نتایج جستجو برای: homogeneously staining regions dmin

تعداد نتایج: 428768  

Journal: :Cancer research 1984
F Gilbert M Feder G Balaban D Brangman D K Lurie R Podolsky V Rinaldt N Vinikoor J Weisband

Structural rearrangements of chromosome 1p have been reported previously as a frequent finding in human neuroblastomas. In a review of karyotypes from 35 neuroblastomas (including 29 published cases and 6 unpublished tumors and cell lines), it was found that, in addition to the abnormalities of chromosome 1p (found in approximately 70% of cases), abnormalities involving only 2 other chromosome ...

Journal: :Cancer research 1984
J M Trent F H Thompson C Ludwig

Cytogenetic analysis of tumor cells from a human malignant melanoma was performed on both the primary tumor colony-forming cells and a cell line (HA-A) established subsequently from the clonogenic population. Chromosome-banding analysis demonstrated identical karyotypic alterations in both the tumor colony-forming cells and the HA-A cell line, documenting their origin from a common precursor. T...

Journal: :Haematologica 2003
Blanca Espinet Lourdes Florensa Marta Salido Francesc Solé

Recent reports have emphasized the role of MLL rearrangements in T and B lineage acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). Abnormalities of the MLL gene, located at 11q23, have been frequently described in acute leukemias (either as reciprocal translocations or as amplifications). Reciprocal translocations are the most common type, with over 30 different partner sites...

2013
Naoya Okada Noriaki Shimizu

Gene amplification plays a pivotal role in malignant transformation of human cells. A plasmid with both a mammalian replication-initiation region (IR)/origin/replicator and a nuclear matrix-attachment region (MAR) is spontaneously amplified in transfected cells by a mechanism that involves amplification at the extrachromosomal site, followed by amplification at the chromosomal arm, ultimately g...

Journal: :Human molecular genetics 2006
Clelia Tiziana Storlazzi Thoas Fioretos Cecilia Surace Angelo Lonoce Angela Mastrorilli Bodil Strömbeck Pietro D'Addabbo Francesco Iacovelli Crescenzio Minervini Anna Aventin Nicole Dastugue Christa Fonatsch Anne Hagemeijer Martine Jotterand Dominique Mühlematter Marina Lafage-Pochitaloff Florence Nguyen-Khac Claudia Schoch Marilyn L Slovak Arabella Smith Francesc Solè Nadine Van Roy Bertil Johansson Mariano Rocchi

Double minutes (dmin)-circular, extra-chromosomal amplifications of specific acentric DNA fragments-are relatively frequent in malignant disorders, particularly in solid tumors. In acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), dmin are observed in approximately 1% of the cases. Most of them consist of an amplified segment from chromosome band 8q24, always including the MYC g...

Journal: :Cancer research 1987
R Klingel A Mincheva T Kahn L Gissmann W Dippold K H Meyer zum Büschenfelde H zur Hausen

By partial homology with the DNA of human papillomavirus type 9 a cellular amplification unit was detected which is amplified in melanoma cells but not in Epstein-Barr virus-transformed B cells of two melanoma patients. A 2.4-kilobase EcoRI fragment of this amplification unit was cloned and designated mel/HPV9. At the chromosomal level we detected mel/HPV9 in homogeneously staining regions or i...

Journal: :Cancer research 1993
M L Slovak J P Ho G Bhardwaj E U Kurz R G Deeley S P Cole

Two doxorubicin-selected human tumor cell lines, H69AR and HT1080/DR4, display a multidrug resistance phenotype but do not overexpress P-glycoprotein. Recently, a 6.5-kilobase mRNA encoding a novel member of the ATP-binding cassette superfamily of transport proteins, designated multidrug resistance-associated protein (MRP), has been identified in the H69AR cell line. In the present study, the l...

Journal: :Cancer research 1995
R Corvi L Savelyeva M Schwab

Amplification of the human N-MYC proto-oncogene is frequently seen either in extrachromosomal double minutes or in homogeneously staining regions of aggressively growing neuroblastomas. N-MYC maps to chromosome 2 band p23-24, but homogeneously staining regions have never been observed at this band, suggesting transposition of N-MYC during amplification. Previous studies had suggested that in ce...

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