Zobrazeno 1 - 9
of 9
pro vyhledávání: '"W D, Fergusson"'
Autor:
G. M. Taylor, JM Birch, W D Fergusson, Tracy Lightfoot, Christine J. Harrison, Adiba Hussain, Pamela D. Thompson, G Watkins, V Verhage
Publikováno v:
Leukemia. 23:863-869
We previously reported that susceptibility to childhood B cell precursor ALL (BCP ALL) is associated with HLA-DPB1 alleles having glutamic acid (E) rather than lysine (K) in the P4 antigenic peptide-binding pocket. Clustering approximately 90% of DPB
Autor:
W. D. Fergusson, S. P. Dearden, W. Ollier, Osborn B. Eden, G M Taylor, Richard F. Stevens, Jillian M. Birch, D A Gokhale, K. Ghodsi
Publikováno v:
British Journal of Haematology. 102:1279-1283
Previous serological studies documenting an association between acute lymphoblastic leukaemia (ALL) and HLA-Cw antigens suggested that the HLA-C locus might influence susceptibility to ALL. However, associations with more than one Cw antigen suggest
Autor:
P. E. C. Brenchley, S. W. D'souza, D. Braddock, G M Taylor, A. J. Robson, D. P. Duckett, W. D. Fergusson
Publikováno v:
Clinical and Experimental Immunology. 81:501-506
SUMMARY Monosomy 21 (M21) is a rare aneuploid condition which in certain cases leads to reduced levels of chromosome 21 gene products. We have prepared an Epstein-Barr virus lymphoblastoid cell-line (LCL) from patient with M21 who has immunological a
Autor:
W. D. Fergusson, G. Morrell, Andrew M. Will, D. I. K. Evans, G. M. Taylor, S. P. Dearden, M. Super, S. Simon, R. F. Stevens, I. H. Brown
Publikováno v:
Archives of Disease in Childhood. 73:453-455
The successful correction of infantile osteopetrosis in an Asian child by bone marrow transplantation (BMT) from an HLA-A,B matched cousin donor is reported. Retrospective HLA molecular analysis revealed that patient and donor were incompatible for H
Autor:
K, Ghodsi, G M, Taylor, D A, Gokhale, S, Dearden, R F, Stevens, J M, Birch, W D, Fergusson, O B, Eden, W, Ollier
Publikováno v:
British journal of haematology. 102(5)
Previous serological studies documenting an association between acute lymphoblastic leukaemia (ALL) and HLA-Cw antigens suggested that the HLA-C locus might influence susceptibility to ALL. However, associations with more than one Cw antigen suggest
Autor:
G. M. Taylor, Andrew M. Will, Peter D. Arkwright, Guy Makin, W. D. Fergusson, Gokhale Da, M. Ayres
X linked lymphoproliferative disease (XLP; Duncan's disease) is a rare disorder affecting boys and characterised by a defective immune response to Epstein- Barr virus caused by a mutation in a gene located at chromosome Xq25. Three siblings with XLP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90958bee155eeb40bdf6d19b3e28314
https://europepmc.org/articles/PMC1717619/
https://europepmc.org/articles/PMC1717619/
Publikováno v:
British Journal of Cancer
The expression of allogenic lymphocyte-activating determinants (LAD) on 25 acute leukaemias has been compared with the expression of cell-surface antigens identified by HLA-DR allo- and xeno-antisera. The close correlation between LAD and DR known to
Publikováno v:
Clinical and experimental immunology. 35(1)
Autologous acute myeloid leukaemia (AML), cells caused the suppression of incorporation of 3H-thymidine (3H-Tdr) by remission lymphocytes stimulated with allogeneic cells. In five patients, autologous AML cells suppressed 3H-Tdr uptake by lymphocytes
Publikováno v:
Cancer Immunology Immunotherapy. 16
We describe an acute myelomonocytic leukaemia (E72) devoid of cell-surface HLA-DR antigens, but capable of inducing cellular responses. Leukaemia E72 induced proliferation of normal lymphocytes in primary mixed lymphocyte culture (MLC), which was onl