Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Hanne K. Høifødt"'
Autor:
Nils, Eide, Ragnar S, Faye, Hanne K, Høifødt, Berit, Sandstad, Geir, Qvale, Rowan, Faber, Peter, Jebsen, Gunnar, Kvalheim, Øystein, Fodstad
Publikováno v:
Acta Ophthalmologica. 93:59-66
Our objective was to study survival rates with the bone marrow (BM) results in a cohort of uveal melanoma patients with long follow-up.Mononuclear cell fractions isolated from BM were examined for tumour cells using our immunomagnetic separation (IMS
Autor:
Leiv Sandvik, Peter Jebsen, Nils Eide, Øystein Fodstad, Rowan Thomas Faber, Geir A. Qvale, Hanne K. Høifødt, Gunnar Kvalheim, Ragnar S. Faye
Publikováno v:
Pathology oncology research : POR. 25(1)
Approximately 50% of uveal melanoma patients develop metastases. We want to evaluate the effect of stricter criteria on our data from our previous study correlating survival and bone marrow (BM) micrometastasis results using our immunomagnetic separa
Autor:
Peter Jebsen, Rowan Thomas Faber, B. Sandstad, Nils Eide, Geir A. Qvale, Ragnar S. Faye, Gunnar Kvalheim, Hanne K. Høifødt, Øystein Fodstad
Publikováno v:
Acta Ophthalmologica. 87:830-836
Our objective was to introduce immunomagnetic separation (IMS) in ocular research by evaluating the possibility of detecting tumour cells in bone marrow (BM) and peripheral blood (PB) samples and validating the captured cells as melanocytic cells.Mon
Autor:
Øystein Fodstad, Wolfgang Lilleby, Piet J. Boender, Ase Bratland, Anne Hansen Ree, Mengyu Wang, Jens P. Berg, Hanne K. Høifødt, Rob Ruijtenbeek, Ingrid H.G. Østensen
Publikováno v:
Clinical & Experimental Metastasis. 26:485-496
Bone metastases in prostate cancer are predominantly osteoblastic. To study regulatory mechanisms underlying the establishment of prostate cancer within an osteoblastic microenvironment, human androgen-sensitive prostate carcinoma cells (LNCaP) were
Autor:
Ragnar S. Faye, Gunhild Mari Mælandsmo, Hanne K. Høifødt, Steinar Aamdal, Elisabeth Paus, Aasmund Berner, Øystein Fodstad
Publikováno v:
Melanoma Research. 18:134-140
The aim of this study was to evaluate S100B in bone marrow (BM) plasma from malignant melanoma patients. BM aspirates and peripheral blood (PB) plasma from 56 patients and BM aspirates from 29 healthy volunteers were collected. S100B was measured usi
Publikováno v:
Clinical Cancer Research. 11:4666-4673
Bone marrow and peripheral blood samples from 60 patients with suspected bone sarcoma were examined for the presence and number of micrometastatic osteosarcoma cells by a sensitive immunomagnetic detection assay, using in parallel two osteosarcoma-as
Autor:
Linn Holstad, Øystein Fodstad, Erling Jacobsen, Steinar Aamdal, Eva Skovlund, Ragnar S. Faye, Hanne K. Høifødt
Publikováno v:
Clinical Cancer Research. 10:4134-4139
Purpose: Positive associations between the presence of micrometastatic tumor cells and disease aggressiveness have been reported in several tumor types, but the clinical implications are still not established. We wanted to test a new, sensitive immun
Autor:
Olav Engebråten, Hanne K. Høifødt, Gunhild Mari Mælandsmo, Hans Petter Gullestad, Zhenhe Suo, Steinar Aamdal, Nirma Skrbo, Øystein Fodstad, Lina Prasmickaite
Publikováno v:
Pigment Cell & Melanoma Research. 23:449-451
Department of Tumour Biology, Oslo University Hospital Radiumhospital, Oslo, Norway Department of Pathology, Oslo University Hospital Radiumhospital, Oslo, Norway Faculty Division, The Norwegian Radium Hospital, University of Oslo, Oslo, Norway Depar
Publikováno v:
Molecular Pathology. 52:68-74
AIM: The presence of malignant cells in the blood and bone marrow of patients with cancer at the time of surgery may be indicative of early relapse. In addition to their numbers, the phenotypes of the micrometastatic cells might be essential in deter
Autor:
Anne Hansen Ree, Geir Olav Hjortland, Eivind Hovig, Klaus Beiske, Leonardo A. Meza-Zepeda, Sigbjørn Smeland, Øystein Fodstad, Per Johannes Bøhler, Knut Håkon Hole, Ola Myklebost, Siri Tveito, Hanne K. Høifødt
Publikováno v:
BMC Cancer, Vol 11, Iss 1, p 455 (2011)
BMC Cancer
BMC Cancer
Background Metastatic progression due to development or enrichment of therapy-resistant tumor cells is eventually lethal. Molecular characterization of such chemotherapy resistant tumor cell clones may identify markers responsible for malignant progr