نتایج جستجو برای: cdkn2b

تعداد نتایج: 500  

Aberrant DNA methylation has been reported as an important phenotype in acute myeloid leukemia. However the clinical significance of methylation changes has not been clear yet. In this study methylation Specific Melting Curve Analysis (MS-MCA) and real time PCR was used to assess the CDKN2B promoter hyper-methylation and gene expression in 59 Iranian acute myeloid leukemia (AML) patients. The i...

Aberrant DNA methylation has been reported as an important phenotype in acute myeloid leukemia. However the clinical significance of methylation changes has not been clear yet. In this study methylation Specific Melting Curve Analysis (MS-MCA) and real time PCR was used to assess the CDKN2B promoter hyper-methylation and gene expression in 59 Iranian acute myeloid leukemia (AML) patients. The i...

2017
Esmat Kamali Dolatabadi Mohammadreza Ostadali Dehaghi Naser Amirizadeh Kazem Parivar Reza Mahdian

Aberrant DNA methylation has been reported as an important phenotype in acute myeloid leukemia. However the clinical significance of methylation changes has not been clear yet. In this study methylation Specific Melting Curve Analysis (MS-MCA) and real time PCR was used to assess the CDKN2B promoter hyper-methylation and gene expression in 59 Iranian acute myeloid leukemia (AML) patients. The i...

2017
Peng Gao Jiyuan Si Bin Yang Jixiang Yu

BACKGROUND The objective of the present study was to identify the association between miR-15a-5p and CDKN2B, and their roles in regulating the development of abdominal aortic aneurysm (AAA). MATERIAL AND METHODS We searched the miRNA database online (www.mirdb.org) and used a luciferase reporter assay system to study the regulatory relationship between miR-15a-5p and CDKN2B. We also conducted r...

2017
Jiangeng Yang Yuchen Liu Anbang He Yuhan Liu Jianting Wu Xinhui Liao Zhaojie Lv Feng Wang Hongbing Mei

BACKGROUND AND OBJECTIVES Hsa-miR-429 is increased in bladder cancer. Its roles in bladder cancer are poorly understood. METHODS The expression levels of hsa-miR-429 and cyclin-dependent kinase inhibitor 2B (CDKN2B) were determined using Real-Time qPCR in a total of 50 patients with bladder cancer. Bladder cancer T24 and 5637 cells were transfected CDKN2B siRNA or hsa-miR-429 mimic. CDKN2B ex...

2017
Tengyue Zhang Kelong Ma Jin Huang Shitang Wang Yabei Liu Gaofei Fan Miao Liu Guangshan Yang Cheng Wang Pingsheng Fan

In this study, we explored the function and mechanism of CDKN2B genes in verapamil (VER)-induced reversal of resistance to doxorubicin (ADM) chemotherapy in hepatocellular carcinoma (HCC). We examined 4 HCC cell lines and found that the expression levels of CDKN2B genes correlated with the level of apoptosis induced by ADM+VER. Overexpression of CDKN2B genes promoted apoptosis in cells treated ...

2017
Qian Hu Xiaowen Chen Sixi Liu Ruiqi Wen Xiuli Yuan Dandan Xu Guosheng Liu Feiqiu Wen

The aim of the present study was to investigate the association between methylation of cyclin-dependent kinase inhibitor 2B (CDKN2B) CpG islands and telomerase activity in children with acute lymphoblastic leukemia (ALL). A total of 72 children with ALL and 12 children with immune thrombocytopenia (ITP) were subjected to bone marrow aspiration and methylation-specific polymerase chain reaction ...

Journal: :Cancer discovery 2015
Mariam Jafri Naomi C Wake David B Ascher Douglas E V Pires Dean Gentle Mark R Morris Eleanor Rattenberry Michael A Simpson Richard C Trembath Astrid Weber Emma R Woodward Alan Donaldson Tom L Blundell Farida Latif Eamonn R Maher

UNLABELLED Familial renal cell carcinoma (RCC) is genetically heterogeneous and may be caused by mutations in multiple genes, including VHL, MET, SDHB, FH, FLCN, PTEN, and BAP1. However, most individuals with inherited RCC do not have a detectable germline mutation. To identify novel inherited RCC genes, we undertook exome resequencing studies in a familial RCC kindred and identified a CDKN2B n...

Journal: :Journal of lipid research 2013
Stuart D Horswell Lee G D Fryer Claire E Hutchison Dlear Zindrou Helen E Speedy Margaret-M Town Emma J Duncan Rasheeta Sivapackianathan Hetal N Patel Emma L Jones Adam Braithwaite Max P A Salm Claire K Y Neuwirth Elizabeth Potter Jonathan R Anderson Kenneth M Taylor Mary Seed D John Betteridge Martin A Crook Anthony S Wierzbicki James Scott Rossi P Naoumova Carol C Shoulders

The purpose of this study was to determine the core biological processes perturbed in the subcutaneous adipose tissue of familial combined hyperlipidemia (FCHL) patients. Annotation of FCHL and control microarray datasets revealed a distinctive FCHL transcriptome, characterized by gene expression changes regulating five overlapping systems: the cytoskeleton, cell adhesion and extracellular matr...

2014
Per-Arne Svensson Björn Wahlstrand Maja Olsson Philippe Froguel Mario Falchi Richard N. Bergman Philip G. McTernan Thomas Hedner Lena M.S. Carlsson Peter Jacobson

Risk alleles within a gene desert at the 9p21 locus constitute the most prevalent genetic determinant of cardiovascular disease. Previous research has demonstrated that 9p21 risk variants influence gene expression in vascular tissues, yet the biological mechanisms by which this would mediate atherosclerosis merits further investigation. To investigate possible influences of this locus on other ...

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