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PREPL gene

Known as: KIAA0436, PREPL, PROLYL ENDOPEPTIDASE-LIKE 
National Institutes of Health

Papers overview

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2018
2018
Hypotonia-cystinuria syndrome is a very rare autosomal recessive contiguous gene deletion syndrome of PREPL and SLC3A1 at 2p21… 
2009
2009
PURPOSE In the TG-21 dosimetry protocol, for cylindrical chambers in electron beams the replacement correction factor Prepl (or… 
2009
2009
Hypotonia–cystinuria syndrome (HCS) and 2p21 deletion syndrome are two recessive contiguous gene deletion syndromes associated… 
Review
2008
Review
2008
Cystinuria type I is an autosomal recessive disorder with an exclusively renal phenotype caused by inactivating mutations in… 
2008
2008
The replacement correction factor (Prepl ) in ion chamber dosimetry accounts for the effects of the medium being replaced by the… 
2001
2001
In electron beam dosimetry with an ionization chamber, a factor that corrects for the cavity perturbation of the medium, Prepl… 
1991
1991
The tables of the mean restricted collision mass stopping power ratios for water, polystyrene and acrylic relative to air given…