نتایج جستجو برای: masserann kit

تعداد نتایج: 29130  

2015
Richard Gedrich Scott Seibel Theresa LaVallee Joseph Paul Eder

Mast cell infiltrates are associated with tumors, though their role in the tumor microenvironment remains unclear. Mast cells express high levels of KIT throughout differentiation and as mature cells. Mast cells in tumors have been shown to release proinflammatory cytokines and promote angiogenesis, increasing tumor growth and metastasis. KIT signaling and mast cells also appear to modulate myl...

Journal: :Blood 2007
Thomas Jahn Erica Leifheit Stacie Gooch Simran Sindhu Kenneth Weinberg

In addition to its physiologic role as central regulator of the hematopoietic and reproductive systems, the Kit receptor tyrosine kinase (RTK) is pathologically overexpressed in some forms of leukemia and constitutively activated by oncogenic mutations in mast-cell proliferations and gastrointestinal stromal tumors. To gain insight into the general activation and signaling mechanisms of RTKs, w...

2017
A. Nazifah Abdullah M. Asri Jusoh Norkharziana Mohd Nayan

This paper presents design and analysis of Multi-output Portable Universal Power Supply Kit (EPS Kit). This EPS Kit is intended as an alternative power supply kit to reduce the issue of a power outage. Lead Acid Battery which is considered one of the easiest sources that can be found during an emergency state is the best alternative energy source. The EPS Kit is designed to store the power in L...

2013
Angelique Ale Frank Siebenhaar Katja Kosanke Michaela Aichler Karin Radrich Sina Heydrich Matthias Schiemann Isabella Bielicki Peter B. Noel Rickmer Braren Marcus Maurer Axel K. Walch Ernst J. Rummeny Vasilis Ntziachristos Moritz Wildgruber

Cardiomyocyte loss via apoptosis plays a crucial role in ventricular remodeling following myocardial infarction (MI). Cell-based therapy approaches using bone marrow derived c-kit⁺ pluripotent cells may attenuate apoptosis following ischemic injury. We therefore thought to examine the early course of apoptosis following myocardial infarction - in-vivo - and non-invasively determine the effect o...

2016
Jing Gao Jian Li Yanyan Li Zhongwu Li Jifang Gong Jian Wu Na Liu Bin Dong Changsong Qi Jie Li Lin Shen

OBJECTIVE Gastrointestinal stromal tumors (GISTs) with no mutations in exons 9, 11, 13, and 17 of the KIT gene and exons 12, and 18 of the PDGFRA gene were defined as KIT/PDGFRA wild-type and they accounted for ~15-20% of GISTs. However, some KIT/PDGFRA wild-type GISTs with KIT mutations in other exons were occasionally reported. We therefore assessed GISTs to understand the whole genomic genot...

2011
Yan Kong Lu Si Yanyan Zhu Xiaowei Xu Christopher L. Corless Keith T. Flaherty Li Li Haifu Li Xinan Sheng Chuanliang Cui Zhihong Chi Siming Li Mei Han Lili Mao Aiping Lu Jun Guo

Purpose: KIT aberrations were described in acral and mucosal melanomas in largely Caucasian populations. Asian populations are more prone to develop acral and mucosal than cutaneous melanomas, and may harbor a high frequency of KIT aberrations. Experimental Design: Melanoma subtypes (n 1⁄4 502) were analyzed histologically to determine melanoma subtype. Tissue samples were analyzed for mutation...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Yue-Ying Wang Li-Juan Zhao Chuan-Feng Wu Ping Liu Lin Shi Yang Liang Shu-Min Xiong Jian-Qing Mi Zhu Chen Ruibao Ren Sai-Juan Chen

The full-length AML1-ETO (AE) fusion gene resulting from t(8;21)(q22;q22) in human acute myeloid leukemia (AML) is not sufficient to induce leukemia in animals, suggesting that additional mutations are required for leukemogenesis. We and others have identified activating mutations of C-KIT in nearly half of patients with t(8;21) AML. To test the hypothesis that activating C-KIT mutations cooper...

Journal: :Cancer research 2006
Elliot B Sambol Grazia Ambrosini Rula C Geha Peter T Kennealey Penelope Decarolis Rachael O'connor Yuhsin V Wu Monica Motwani Jin-Hong Chen Gary K Schwartz Samuel Singer

Gastrointestinal stromal tumors (GIST) are characterized by activating mutations in the c-KIT gene which confers ligand-independent activation of the KIT receptor. Imatinib mesylate has been shown to effectively block constitutively active KIT and delay tumor growth. However, resistance to imatinib mesylate is emerging as a major clinical problem and novel therapies are needed. We report that t...

2016
Mingjun Du Sebastian Schmull Wentian Zhang Chenxi Wang Feng Lian Yao Chen Song Xue

Although the bone marrow mononuclear cell (BMMNC) is known as an ideal cell type for cell-based therapy for MI treatment, the effective subpopulation still remains unknown. Our study aimed at identifying the optimal subset of BMMNCs suited for cardiac regeneration. In this study, we observed that MI led to (i) a significant increase of the c-kit(+)AT2R(+) BMMNC subpopulation in mice and (ii) a ...

2014
Ying-Yu Ma Sheng Yu Xu-Jun He Yuan Xu Fang Wu Ying-Jie Xia Kun Guo Hui-Ju Wang Zai-Yuan Ye Wei Zhang Hou-Quan Tao

The aim of this study was to discuss the role of c-KIT mutation in the pathogenesis of gastrointestinal stromal tumors (GISTs) and analyze its correlation with proliferation and apoptosis. c-KIT and PDGFRA genotypes were examined by deoxyribonucleic acid sequencing. Immunohistochemistry was performed to determine the expression levels of Kit, Ki-67 (proliferation marker), and apoptotic protease...

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