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AGBL5 gene

Known as: AGBL5, CCP5, FLJ21839 
 
National Institutes of Health

Papers overview

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2019
2019
PURPOSE To identify the accurate clinical diagnosis of rare syndromic inherited retinal diseases (IRDs) based on the combination… Expand
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2019
2019
Sperm cells are highly specialized mammalian cells, and their biogenesis requires unique intracellular structures. Perturbation… Expand
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2017
2017
Proteins may undergo a type of posttranslational modification - polyglutamylation, where a glutamate residue is enzymatically… Expand
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2016
2016
Purpose:Retinal dystrophies (RD) are heterogeneous hereditary disorders of the retina that are usually progressive in nature. The… Expand
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Review
2016
Review
2016
Purpose AGBL5, encoding ATP/GTP binding protein-like 5, was previously proposed as an autosomal recessive retinitis pigmentosa… Expand
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2015
2015
PURPOSE Retinitis pigmentosa (RP) is the most common inherited retinal disease with high genetic heterogeneity and variable… Expand
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2014
2014
My research project is focused around a specific gene—cytosolic carboxypeptidase 5 (CCP5). Previous research suggests that the… Expand
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2013
2013
Cytosolic carboxypeptidase 5 (CCP5) is a member of a subfamily of enzymes that cleave C-terminal and/or side chain amino acids… Expand
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