Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Jessica Furriol"'
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 10, Iss 5, Pp n/a-n/a (2024)
Abstract Angiogenesis is recognized as a hallmark of cancer, and vascular endothelial growth factor (VEGF) is a key regulator of the angiogenic process and is related to cancer progression. Anti‐VEGF therapy has been tried but with limited success
Externí odkaz:
https://doaj.org/article/94ec628e280244a78e1f2c98c912dad2
Autor:
Hassan Osman Alhassan Elsaid, Mariell Rivedal, Eleni Skandalou, Einar Svarstad, Camilla Tøndel, Even Birkeland, Øystein Eikrem, Janka Babickova, Hans-Peter Marti, Jessica Furriol
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-15 (2023)
Abstract Background Fabry disease (FD) is a rare lysosomal storage disorder caused by mutations in the GLA gene, resulting in reduced or lack of α-galactosidase A activity. This results in the accumulation of globotriaosylceramide (Gb3) and other gl
Externí odkaz:
https://doaj.org/article/4ff8c0c1e6f84277b262dad7adbc6a2e
Autor:
Anne Kipp, Hans-Peter Marti, Janka Babickova, Sigrid Nakken, Sabine Leh, Thea A. S. Halden, Trond Jenssen, Bjørn Egil Vikse, Anders Åsberg, Giulio Spagnoli, Jessica Furriol
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-15 (2023)
Abstract Background Diabetes mellitus (DM), either preexisting or developing after transplantation, remains a crucial clinical problem in kidney transplantation. To obtain insights into the molecular mechanisms underlying PTDM development and early g
Externí odkaz:
https://doaj.org/article/df15af6c0222407f83ce8558b2e5a24e
Autor:
Ole Petter Nordbø, Lea Landolt, Øystein Eikrem, Andreas Scherer, Sabine Leh, Jessica Furriol, Terje Apeland, Piotr Mydel, Hans‐Peter Marti
Publikováno v:
Physiological Reports, Vol 11, Iss 19, Pp n/a-n/a (2023)
Abstract Hypertensive nephrosclerosis (HN) and Type 2 diabetic nephropathy (T2DN) are the leading causes of chronic kidney disease (CKD). To explore shared pathogenetic mechanisms, we analyzed transcriptomes of kidney biopsies from patients with HN o
Externí odkaz:
https://doaj.org/article/f2b04b1557c248e98bfb3675c6a055b6
Autor:
Philipp Strauss, Mariell Rivedal, Andreas Scherer, Øystein Eikrem, Sigrid Nakken, Christian Beisland, Leif Bostad, Arnar Flatberg, Eleni Skandalou, Vidar Beisvåg, Jessica Furriol, Hans-Peter Marti
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Clear cell renal cell carcinoma (ccRCC) is the most common renal cancer. Identification of ccRCC likely to progress, despite an apparent low risk at the time of surgery, represents a key clinical issue. From a cohort of adult ccRCC patients
Externí odkaz:
https://doaj.org/article/4eeaf6c69c79445dafaf83fb89e0844a
Autor:
Sigrid Nakken, Øystein Eikrem, Hans-Peter Marti, Christian Beisland, Leif Bostad, Andreas Scherer, Arnar Flatberg, Vidar Beisvag, Eleni Skandalou, Jessica Furriol, Philipp Strauss
Publikováno v:
Cancer Cell International, Vol 21, Iss 1, Pp 1-12 (2021)
Abstract Background Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cancer and one of the most common cancers. While survival for localized ccRCC is good, the survival of metastatic disease is not, and thirty percent of pa
Externí odkaz:
https://doaj.org/article/833c96fba2c94c27b5517c4efa0a602b
Autor:
Hassan O.A. Elsaid, Jessica Furriol, Maria Blomqvist, Mette Diswall, Sabine Leh, Naouel Gharbi, Jan Haug Anonsen, Janka Babickova, Camilla Tøndel, Einar Svarstad, Hans-Peter Marti, Maximilian Krause
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100851- (2022)
Fabry disease (FD) is a rare genetic lysosomal storage disorder, resulting from partial or complete lack of alpha-galactosidase A (α-GAL) enzyme, leading to systemic accumulation of substrate glycosphingolipids with a broad range of tissue damage. C
Externí odkaz:
https://doaj.org/article/c08f3649e3f54978ad9b9e0bc4ebe0e1
Autor:
Øystein Eikrem, Bjørnar Lillefosse, Nicolas Delaleu, Philipp Strauss, Tarig Osman, Bjørn Egil Vikse, Hanna Debiec, Pierre Ronco, Miroslav Sekulic, Even Koch, Jessica Furriol, Sabine Maria Leh, Hans-Peter Marti
Publikováno v:
Biomedicines, Vol 11, Iss 1, p 226 (2023)
Background: Minimal change disease (MCD), a major cause of nephrotic syndrome, is usually treated by corticosteroid administration. MCD unresponsiveness to therapy and recurrences are nonetheless frequently observed, particularly in adults. To explor
Externí odkaz:
https://doaj.org/article/23790acbf08e4523a975de3dc95e9ace
Autor:
Tony J. Chen, Piotr Mydel, Małgorzata Benedyk‐Machaczka, Marta Kamińska, Urszula Kalucka, Magnus Blø, Jessica Furriol, Gro Gausdal, James Lorens, Tarig Osman, Hans‐Peter Marti
Publikováno v:
Physiological Reports, Vol 9, Iss 23, Pp n/a-n/a (2021)
Abstract AXL tyrosine kinase activation enhances cancer cell survival, migration, invasiveness, and promotes drug resistance. AXL overexpression is typically detected in a high percentage of renal cell carcinomas (RCCs) and is strongly associated wit
Externí odkaz:
https://doaj.org/article/4d5c7281b2d740ccbc2c6acd539e343d
Autor:
Hassan Osman Alhassan Elsaid, Håkon Tjeldnes, Mariell Rivedal, Camille Serre, Øystein Eikrem, Einar Svarstad, Camilla Tøndel, Hans-Peter Marti, Jessica Furriol, Janka Babickova
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 1, p 358 (2022)
Fabry disease (FD) is an X-linked inborn metabolic disorder due to partial or complete lysosomal α-galactosidase A deficiency. FD is characterized by progressive renal insufficiency and cardio- and cerebrovascular involvement. Restricted access on G
Externí odkaz:
https://doaj.org/article/a5917da9ab344f67a1061aac06dfab58