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Neuroprotectin D1 upregulates Iduna expression and provides protection in cellular uncompensated oxidative stress and in experimental ischemic stroke.Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probandsMolecular mechanisms of signaling via the docosanoid neuroprotectin D1 for cellular homeostasis and neuroprotection.The phenotypic variability of HK1-associated retinal dystrophy.Diagnosis of a mild peroxisomal phenotype with next-generation sequencing.A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa.Investigating the disease association of USH2A p.C759F variant by leveraging large retinitis pigmentosa cohort data.Photoreceptor glucose metabolism determines normal retinal vascular growth.Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario.ADIPOR1 is essential for vision and its RPE expression is lost in the Mfrp mouse
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description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 12 December 2015
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa
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ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa.
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type
label
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa
@en
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa.
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prefLabel
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa
@en
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa.
@nl
P2093
P2860
P356
P1433
P1476
ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa
@en
P2093
Aiden Eblimit
Lee-Jun C Wong
Mingchu Xu
Ningna Xiao
Richard A Lewis
P2860
P304
P356
10.1002/HUMU.22940
P577
2015-12-12T00:00:00Z