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KLKB1 wt Allele

Known as: KLK3, Kallikrein B, Plasma (Fletcher Factor) 1 wt Allele, PPK 
Human KLKB1 wild-type allele is located in the vicinity of 4q35 and is approximately 49 kb in length. This allele, which encodes plasma kallikrein… 
National Institutes of Health

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4q35Blood coagulationHydrolysisKLK3 gene

Broader (1)

KLKB1 gene

Papers overview

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2018
2018
SLURP‐1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
Mal de Meleda (MDM) is a rare inherited autosomal recessive genodermatosis characterized by palmoplantar keratoderma (PPK) with… 
2014
2014
Palmoplantar keratosis in oculodentodigital dysplasia with a GJA1 point mutation out of the C‐terminal region of connexin 43
Gap junction proteins are composed of 21 genes of the connexin (Cx) family. They play important roles in cell–cell contact by… 
2013
2013
Very low PSA concentrations and deletions of the KLK3 gene.
BACKGROUND Prostate-specific antigen (PSA), a widely used biomarker for prostate cancer (PCa), is encoded by a kallikrein gene… 
2010
2010
Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutations.
2008
2008
Major Role of Human KLK14 in Seminal Clot Liquefaction*
Liquefaction of human semen involves proteolytic degradation of the seminal coagulum and release of motile spermatozoa. Several… 
2008
2008
"Nagashima-type" keratosis as a novel entity in the palmoplantar keratoderma category.
BACKGROUND "Nagashima-type" keratosis is characterized by transgressive and nonprogressive palmoplantar keratoderma (PPK) with an… 
Highly Cited
2002
Highly Cited
2002
The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family
Dominant mutations in the GJB2 gene encoding connexin 26 (Cx26) can cause non‐syndromic hearing impairment alone or in… 
1997
1997
Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosis.
The Papillon-Lefèvre and Haim Munk syndromes are characterized by the presence of both palmoplantar hyperkeratosis (PPK) and… 
1996
1996
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).
Focal non-epidermolytic palmoplantar keratoderma (PPK or palmoplantar ectodermal dysplasia type III) is associated with… 
Highly Cited
1993
Highly Cited
1993
Cloning, sequence and characterization of the polyphosphate kinase-encoding gene (ppk) of Klebsiella aerogenes.
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