Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Janes Efing"'
Autor:
Barnabas Irmer, Janes Efing, Lea Elisabeth Reitnauer, Allegra Angenendt, Saskia Heinrichs, Antonia Schubert, Matthias Schulz, Claudia Binder, Joke Tio, Uwe Hansen, Christiane Geyer, Mirjam Gerwing, Annalen Bleckmann, Kerstin Menck
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-19 (2023)
Abstract Background Extracellular vesicles (EVs) harbor a plethora of different biomolecules, which they can transport across cells. In cancer, tumor-derived EVs thereby support the creation of a favorable tumor microenvironment. So far, EV uptake an
Externí odkaz:
https://doaj.org/article/2d48326b02b54a75a3384e4a27350f60
Autor:
Nourhan Hassan, Nico Bückreiß, Janes Efing, Marie Schulz-Fincke, Philipp König, Burkhard Greve, Gerd Bendas, Martin Götte
Publikováno v:
Cells, Vol 12, Iss 6, p 910 (2023)
Syndecan-1 (Sdc-1) upregulation is associated with poor prognosis in breast cancer. Sdc-1 knockdown results in reduced angiogenesis and the dysregulation of tissue factor (TF) pathway constituents. Here, we evaluate the regulatory mechanisms and func
Externí odkaz:
https://doaj.org/article/dcd1ba93aa3845a7ac7ca753d5f42768
Autor:
A. Katharina Kolonko, Janes Efing, Yadira González-Espinosa, Nadine Bangel-Ruland, Willy van Driessche, Francisco M. Goycoolea, Wolf-Michael Weber
Publikováno v:
Biomedicines, Vol 8, Iss 9, p 364 (2020)
Cystic fibrosis (CF), a lethal hereditary disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene coding for an epithelial chloride channel, is characterized by an imbalanced homeostasis of ion and water tra
Externí odkaz:
https://doaj.org/article/6c6698f1e0da44bc8224dbc7b87138ce
Publikováno v:
Cancers. 15:1524
Historically, the only focus on tissue factor (TF) in clinical pathophysiology has been on its function as the initiation of the extrinsic coagulation cascade. This obsolete vessel-wall TF dogma is now being challenged by the findings that TF circula
Autor:
Janes Efing, Francisco M. Goycoolea, Nadine Bangel-Ruland, Willy Van Driessche, Yadira González-Espinosa, A Katharina Kolonko, Wolf-Michael Weber
Publikováno v:
Biomedicines, Vol 8, Iss 364, p 364 (2020)
Biomedicines
Volume 8
Issue 9
Biomedicines
Volume 8
Issue 9
Cystic fibrosis (CF), a lethal hereditary disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene coding for an epithelial chloride channel, is characterized by an imbalanced homeostasis of ion and water tra