About: José-Alain Sahel

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie)
Life Event	http://www.idref.fr/074683284/birth
preferred label	Sahel, José-Alain (1955-.... ; professeur en ophtalmologie)
name	José-Alain Sahel
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000077169606
Given name	José-Alain
familyName	Sahel
has biographical i...tion (Deprecated)	Médecin ophtalmologiste, universitaire et créateur d'entreprise français. - Membre de l'Académie des Sciences, lauréat de la médaille de l'innovation du CNRS 2012 Professeur au Collège de France (2015-2016) du cours : \"Rapprocher les regards\" dans le cadre de la chaire annuelle \"Innovation technologique Liliane Bettencourt\"
gender	male
ORCID iD	0000-0002-4831-1153
is sameAs of	Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie) Sahel, José-Alain (1955-.... ; professeur en ophtalmologie)
is Thesis advisor of	http://www.sudoc.fr/181562618/id http://www.sudoc.fr/040942686/id http://www.sudoc.fr/043134610/id http://www.sudoc.fr/043228364/id http://www.sudoc.fr/204688507/id http://www.sudoc.fr/043291023/id http://www.sudoc.fr/082550417/id http://www.sudoc.fr/043352006/id http://www.sudoc.fr/098532928/id http://www.sudoc.fr/074685163/id http://www.sudoc.fr/257945229/id http://www.sudoc.fr/249457849/id http://www.sudoc.fr/280002599/id
is Praeses of	http://www.sudoc.fr/190901160/id http://www.sudoc.fr/196905613/id
is Author of	http://www.sudoc.fr/119994739/id http://www.sudoc.fr/146843762/id http://www.sudoc.fr/061410977/id http://www.sudoc.fr/188480056/id http://www.sudoc.fr/195599152/id http://www.sudoc.fr/195628942/id http://www.sudoc.fr/227155467/id IL-1β induces rod degeneration through the disruption of retinal glutamate homeostasis Taurine deficiency damages retinal neurones: cone photoreceptors and retinal ganglion cells A New Method for Visualizing Drusen and Their Progression in Flood-Illumination Adaptive Optics Ophthalmoscopy Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 gene mRNA trans -splicing in gene therapy for genetic diseases Towards optogenetic vision restoration with high resolution Partial recovery of visual function in a blind patient after optogenetic therapy Spatiotemporal response of rat visual cortex during moving stimuli using Functional Ultrasound (fUS) Imaging http://www.sudoc.fr/233285296/id LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans -Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa Early and late stage gene therapy interventions for inherited retinal degenerations Vision Restoration by Optogenetic Therapy and Developments Toward Sonogenetic Therapy PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT Quality versus quantity: assessing individual research performance. http://hub.abes.fr/edp/periodical/medsci/2010/volume_26/issue_3/medsci2010263p241/w AAV-mediated gene therapy in Dystrophin-Dp71 deficient mouse leads to blood-retinal barrier restoration and oedema reabsorption Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision Identification of an Alternative Splicing Product of the Otx2 Gene Expressed in the Neural Retina and Retinal Pigmented Epithelial Cells Pulsatile microvascular blood flow imaging by short-time Fourier transform analysis of ultrafast laser holographic interferometry Foxg1-Cre Mediated Lrp2 Inactivation in the Developing Mouse Neural Retina, Ciliary and Retinal Pigment Epithelia Models Congenital High Myopia Apolipoprotein E promotes subretinal mononuclear phagocyte survival and chronic inflammation in age-related macular degeneration Mo-derived perivascular macrophage recruitment protects against endothelial cell death in retinal vein occlusion MERTK mutation update in inherited retinal diseases Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study The development of white matter structural changes during the process of deterioration of the visual field The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte Elimination Hypoxia Inhibits Subretinal Inflammation Resolution Thrombospondin-1 Dependently https://archive-ouverte.unige.ch/unige:1451#id Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndrome Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy Is indocyanine green angiography useful for the diagnosis of macular telangiectasia type 2? Functional ultrasound imaging of deep visual cortex in awake nonhuman primates Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patients Relative Frequencies of Inherited Retinal Dystrophies and Optic Neuropathies in Southern France: Assessment of 21-year Data Management Prevalence of ABCA4 Deep-Intronic Variants and Related Phenotype in An Unsolved “One-Hit” Cohort with Stargardt Disease A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family. Near-infrared fundus autofluorescence alterations correlate with swept-source optical coherence tomography angiography findings in patients with retinitis pigmentosa Carotenoid composition and conformation in retinal oil droplets of the domestic chicken Foveal Shape and Structure in a Normal Population Rod-derived cone viability factor for treating blinding diseases: from clinic to redox signaling. ℮-conome: an automated tissue counting platform of cone photoreceptors for rodent models of retinitis pigmentosa. http://journals.openedition.org/lettre-cdf/3199#id https://serval.unil.ch/notice/serval:BIB_E9379337ECE2#id

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