Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Frida, Abel"'
Autor:
Sinan Karakaya, Lisa Gunnesson, Erik Elias, Paula Martos-Salvo, Mercedes Robledo, Ola Nilsson, Bo Wängberg, Frida Abel, Sven Påhlman, Andreas Muth, Sofie Mohlin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare neuroendocrine tumors. PGLs can further be divided into sympathetic (sPGLs) and head-and-neck (HN-PGLs). There are virtually no treatment options, and no cure, for metastatic PCCs a
Externí odkaz:
https://doaj.org/article/bab3867431174edda96dfadd196f72e5
Autor:
Tajana Tešan Tomić, Josefin Olausson, Anna Rehammar, Lily Deland, Andreas Muth, Katarina Ejeskär, Staffan Nilsson, Erik Kristiansson, Ola Nilsson Wassén, Frida Abel
Publikováno v:
PLoS Genetics, Vol 16, Iss 6, p e1008803 (2020)
Identification of additional cancer-associated genes and secondary mutations driving the metastatic progression in pheochromocytoma and paraganglioma (PPGL) is important for subtyping, and may provide optimization of therapeutic regimens. We recently
Externí odkaz:
https://doaj.org/article/a6a4615944944cec979301003fb01ffb
Autor:
Tajana Tešan Tomić, Josefin Olausson, Annica Wilzén, Magnus Sabel, Katarina Truvé, Helene Sjögren, Sándor Dósa, Magnus Tisell, Birgitta Lannering, Fredrik Enlund, Tommy Martinsson, Pierre Åman, Frida Abel
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0175638 (2017)
Pilocytic astrocytoma (PA) is the most common pediatric brain tumor. A recurrent feature of PA is deregulation of the mitogen activated protein kinase (MAPK) pathway most often through KIAA1549-BRAF fusion, but also by other BRAF- or RAF1-gene fusion
Externí odkaz:
https://doaj.org/article/602d8a80ec34443192a88cb2a6baca18
Autor:
Tajana Tešan Tomić, Josefin Olausson, Annica Wilzén, Magnus Sabel, Katarina Truvé, Helene Sjögren, Sándor Dósa, Magnus Tisell, Birgitta Lannering, Fredrik Enlund, Tommy Martinsson, Pierre Åman, Frida Abel
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184715 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0175638.].
Externí odkaz:
https://doaj.org/article/822b4d2c56cf4b7aaffee268d1c7880d
Autor:
Lily, Deland, Simon, Keane, Thomas Olsson, Bontell, Henrik, Fagman, Helene, Sjögren, Anders E, Lind, Helena, Carén, Magnus, Tisell, Jonas A, Nilsson, Katarina, Ejeskär, Magnus, Sabel, Frida, Abel
Publikováno v:
Cancer Genomics Proteomics
Background/Aim: Although fusion genes involving the proto-oncogene receptor tyrosine kinase ROS1 are rare in pediatric glioma, targeted therapies with small inhibitors are increasingly being approved for histology-agnostic fusion-positive solid tumor
Autor:
Sinan Karakaya, Lisa Gunnesson, Erik Elias, Paula Martos Salvo, Mercedes Robledo, Ola Nilsson, Bo Wängberg, Frida Abel, Sven Påhlman, Andreas Muth, Sofie Mohlin
Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare neuroendocrine tumors. PGLs can further be divided into sympathetic (sPGLs) and head-and-neck (HN-PGLs). There are virtually no treatment options, and no cure, for metastatic PCCs and PGLs (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae887625ee735f020682679945f7ac3c
https://doi.org/10.1101/2022.05.27.493680
https://doi.org/10.1101/2022.05.27.493680
Autor:
LILY DELAND, SIMON KEANE, THOMAS OLSSON BONTELL, HENRIK FAGMAN, HELENE SJÖGREN, ANDERS E. LIND, HELENA CARÉN, MAGNUS TISELL, JONAS A. NILSSON, KATARINA EJESKÄR, MAGNUS SABEL, FRIDA ABEL
BACKGROUND/AIM: Although fusion genes involving the proto-oncogene receptor tyrosine kinase ROS1 are rare in pediatric glioma, targeted therapies with small inhibitors are increasingly being approved for histology-agnostic fusion-positive solid tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d76905c783246a995ac43a1144e0940b
http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-22033
http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-22033
Autor:
Tajana Tešan Tomić, Frida Abel, Erik Kristiansson, Anna Rehammar, Annica Wilzén, Bo Wängberg, Ola Nilsson, Andreas Muth
Publikováno v:
International Journal of Cancer. 138:2201-2211
One out of ten patients with pheochromocytoma (PCC) and paraganglioma (PGL) develop malignant disease. Today there are no reliable pathological methods to predict malignancy at the time of diagnosis. Tumors harboring mutations in the succinate dehydr
Autor:
Katarina Truvé, Frida Abel, Sándor Dósa, Tajana Tešan Tomić, Annica Wilzén, Magnus Tisell, Tommy Martinsson, Josefin Olausson, Fredrik Enlund, Helene Sjögren, Birgitta Lannering, Pierre Åman, Magnus Sabel
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184715 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0175638.].
Publikováno v:
International Journal of Oncology. 42:609-616
The phosphoinositide-3 kinase (PI3K) pathway plays a critical role in cancer cell growth and survival and has also been implicated in the development of the childhood cancer neuroblastoma. In neuroblastoma high mRNA expression of the PI3K catalytic i