Zobrazeno 1 - 10
of 516
pro vyhledávání: '"C. Rudduck"'
Autor:
Puay Hoon Tan, Chow Yin Wong, Danny C. T. Ong, C Rudduck, Kong-Weng Eu, D K H Lie, F Seow-Choen, Joe W. Gray, Koei Chin, Wen-Lin Kuo, Ann S. G. Lee, Y M Ho, G S Hong, C L M Chua
Publikováno v:
Oncogene. 28:4189-4200
Deletion of 11q23-q24 is frequent in a diverse variety of malignancies, including breast and colorectal carcinoma, implicating the presence of a tumor suppressor gene at that chromosomal region. We examined a 6-Mb region on 11q23 by high-resolution d
Autor:
Fiona M. Ross, Gareth J. Morgan, Gianpaolo Dagrada, T Parker, C Rudduck, A Wechalekar, Rebecca K.M. Protheroe, E.D. Cabanas, A H Ibrahim, Mathew Nightingale, Kim Orchard, Christine J. Harrison, Nicholas C.P. Cross, Kan Luk Cheung, Laura Chiecchio
Publikováno v:
Leukemia. 20:1610-1617
In myeloma, the prognostic impact of different strategies used to detect chromosome 13 deletion (Delta13) remains controversial. To address this, we compared conventional cytogenetics and interphase fluorescence in situ hybridization (iFISH) in a lar
Autor:
C. Rudduck-Sivaswaren, D. K. H. Lie, P. Lim, Sim-Leng Tien, E. Lim, A. S. G. Lee, Patrick Tan
Publikováno v:
Clinical Genetics. 68:461-465
Evidence for deletion of 9q as a two-step process in chronic myeloid leukemia. Chronic myeloid leukemia (CML) is characterized by the Philadelphia translocation t(9;22)(q34;q11) resulting in the BCR/ABL fusion gene. Submicroscopic deletion of the der
Autor:
S. Ohta, D. Simon, J.H. Kurth, C.N. Hahn, B.K. May, M.C. Kurth, I. Rodriguez de Ledesma, Y.D. Patel, C. Steinlein, B.D. Harris, J.P. Banga, S. Mazan, B. Weiffenbach, D.S. Gallagher, O.M. Garson, J.E. Womack, Z. Tümer, H. Nishi, H.M. Kozman, E.J.M. Schuurman, T. Sasazuki, N. Aoki, A. Pellicer, H.A. Phillips, A.A.B. Bergen, G.J.B. van Ommen, J.C. Mulley, J.A. Padilla, A. Kato, C. Jeanpierre, N. Roeckel, A.P. Monaco, C. Rudduck, D. Sheer, T.A. Jones, E. Austruy, C. Junien, R. Espinosa, A.M. Ryan, G.R. Sutherland, J.-P. Bachellerie, Ca. Westbrook, M. Schmid, H. Lerach, E. Dietzsch, A. Rabasco, D.F. Callen, L. Sottrup-Jensen, M. Cohen-Salmon, T. Kristensen, M M Le Beau, S. Hirosawa, A.M. McGregor, J.J. Pérez-Regadera, E. Bakker, P. Laslo, J.L. Fernández-García, L.-H. Qu, M.C. Wapenaar, M. Dixon, L.M. Duncan, R.H. Martin, R.I. Barnes, A. Kimura, E.M. Bleeker-Wagemakers, A.M. Bowcock, S.A. Whitmore, N. Tommerup, B.B. Knowles, J. Santos, J.L. Omdahl, W.L. Neuman, M. Guttenbach, A.N. Silahtaroglu, P.S. Barnett, M.-G. Mattéi, L. Iannuzzi, Y. Nakamura, E. Baker, P.J. Diergaarde, G.P. Di Meo, M. Martínez-Trancón, S. Toyota
Publikováno v:
Cytogenetic and Genome Research. 62:I-IV
Autor:
O.M. Garson, Ursula R. Kees, M.C.N. Willoughby, C. Rudduck, John Papadimitriou, Jette Ford, Dominic V. Spagnolo
Publikováno v:
Genes, Chromosomes and Cancer. 4:195-204
A 6-year-old girl presented with a tumor of the right shoulder involving bone, adjacent soft tissue, and regional lymph nodes. The conventional histologic diagnosis was ambiguous, initially suggesting lymphoma. After relapse on lymphoma therapy, reev
Publikováno v:
Cancer Genetics and Cytogenetics. 58:55-59
G-banded chromosome analysis of neuroblastoma cells from two children revealed homogeneously staining regions (hsr) in one patient and double minutes (dmin) in the other. Subsequently, both abnormalities were confirmed as areas of N-myc amplification
Autor:
Bruce Bennetts, Carolyn Ellaway, Bridget Wilcken, Shanti Balasubramaniam, C. Rudduck, Gregory Peters
Publikováno v:
Molecular genetics and metabolism. 99(1)
OTC deficiency, a partially dominant X-linked trait, is the most frequent inborn error of the urea cycle. We describe a female patient with a contiguous gene deletion syndrome encompassing the OTC, DMD, RPGR, CYBB and XK genes, amongst others, only m
Publikováno v:
Cytogenetics and cell genetics. 62(4)
A simple G-banding protocol has been found to be compatible with a nonisotopic in situ hybridization technique utilizing a biotin-streptavidin-polyalkaline phosphatase complex. The chromosomes are banded following detection of the hybridization signa
Publikováno v:
Cancer genetics and cytogenetics. 59(2)
A non-radioactive chromosomal in situ hybridization technique utilizing a biotin-streptavidin-polyalkaline-phosphatase complex was successfully applied to three neuroblastoma cell lines for detection of MYCN amplification. These cell lines, designate
Publikováno v:
Biochimica et biophysica acta. 1097(4)
In situ hybridization studies were performed on a series of chronic progressive external ophthalmoplegia patients harbouring large mitochondrial DNA deletions, using intra- and extra-deletional probes. Clear differences in the distribution of wild ty