Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Evgeniya, Petrova"'
Autor:
Evgeniya Petrova, Jesús María López-Gay, Matthias Fahrner, Florent Leturcq, Jean-Pierre de Villartay, Claire Barbieux, Patrick Gonschorek, Lam C. Tsoi, Johann E. Gudjonsson, Oliver Schilling, Alain Hovnanian
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-24 (2024)
Abstract Netherton syndrome (NS) is a rare skin disease caused by loss-of-function mutations in the serine peptidase inhibitor Kazal type 5 (SPINK5) gene. Disease severity and the lack of efficacious treatments call for a better understanding of NS m
Externí odkaz:
https://doaj.org/article/a4b9cbf4d219401da0ec2c2e31fec3de
Autor:
Evgeniya Petrova, Varvara Preter
Publikováno v:
Antropologicheskij forum. 18:11-36
The article analyzes the phenomenon that we call the “last Soviet TV viewers” in the Russian rural areas. This is the generation of people over 50 years old who were the first for whom television became the primary medium from a young age, and wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::547a619c847ab98dcf2e0271330d4f56
https://doi.org/10.31250/1815-8870-2022-18-54-11-36
https://doi.org/10.31250/1815-8870-2022-18-54-11-36
Publikováno v:
Viruses, Vol 11, Iss 1, p 68 (2019)
Flaviviruses, such as dengue (DENV), West Nile (WNV), yellow fever (YFV) and Zika (ZIKV) viruses, are mosquito-borne pathogens that present a major risk to global public health. To identify host factors that promote flavivirus replication, we perform
Externí odkaz:
https://doaj.org/article/dce8601e38274394a2e3d75c912986b8
Autor:
Alain Hovnanian, Evgeniya Petrova
Publikováno v:
Expert Opinion on Orphan Drugs. 8:455-487
Introduction: Netherton syndrome (NS) is a rare and severe ichthyosis characterized by superficial scaling, skin inflammation, a specific hair shaft defect, severe atopic manifestations and multisy...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::963b590104f8d2d959a1db7dbe2538b5
https://doi.org/10.1080/21678707.2020.1857724
https://doi.org/10.1080/21678707.2020.1857724
The content of heavy metals in the bottom sediments of the Uglovoy Bay (Peter the Great Gulf, Sea of Japan) was studied based on the surveys carried out in 2016-2021. The contamination of sediments in the bay was compared to the background concentrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c2b83ab53ceab759019d4bc6b5f6b8a
https://doi.org/10.21203/rs.3.rs-1452427/v1
https://doi.org/10.21203/rs.3.rs-1452427/v1
Publikováno v:
Zhurnal Sotsiologii i Sotsialnoy Antropologii (The Journal of Sociology and Social Anthropology).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f054ca3506b49c056329264d84c442a8
https://doi.org/10.31119/jssa.2022.25.1.4
https://doi.org/10.31119/jssa.2022.25.1.4
Publikováno v:
Disease Models & Mechanisms, Vol 5, Iss 4, Pp 553-561 (2012)
SUMMARY Skin papillomas arise as a result of clonal expansion of mutant cells. It has been proposed that the expansion of pretumoral cell clones is propelled not only by the increased proliferation capacity of mutant cells, but also by active cell se
Externí odkaz:
https://doaj.org/article/1f905455328f49769aff5bbd4daa3502
Autor:
Claire, Barbieux, Mathilde, Bonnet des Claustres, Matthias, Fahrner, Evgeniya, Petrova, Lam C, Tsoi, Olivier, Gouin, Florent, Leturcq, Pascale, Nicaise-Roland, Christine, Bole, Vivien, Béziat, Emmanuelle, Bourrat, Oliver, Schilling, Johann E, Gudjonsson, Alain, Hovnanian
Publikováno v:
The Journal of allergy and clinical immunology. 149(4)
Netherton syndrome (NS) is a rare recessive skin disorder caused by loss-of-function mutations in SPINK5 encoding the protease inhibitor LEKTI (lymphoepithelial Kazal-type-related inhibitor). NS patients experience severe skin barrier defects, displa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6aabf5442347f0f44167283c2f1f650
https://pubmed.ncbi.nlm.nih.gov/35218769
https://pubmed.ncbi.nlm.nih.gov/35218769
Autor:
Lucian Beer, Polina Kalinina, Adelheid Elbe-Bürger, Alain Hovnanian, Vera Vorstandlechner, Michael Mildner, Erwin Tschachler, Barbara Sterniczky, Leopold Eckhart, Dagmar Födinger, Barbara Lengauer, Maria Laggner, Evgeniya Petrova, Bahar Golabi, Maria Buchberger, Manuela Hiess
Publikováno v:
The Journal of investigative dermatology. 141(5)
WFDC proteins such as peptidase inhibitor 3 and SLPI inhibit proteases in the epidermis and other tissues. In this study, we tested the hypothesis that further WFDC protein family members might contribute to epidermal homeostasis. We found that in ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67528d803e1bc1510a3c9510ec1334c2
https://pubmed.ncbi.nlm.nih.gov/33157095
https://pubmed.ncbi.nlm.nih.gov/33157095