Robert S. Molday
Affiliations: | University of British Columbia, Vancouver, Vancouver, BC, Canada |
Area:
Biochemistry, Neuroscience BiologyGoogle:
"Robert Molday"Mean distance: 53433
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Publications
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| Xu T, Molday LL, Molday RS. (2023) Retinal-phospholipid Schiff-base conjugates and their interaction with ABCA4, the ABC transporter associated with Stargardt disease. The Journal of Biological Chemistry. 299: 104614 |
| Molday RS, Garces FA, Scortecci JF, et al. (2021) Structure and function of ABCA4 and its role in the visual cycle and Stargardt macular degeneration. Progress in Retinal and Eye Research. 101036 |
| Skiba NP, Cady MA, Molday L, et al. (2021) TMEM67, TMEM237 and embigin in the complex with lactate transporter MCT1 are unique components of the photoreceptor outer segment plasma membrane. Molecular & Cellular Proteomics : McP. 100088 |
| Garces FA, Scortecci JF, Molday RS. (2020) Functional Characterization of ABCA4 Missense Variants Linked to Stargardt Macular Degeneration. International Journal of Molecular Sciences. 22 |
| Curtis SB, Molday LL, Garces FA, et al. (2020) Functional Analysis and Classification of Homozygous and Hypomorphic ABCA4 Variants Associated with Stargardt Macular Degeneration. Human Mutation |
| Ennishi D, Healy S, Bashashati A, et al. (2020) TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma. Nature Medicine |
| Novales Flamarique I, Ahmed AS, Cheng CL, et al. (2019) Growth hormone regulates opsin expression in the retina of a salmonid fish. Journal of Neuroendocrinology. e12804 |
| Guissart C, Harrison AN, Benkirane M, et al. (2019) ATP8A2-related disorders as recessive cerebellar ataxia. Journal of Neurology |
| Dyka FM, Molday LL, Chiodo V, et al. (2019) Dual ABCA4-AAV vector treatment reduces pathogenic retinal A2E accumulation in a mouse model of autosomal recessive Stargardt Disease. Human Gene Therapy |
| Choi H, Andersen JP, Molday RS. (2019) Expression and Functional Characterization of Missense Mutations in ATP8A2 Linked to Severe Neurological Disorders. Human Mutation |