, Michelangelo; McFarland, Robert; Sue, Carolyn M; Suomalainen, Anu; Taylor, Robert W; Thorburn, David R; Turnbull, Doug M Journal: Lancet neurology Issue: Volume 20:Issue 7(2021) Page Start: 573 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. Mitochondrial DNA mutations induce mitochondrial biogenesis and increase the tumorigenic potential of Hodgkin and Reed–Sternberg cells. (7th April 2020) Authors: Haumann, Sophie; Boix, Julia; Knuever, Jana; Bieling, Angela; Vila Sanjurjo, Anton; Elson, Joanna L; Blakely, Emma L; Taylor, Robert W; Riet, Nicole; Abken, Hinrich; Kashkar, Hamid; Hornig-Do, Hue-Tran; Wiesner, Rudolf J Journal: Carcinogenesis Issue: Volume 41:Number 12(2020) Page Start: 1735 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease. (22nd August 2019) Authors: Oláhová, Monika; Berti, Camilla Ceccatelli; Collier, Jack J; Alston, Charlotte L; Jameson, Elisabeth; Jones, Simon A; Edwards, Noel; He, Langping; Chinnery, Patrick F; Horvath, Rita; Goffrini, Paola; Taylor, Robert W; Sayer, John A Journal: Human molecular genetics Issue: Volume 28:Number 22(2019) Page Start: 3766 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. MtDNA disease for the neurologist. (January 2011) Authors: Nesbitt, Victoria; Whittaker, Roger G; Turnbull, Douglass M; McFarland, Robert; Taylor, Robert W Journal: Future neurology Issue: Volume 6:Number 1(2011) Page Start: 63 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy. (24th August 2018) Authors: Pacheu-Grau, David; Callegari, Sylvie; Emperador, Sonia; Thompson, Kyle; Aich, Abhishek; Topol, Sarah E; Spencer, Emily G; McFarland, Robert; Ruiz-Pesini, Eduardo; Torkamani, Ali; Taylor, Robert W; Montoya, Julio; Rehling, Peter Journal: Human molecular genetics Issue: Volume 27:Number 23(2018:Dec. 01) Page Start: 4135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗