Functional characterization of all‐trans retinoic acid‐induced differentiation factor (ATRAID)

por Mehrasa, Roya, Cristea, Ileana, Bredrup, Cecilie, Rødahl, Eyvind, Bruland, Ove
Publicado 2023

Haplotype Analysis of Norwegian and Swedish Patients with Acute Intermittent Porphyria (AIP): Extreme Haplotype Heterogeneity for the Mutation R116W

por Tjensvoll, Kjersti, Bruland, Ove, Floderus, Ylva, Skadberg, Øyvind, Sandberg, Sverre, Apold, Jaran
Publicado 2003

S100A14 Interacts with S100A16 and Regulates Its Expression in Human Cancer Cells

por Sapkota, Dipak, Costea, Daniela Elena, Ibrahim, Salah O., Johannessen, Anne C., Bruland, Ove
Publicado 2013

Gamma Knife Radiosurgery does not alter the copy number aberration profile in sporadic vestibular schwannoma

por Håvik, Aril Løge, Bruland, Ove, Dhayalan, Dhanushan, Lund-Johansen, Morten, Knappskog, Per-Morten
Publicado 2020

Corneal Vascularization Associated With a Novel PDGFRB Variant

por Gladkauskas, Titas, Bruland, Ove, Abu Safieh, Leen, Edward, Deepak P., Rødahl, Eyvind, Bredrup, Cecilie
Publicado 2023

Adenoviral Mediated Expression of BMP2 by Bone Marrow Stromal Cells Cultured in 3D Copolymer Scaffolds Enhances Bone Formation

por Sharma, Sunita, Sapkota, Dipak, Xue, Ying, Sun, Yang, Finne-Wistrand, Anna, Bruland, Ove, Mustafa, Kamal
Publicado 2016

The SH3PXD2A-HTRA1 fusion transcript is extremely rare in Norwegian sporadic vestibular schwannoma patients

por Taule-Sivertsen, Peter, Bruland, Ove, Håvik, Aril Løge, Bratland, Eirik, Lund-Johansen, Morten, Knappskog, Per Morten
Publicado 2021

Serum BAFF and APRIL Levels, T-Lymphocyte Subsets, and Immunoglobulins after B-Cell Depletion Using the Monoclonal Anti-CD20 Antibody Rituximab in Myalgic Encephalopathy/Chronic Fa...

por Lunde, Sigrid, Kristoffersen, Einar K., Sapkota, Dipak, Risa, Kristin, Dahl, Olav, Bruland, Ove, Mella, Olav, Fluge, Øystein
Publicado 2016

S100A16 promotes differentiation and contributes to a less aggressive tumor phenotype in oral squamous cell carcinoma

por Sapkota, Dipak, Bruland, Ove, Parajuli, Himalaya, Osman, Tarig A., Teh, Muy-Teck, Johannessen, Anne C., Costea, Daniela Elena
Publicado 2015

Inverse correlation between PDGFC expression and lymphocyte infiltration in human papillary thyroid carcinomas

por Bruland, Ove, Fluge, Øystein, Akslen, Lars A, Eiken, Hans G, Lillehaug, Johan R, Varhaug, Jan E, Knappskog, Per M
Publicado 2009

Evidence for anticipation in Beckwith–Wiedemann syndrome

por Berland, Siren, Appelbäck, Mia, Bruland, Ove, Beygo, Jasmin, Buiting, Karin, Mackay, Deborah J G, Karen Temple, I, Houge, Gunnar
Publicado 2013

Genetic alterations associated with malignant transformation of sporadic vestibular schwannoma

por Håvik, Aril Løge, Bruland, Ove, Miletic, Hrvoje, Poulsgaard, Lars, Scheie, David, Fugleholm, Kåre, Lund-Johansen, Morten, Knappskog, Per-Morten
Publicado 2021

Activity monitoring and patient-reported outcome measures in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients

por Rekeland, Ingrid G., Sørland, Kari, Bruland, Ove, Risa, Kristin, Alme, Kine, Dahl, Olav, Tronstad, Karl J., Mella, Olav, Fluge, Øystein
Publicado 2022

Xeno-free generation of human induced pluripotent stem cells from donor-matched fibroblasts isolated from dermal and oral tissues

por Ali, Hassan R. W., Suliman, Salwa, Osman, Tarig Al-Hadi, Carrasco, Manuel, Bruland, Ove, Costea, Daniela-Elena, Ræder, Helge, Mustafa, Kamal
Publicado 2023

Benefit from B-Lymphocyte Depletion Using the Anti-CD20 Antibody Rituximab in Chronic Fatigue Syndrome. A Double-Blind and Placebo-Controlled Study

por Fluge, Øystein, Bruland, Ove, Risa, Kristin, Storstein, Anette, Kristoffersen, Einar K., Sapkota, Dipak, Næss, Halvor, Dahl, Olav, Nyland, Harald, Mella, Olav
Publicado 2011

B-Lymphocyte Depletion in Myalgic Encephalopathy/ Chronic Fatigue Syndrome. An Open-Label Phase II Study with Rituximab Maintenance Treatment

por Fluge, Øystein, Risa, Kristin, Lunde, Sigrid, Alme, Kine, Rekeland, Ingrid Gurvin, Sapkota, Dipak, Kristoffersen, Einar Kleboe, Sørland, Kari, Bruland, Ove, Dahl, Olav, Mella, Olav
Publicado 2015

GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies

por Haugarvoll, Kristoffer, Johansson, Stefan, Rodriguez, Carlos E., Boman, Helge, Haukanes, Bjørn Ivar, Bruland, Ove, Roque, Francisco, Jonassen, Inge, Blomqvist, Maria, Telstad, Wenche, Månsson, Jan-Eric, Knappskog, Per Morten, Bindoff, Laurence A.
Publicado 2017

Temperature-dependent autoactivation associated with clinical variability of PDGFRB Asn666 substitutions

por Bredrup, Cecilie, Cristea, Ileana, Safieh, Leen Abu, Di Maria, Emilio, Gjertsen, Bjørn Tore, Tveit, Kåre Steinar, Thu, Frode, Bull, Nils, Edward, Deepak P, Hennekam, Raoul C M, Høvding, Gunnar, Haugen, Olav H, Houge, Gunnar, Rødahl, Eyvind, Bruland, Ove
Publicado 2021

STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

por Heimdal, Ketil, Sanchez-Guixé, Monica, Aukrust, Ingvild, Bollerslev, Jens, Bruland, Ove, Jablonski, Greg Eigner, Erichsen, Anne Kjersti, Gude, Einar, Koht, Jeanette A, Erdal, Sigrid, Fiskerstrand, Torunn, Haukanes, Bjørn Ivar, Boman, Helge, Bjørkhaug, Lise, Tallaksen, Chantal ME, Knappskog, Per M, Johansson, Stefan
Publicado 2014