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SPINK5 gene

Known as: NS, LEKTI, SPINK5 
National Institutes of Health

Papers overview

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2016
2016
A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in… 
2015
2015
A large proportion of cancer-related deaths are caused by thrombosis and general organ failure. Although the awareness of tumor… 
2014
2014
To study the relationship between the biological and morphological characteristics of oral intraepithelial neoplasms (OINs), we… 
2013
2013
textabstractNetherton syndrome (NS) is a rare autosomal recessive genodermatosis caused by SPINK-5 mutations. The SPINK-5 gene… 
Review
2013
Review
2013
Netherton syndrome (NS, OMIM 256500) is a rare autosomal recessive disorder manifesting with congenital ichthyosis, a specific… 
2011
2011
Abstract:  A balanced proteolytic activity in the epidermis is vital to maintain epidermal homoeostasis and barrier function… 
2005
2005
Background  Netherton syndrome (NS) is a severe autosomal recessive disorder characterized by ichthyosiform erythroderma, bamboo… 
Review
2002
Review
2002
Abstract Based on the isolation of a 55 amino acid peptide from human hemofiltrate, we cloned the cDNA for a novel human 15…