Zobrazeno 1 - 10
of 531
pro vyhledávání: '"SVERRE HEIM"'
Autor:
Marta Brunetti, Kristin Andersen, Signe Spetalen, Andrea Lenartova, Liv Toril Nygård Osnes, Helen Vålerhaugen, Sverre Heim, Francesca Micci
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionAlterations of the NUP214 gene (9q34) are recurrent in acute leukemias. Rearrangements of chromosomal band 9q34 targeting this locus can be karyotypically distinct, for example t(6;9)(p22;q34)/DEK::NUP214, or cryptic, in which case no vis
Externí odkaz:
https://doaj.org/article/6e54dab0855646e29369ccaf4222b21f
Autor:
Marine Jeanmougin, Annette B. Håvik, Lina Cekaite, Petter Brandal, Anita Sveen, Torstein R. Meling, Trude H. Ågesen, David Scheie, Sverre Heim, Ragnhild A. Lothe, Guro E. Lind
Publikováno v:
Molecular Oncology, Vol 14, Iss 5, Pp 1016-1027 (2020)
Glioblastoma (GBM), the most aggressive form of brain cancer, is characterized by a high level of molecular heterogeneity, and infiltration by various immune and stromal cell populations. Important advances have been made in deciphering the microenvi
Externí odkaz:
https://doaj.org/article/50f176e97628490093af05af0a6840dd
Autor:
Ioannis Panagopoulos, Marta Brunetti, Margrethe Stoltenberg, Rønnaug A. U. Strandabø, Julie Staurseth, Kristin Andersen, Ilyá Kostolomov, Tarjei S. Hveem, Susanne Lorenz, Tove Anita Nystad, Trond Flægstad, Francesca Micci, Sverre Heim
Publikováno v:
Experimental Hematology & Oncology, Vol 8, Iss 1, Pp 1-8 (2019)
Abstract Background Many cases of acute lymphoblastic leukemia (ALL) carry visible acquired chromosomal changes of pathogenetic, diagnostic, and prognostic importance. Nevertheless, from one-fourth to half of newly diagnosed ALL patients have no visi
Externí odkaz:
https://doaj.org/article/13b4b065f7d140f5873cb80ec0e7758d
Autor:
Ioannis Panagopoulos, Ludmila Gorunova, Hege Kilen Andersen, Astrid Bergrem, Anders Dahm, Kristin Andersen, Francesca Micci, Sverre Heim
Publikováno v:
Experimental Hematology & Oncology, Vol 7, Iss 1, Pp 1-7 (2018)
Abstract Background Acquired primary chromosomal changes in cancer are sometimes found as sole karyotypic abnormalities. They are specifically associated with particular types of neoplasia, essential in establishing the neoplasm, and they often lead
Externí odkaz:
https://doaj.org/article/8d5d0c31fd764089b4c8ed35d9bbe187
Autor:
Marianne Lislerud Smebye, Antonio Agostini, Bjarne Johannessen, Jim Thorsen, Ben Davidson, Claes Göran Tropé, Sverre Heim, Rolf Inge Skotheim, Francesca Micci
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-10 (2017)
Abstract Background A fusion gene is a hybrid gene consisting of parts from two previously independent genes. Chromosomal rearrangements leading to gene breakage are frequent in high-grade serous ovarian carcinomas and have been reported as a common
Externí odkaz:
https://doaj.org/article/87dbcd2ce34d4b30af8c842afc00eb0a
Autor:
Ioannis Panagopoulos, Ludmila Gorunova, Eva-Marie Jacobsen, Kristin Andersen, Francesca Micci, Sverre Heim
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0196181 (2018)
Leukemic cells often carry chromosome aberrations which generate chimeric genes of pathogenetic, diagnostic, and prognostic importance. New rearrangements giving rise to novel fusion genes define hitherto unrecognized genetic leukemia subgroups. G-ba
Externí odkaz:
https://doaj.org/article/b19cc9729f3643218e176b4e62f1c8f3
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124288 (2015)
Retroperitoneal leiomyoma is a rare benign smooth muscle tumor almost exclusively found in women and with histopathological features similar to uterine leiomyomas. The pathogenesis of retroperitoneal leiomyoma is unclear and next to nothing is known
Externí odkaz:
https://doaj.org/article/b62805e8a22d462c9cc2639e9b8ff15e
Publikováno v:
PLoS ONE, Vol 10, Iss 1, p e0117010 (2015)
Retroperitoneal leiomyoma is a rare type of benign smooth muscle tumor almost exclusively found in women and with histopathological features similar to uterine leiomyomas. The pathogenesis of retroperitoneal leiomyoma is unclear and next to nothing i
Externí odkaz:
https://doaj.org/article/a7321b72fc7441c1b96b975056c19f4a
Autor:
Synne Torkildsen, Ludmila Gorunova, Klaus Beiske, Geir E Tjønnfjord, Sverre Heim, Ioannis Panagopoulos
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132736 (2015)
RNA-sequencing of a case of acute myeloid leukemia with the bone marrow karyotype 46,XY,t(2;14)(q22;q32)[5]/47,XY,idem,+?4,del(6)(q13q21)[cp6]/46,XY[4] showed that the t(2;14) generated a ZEB2-BCL11B chimera in which exon 2 of ZEB2 (nucleotide 595 in
Externí odkaz:
https://doaj.org/article/2713518e0f46434c93783ca957b1f4f6
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 6, Iss 5, Pp 578-583 (2004)
Tenosynovial giant cell tumor (TSGCT) is a disease of disputed etiology and pathogenesis. Some investigations indicate a neoplastic origin of the tumors; others indicate that they are polyclonal and inflammatory. The cytogenetic and molecular genetic
Externí odkaz:
https://doaj.org/article/a3a69f53db6d4828bdce9dc6e95ffb72