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OLFM3 gene

Known as: NOE3, OLFM3, OLFACTOMEDIN 3 
 
National Institutes of Health

Papers overview

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2018
2018
Malformations of cortical development (MCD) are a common cause of intractable seizures in humans. Among these, focal cortical… Expand
2017
2017
  • M. Fini
  • Investigative ophthalmology & visual science
  • 2017
  • Corpus ID: 4055021
MYOC, encoding the secreted protein myocilin, was the first gene linked to familial forms of primary open angle glaucoma (POAG… Expand
2012
2012
Three clonal subpopulations of DLKP, a poorly differentiated squamous lung carcinoma cell line, display striking differences in… Expand
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2011
2011
Myocilin, trabecular meshwork inducible glucocorticoid response, also known as MYOC, is encoded by the MYOC gene in humans. The… Expand
2011
2011
PURPOSE Olfactomedin 2 (OLFM2) belongs to the family of olfactomedin domain-containing proteins. Genetic data suggest its… Expand
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2008
2008
The elucidation of mechanisms underlying telencephalic neural development has been limited by the lack of knowledge regarding the… Expand
2007
2007
Optimedin, also known as olfactomedin 3, belongs to a family of olfactomedin domain-containing proteins. It is expressed in… Expand
2005
2005
The Optimedin gene, also known as Olfactomedin 3, encodes an olfactomedin domain-containing protein. There are two major splice… Expand
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2004
2004
PURPOSE To identify olfactomedin domain containing proteins, which are expressed in the eye and have similarity to myocilin, to… Expand
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Highly Cited
2002
Highly Cited
2002
Mutations in the MYOC gene may lead to juvenile open-angle glaucoma with high intraocular pressure, and are detected in about 4… Expand
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