Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anna Strobl"'
Autor:
Esther Schamschula, Angelika Lahnsteiner, Yassen Assenov, Wolfgang Hagmann, Nadja Zaborsky, Markus Wiederstein, Anna Strobl, Frauke Stanke, Thomas Muley, Christoph Plass, Burkhard Tümmler, Angela Risch
Publikováno v:
Epigenetics, Vol 17, Iss 8, Pp 837-860 (2022)
Cystic fibrosis (CF) is a monogenic disease, characterized by massive chronic lung inflammation. The observed variability in clinical phenotypes in monozygotic CF twins is likely associated with the extent of inflammation. This study sought to invest
Externí odkaz:
https://doaj.org/article/c7a930fa9d8f4925abc3c509791603ca
Autor:
Solange De Noon, Jannat Ijaz, Tim HH Coorens, Fernanda Amary, Hongtao Ye, Anna Strobl, Iben Lyskjær, Adrienne M Flanagan, Sam Behjati
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 7, Iss 5, Pp 425-431 (2021)
Abstract Osteosarcoma, the most common primary malignant tumour of bone, affects both children and adults. No fundamental biological differences between paediatric and adult osteosarcoma are known. Here, we apply multi‐region whole‐genome sequenc
Externí odkaz:
https://doaj.org/article/16b98de9749b4c9abdc0e03213cd875e
Autor:
Thomas Muley, Angelika Lahnsteiner, Anna Strobl, Wolfgang Hagmann, Burkhard Tümmler, Esther Schamschula, Nadja Zaborsky, Christoph Plass, Frauke Stanke, Markus Wiederstein, Yassen Assenov, Angela Risch
Publikováno v:
Epigenetics. 17:837-860
Cystic fibrosis (CF) is a monogenic disease, characterized by massive chronic lung inflammation. The observed variability in clinical phenotypes in monozygotic CF twins is likely associated with the extent of inflammation. This study sought to invest
Autor:
Esther, Schamschula, Angelika, Lahnsteiner, Yassen, Assenov, Wolfgang, Hagmann, Nadja, Zaborsky, Markus, Wiederstein, Anna, Strobl, Frauke, Stanke, Thomas, Muley, Christoph, Plass, Burkhard, Tümmler, Angela, Risch
Publikováno v:
Epigenetics. 17(8)
Cystic fibrosis (CF) is a monogenic disease, characterized by massive chronic lung inflammation. The observed variability in clinical phenotypes in monozygotic CF twins is likely associated with the extent of inflammation. This study sought to invest
Autor:
Victoria Strobl, Georg Stockmaier, Suzana Tesanovic, Florian Wolff, Wolfgang Gruber, Fritz Aberger, David Licha, Roland Reischl, Sandra Grund-Groeschke, Angela Risch, Markus Wiederstein, Christina Sternberg, Jutta Horejs-Hoeck, Dominik P. Elmer, Anna Strobl, Richard Moriggl, Hieu-Hoa Dang, Christian G. Huber
Pharmacological targeting of Hedgehog (HH)/GLI has proven effective for certain blood, brain and skin cancers including basal cell carcinoma (BCC). However, limited response rates and the development of drug resistance call for improved anti-HH thera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32448f1f2e19119eb91a0246f60b9ba
Circulating Wnt inhibitory factor 1 levels are associated with development of cardiovascular disease
Autor:
Karin Salzmann, Anna Strobl, Georg Goebel, Bernhard Iglseder, Mariya Paulweber, K Rufinatscha, Herbert Tilg, Susanne Kaser, Bernhard Paulweber, Alexander Tschoner, Gabriele Staudacher, Ludmilla Kedenko, Claudia Ress, Karin Willeit
Publikováno v:
Atherosclerosis. 273
Background and aims Wnt signaling is involved in atherosclerotic plaque formation directly and indirectly by modulating cardiovascular risk factors. We investigated whether circulating concentrations of Wnt inhibitors are associated with cardiovascul
Autor:
Josef Thalhamer, Anna Strobl, Theresa Thalhamer, Martin Steiner, Sandra Scheiblhofer, Veronika Hoepflinger, Richard Weiss
Publikováno v:
Vaccine. 35(14)
Background Methods to deliver an antigen into the skin in a painless, defined, and reproducible manner are essential for transcutaneous immunization (TCI). Here, we employed an ablative fractional infrared laser (P.L.E.A.S.E. Professional) to introdu
Autor:
Carine Bonnard, Nurten A. Akarsu, Anna Strobl, Hane Lee, Barry Merriman, Mohammad Shboul, Bruno Reversade, Hülya Kayserili, Hanan Hamamy
Publikováno v:
Differentiation. 80:S52
A novel autosomal recessive syndrome with congenital heart, blood, bone and craniofacial defects was delineated by homozygosity mapping in two inbred families. Independent disease-causing mutations were found in one of the Iroquois (IRX) transcriptio