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KLK5 gene

Known as: SCTE, KALLIKREIN-RELATED PEPTIDASE 5, KALLIKREIN 5 
 
National Institutes of Health

Papers overview

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Review
2013
Review
2013
Netherton syndrome (NS) is a rare autosomal recessive skin disease with severe skin inflammation and scaling, a specific hair… Expand
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Highly Cited
2009
Highly Cited
2009
A previously unreported Kazal-type serine protease inhibitor, serine protease inhibitor Kazal type 9 (SPINK9), was identified in… Expand
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Highly Cited
2008
Highly Cited
2008
Proteinase-activated receptor-2 (PAR2) is a seven transmembrane spanning, G-protein-coupled receptor, present on the membrane of… Expand
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Highly Cited
2007
Highly Cited
2007
Acne rosacea is an inflammatory skin disease that affects 3% of the US population over 30 years of age and is characterized by… Expand
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Highly Cited
2007
Highly Cited
2007
LEKTI is a 15-domain serine proteinase inhibitor whose defective expression underlies the severe autosomal recessive… Expand
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Highly Cited
2007
Highly Cited
2007
Desquamation of the stratum corneum is a serine protease-dependent process. Two members of the human tissue kallikrein (KLK… Expand
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Highly Cited
2007
Highly Cited
2007
Abstract:  Human tissue kallikreins are a family of 15 trypsin‐ or chymotrypsin‐like secreted serine proteases (KLK1–KLK15). Many… Expand
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Highly Cited
2005
Highly Cited
2005
Lympho-epithelial Kazal-type-related inhibitor (LEKTI) is a putative serine protease inhibitor encoded by serine protease… Expand
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Highly Cited
2004
Highly Cited
2004
Corneodesmosin (CDSN), desmoglein 1 (DSG1), and desmocollin 1 (DSC1) are adhesive proteins of the extracellular part of the… Expand
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Highly Cited
2001
Highly Cited
2001
Kallikrein gene 5 (KLK5, also known as KLK-L2), located on chromosome 19q13.4, is one of the newly identified members of the… Expand
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