OPTN gene

Known as: 14.7K-INTERACTING PROTEIN, GLC1E GENE, TFIIIA-INTP 
This gene plays a role in both neuroprotection and Golgi maintenance

Topic mentions per year

Topic mentions per year

1989-2018
0204019892018

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Amyotrophic Lateral Sclerosis (ALS) is the most frequent motor neuron disease in adults. Classical ALS is characterized by the… (More)
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Highly Cited
2011
Highly Cited
2011
Selective autophagy can be mediated via receptor molecules that link specific cargoes to the autophagosomal membranes decorated… (More)
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Highly Cited
2010
Highly Cited
2010
Amyotrophic lateral sclerosis (ALS) has its onset in middle age and is a progressive disorder characterized by degeneration of… (More)
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Highly Cited
2010
Highly Cited
2010
Paget's disease of bone (PDB) is a common disorder with a strong genetic component characterized by focal increases in bone… (More)
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Highly Cited
2007
Highly Cited
2007
NF-kappaB essential modulator (NEMO), the regulatory subunit of the IkappaB kinase (IKK) that activates NF-kappaB, is essential… (More)
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Highly Cited
2006
Highly Cited
2006
BACKGROUND To expand the opportunity for paired live donor kidney transplantation, computerized matching algorithms have been… (More)
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2006
2006
PURPOSE Optineurin gene (OPTN) mutations are reported in primary open angle glaucoma patients (POAG) from different populations… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND & AIMS A consensus has been reached that liver donor allocation should be based primarily on liver disease severity… (More)
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Highly Cited
2002
Highly Cited
2002
Primary open-angle glaucoma (POAG) affects 33 million individuals worldwide and is a leading cause of blindness. In a study of 54… (More)
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