Zobrazeno 1 - 10
of 21
pro vyhledávání: '"M O, Diaz"'
Publikováno v:
Blood. 83:641-644
Rearrangements of chromosome band 11q23 are common in infant leukemias, comprising more than 70% of the observed chromosome abnormalities in children less than 1 year of age. The MLL gene, which is located at the 11q23 breakpoint in infant, childhood
Publikováno v:
Blood. 80:744-749
Homozygous and hemizygous deletions of the interferon A (IFNA) and IFNB genes have been frequently observed in acute leukemia cell lines, primary acute leukemia cases, and gliomas. Because IFNs have an antiproliferative effect, selection against the
Autor:
O R Colamonici, L M Pfeffer, F D'Alessandro, L C Platanias, S A Gregory, A Rosolen, R Nordan, R A Cruciani, M O Diaz
Publikováno v:
The Journal of Immunology. 148:2126-2132
The structure of IFN-alpha receptor was studied by 1) developing antibodies against the receptor, and 2) screening a number of cell lines by affinity cross-linking to identify cells that express different IFN-alpha 2 receptor structures. We report th
Publikováno v:
Cancer research. 61(11)
Translocations involving the MLL gene at 11q23 are a frequent finding in therapy-related leukemia and are concentrated within a short, 8.3-kb tract of DNA, the breakpoint cluster region. In addition, a specific site adjacent to exon 12 within this re
Publikováno v:
Genes, chromosomescancer. 20(4)
The MOLT-16 cell line was established from the leukemic cells of a patient with T-cell acute lymphoblastic leukemia and contains a t(8;14)(q24;q11) resulting in juxtaposition of sequences downstream of the MYC gene on chromosome 8 and the J region of
Autor:
H G, Super, P L, Strissel, O M, Sobulo, D, Burian, S C, Reshmi, B, Roe, N J, Zeleznik-Le, M O, Diaz, J D, Rowley
Publikováno v:
Genes, chromosomescancer. 20(2)
The MLL gene at chromosome 11, band q23, is involved in translocations with as many as 40 different chromosomal bands. Virtually all breakpoints occur within an 8.3 kb BamHI fragment and result in 5' MLL fused to partner genes in a 5'-3' orientation.
Publikováno v:
Leukemia. 10(4)
The CDKN2 gene has been recently localized to a chromosomal region found to be deleted in leukemias and solid tumors. CDKN2 encodes a 16 kDa protein product (p16INK4A), which functions as a specific inhibitor or the cyclin-dependent kinases 4 and 6.
Autor:
O R, Colamonici, B, Porterfield, P, Domanski, R K, Handa, S, Flex, C E, Samuel, R, Pine, M O, Diaz
Publikováno v:
The Journal of biological chemistry. 269(44)
Two interferon (IFN) alpha-regulated genes, IRF1/ISGF2 and PKR/p68 kinase, may function as tumor suppressor genes suggesting that the IFN system may function as a tumor suppressor system. We report that the expression of the alpha subunit of the type
Autor:
W, Stock, M J, Thirman, R K, Dodge, J D, Rowley, M O, Diaz, D, Wurster-Hill, R E, Sobol, F R, Davey, R A, Larson, C A, Westbrook
Publikováno v:
Leukemia. 8(11)
Specific structural rearrangements involving chromosome band 11q23 occur in a variety of hematologic malignancies, including an estimated 2-7% of patients with acute lymphoblastic leukemia (ALL). Translocations involving chromosome band 11q23 have be
Publikováno v:
Blood. 84(4)
Previously we had characterized the t(1;7)(p34;q34) translocation from HSB-2. This translocation fused the beta T-cell receptor gene (TCRB) constant region and transcriptional enhancer with the type I transcription unit of the LCK gene on the derivat