Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Martin Wölker"'
Publikováno v:
Zeitschrift für Hochschulentwicklung (2016)
Obwohl Problembasiertes Lernen inzwischen an Hochschulen praktiziert wird, spielt diese Methode in technisch ausgerichteten Studiengängen noch eine untergeordnete Rolle. Hochschulzugangsberechtigungen sind vielfältig geworden und eine heterogene St
Externí odkaz:
https://doaj.org/article/9e10757e25c34a09a3bdb7ec57211e7b
Autor:
Bedair Dewidar, Lucia Mastrototaro, Cornelia Englisch, Claudia Ress, Cesare Granata, Elisabeth Rohbeck, Dominik Pesta, Geronimo Heilmann, Martin Wolkersdorfer, Irene Esposito, Michelle Reina Do Fundo, Fariba Zivehe, Aslihan Yavas, Michael Roden
Publikováno v:
EBioMedicine, Vol 94, Iss , Pp 104714- (2023)
Summary: Background: Disturbed hepatic energy metabolism contributes to non-alcoholic fatty liver (NAFLD), but the development of changes over time and obesity- or diabetes-related mechanisms remained unclear. Methods: Two-day old male C57BL/6j mice
Externí odkaz:
https://doaj.org/article/2ea07f5ef7394e27b4129d4349050a24
Autor:
Christina Guttmann-Gruber, Josefina Piñón Hofbauer, Birgit Tockner, Victoria Reichl, Alfred Klausegger, Peter Hofbauer, Martin Wolkersdorfer, Khek-Chian Tham, Seong Soo Lim, John E. Common, Anja Diem, Katharina Ude-Schoder, Wolfgang Hitzl, Florian Lagler, Julia Reichelt, Johann W. Bauer, Roland Lang, Martin Laimer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Wound management is a critical factor when treating patients with the inherited skin fragility disease dystrophic epidermolysis bullosa (DEB). Due to genetic defects in structural proteins, skin and mucous epithelia are prone to b
Externí odkaz:
https://doaj.org/article/97b40c2da2df4214a64bb591a0e70e81
Autor:
Michael Ablinger, Thomas K. Felder, Monika Wimmer, Roland Zauner, Peter Hofbauer, Thomas Lettner, Martin Wolkersdorfer, Florian B. Lagler, Anja Diem, Johann W. Bauer, Verena Wally
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-5 (2018)
Abstract Generalized severe epidermolysis bullosa simplex (EBS-gen sev) is caused by mutations within either the KRT5 or KRT14 gene, phenotypically resulting in blistering and wounding of the skin and mucous membranes after minor mechanical friction.
Externí odkaz:
https://doaj.org/article/a16c6bdbae734703b4e43d830870d4d9