Zobrazeno 1 - 10
of 3 588
pro vyhledávání: '"A, Sarasin"'
Autor:
Leticia K. Lerner, Dorine Bonte, Morwenna Le Guillou, Mahwish Mian Mohammad, Zeinab Kasraian, Alain Sarasin, Emmanuelle Despras, Said Aoufouchi
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/9d02092ecc5f4325948657a53eee289a
Autor:
Andrey. A. Yurchenko, Brice Fresneau, Bruno Borghese, Fatemeh Rajabi, Zora Tata, Catherine Genestie, Alain Sarasin, Sergey I. Nikolaev
Publikováno v:
Communications Medicine, Vol 3, Iss 1, Pp 1-8 (2023)
Abstract Background Xeroderma pigmentosum (XP) is a group of rare hereditary disorders with highly increased risk of skin tumors due to defective DNA repair. Recently we reported 34-fold increased risk of internal tumors in XP patients in comparison
Externí odkaz:
https://doaj.org/article/173eb58c3ebc4c67a77cceb3fa486a2a
Autor:
Romain Betend, Laurent Suppan, Michele Chan, Simon Regard, François Sarasin, Christophe A. Fehlmann
Publikováno v:
Swiss Medical Weekly, Vol 153, Iss 12 (2023)
BACKGROUND: Clinical experience has been shown to affect many patient-related outcomes but its impact in the prehospital setting has been little studied. OBJECTIVES:To determine whether rates of discharge at scene, handover to paramedics and superv
Externí odkaz:
https://doaj.org/article/92ddd6357887458fa016ab4066353cfc
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Andrey A. Yurchenko, Fatemeh Rajabi, Tirzah Braz-Petta, Hiva Fassihi, Alan Lehmann, Chikako Nishigori, Jinxin Wang, Ismael Padioleau, Konstantin Gunbin, Leonardo Panunzi, Fanny Morice-Picard, Pierre Laplante, Caroline Robert, Patricia L. Kannouche, Carlos F. M. Menck, Alain Sarasin, Sergey I. Nikolaev
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-17 (2023)
Abstract Xeroderma pigmentosum (XP) is a genetic disorder caused by mutations in genes of the Nucleotide Excision Repair (NER) pathway (groups A-G) or in Translesion Synthesis DNA polymerase η (V). XP is associated with an increased skin cancer risk
Externí odkaz:
https://doaj.org/article/43ea5e8dbf97496ea865d7ad15fce1e5
Autor:
Matthieu Lyon, Christophe Alain Fehlmann, Marc Augsburger, Thomas Schaller, Catherine Zimmermann-Ivol, Julien Celi, Birgit Andrea Gartner, Nicolas Lorenzon, François Sarasin, Laurent Suppan
Publikováno v:
JMIR Formative Research, Vol 7, p e48057 (2023)
BackgroundCarbon monoxide (CO) poisoning is an important cause of morbidity and mortality worldwide. Symptoms are mostly aspecific, making it hard to identify, and its diagnosis is usually made through blood gas analysis. However, the bulkiness of ga
Externí odkaz:
https://doaj.org/article/02aca060eafd467c99e965017fbcae85
Autor:
P. Sarasin
Publikováno v:
Geographica Helvetica, Vol 78, Pp 131-133 (2023)
Externí odkaz:
https://doaj.org/article/7c4596979b9c4a64bc5b40c0ff67041b
Autor:
Vimolmas Tansathitaya, Witchana Sarasin, Tanapati Phakham, Vorthon Sawaswong, Prangwalai Chanchaem, Sunchai Payungporn
Publikováno v:
Journal of Pure and Applied Microbiology, Vol 16, Iss 2, Pp 1130-1137 (2022)
The microbiome, a community of microorganisms in the body, is currently used as a biomarker in many disease prognoses. Prevotella, Turicibacte, Bacteroides, Firmicutes/Bacteroidetes are frequently used as a biomarker for rheumatoid arthritis, colorec
Externí odkaz:
https://doaj.org/article/78e8713e6bef4351bbdf3c193fa25e1f
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Xeroderma pigmentosum (XP) is a rare, autosomal, recessive DNA repair-deficiency disorder with a frequency of 1–3 per million livebirths in Europe and USA but with higher frequencies in isolated islands or in countries with a hi
Externí odkaz:
https://doaj.org/article/382e0433cf2e44739c87a5359aee2590
Autor:
Goltermann, Svenja, Sarasin, Philipp
Publikováno v:
Geschichte und Gesellschaft, 2021 Jan 01. 47(1), 157-162.
Externí odkaz:
https://www.jstor.org/stable/27032377