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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… Expand
National Institutes of Health

Papers overview

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Review
2015
Review
2015
Olmsted syndrome (OS) is a rare genodermatosis classically characterized by the combination of bilateral mutilating transgredient… Expand
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Review
2014
Review
2014
Palmoplantar keratodermas (PPK) comprise a heterogeneous group of keratinization disorders with hyperkeratotic thickening of… Expand
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2013
2013
Phacomatosis pigmentokeratotica (PPK) is a rare epidermal nevus syndrome characterized by the co-occurrence of a sebaceous nevus… Expand
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2008
2008
Liquefaction of human semen involves proteolytic degradation of the seminal coagulum and release of motile spermatozoa. Several… Expand
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2005
2005
We describe a large inbred Sicilian family that includes four 46, XX (SRY-) brothers. Palmoplantar hyperkeratosis (PPK) and an… Expand
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Highly Cited
2002
Highly Cited
2002
Synthesis of inorganic polyphosphate (poly P) from the terminal phosphate of ATP is catalyzed reversibly by poly P kinase (PPK… Expand
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1997
1997
The Papillon-Lefèvre and Haim Munk syndromes are characterized by the presence of both palmoplantar hyperkeratosis (PPK) and… Expand
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1996
1996
Focal non-epidermolytic palmoplantar keratoderma (PPK or palmoplantar ectodermal dysplasia type III) is associated with… Expand
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1994
1994
Mutations in keratin 9 have been found in families with an epidermolytic form of palmar-plantar keratoderma (PPK). In another… Expand
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1993
1993
Polyphosphate kinase (PPK) catalyzes the formation of polyphosphate (polyP). The PPK-encoding gene (ppk) has been cloned from… Expand
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