Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Deeqa Ahmed"'
Autor:
Heidi M. Namløs, Magne Skårn, Deeqa Ahmed, Iwona Grad, Kim Andresen, Stine H. Kresse, Else Munthe, Massimo Serra, Katia Scotlandi, Antonio Llombart-Bosch, Ola Myklebost, Guro E. Lind, Leonardo A. Meza-Zepeda
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Osteosarcoma is the most common primary malignant tumour of bone occurring in children and young adolescents and is characterised by complex genetic and epigenetic changes. The miRNA miR-486-5p has been shown to be downregulated i
Externí odkaz:
https://doaj.org/article/b508152fbe6b4d9db3a0cc3f2bf17690
Autor:
Teresia Wangensteen, Caroline Nangota Felde, Deeqa Ahmed, Lovise Mæhle, Sarah Louise Ariansen
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-8 (2019)
Abstract Background Pathogenic variants in BRCA1 and BRCA2 cause hereditary breast and ovarian cancer. Screening of these genes has become easily accessible in diagnostic laboratories. Sequencing and copy number analyses are used to detect pathogenic
Externí odkaz:
https://doaj.org/article/d7e72994ac3b468cb0e5e50b7ae3fab3
Autor:
Namløs, Heidi Maria, Skårn, Magne Nordang, Ali, Deeqa Ahmed Mohamed, Grad, Iwona, Andresen, Kim, Kresse, Stine Henrichson, Munthe, Else, Serra, Massimo, Scotlandi, Katia, Llombart-Bosch, Antonio, Myklebost, Ola, Lind, Guro Elisabeth, Meza, Leonardo Zepeda
Externí odkaz:
https://hdl.handle.net/11250/3025159
Autor:
Heidi M. Namløs, Magne Skårn, Deeqa Ahmed, Iwona Grad, Kim Andresen, Stine H. Kresse, Else Munthe, Massimo Serra, Katia Scotlandi, Antonio Llombart-Bosch, Ola Myklebost, Guro E. Lind, Leonardo A. Meza-Zepeda
Publikováno v:
BMC Genomics
Background Osteosarcoma is the most common primary malignant tumour of bone occurring in children and young adolescents and is characterised by complex genetic and epigenetic changes. The miRNA miR-486-5p has been shown to be downregulated in osteosa
Autor:
Heidi Namløs, Magne Skårn, Deeqa Ahmed, Iwona Grad, Kim Andresen, Stine Kresse, Massimo Serra, Katia Scotlandi, Antonio Llombart-Bosch, Ola Myklebost, Guro Lind, Leonardo Meza-Zepeda
Osteosarcoma is the most common primary malignant tumour of bone occurring in children and young adolescents, and is characterised by complex genetic and epigenetic changes. The miRNA miR-486-5p has been shown to be downregulated in osteosarcoma and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f38b1fde001e3a17bdec9aa0d8c3731
https://doi.org/10.21203/rs.3.rs-112581/v1
https://doi.org/10.21203/rs.3.rs-112581/v1
Autor:
Guro Elisabeth Lind, Torleiv O. Rognum, Ragnhild A. Lothe, Hilde Honne, Gunn Iren Meling, Stine A. Danielsen, Deeqa Ahmed, Edgar Rivedal, Edward Leithe, Solveig Sirnes
Publikováno v:
Epigenetics. 6:602-609
Gap junctions are specialized plasma membrane domains consisting of channels formed by members of the connexin protein family. Gap junctional intercellular communication is often lost in cancers due to aberrant localization or downregulation of conne
Autor:
Peter W. Eide, Mette Eknæs, Ina A. Eilertsen, Stine A. Danielsen, Deeqa Ahmed, Ragnhild A. Lothe, Guro Elisabeth Lind, Merete Hektoen
Publikováno v:
Oncogenesis
Cell lines are invaluable biomedical research tools, and recent literature has emphasized the importance of genotype authentication and characterization. In the present study, 24 out of 27 cell line identities were confirmed by short tandem repeat pr
Autor:
Trude H. Aagesen, Guro Elisabeth Lind, Michael Bretthauer, Arild Nesbakken, Torleiv O. Rognum, Geir Hoff, Espen Thiis-Evensen, Stine A. Danielsen, Deeqa Ahmed, Ragnhild A. Lothe
Publikováno v:
Clinical and Translational Gastroenterology
OBJECTIVES: We recently identified a six-gene methylation-based biomarker panel suitable for early detection of colorectal cancer (CRC). In this study, we compared the performance of this novel epi-panel with that of previously identified DNA methyla
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 21:1889-1889
We read with great interest the recent article of Moinova and colleagues reporting that aberrant methylation of exon-1 of the vimentin ( VIM ) gene is a highly common epigenetic alteration in neoplasia of the upper (esophagus and gastric) and the low
Autor:
Arild Nesbakken, Geir Hoff, Guro Elisabeth Lind, Stine A. Danielsen, Michael Bretthauer, Deeqa Ahmed, Ragnhild A. Lothe, Espen Thiis-Evensen, Torleiv O. Rognum, Trude H. Ågesen
Publikováno v:
Annals of Oncology. 23:iv23
Introduction Colorectal cancer is a common disease with a world-wide annual incidence of 1.2 million. The mortality rate is high, especially for patients diagnosed with an advanced tumor stage. We recently identified DNA methylation based biomarkers