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Brain Research, ISSN 0006-8993, 11/2019, Volume 1723, pp. 146391 - 146391
Recent researches suggest that autophagic degradation declines with age, and this leads to an accumulation of damage that contributes to age-related cellular... 
Neuroprotection | Ischemic stroke | NMNAT1 | Autophagy | Index Medicus
Journal Article
Neuroscience Letters, ISSN 0304-3940, 02/2007, Volume 413, Issue 1, pp. 46 - 51
The chimeric Wld protein consisting of the N-terminal 70 amino acids of Ufd2 and the complete sequence of nicotinamide mononucleotide adenylyltransferase1... 
NAD | Nmnat1 | Axon degeneration
Journal Article
Experimental eye research, ISSN 0014-4835, 3/2013, Volume 108, pp. 76 - 83
Light-induced retinal damage (LD) occurs after surgery or sun exposure. We previously showed that zinc (Zn 2+ ) accumulated in photoreceptors and RPE cells... 
mouse | rat | sirtuin | NMNAT1
Journal Article
Journal Article
Journal Article
Molecular Neurodegeneration, 2012, Volume 7, Issue 1
Journal Article
Neuroscience Letters, ISSN 0304-3940, 2007, Volume 413, Issue 1, pp. 46 - 51
The chimeric Wld protein consisting of the N-terminal 70 amino acids of Ufd2 and the complete sequence of nicotinamide mononucleotide adenylyltransferase1... 
NAD | Nmnat1 | Axon degeneration
Journal Article
Cell Reports, ISSN 2211-1247, 09/2016, Volume 17, Issue 1, pp. 69 - 85
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 8279 - 11
Leber congenital amaurosis (LCA) is a genetically and clinically heterogeneous disease, and represents the most severe form of inherited retinal dystrophy... 
CLINICAL DEFINITION | REFINEMENT | NMNAT1 | ONSET RETINAL DYSTROPHY | RPGRIP1 GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | RECESSIVE RETINITIS-PIGMENTOSA | GENETIC-HETEROGENEITY | COHORT | MUTATIONS | Polymerase chain reaction | Copy number | Blindness | Retinal degeneration | Retina | Diagnosis | Mutation | Dystrophy
Journal Article
Journal Article
Ophthalmology, ISSN 0161-6420, 2017, Volume 124, Issue 7, pp. 992 - 1003
Journal Article