1. AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicity. (20th March 2020) Authors: Aguilà, Monica; Bellingham, James; Athanasiou, Dimitra; Bevilacqua, Dalila; Duran, Yanai; Maswood, Ryea; Parfitt, David A; Iwawaki, Takao; Spyrou, Giannis; Smith, Alexander J; Ali, Robin R; Cheetham, Michael E Journal: Human molecular genetics Issue: Volume 29:Number 8(2020) Page Start: 1310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis. Issue 1 (January 2019) Authors: Mole, Sara E; Anderson, Glenn; Band, Heather A; Berkovic, Samuel F; Cooper, Jonathan D; Kleine Holthaus, Sophia-Martha; McKay, Tristan R; Medina, Diego L; Rahim, Ahad A; Schulz, Angela; Smith, Alexander J Journal: Lancet neurology Issue: Volume 18:Issue 1(2019) Page Start: 107 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CT appearance of presumptively normal intrathoracic lymph nodes in cats. Issue 10 (October 2020) Authors: Smith, Alexander J; Sutton, Dawn R; Major, Alison C Journal: Journal of feline medicine and surgery Issue: Volume 22:Issue 10(2020) Page Start: 875 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Nanotube‐like processes facilitate material transfer between photoreceptors. (8th September 2021) Authors: Kalargyrou, Aikaterini A; Basche, Mark; Hare, Aura; West, Emma L; Smith, Alexander J; Ali, Robin R; Pearson, Rachael A Journal: EMBO reports Issue: Volume 22:Number 11(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease. (6th September 2019) Authors: kleine Holthaus, Sophia-Martha; Herranz-Martin, Saul; Massaro, Giulia; Aristorena, Mikel; Hoke, Justin; Hughes, Michael P; Maswood, Ryea; Semenyuk, Olha; Basche, Mark; Shah, Amna Z; Klaska, Izabela P; Smith, Alexander J; Mole, Sara E; Rahim, Ahad A; Ali, Robin R Journal: Human molecular genetics Issue: Volume 28:Number 23(2019) Page Start: 3867 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Retinal gene therapy. Issue 1 (1st March 2018) Authors: Kumaran, Neruban; Michaelides, Michel; Smith, Alexander J; Ali, Robin R; Bainbridge, James W B Journal: British medical bulletin Issue: Volume 126:Issue 1(2018) Page Start: 13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP). (23rd December 2020) Authors: Moreno-Leon, Laura; West, Emma L; O'Hara-Wright, Michelle; Li, Linjing; Nair, Rohini; He, Jie; Anand, Manisha; Sahu, Bhubanananda; Chavali, Venkat Ramana Murthy; Smith, Alexander J; Ali, Robin R; Jacobson, Samuel G; Cideciyan, Artur V; Khanna, Hemant Journal: Human molecular genetics Issue: Volume 29:Number 22(2020) Page Start: 3706 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. RPGR-associated retinopathy: clinical features, molecular genetics, animal models and therapeutic options. Issue 8 (3rd February 2016) Authors: Tee, James J L; Smith, Alexander J; Hardcastle, Alison J; Michaelides, Michel Journal: British journal of ophthalmology Issue: Volume 100:Issue 8(2016) Page Start: 1022 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗