A number of studies provide strong evidence that KLK5 is one of the most important serine proteases in the epidermis and is involved in processes such as desquamation, processing of antimicrobial peptides or induction of inflammatory reaction. The role of KLK5 has been deduced from in vitro experiments and thus its functions should be verified in vivo. This work aimed to develop a specific tissue targeting strategy to study the role of murine kallikreins in the epidermal compartment in vivo and to generate a transgenic model overexpressing mKlk5 in the mouse epidermis. Using the modified promoter of human involucrin, transgenic mice expressing the fluorescent marker, tdTomato, were generated in the first step. This transgenic reporter mouse...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibito...
Kallikrein-related peptidases (KLKs) constitute a highly conserved serine protease family. Based on ...
Kallikrein-related peptidases (KLKs) constitute a family of closely related serine proteases encoded...
Epidermal homeostasis, including proper turnover of keratinocytes, plays important role in the barri...
International audienceThe development of three‐dimensional models of reconstituted mouse epidermis (...
Kallikrein-related peptidases (KLKs) are a subgroup of serine proteases of undisputable importance f...
The regulatory elements of the human keratin K1 gene have been used to target expression of the v-Ha...
<p><i>In situ</i> zymography using fluorescence-quenched casein (<b>A)</b> or elastin (<b>B</b>). Sk...
To produce conditional expression of genes in the mouse epidermis we have generated transgenic mouse...
AbstractLGR5 is a known marker of embryonic and adult stem cells in several tissues. In a mouse mode...
Keratins are the major structural proteins of keratinocytes, which are the most abundant cell type i...
Mouse tissue kallikreins (Klks) are members of a large, multigene family consisting of 37 genes, 26 ...
Background: Transgenic animals have greatly enhanced our understanding of the contribution of variou...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibito...
Kallikrein-related peptidases (KLKs) constitute a highly conserved serine protease family. Based on ...
Kallikrein-related peptidases (KLKs) constitute a family of closely related serine proteases encoded...
Epidermal homeostasis, including proper turnover of keratinocytes, plays important role in the barri...
International audienceThe development of three‐dimensional models of reconstituted mouse epidermis (...
Kallikrein-related peptidases (KLKs) are a subgroup of serine proteases of undisputable importance f...
The regulatory elements of the human keratin K1 gene have been used to target expression of the v-Ha...
<p><i>In situ</i> zymography using fluorescence-quenched casein (<b>A)</b> or elastin (<b>B</b>). Sk...
To produce conditional expression of genes in the mouse epidermis we have generated transgenic mouse...
AbstractLGR5 is a known marker of embryonic and adult stem cells in several tissues. In a mouse mode...
Keratins are the major structural proteins of keratinocytes, which are the most abundant cell type i...
Mouse tissue kallikreins (Klks) are members of a large, multigene family consisting of 37 genes, 26 ...
Background: Transgenic animals have greatly enhanced our understanding of the contribution of variou...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
The analysis of keratin 6 expression is complicated by the presence of multiple isoforms that are ex...
Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibito...