نتایج جستجو برای: hmga2

تعداد نتایج: 735  

Journal: :Anticancer research 2006
Takahiro Kubo Yoshito Matsui Tomohiro Goto Kiminori Yukata Kenji Endo Ryosuke Sato Takahiko Tsutsui Natsuo Yasui

BACKGROUND The magnetic resonance (MR) characteristics of parosteal lipomas with the HMGA2-LPP fusion transcripts are described. PATIENTS AND METHODS The expression of HMGA2-LPP fusion transcripts was determined using the reverse transcription-polymerase chain reaction method. RESULTS MR images of two cases with the fusion transcripts, a 56-year-old man and a 50-year-old woman, revealed het...

2014
Keqiang Zhang Hanlin Gao Xiwei Wu Jinhui Wang Wendi Zhou Guihua Sun Jinghan Wang Yafan Wang Bing Mu Charles Kim Peiguo Chu Donald M. Ho David K. Ann Tai-Tong Wong Yun Yen

Purpose: Atypical teratoid/rhabdoid tumors (AT/RT) are highly aggressive pediatric malignancies characterized by biallelic inactivation of the SMARCB1 tumor suppressor gene. We searched for novel genomic aberrations by investigating the copy number and expression alterations of let-7a3/let-7b microRNA (miRNA) and correlated these with expression of high-mobility group AT-hook 2 (HMGA2) oncoprot...

2012
A. A. Ismail S. Wagner H. Murua Escobar S. Willenbrock K. A. Sterenczak M. T. Samy A. M. Abd El-Aal I. Nolte P. Wefstaedt

Multipotency and self-renewal are considered as most important features of stem cells to persist throughout life in tissues. In this context, the role of HMGA proteins to influence proliferation of adipose-derived mesenchymal stem cell (ASCs) while maintaining their multipotent and self-renewal capacities has not yet been investigated. Therefore, extracellular HMGA1 and HMGA2 application alone ...

Journal: :European journal of endocrinology 2011
Darya Gorbenko del Blanco Laura C G de Graaff Dirk Posthouwer Theo J Visser Anita C S Hokken-Koelega

OBJECTIVE In most patients, the genetic cause of isolated GH deficiency (IGHD) is unknown. By identifying several genes associated with height variability within the normal population, three separate genome-wide association studies provided new candidate genes for human growth disorders. We selected two of them for genetic screening of our IGHD population. AIM We aimed to determine whether hi...

Journal: :Blood 2014
Kentson Lam Alexander Muselman Randal Du Yuka Harada Amanda G Scholl Ming Yan Shinobu Matsuura Stephanie Weng Hironori Harada Dong-Er Zhang

RUNX1 is a master transcription factor in hematopoiesis and mediates the specification and homeostasis of hematopoietic stem and progenitor cells (HSPCs). Disruptions in RUNX1 are well known to lead to hematologic disease. In this study, we sought to identify and characterize RUNX1 target genes in HSPCs by performing RUNX1 chromatin immunoprecipitation with high-throughput sequencing (ChIP-seq)...

Journal: :Cancer research 2010
Joern Bullerdiek Birgit Rommel

To the Editor: Recently, Li and colleagues (1) have presented evidence for the impairment of nonhomologous and joining repair (NHEJ) of DNA damage by the chromatin binding protein HMGA2. In this interesting article, the cytogenetic stability of fibroblasts transfected by a construct encoding HMGA2 was analyzed as a hallmark of deficient NHEJ. Twenty-five metaphases of these fibroblasts were kar...

2018
Zhi-Hua Ye Ding-Wen Gui

Renal cell carcinoma (RCC) is one of the most common urinary malignancies with a high rate of morbidity. MicroRNAs (miRNAs) have been shown to be critical post‑transcriptional regulators in tumorigenesis. The present study aimed to investigate the effect of miRNA (miR)‑539 on the proliferation and apoptosis of RCC. The expression of miR‑539 and high mobility group AT‑hook 2(HMGA2) were examined...

Journal: :Cancer research 2003
Bradley J Quade Stanislawa Weremowicz David M Neskey Roberta Vanni Carll Ladd Paola Dal Cin Cynthia C Morton

Uterine leiomyomata are one of several benign tumors characterized by frequent chromosomal rearrangement involving 12q15. The 12q15 rearrangement in leiomyomata typically is manifested as t(12;14)(q15;q23-24), which has been hypothesized to create pathobiologically significant fusion transcripts derived from HMGA2 and RAD51L1. To explore further this hypothesis, we mapped chromosomal breakpoint...

2016
Xiaoling Zhong Xuan Liu Yamu Li Man Cheng Wen Wang Kuan Tian Lili Mu Tao Zeng Ying Liu Xiaobing Jiang Luyang Yu Liang Gao Yan Zhou

Glioblastoma multiforme (GBM) is the most common type of brain tumors with dismal outcomes. The mesenchymal phenotype is the hallmark of tumor aggressiveness in GBMs. Perivascular smooth muscle cells (pericytes) are essential in homeostasis of normal and glioma tissues. Here we found HMGA2, an architectural transcription factor that promotes mesenchymal phenotypes in a number of solid tumors, i...

2012
Qiong Zou Li Xiong Zhulin Yang Fang Lv Leping Yang Xiongying Miao

BACKGROUND The objective of this study was to investigate CD9 and HMGA2 expression and its clinicopathological significance in benign and malignant lesion tissues of the gallbladder. METHODS The resected specimens of 108 cases of gallbladder adenocarcinoma, 46 cases of adjacent tissue, 15 cases of polyps and 35 cases of chronic cholecystitis were made into conventional paraffin-embedded secti...

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