Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fiona, Watkins"'
Autor:
Fiona Watkins
Publikováno v:
Journal of Learning Development in Higher Education, Iss 29 (2023)
Models of information literacy (Coonan et al., 2018; SCONUL, 2011) are explicit: critical thinking and ethical information use are essential skills within higher education (HE). Referencing is key to this, demonstrating how students select and apply
Externí odkaz:
https://doaj.org/article/bce56b075e3446178f76f068f3ffb919
Autor:
Markus Kostrzewa, Jacqueline Boultwood, Amanda J. Strickson, James S. Wainscoat, Carrie Fidler, Ulrich Müller, Rina J. Jaju, Fiona Watkins
The 5q- syndrome is a myelodysplastic syndrome with the 5q deletion ¿del(5q) as the sole karyotypic abnormality. We are using the expressed sequence tag (EST) resource as our primary approach to identifying novel candidate genes for the 5q- syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c33d28c45835bbb98d85e19a56249e8
https://doi.org/10.1006/geno.2000.6193
https://doi.org/10.1006/geno.2000.6193
Autor:
Lyndal Kearney, Nicholas C.P. Cross, James S. Wainscoat, Fiona Watkins, Peter D. Aplan, Jan Fang Cheng, Oskar A. Haas, Rina J. Jaju, Carrie Fidler, Kevin Clark, Amanda J. Strickson, Jacqueline Boultwood
The recurrent translocation t(5;11)(q35;p15.5) associated with a 5q deletion, del(5q), has been reported in childhood acute myeloid leukemia (AML). We report the cloning of the translocation breakpoints in de novo childhood AML harboring a cryptic t(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e5e3ff42ba64dc6ed8f623e804ae56
https://ora.ox.ac.uk/objects/uuid:0dd8f9d5-d684-4096-8d60-4a5da7e2699f
https://ora.ox.ac.uk/objects/uuid:0dd8f9d5-d684-4096-8d60-4a5da7e2699f
Autor:
Lisa J. Campbell, Carrie Fidler, Helen Eagleton, Jacqueline Boultwood, Tim Littlewood, Andrea Pellagatti, Fiona Watkins, Noor Esoof, James S. Wainscoat, Nicholas C.P. Cross
Publikováno v:
British Journal of Haematology. 126:508-511
The putative tumour suppressor gene gravin is down-regulated in several solid tumours and is implicated in tumorigenesis. We have evaluated the expression levels of the gravin gene in the CD34(+)/blast cells of a range of myeloid malignancies as comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecd71d5916615f60ee6c88b5a5f5e12d
https://doi.org/10.1111/j.1365-2141.2004.05067.x
https://doi.org/10.1111/j.1365-2141.2004.05067.x
Autor:
David Vetrie, Peter M. Gordon, Beena Pushkaran, Lisa J. Campbell, Mark Kwan, Helen Eagleton, Barrie Woodcock, Cordelia Langford, Andrea Pellagatti, James D. Cavenagh, Carrie Fidler, Noor Esoof, James S. Wainscoat, Fiona Watkins, Jacqueline Boultwood
Publikováno v:
British Journal of Haematology. 125:576-583
The myelodysplastic syndromes (MDS) comprise a heterogeneous group of clonal disorders of the haematopoietic stem cell and primarily involve cells of the myeloid lineage. Using cDNA microarrays comprising 6000 human genes, we studied the gene express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f91155a3361f84703cc6ad0b25ab87
https://doi.org/10.1111/j.1365-2141.2004.04958.x
https://doi.org/10.1111/j.1365-2141.2004.04958.x
Autor:
Stefano Pileri, Ming-Qing Du, Fiona Watkins, David Y. Mason, Margaret Jones, Fabio Facchetti, Peter G. Isaacson, Tim C. Diss, Michela Pozzobon, Teresa Marafioti, Amanda J. Strickson, Soo Yong Tan
Publikováno v:
Blood. 102:2868-2876
We describe large B cells, many of which have a stellate or dendritic morphology, found in the interfollicular T-cell-rich areas of human peripheral lymphoid tissue. These B cells probably require CD40/CD40 ligand signaling for their generation and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::444788400b26fe53a509220a59feccae
https://doi.org/10.1182/blood-2003-03-0692
https://doi.org/10.1182/blood-2003-03-0692
Autor:
James S. Wainscoat, Paul McGale, Patricia Shepherd, J Boultwood, Susan Richards, Andrew Peniket, Fiona Watkins, Carrie Fidler, Timothy Littlewood
Publikováno v:
Blood. 96:358-361
Telomere shortening is associated with disease evolution in chronic myelogenous leukemia (CML). We have examined the relationship between diagnostic telomere length and outcome in 59 patients with CML who entered into the MRC CMLIII Trial by Southern
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd0c33e65a046a19f21c1fc2ff3aaf3d
https://doi.org/10.1182/blood.v96.1.358
https://doi.org/10.1182/blood.v96.1.358
Autor:
James S. Wainscoat, A. Gaiger, Carrie Fidler, Andrew Peniket, Joanna Snowball, J Boultwood, Sara Haynes, Timothy Littlewood, Fiona Watkins, Patricia Shepherd, Rajko Kusec
Publikováno v:
American Journal of Hematology. 61:5-9
We studied telomere length in the peripheral blood leukocyte samples of a large group of patients with chronic myelogenous leukemia (CML) by Southern blot hybridization using the (TTAGGG)4 probe. The average telomere length expressed as the peak telo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f2f56dbe92c5d0d8fdba43d7733ad1
https://doi.org/10.1002/(sici)1096-8652(199905)61:1<5::aid-ajh2>3.0.co
https://doi.org/10.1002/(sici)1096-8652(199905)61:1<5::aid-ajh2>3.0.co
Autor:
Carrie, Fidler, Fiona, Watkins, David T, Bowen, Timothy J, Littlewood, James S, Wainscoat, Jacqueline, Boultwood
Publikováno v:
Haematologica. 89(7)
Mutations of the NRAS and TP53 genes and internal tandem duplication (ITD) of the FLT3 gene are among the most frequently observed molecular abnormalities in the myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). We sought to determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a8a17e88880ac6085c405786d095479
https://pubmed.ncbi.nlm.nih.gov/15257941
https://pubmed.ncbi.nlm.nih.gov/15257941