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1. AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicity. (20th March 2020)

3. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021)

5. Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies. Issue 4 (9th September 2022)

6. New variants and in silico analyses in GRK1 associated Oguchi disease. Issue 2 (30th November 2020)

7. New variants and in silico analyses in GRK1 associated Oguchi disease. Issue 2 (30th November 2020)

8. REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking. (5th May 2017)

9. The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6. (16th January 2018)

10. The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6. (26th August 2017)