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Showing results 1-8 of 8

2023
1 Noren-Nystrom, Ulrika; Andersen, Mette K.; Barbany, Gisela; Dirse, Vaidas; Eilert-Olsen, Martine; Engvall, Marie; Harila-Saari, Arja; Heyman, Mats; Hovland, Randi; Haikio, Satu; Jonsson, Jon J.; Karhu, Ritva; Kjeldsen, Eigil; Norberg, Anna; Preiss, Birgitte S.; Pulkkinen, Kati; Quist-Paulsen, Petter; Rasanen, Hannele; Schmiegelow, Kjeld; Seitsonen, Anne; Sjogren, Helene; Tammur, Pille; Johansson, Bertil.
Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old with Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial. HemaSphere 2023 ;Volume 7.(5) p. E883-
OUS HAUKELAND STO Untitled
 
2022
2 Panagopoulos, Ioannis; Andersen, Kristin; Gorunova, Ludmila; Eilert-Olsen, Martine; Lund-Iversen, Marius; Wessel-Aas, Trygve; Lloret, Isabel; Micci, Francesca; Heim, Sverre.
Presence of a t(12;18)(q14;q21) Chromosome Translocation and Fusion of the Genes for High-mobility Group AT-Hook 2 ( HMGA2 ) and WNT Inhibitory Factor 1 ( WIF1 ) in Infrapatellar Fat Pad Cells from a Patient With Hoffas Disease. Cancer Genomics & Proteomics 2022 ;Volume 19.(5) p. 584-590
OUS Untitled
 
2021
3 Panagopoulos, Ioannis; Andersen, Kristin; Eilert-Olsen, Martine; Rognlien, Anne Gro Wesenberg; Munthe-Kaas, Monica Cheng; Micci, Francesca; Heim, Sverre.
Rare KMT2A-ELL and novel ZNF56-KMT2A fusion genes in pediatric T-cell acute lymphoblastic leukemia. Cancer Genomics & Proteomics 2021 ;Volume 18.(2) p. 121-131
UiO OUS Untitled
 
4 Panagopoulos, Ioannis; Andersen, Kristin; Eilert-Olsen, Martine; Zeller, Bernward; Munthe-Kaas, Monica Cheng; Buechner, Jochen; Osnes, Liv T. N.; Micci, Francesca; Heim, Sverre.
Therapy-induced deletion in 11q23 leading to fusion of KMT2A with ARHGEF12 and development of B lineage acute lymphoplastic leukemia in a child treated for acute myeloid leukemia caused by t(9;11)(p21;q23)/ KMT2A-MLLT3. Cancer Genomics & Proteomics 2021 ;Volume 18.(1) p. 67-81
OUS UiO Untitled
 
2019
5 Eilert-Olsen, Martine; Hjukse, Jarand Berg; Thoren, Anna; Tang, Wannan; Enger, Rune; Jensen, Vidar; Pettersen, Klas Henning; Nagelhus, Erlend Arnulf.
Astroglial endfeet exhibit distinct Ca2+ signals during hypoosmotic conditions. Glia 2019 ;Volume 67.(12) p. 2399-2409
UiO OUS Untitled
 
2012
6 Eilert-Olsen, Martine; Haj Yasein, Nadia Nabil; Vindedal, Gry Fluge; Enger, Rune; Gundersen, Georg Andreas; Hoddevik, Eystein Hellstrøm; Petersen, Petur Henry; Haug, Finn-Mogens Smejda; Skare, Øivind; Adams, Marvin E.; Froehner, Stanley C.; Burkhardt, John Michael; Thoren, Anna; Nagelhus, Erlend Arnulf.
Deletion of aquaporin-4 changes the perivascular glial protein scaffold without disrupting the brain endothelial barrier. Glia 2012 ;Volume 60.(3) p. 432-440
OUS FHI UiO UiB Untitled
 
7 Enger, Rune; Gundersen, Georg Andreas; Haj-Yasein, Nadia Nabil; Eilert-Olsen, Martine; Thoren, Anna; Vindedal, Gry Fluge; Petersen, Petur Henry; Skare, Øivind; Nedergaard, Maiken; Ottersen, Ole Petter; Nagelhus, Erlend Arnulf.
Molecular scaffolds underpinning macroglial polarization: An analysis of retinal Muller cells and brain astrocytes in mouse. Glia 2012 ;Volume 60.(12) p. 2018-2026
STAMI UiO OUS Untitled
 
2011
8 Haj Yasein, Nadia Nabil; Vindedal, Gry Fluge; Eilert-Olsen, Martine; Gundersen, Georg Andreas; Skare, Øivind; Laake, Petter; Klungland, Arne; Thoren, Anna; Burkhardt, John Michael; Ottersen, Ole Petter; Nagelhus, Erlend Arnulf.
Glial-conditional deletion of aquaporin-4 (Aqp4) reduces blood-brain water uptake and confers barrier function on perivascular astrocyte endfeet. Proceedings of the National Academy of Sciences of the United States of America 2011 ;Volume 108.(43) p. 17815-17820
UiO OUS Untitled