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KRT16 gene

Known as: keratin 16, NEPPK, KERATIN 16, TYPE I 
This gene plays a role in the formation of both skin and hair.
National Institutes of Health

Papers overview

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2019
2019
La paquioniquia congenita forma parte de un grupo heterogeneo de  enfermedades geneticas caracterizadas por alteraciones en el… 
2017
2017
239430_at IGFL1 IGF-like family member 1 chr19q13.32 231033_at . . . Full-length insert cDNA clone YI40A07 . . . 1559607_s_at… 
2017
2017
Introduction Pachyonychia Congenital is a rare, but well-characterized autosomal dominant disorder of keratinization… 
2016
2016
Importance: This post-marketing surveillance study was conducted to evaluate real-world information about the efficacy and… 
2014
2014
Pachyonychia congenital (PC), consist of a group of rare autosomal-dominant ectodermal disorders. Symmetrically thickened… 
2013
2013
OBJECTIVE To investigate the expression of KRT16 in laryngeal squamous cell carcinoma(LSCC) and their relationship with… 
2005
2005
Objective To detect the polymorphisms of the KRT6A and KRT16 genes in two Chinese families with pachyonychia congenita type I… 
2004
2004
Tylosis (focal non-epidermolytic palmoplantar keratoderma) is associated with the early onset of squamous cell oesophageal cancer…