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Quoted phrase not found in phrase index: "Rearrangement of 8q21"
Page 1
Herpes virus type 8-negative primary effusion lymphoma associated with PAX-5 gene rearrangement and hepatitis C virus: a case report and review of the literature.
Ichinohasama R, Miura I, Kobayashi N, Saitoh Y, DeCoteau JF, Saiki Y, Mori S, Kadin ME, Ooya K. Ichinohasama R, et al. Am J Surg Pathol. 1998 Dec;22(12):1528-37. doi: 10.1097/00000478-199812000-00010. Am J Surg Pathol. 1998. PMID: 9850179 Review.
At present, there is no case report of HHV8- primary effusion lymphoma (PEL) with t(9;14)(p13;q32) involving both PAX-5 and immunoglobulin heavy chain gene rearrangement, which is a rare translocation in B-cell non-Hodgkin's lymphoma, in an HIV- patient. ...This cas …
At present, there is no case report of HHV8- primary effusion lymphoma (PEL) with t(9;14)(p13;q32) involving both PAX-5 and immunoglobulin h …
Low-level c-myc amplification in human colonic carcinoma cell lines and tumors: a frequent, p53-independent mutation associated with improved outcome in a randomized multi-institutional trial.
Augenlicht LH, Wadler S, Corner G, Richards C, Ryan L, Multani AS, Pathak S, Benson A, Haller D, Heerdt BG. Augenlicht LH, et al. Cancer Res. 1997 May 1;57(9):1769-75. Cancer Res. 1997. PMID: 9135021 Clinical Trial.
Human colonic cancer is associated with multiple genetic deletions, mutations, and alterations in gene expression; in contrast, gene amplification has not been recognized as a prominent characteristic of human colonic tumors. Although the c-myc gene is overex …
Human colonic cancer is associated with multiple genetic deletions, mutations, and alterations in gene expression; in contrast, ge …
A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements.
Lim CK, Cho JW, Kim JY, Kang IS, Shim SH, Jun JH. Lim CK, et al. Fertil Steril. 2008 Nov;90(5):1680-4. doi: 10.1016/j.fertnstert.2007.08.016. Epub 2008 Feb 20. Fertil Steril. 2008. PMID: 18076880 Free article.
OBJECTIVE: To report a live birth after successful preimplantation genetic diagnosis (PGD) for carriers of complex chromosomal rearrangements (CCRs) with translocation and deletion. DESIGN: Fluorescent in situ hybridization (FISH) was applied to PGD for CCR carriers. ...
OBJECTIVE: To report a live birth after successful preimplantation genetic diagnosis (PGD) for carriers of complex chromosomal rearrangem …
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome.
Miozzo M, Castorina P, Riva P, Dalprà L, Fuhrman Conti AM, Volpi L, Hoe TS, Khoo A, Wiegant J, Rosenberg C, Larizza L. Miozzo M, et al. Int J Cancer. 1998 Aug 12;77(4):504-10. doi: 10.1002/(sici)1097-0215(19980812)77:4<504::aid-ijc5>3.0.co;2-y. Int J Cancer. 1998. PMID: 9679749 Free article.
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive genodermatosis associated with increased risk of mesenchymal tumors. The putative gene has been provisionally assigned to chromosome 8. Using a cytogenetic-molecular approach, we studied lymphocytes, fibroblasts …
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive genodermatosis associated with increased risk of mesenchymal tumors. The putat …