Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Zuzana Ileninova"'
Autor:
Petr Kasparek, Zuzana Ileninova, Olga Zbodakova, Ivan Kanchev, Oldrich Benada, Karel Chalupsky, Maria Brattsand, Inken M Beck, Radislav Sedlacek
Publikováno v:
PLoS Genetics, Vol 13, Iss 1, p e1006566 (2017)
Netherton syndrome (NS) is a severe skin disease caused by the loss of protease inhibitor LEKTI, which leads to the dysregulation of epidermal proteases and severe skin-barrier defects. KLK5 was proposed as a major protease in NS pathology, however i
Externí odkaz:
https://doaj.org/article/bd44d971be1a4155b195a02dcfec4518
Autor:
Radka Haneckova, Zuzana Ileninova, Petr Kasparek, Irena Jenickova, Ivan Kanchev, Radislav Sedlacek
Publikováno v:
Biological chemistry. 397(12)
Netherton syndrome (NS) is caused by mutations in the SPINK5 gene. Several Spink5-deficient mouse models were generated to understand the mechanisms of NS in vivo. However, Spink5-deficiency in mice is associated with postnatal lethality that hampers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b0bf620fe068e2028e933414334bcd9
https://pubmed.ncbi.nlm.nih.gov/27543783
https://pubmed.ncbi.nlm.nih.gov/27543783
Autor:
Karel Chalupsky, Inken M. Beck, Radislav Sedlacek, Zuzana Ileninova, Ivan Kanchev, Olga Zbodakova, Oldrich Benada, Maria Brattsand, Petr Kasparek
Publikováno v:
PLoS Genetics, Vol 13, Iss 1, p e1006566 (2017)
PLoS Genetics
PLoS Genetics
Netherton syndrome (NS) is a severe skin disease caused by the loss of protease inhibitor LEKTI, which leads to the dysregulation of epidermal proteases and severe skin-barrier defects. KLK5 was proposed as a major protease in NS pathology, however i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5df2b8804f878e4c4899f20a96247b09
https://doi.org/10.1371/journal.pgen.1006566
https://doi.org/10.1371/journal.pgen.1006566