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Times Cited: 508
Times Cited: 508
Times Cited
Times Co-cited
Similarity
Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.
P M D'Cruz, D Yasumura, J Weir, M T Matthes, H Abderrahim, M M LaVail, D Vollrath. Hum Mol Genet 2000
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An RCS-like retinal dystrophy phenotype in mer knockout mice.
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Phagocytosis and clearance of apoptotic cells is mediated by MER.
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Loss of synchronized retinal phagocytosis and age-related blindness in mice lacking alphavbeta5 integrin.
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Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis.
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Mertk triggers uptake of photoreceptor outer segments during phagocytosis by cultured retinal pigment epithelial cells.
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Diurnal, localized exposure of phosphatidylserine by rod outer segment tips in wild-type but not Itgb5-/- or Mfge8-/- mouse retina.
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Differential TAM receptor-ligand-phospholipid interactions delimit differential TAM bioactivities.
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A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases.
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Understanding photoreceptor outer segment phagocytosis: use and utility of RPE cells in culture.
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Essential role for MFG-E8 as ligand for alphavbeta5 integrin in diurnal retinal phagocytosis.
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TAM receptors regulate multiple features of microglial physiology.
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The anticoagulation factor protein S and its relative, Gas6, are ligands for the Tyro 3/Axl family of receptor tyrosine kinases.
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Activated microglia in human retinitis pigmentosa, late-onset retinal degeneration, and age-related macular degeneration.
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Rod outer segment disk shedding in rat retina: relationship to cyclic lighting.
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Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa.
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10
Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS rats.
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Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
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Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration.
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7
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.