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Gerard A. Lutty

Researcher at Johns Hopkins University School of Medicine

Publications -  214
Citations -  13767

Gerard A. Lutty is an academic researcher from Johns Hopkins University School of Medicine. The author has contributed to research in topics: Retina & Retinal. The author has an hindex of 64, co-authored 211 publications receiving 12338 citations. Previous affiliations of Gerard A. Lutty include Johns Hopkins University & University of California, Davis.

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Understanding age-related macular degeneration (AMD): Relationships between the photoreceptor/retinal pigment epithelium/Bruch’s membrane/choriocapillaris complex

TL;DR: The mutualistic symbiotic relationship within the photoreceptor/RPE/BrMb/CC complex is lost in both forms of AMD, and loss of this functionally integrated relationship results in death and dysfunction of all of the components in the complex.
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Measurement of endothelial cell free radical generation: evidence for a central mechanism of free radical injury in postischemic tissues

TL;DR: In this paper, electron paramagnetic resonance measurements with the spin trap 5,5'-dimethyl-1-pyrroline-N-oxide (DMPO) demonstrate that bovine endothelial cells subjected to anoxia and reoxygenation become potent generators of superoxide and hydroxyl free radicals.
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Relationship between RPE and choriocapillaris in age-related macular degeneration.

TL;DR: The primary insult in GA appears to be at the level of the RPE, and there is an intimate relationship between retinal pigment epithelial atrophy and secondary CC degeneration.
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Enhanced expression of intracellular adhesion molecule-1 and P-selectin in the diabetic human retina and choroid.

TL;DR: It is demonstrated that ICAM-1 and P-selectin are constitutively expressed in the normal choroid and are upregulated in the choroidal vasculature in diabetes, but only IC AM-1 was up regulated in the retina of diabetic subjects.
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Choriocapillaris degeneration and related pathologic changes in human diabetic eyes.

TL;DR: The percentage of choroid with focal CCD in group 1 choroids was more than 4-fold greater than that in nondiabetic Choroids, and the presence of CCD was related to basal laminar deposits and, in some cases, to choroidal neovascularization.