نتایج جستجو برای: c kit

تعداد نتایج: 1076403  

Journal: :The Journal of Experimental Medicine 1991
M Ogawa Y Matsuzaki S Nishikawa S Hayashi T Kunisada T Sudo T Kina H Nakauchi

The expression and function of a receptor tyrosine kinase, c-kit, in the adult bone marrow of the mouse were investigated by using monoclonal antibodies (mAbs) against the extracellular domain of murine c-kit. In adult C57BL/6 mouse, 7.8% of total bone marrow cells express c-kit on their surface. Half of the c-kit+ cells do not express lineage markers including Mac-1, Gr-1, TER-119, and B220, w...

2018
Weiwei Yan Zhenyu Zhu Fei Pan Ang Huang Guang-hai Dai

Background To explore new biomarkers for indicating the recurrence and prognosis in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients after tumor resection, we investigated the expression and prognostic value of c-kit(CD117) in HBV-related HCC. Materials and methods Immunohistochemistry was used to estimate the expression of c-kit(CD117) and CD34 in the liver cancer tiss...

Journal: :Circulation Research 2018

2013
Leandro C. BARCHI Joaquim GAMA-RODRIGUES Fábio APM CARVALHO Marcelo C. BARCHI Olivia C. Grimaldi OLIVEIRA Marcelo F. CARNEIRO Joaquim Gama-Rodrigues

Gastrointestinal stromal tumors (GIST) are rare, representing less than 1% of all gastrointestinal tumors. However, this is the most frequent nonepithelial neoplasm of the digestive tract. Mean age at diagnose is 58 years old, and the two structures usually involved are stomach and bowel12. The main symptoms are abdominal pain and digestive bleeding2, while the most frequent presentation are so...

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...

2015
Nishat Sultana Lu Zhang Jianyun Yan Jiqiu Chen Weibin Cai Shegufta Razzaque Dongtak Jeong Wei Sheng Lei Bu Mingjiang Xu Guo-Ying Huang Roger J. Hajjar Bin Zhou Anne Moon Chen-Leng Cai

Identifying a bona fide population of cardiac stem cells (CSCs) is a critical step for developing cell-based therapies for heart failure patients. Previously, cardiac c-kit(+) cells were reported to be CSCs with a potential to become myocardial, endothelial and smooth muscle cells in vitro and after cardiac injury. Here we provide further insights into the nature of cardiac c-kit(+) cells. By t...

Journal: :Head & neck 2009
Rebecca D Chernock Arie Perry John D Pfeifer Joseph A Holden James S Lewis

BACKGROUND Our objective was to identify the expression of epidermal growth factor receptor (EGFR), c-KIT (CD117), and HER2/neu in sinonasal undifferentiated carcinoma (SNUC). METHODS Immunohistochemistry for c-KIT (CD117), EGFR, and HER2/neu was performed on paraffin-embedded tissue from SNUC cases. A search for activating mutations in c-kit exons 9, 11, 13, and 17 or gene amplification was ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2001
B Scappini F Onida H M Kantarjian L Dong S Verstovsek M J Keating M Beran

STI571 is a 2-phenylalaminopyrimidine derivative that inhibits c-abl, Bcr-Abl, and platelet-derived growth factor receptor tyrosine kinases. Recently, inhibition of stem cell factor (SCF)-induced c-kit phosphorylation and cell proliferation by STI571 was reported in the human myeloid cell line MO7e. Because approximately 70% of acute myelogenous leukemia (AML) cases are c-kit positive, we evalu...

Journal: :Molecular cancer therapeutics 2007
Kathryn G Roberts Adam F Odell Ellen M Byrnes Rosa M Baleato Renate Griffith Alan Bruce Lyons Leonie K Ashman

Certain mutations within c-KIT cause constitutive activation of the receptor and have been associated with several human malignancies. These include gastrointestinal stromal tumors (GIST), mastocytosis, acute myelogenous leukemia, and germ cell tumors. The kinase inhibitor imatinib potently inhibits c-KIT and is approved for treatment of GIST. However, secondary point mutations can develop with...

2017
Xuhui Ma Yunteng Wu Tian Zhang Hao Song Houyu Jv Wei Guo Guoxin Ren

c-Kit mutations are frequently detected in mucosal melanomas, but their clinical significance in metastatic oral mucosal melanomas (OMM) remains unclear. The main purpose of this study was to investigate the clinical and pathological features of metastatic OMMs with c-Kit mutations and the efficiency of the tyrosine kinase inhibitor imatinib in treating metastatic OMMs. We found thatresidual pr...

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