Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Atle Brendehaug"'
Autor:
Caroline Engen, Monica Hellesøy, Tim Grob, Adil Al Hinai, Atle Brendehaug, Line Wergeland, Siv Lise Bedringaas, Randi Hovland, Peter J. M. Valk, Bjørn T. Gjertsen
Publikováno v:
Molecular Oncology, Vol 15, Iss 9, Pp 2300-2317 (2021)
Recurrent somatic internal tandem duplications (ITD) in the FMS‐like tyrosine kinase 3 (FLT3) gene characterise approximately one third of patients with acute myeloid leukaemia (AML), and FLT3‐ITD mutation status guides risk‐adapted treatment s
Externí odkaz:
https://doaj.org/article/5c847808f7ca4069b952cc2692905f06
Autor:
Line Wergeland, Siv Lise Bedringaas, Peter J. M. Valk, Adil Al Hinai, Atle Brendehaug, Monica Hellesøy, Caroline Engen, Tim Grob, Bjørn Tore Gjertsen, Randi Hovland
Publikováno v:
Molecular Oncology, 15(9), 2300-2317. John Wiley & Sons Ltd.
Molecular Oncology
Molecular Oncology, Vol 15, Iss 9, Pp 2300-2317 (2021)
Molecular Oncology
Molecular Oncology, Vol 15, Iss 9, Pp 2300-2317 (2021)
Recurrent somatic internal tandem duplications (ITD) in the FMS‐like tyrosine kinase 3 (FLT3) gene characterise approximately one third of patients with acute myeloid leukaemia (AML), and FLT3‐ITD mutation status guides risk‐adapted treatment s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::537b99528ae4696620686c3be73f6d88
https://doi.org/10.1002/1878-0261.12961
https://doi.org/10.1002/1878-0261.12961
Autor:
Peter J. M. Valk, Tim Grob, Atle Brendehaug, Randi Hovland, Siv Lise Bedringaas, Line Wergeland, Bjørn Tore Gjertsen, Caroline Engen, Adil S.A. Al Hinai, Monica Hellesøy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::459589119e008dbeb9f5d30205678c8e
https://doi.org/10.1002/1878-0261.12961/v2/response1
https://doi.org/10.1002/1878-0261.12961/v2/response1
Autor:
Atle Brendehaug, Riikka Karjalainen, Tara Helen Dowling, Stein-Erik Gullaksen, Caroline A. Heckman, Monica Hellesøy, Emmet McCormack, Øystein Bruserud, Eline Mejlænder-Andersen, Randi Hovland, Muntasir Mamun Majumder, Mihaela Popa, Samuli Eldfors, Bjørn Tore Gjertsen, Caroline Engen, Jonathan M. Irish, Kimmo Porkka, Brent Ferrell
SUMMARYAcute myeloid leukaemia (AML) is a highly heterogeneous disease. Here, we decipher the disease composition of a single AML patient through longitudinal sampling scrutinized by high-resolution genetic and phenotypic approaches, including sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9e217a2e82c99a265696b6e51262865
https://doi.org/10.1101/2020.11.03.20222885
https://doi.org/10.1101/2020.11.03.20222885
Autor:
Liv T. N. Osnes, Trude Høysæter, Signe Spetalen, Trine Prescott, Atle Brendehaug, Anette K Eek, Rakel Brendsdal Forthun, Randi Hovland, Monica Cheng Munthe-Kaas
Publikováno v:
Journal of pediatric hematology/oncology. 43(4)
Dysregulated tyrosine kinases in myeloid/lymphoid neoplasms with eosinophilia are rare, but do occur in children. To increase awareness of this diagnosis, we present a child who was diagnosed after a 3-year disease history. The patient was initially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb5c604d606ecd3302bc792f616e527
https://pubmed.ncbi.nlm.nih.gov/32852395
https://pubmed.ncbi.nlm.nih.gov/32852395
Autor:
Emmet McCormack, Stein-Erik Gullaksen, Mihaela Popa, Vibeke Andresen, Atle Brendehaug, Randi Hovland, Pilar Ayuda-Durán, Bjørn Tore Gjertsen, Jorrit M. Enserink, Maria Omsland
Publikováno v:
The FASEB Journal
Chronic myeloid leukemia (CML) is a stem cell disease of the bone marrow where mechanisms of inter‐leukemic communication and cell‐to‐cell interactions are proposed to be important for optimal therapy response. Tunneling nanotubes (TNTs) are no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcaef4ed815ce78889eb5a351e66a65b
https://hdl.handle.net/11250/2755521
https://hdl.handle.net/11250/2755521
Publikováno v:
Clinical Case Reports
Key Clinical Message We report a Norwegian girl with mild clinical features of Kagami–Ogata syndrome (KOS) and mosaic upd(14)pat. To our knowledge, this is the first report describing a mosaic patient with KOS. These results imply that mosaic unipa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2191aa3b4f92424e19a1f2c53022bfb1
https://doi.org/10.1002/ccr3.1300
https://doi.org/10.1002/ccr3.1300
Autor:
Gyri Aasland Gradek, Olaug K. Rødningen, Bjørn Ivar Haukanes, Atle Brendehaug, Gunnar Helland, Gunnar Houge, Siren Berland, Ernie M.H.F. Bongers, Rolph Pfundt, Nicole de Leeuw, Randi Hovland, Stefan Johansson, Madeleine Fannemel
Publikováno v:
American Journal of Medical Genetics. Part A, 164, 7, pp. 1622-6
American Journal of Medical Genetics. Part A, 164, 1622-6
American Journal of Medical Genetics. Part A, 164, 1622-6
Item does not contain fulltext MEIS2 is a homeodomain-containing transcription factor of the TALE superfamily that has been proven important for development. We confirm and extend a recent single clinical report stating that deletions in MEIS2 can ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdf855f5eff49f9555f5ed17329323a3
https://hdl.handle.net/2066/138141
https://hdl.handle.net/2066/138141
Autor:
Atle Brendehaug, Darya P. Vanichkina, Chirag Nepal, Helle Lybæk, Anke H A den Engelsman-van Dijk, Gunnar Houge, Diederik R.H. de Bruijn
Publikováno v:
Epigenetics
It was recently shown that duplications of the RevSex element, located 0.5 Mb upstream of SOX9, cause XX-disorder of sex development (DSD), and that deletions cause XY-DSD. To explore how a 148 kb RevSex duplication could have turned on gonadal SOX9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c195e79914e9e5d09a2f3e33bbf170ab
https://doi.org/10.4161/epi.27474
https://doi.org/10.4161/epi.27474
Publikováno v:
Molecular Syndromology. 1:294-300
In a 16-year-old girl with intellectual disability, irregular teeth, slight body asymmetry, and striated skin pigmentation, highly skewed X-inactivation increased the likelihood of an X-linked cause of her condition. Among these, prominent supraorbit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4bd31545211c74fbc7d639474659179
https://doi.org/10.1159/000330111
https://doi.org/10.1159/000330111