1. B17 Blood transcriptome replicates dysregulation found in human huntington's disease brain and shares an immune signature with alzheimer's disease. (13th September 2016) Authors: Flower, Michael; Moss, Davina Hensman; Lo, Kitty K; Miller, James; Omen, Gert-Jan van; 't Hoen, Peter AC; Stone, Timothy; Guinee, Amelia; Langbehn, Doug; Jones, Lesley; Plagnol, Vincent; van Roon-Mom, Willeke MC; Holmans, Peter; Tabrizi, Sarah J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. B48 DNA repair pathways as a common genetic mechanism modulating the age at onset in polyglutamine diseases. (13th September 2016) Authors: Bettencourt, Conceição; Moss, Davina Hensman; Flower, Michael; Wiethoff, Sarah; Brice, Alexis; Goizet, Cyril; Stevanin, Giovanni; Koutsis, Georgios; Karadima, Georgia; Panas, Marios; Yescas-Gómez, Petra; García-Velázquez, Lizbeth Esmeralda; Alonso-Vilatela, María Elisa; Lima, Manuela; Raposo, Maf... Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. B49 Genetic modifiers of huntington's disease progression. (13th September 2016) Authors: Moss, Davina J Hensman; Pardiñas, Antonio F; Flower, Michael; Miller, James; Lo, Kitty; Plagnol, Vincent; Holmans, Peter; Jones, Lesley; Langbehn, Douglas; Tabrizi, Sarah J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. C04 FAN1 controls cag repeat expansion in Huntington's disease by dual functions, MLH1 retention and nuclease activity. (12th September 2022) Authors: Goold, Robert; Hamilton, Joseph; Menneteau, Thomas; Flower, Michael; Bunting, Emma; Aldous, Sarah; Porro, Antonio; Vicente, José; Allen, Nicholas; Wilkinson, Hilary; Bates, Gillian; Sartori, Alessandro; Thalassinos, Konstantinos; Balmus, Gabriel; Tabrizi, Sarah Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 93(2022)Supplement 1 Page Start: A17 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. C06 Genetic variation in MSH3 that lowers its expression ameliorates disease course and limits repeat expansion in huntington's disease and myotonic dystrophy type 1. (September 2018) Authors: Flower, Michael; Lomeikaite, Vilija; Ciosi, Marc; Morales, Fernando; Lo, Kitty; Moss, Davina Hensman; Jones, Lesley; Holmans, Peter; Tabrizi, Sarah J; Monckton, Darren G Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 89(2018)Supplement 1 Page Start: A28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. C07 A CRISPRI platform to assess the role of HD risk modifiers in CAG repeat expansion in iPSC derived striatal neurons. (12th September 2022) Authors: Ferguson, Ross; Flower, Michael; Tabrizi, Sarah J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 93(2022)Supplement 1 Page Start: A18 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cover Image, Volume 70, Issue 3. Issue 3 (5th January 2022) Authors: Lange, Jenny; Gillham, Olivia; Alkharji, Reem; Eaton, Simon; Ferrari, Giulia; Madej, Monika; Flower, Michael; Tedesco, Francesco Saverio; Muntoni, Francesco; Ferretti, Patrizia Journal: Glia Issue: Volume 70:Issue 3(2022) Page Start: C1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. DNA REPAIR PATHWAYS MODULATE ONSET IN POLYGLUTAMINE DISEASES. Issue 12 (15th November 2016) Authors: Bettencourt, Conceição; Moss, Davina Hensman; Flower, Michael; Wiethoff, Sarah; Giunti, Paola; Durr, Alexandra; Holmans, Peter; Houlden, Henry; Tabrizi, Sarah; Jones, Lesley Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87:Issue 12(2016) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Issue 6 (6th May 2016) Authors: Bettencourt, Conceição; Hensman‐Moss, Davina; Flower, Michael; Wiethoff, Sarah; Brice, Alexis; Goizet, Cyril; Stevanin, Giovanni; Koutsis, Georgios; Karadima, Georgia; Panas, Marios; Yescas‐Gómez, Petra; García‐Velázquez, Lizbeth Esmeralda; Alonso‐Vilatela, María Elisa; Lima, Manuela; Raposo, Maf... Journal: Annals of neurology Issue: Volume 79:Issue 6(2016:Jun.) Page Start: 983 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Dystrophin deficiency affects human astrocyte properties and response to damage. Issue 3 (13th November 2021) Authors: Lange, Jenny; Gillham, Olivia; Alkharji, Reem; Eaton, Simon; Ferrari, Giulia; Madej, Monika; Flower, Michael; Tedesco, Francesco Saverio; Muntoni, Francesco; Ferretti, Patrizia Journal: Glia Issue: Volume 70:Issue 3(2022) Page Start: 466 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗