Showing results (51-60 of 60) with videos related to
Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
The Journal of Clinical Investigation|October 2, 2023
Perilipin 2-positive mononuclear phagocytes accumulate in the diabetic retina and promote PPARγ-dependent vasodegenerationGuillaume Blot, Rémi Karadayi, Lauriane Przegralek, et al.EMBO Molecular Medicine|October 22, 2013
CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient miceFlorian Sennlaub, Constance Auvynet, Bertrand Calippe, et al.Journal of Neuroinflammation|January 17, 2024
Splenic monocytes drive pathogenic subretinal inflammation in age-related macular degenerationChristophe Roubeix, Caroline Nous, Sébastien Augustin, et al.Progress in Neurobiology|August 15, 2021
P2X7-deficiency improves plasticity and cognitive abilities in a mouse model of TauopathyKevin Carvalho, Elodie Martin, Aurélia Ces, et al.Human Molecular Genetics|September 13, 2013
The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large familyIsabelle Audo, Kinga Bujakowska, Elise Orhan, et al.Immunity|February 24, 2017
Complement Factor H Inhibits CD47-Mediated Resolution of InflammationBertrand Calippe, Sebastien Augustin, Fanny Beguier, et al.Cellular and Molecular Life Sciences : CMLS|July 17, 2023
Autophagy protein 5 controls flow-dependent endothelial functionsPierre Nivoit, Thomas Mathivet, Junxi Wu, et al.Immunity|August 20, 2020
The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte EliminationFanny Beguier, Michael Housset, Christophe Roubeix, et al.The Journal of Clinical Endocrinology and Metabolism|October 8, 2019
Glucagon-like Peptide 1 Receptor Agonists, Diabetic Retinopathy and Angiogenesis: The AngioSafe Type 2 Diabetes StudyBénédicte Gaborit, Jean-Baptiste Julla, Samaher Besbes, et al.American Journal of Human Genetics|November 10, 2009
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindnessIsabelle Audo, Susanne Kohl, Bart P Leroy, et al.Pageof 6