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OLFML3 gene

Known as: OLFML3, olfactomedin like 3, HNOEL-iso 
 
National Institutes of Health

Papers overview

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2019
2019
Goniodysgenesis is a developmental abnormality of the anterior chamber of the eye. It is generally considered to be congenital in… Expand
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2019
2019
PURPOSE Canine primary closed-angle glaucoma (PCAG) is a complex disease caused by multiple genetic factors. A c.590G>A variant… Expand
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2018
2018
Microglia maturation takes place during the postnatal weeks and is characterized by the establishment of a unique microglia… Expand
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Highly Cited
2013
Highly Cited
2013
Purpose: Cancer-associated fibroblasts (CAF) are essential components of the stroma that play a critical role in cancer… Expand
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2012
2012
The Olfactomedin-like 3 (OLFML3) gene has matrix-related function involved in embryonic development. MicroRNA-155 (miR-155), 21… Expand
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2008
2008
Myocilin is a 55-57kDa secreted glycoprotein and member of the olfactomedin family, which is mutated in some forms of primary… Expand
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2007
2007
2,6-Dichlorophenyl methylsulphone and a number of structurally related chemicals are CYP-activated toxicants in the olfactory… Expand
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