نتایج جستجو برای: 11q23 translocation

تعداد نتایج: 47169  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2000
R A Herbst S Mommert U Casper E K Podewski P Kiehl A Kapp J Weiss

Genetic alterations of the long arm of chromosome 11 have been implicated in melanoma pathogenesis, and we recently identified two distinct regions of common allelic loss in chromosomal band 11q23. To establish the point in time of melanoma tumorigenesis at which these two putative tumor suppressor loci become relevant, we investigated allelic loss [loss of heterozygosity (LOH)] in both chromos...

Journal: :Cancer research 1994
Y Gu H Alder T Nakamura S A Schichman R Prasad O Canaani H Saito C M Croce E Canaani

DNA rearrangements caused by chromosome translocations between band 11q23 and various chromosomes can be detected by a single probe, B859, an 859-base pair complementary DNA fragment derived from the human ALL-1 gene. To try to understand why band 11q23 becomes a frequent target of the translocations, we have sequenced the entire breakpoint cluster region, a 8342-base pair BamHI genomic fragmen...

2017
Amanda C. Winters Kathrin M. Bernt

The mixed-lineage leukemia 1 (MLL1) gene (now renamed Lysine [K]-specific MethylTransferase 2A or KMT2A) on chromosome 11q23 is disrupted in a unique group of acute leukemias. More than 80 different partner genes in these fusions have been described, although the majority of leukemias result from MLL1 fusions with one of about six common partner genes. Approximately 10% of all leukemias harbor ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2012
Aimee M Crago Nicholas D Socci Penelope DeCarolis Rachael O'Connor Barry S Taylor Li-Xuan Qin Cristina R Antonescu Samuel Singer

PURPOSE Molecular events underlying progression of well-differentiated liposarcoma (WDLS) to dedifferentiated liposarcoma (DDLS) are poorly defined. This study sought to identify copy number alterations (CNA) associated with dedifferentiation of WDLS, with DDLS morphology, and with patient outcomes. EXPERIMENTAL DESIGN Fifty-five WDLS and 52 DDLS were analyzed using Agilent 244K comparative g...

Journal: :Japanese journal of human genetics 1995

Journal: :Blood 2009
Sarah J Horton Vanessa Walf-Vorderwülbecke Steve J Chatters Neil J Sebire Jasper de Boer Owen Williams

Chromosomal translocations involving 11q23 are frequent in infant acute leukemia and give rise to the formation of MLL fusion genes. The mechanism of leukemic transformation by these fusions has been the subject of numerous investigations. However, the dependence of acute leukemia on MLL fusion activity in vivo and the efficacy of targeting this activity to eliminate disease have not been estab...

2012
Ian G. Cowell Caroline A. Austin

Type II DNA topoisomerases have the ability to generate a transient DNA double-strand break through which a second duplex can be passed; an activity essential for DNA decatenation and unknotting. Topoisomerase poisons stabilize the normally transient topoisomerase-induced DSBs and are potent and widely used anticancer drugs. However, their use is associated with therapy-related secondary leukem...

2009
María Sol Brassesco Ana Paula Montaldi Diana Ester Gras Rosane Gomes de Paula Queiroz Nilce Maria Martinez-Rossi Luiz Gonzaga Tone Elza Tiemi Sakamoto-Hojo

Chromosomal translocations are characteristic of hematopoietic neoplasias and can lead to unregulated oncogene expression or the fusion of genes to yield novel functions. In recent years, different lymphoma/leukemia-associated rearrangements have been detected in healthy individuals. In this study, we used inverse PCR to screen peripheral lymphocytes from 100 healthy individuals for the presenc...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

2012
Jaroslaw Piszcz Lukasz Bolkun Edyta Cichocka Janusz Kloczko

Secondary acute leukaemia (s-ALL) is a destructive complication in patients who have been previously treated for other cancer. Secondary acute lymphoblastic leukaemia is rarely reported whereas secondary acute myeloid leukaemia is much more common. Chromosomal 11q23 abnormality, frequently detected in therapy-related acute myeloid leukaemia, is the most common cytogenetic alteration in secondar...

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