Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nuala Robson"'
Autor:
Julie McGimpsey, Nuala Robson, Ross McMullan, Graeme Greenfield, Mark Catherwood, Mary Frances McMullin
Publikováno v:
Kompass Onkologie. 6:135-142
Hintergrund: Das BCR-ABL1-Fusionsgen, das der Pathogenese der CML zugrunde liegt, kann aus einer Reihe verschiedener Bruchstellen entstehen. Die häufigsten Varianten sind die Transkripte e13a2 und e14a2, die durch Bruchstellen im Bereich von Exon 13
Autor:
Mary Frances McMullin, Mark Catherwood, Graeme Greenfield, Ross McMullan, Julie McGimpsey, Nuala Robson
Publikováno v:
Greenfield, G, McMullan, R, Robson, N, McGimpsey, J, Catherwood, M & McMullin, M F 2019, ' Response to Imatinib therapy is inferior for e13a2 BCR-ABL1 transcript type in comparison to e14a2 transcript type in chronic myeloid leukaemia ', EMJ Hematology, vol. 19, pp. 7 . https://doi.org/10.1186/s12878-019-0139-2
Background: The BCR-ABL1 fusion gene underlying the pathogenesis of CML can arise from a variety of breakpoints. The e13a2 and e14a2 transcripts formed by breakpoints occurring around exon 13 and exon 14 of the BCR gene respectively are the most comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f95572ad1db7e9fa48c7a8fbde407cd0
https://pure.qub.ac.uk/en/publications/c001a958-0796-4f01-8806-ce7c7c02ef55
https://pure.qub.ac.uk/en/publications/c001a958-0796-4f01-8806-ce7c7c02ef55
Autor:
Mervyn Humphreys, Simona Soverini, Nuala Robson, Sarah Lawless, B. Lundy, Peter McGrattan, Mary Frances McMullin, Ken I. Mills, Conal McConville, Mark Catherwood
Publikováno v:
Journal of Hematopathology. 9:155-160
Chronic myeloid leukaemia (CML) is consistently associated with the BCR-ABL1 fusion gene located on the derivative chromosome 22 (Philadelphia chromosome, Ph + ve) as a result of a t(9;22)(q34;q11.2) translocation. We describe a 36-year-old male in b
Autor:
Graeme, Greenfield, Ross, McMullan, Nuala, Robson, Julie, McGimpsey, Mark, Catherwood, Mary Frances, McMullin
Publikováno v:
BMC Hematology
Background The BCR-ABL1 fusion gene underlying the pathogenesis of CML can arise from a variety of breakpoints. The e13a2 and e14a2 transcripts formed by breakpoints occurring around exon 13 and exon 14 of the BCR gene respectively are the most commo
Autor:
Mary Frances McMullin, Maria Luigia Randi, Irene Bertozzi, Elisabetta Cosi, Nuala Robson, Giacomo Biagetti, Mark Catherwood
Publikováno v:
Biagetti, G, Catherwood, M, Robson, N, Bertozzi, I, Cosi, E, McMullin, M F & Randi, M L 2017, ' HFE mutations in idiopathic erythrocytosis ', British Journal of Haematology . https://doi.org/10.1111/bjh.14555