Colocalization of Cystatin M/E and its Target Proteases Suggests a Role in Terminal Differentiation of Human Hair Follicle and Nail

Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome

Stéphane Chavanas, Christine Bodemer, Ariane Rochat et al. · Nature Genetics · 2000 · 845 citations

Life Sciences, Genetics, Molecular Genetics +7

Degradation of Corneodesmosome Proteins by Two Serine Proteases of the Kallikrein Family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7

Cécile Caubet, Nathalie Jonca, Maria Brattsand et al. · Journal of Investigative Dermatology · 2004 · 509 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +14

Cathepsin L deficiency as molecular defect of <i>furless:</i> hyperproliferation of keratinocytes and pertubation of hair follicle cycling

Wera Roth, Jan M. Deussing, Vladimir A. Botchkarev et al. · The FASEB Journal · 2000 · 309 citations

Medicine, Dermatology, Molecular Biology +17

Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C

Thomas C. Hart · Journal of Medical Genetics · 2000 · 227 citations · Full text

Medicine, Dermatology, Molecular Genetics +14

Human Cathepsin V Functional Expression, Tissue Distribution, Electrostatic Surface Potential, Enzymatic Characterization, and Chromosomal Localization

Dieter Brömme, Zhenqiang Li, Michel Barnes et al. · Biochemistry · 1999 · 219 citations

Life Sciences, Biochemistry, Molecular Biology +17