Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Noor, Esoof"'
Autor:
Michale Bouskila, Noor Esoof, Laurie Gay, Emily H. Fang, Maria Deak, Michael J. Begley, Lewis C. Cantley, Alan Prescott, Kate G. Storey, Dario R. Alessi
Publikováno v:
Biochemical Journal. 437:157-167
Mutations that truncate the C-terminal non-catalytic moiety of TTBK2 (tau tubulin kinase 2) cause the inherited, autosomal dominant, SCA11 (spinocerebellar ataxia type 11) movement disorder. In the present study we first assess the substrate specific
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
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
Autor:
Noor Esoof, James S. Wainscoat, Luca Malcovati, Sally Killick, Jacqueline Boultwood, Mario Cazzola, Carlo Aul, Aristoteles Giagounidis, Carrie Fidler, Andrea Pellagatti, David Oscier
Publikováno v:
BLOOD. 108(11)
Myelodysplasia (MDS) is a heterogeneous group of clonal disorders of hematopoietic stem cells characterised by ineffective hematopoiesis and a variable risk of transformation to acute myelogenous leukaemia. We have used Comparative Genomic Hybridisat
Autor:
Andrea, Pellagatti, Noor, Esoof, Fiona, Watkins, Cordelia F, Langford, David, Vetrie, Lisa J, Campbell, Carrie, Fidler, James D, Cavenagh, Helen, Eagleton, Peter, Gordon, Barrie, Woodcock, Beena, Pushkaran, Mark, Kwan, James S, Wainscoat, Jacqueline, Boultwood
Publikováno v:
British journal of haematology. 125(5)
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