نتایج جستجو برای: keywordsgene expressionhematopoietic stem cellsmethylationtumor suppressor genes

تعداد نتایج: 706243  

2013
Nicholas Thompson

Molecular aspects of cancer continue to be uncovered by researchers around the world. Theses aspects will need to be exploited in the next generation of cancer treatments. Specific tumor suppressor genes such as p53 can serve as novel therapeutic targets as well. Although the scientific understanding of the actual steps in tumorigenesis is rather muddled, the differences between cancer and norm...

Journal: :Cancer 2015
Luc G T Morris Timothy A Chan

Carcinogenesis is a multistep process attributable to both gain-of-function mutations in oncogenes and loss-of-function mutations in tumor suppressor genes. Currently, most molecular targeted therapies are inhibitors of oncogenes, because inactivated tumor suppressor genes have proven harder to "drug." Nevertheless, in cancers, tumor suppressor genes undergo alteration more frequently than do o...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1976
H M Laten J Gorman F Webb R M Bock

We have demonstrated in Saccharomyces cerevisiae the transposition of a gene coding for an efficient ochre (UAA) suppressor from a centromere-linked site on chromosome III to two new sites in the yeast genome. One site is on chromosome VI, very close to, if not allelic with, SUP11, one of eight genes coding for a tyrosine-inserting suppressor. The second site is on chromosome III, unlinked to t...

Journal: :Cancer research 2010
Jenny Mattison Jaap Kool Anthony G Uren Jeroen de Ridder Lodewyk Wessels Jos Jonkers Graham R Bignell Adam Butler Alistair G Rust Markus Brosch Catherine H Wilson Louise van der Weyden David A Largaespada Michael R Stratton P Andy Futreal Maarten van Lohuizen Anton Berns Lara S Collier Tim Hubbard David J Adams

Comparative genomic hybridization (CGH) can reveal important disease genes but the large regions identified could sometimes contain hundreds of genes. Here we combine high-resolution CGH analysis of 598 human cancer cell lines with insertion sites isolated from 1,005 mouse tumors induced with the murine leukemia virus (MuLV). This cross-species oncogenomic analysis revealed candidate tumor supp...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Hideaki Mizuno Benjamin T Spike Geoffrey M Wahl Arnold J Levine

Breast cancer comprises a heterogeneous set of diseases distinguishable from one another by pathologic presentation and molecular signatures. However, each breast cancer subtype is also heterogeneous. Some of the heterogeneity may be attributable to genetic instability, but recent data emphasize that developmental plasticity may also contribute. The p53 tumor suppressor could constitute a nodal...

Background: Several studies have examined the presence of DNA methylation of CpG islands in leukemia. Methylation of SOX17 and RUNX3 genes may play a role in leukemogenesis through silencing tumor suppressor genes. We investigated the methylation status of SOX17 and RUNX3 genes in patients with acute leukemia.    Methods: In this case-control study, peripheral blood samples from 100 AML and 10...

Journal: :journal of sciences, islamic republic of iran 2014
sh. mohammad ganji

e-cadherin is among tumor suppressor genes which mostly subjects to the down-regulation in squamous cell carcinoma of esophagus (scce). the gene is tightly associated with the tumor invasion and metastasis in multiple human cancers, especially scce. cpg islands’ methylation in the promoter region of e-cadherin is among the mechanisms that have been suggested for the e-cadherin silencing, howeve...

Journal: :gastroenterology and hepatology from bed to bench 0
ehsan nazemalhosseini mojarad peter jk kuppen hamid asadzadeh aghdaei mohammad reza zali md

it is clear that colorectal cancer (crc) develops through multiple genetic and epigenetic pathways. these pathways may be determined on the basis of three molecular features: (i) mutations in dna mismatch repair genes, leading to a dna microsatellite instability (msi) phenotype, (ii) mutations in apc and other genes that activate wnt pathway, characterized by chromosomal instability (cin) pheno...

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