Zobrazeno 1 - 5
of 5
pro vyhledávání: '"J. E. V. Watson"'
Autor:
Ivonne Archibeque, Steven G. Elliott, Scott Powers, Paul D. Kassner, Leigh Busse, J E V Watson, Norma Rogers, W Brown, Angus M. Sinclair, G E Arnold, Ken C. Q. Nguyen
Publikováno v:
British Journal of Cancer
Erythropoietin receptor (EpoR) has been reported to be overexpressed in tumours and has raised safety concerns regarding the use of erythropoiesis-stimulating agents (ESAs) to treat anaemia in cancer patients. To investigate the potential for EpoR to
Autor:
S. G. Hillier, C. Taylor, John F. Smyth, K. J. Taylor, David J. Porteous, Diane Scott, Adam J.W. Paige, Hani Gabra, J. E. V. Watson, Susan M. Farrington
Publikováno v:
Proceedings of the National Academy of Sciences. 98:11417-11422
We previously reported the construction of a P1-derived artificial chromosome (PAC) contig encompassing a set of homozygous deletions of chromosome 16q23–24.1 found in primary ovarian tumor material and several tumor cell lines. Using these PAC clo
Autor:
David J. Porteous, Paul Perry, Harris Morrison, J. E. V. Watson, John F. Smyth, G. J. Rabiasz, K. J. Taylor, Hani Gabra
Publikováno v:
Scopus-Elsevier
Watson, J E, Gabra, H, Taylor, K J, Rabiasz, G J, Morrison, H, Perry, P, Smyth, J F & Porteous, D J 1999, ' Identification and characterization of a homozygous deletion found in ovarian ascites by representational difference analysis ', Genome Research, vol. 9, no. 3, pp. 226-33 .
Watson, J E, Gabra, H, Taylor, K J, Rabiasz, G J, Morrison, H, Perry, P, Smyth, J F & Porteous, D J 1999, ' Identification and characterization of a homozygous deletion found in ovarian ascites by representational difference analysis ', Genome Research, vol. 9, no. 3, pp. 226-33 .
We have performed representational difference analysis (RDA) on DNA from tumor cells and normal fibroblasts isolated from the ascites of a patient with ovarian cancer. Five of six products of the RDA were homozygously deleted from the tumor DNA. One
Autor:
Samantha J. L. Knight, Ruth N. MacKinnon, A. Roche, J. E. V. Watson, Grant R. Sutherland, Nicholas Stuart Tudor Thomas, T.J. Flint, M. Schmidt, Mark Patterson, Yvonne Boyd, Kay E. Davies, Mark C. Hirst, M. C. Hors-Cayla, J.H.D. Bassett, Y. Nakahori, M. V. Bell, Stephen T. Warren
Publikováno v:
Genomics. 10(1)
We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the fragile site at Xq27.3. So far, no microdissection markers derived from Xq28 material have been found, thus allowing a rapid s
Autor:
Grant R. Sutherland, Ruth N. MacKinnon, C. E. Schwartz, David H. Ledbetter, Mark Patterson, David F. Callen, M. V. Bell, Kay E. Davies, Susan A. Ledbetter, Niklas Dahl, J. E. V. Watson, Mark C. Hirst
Publikováno v:
American journal of medical genetics. 38(2-3)
We have localized the gene encoding a cerebellar degeneration related (CDR) protein to a region proximal to the fragile site close to DXS98 and DXS105. This gene is polymorphic with the enzyme RsaI and therefore also provides a new genetic marker in