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Year Number of Results
2013 2
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2019 2
2020 1
2021 1
2024 0

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Page 1
Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen.
Taylor RL, Poulter JA, Downes SM, McKibbin M, Khan KN, Inglehearn CF, Webster AR, Hardcastle AJ, Michaelides M, Bishop PN, Clark SJ, Black GC; United Kingdom Inherited Retinal Dystrophy Consortium. Taylor RL, et al. Ophthalmology. 2019 Oct;126(10):1410-1421. doi: 10.1016/j.ophtha.2019.03.013. Epub 2019 Mar 21. Ophthalmology. 2019. PMID: 30905644 Free PMC article.
Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes.
Porter LF, Saptarshi N, Fang Y, Rathi S, den Hollander AI, de Jong EK, Clark SJ, Bishop PN, Olsen TW, Liloglou T, Chavali VRM, Paraoan L. Porter LF, et al. Clin Epigenetics. 2019 Jan 14;11(1):6. doi: 10.1186/s13148-019-0608-2. Clin Epigenetics. 2019. PMID: 30642396 Free PMC article.
The eye as a complement dysregulation hotspot.
Clark SJ, Bishop PN. Clark SJ, et al. Semin Immunopathol. 2018 Jan;40(1):65-74. doi: 10.1007/s00281-017-0649-6. Epub 2017 Sep 25. Semin Immunopathol. 2018. PMID: 28948331 Free PMC article. Review.
Complement factor H in host defense and immune evasion.
Parente R, Clark SJ, Inforzato A, Day AJ. Parente R, et al. Cell Mol Life Sci. 2017 May;74(9):1605-1624. doi: 10.1007/s00018-016-2418-4. Epub 2016 Dec 10. Cell Mol Life Sci. 2017. PMID: 27942748 Free PMC article. Review.
19 results