CXCR4/CXCL12 expression and signalling in kidney cancer
暂无分享,去创建一个
M. Probst-Kepper | J. Lauber | J. Buer | M. Mengel | A. Schrader | M. Templin | K. Dittmar | O. Lechner | M Mengel | M Probst-Kepper | A J Schrader | O Lechner | M Templin | K E J Dittmar | S Machtens | A Franzke | T Wollensak | P Gatzlaff | J Atzpodien | J Buer | J Lauber | A. Franzke | J. Lauber | S. Machtens | J. Atzpodien | P. Gatzlaff | T. Wollensak | M. Probst‐Kepper | Patricia Gatzlaff | Andres J. Schrader
[1] Sam W. Lee,et al. Altered Regulation of Cyclin G in Human Breast Cancer and Its Specific Localization at Replication Foci in Response to DNA Damage in p53+/+ Cells* , 1999, The Journal of Biological Chemistry.
[2] H. Kikutani,et al. Molecular cloning and structure of a pre-B-cell growth-stimulating factor. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[3] S. Dudas,et al. Identification and localization of the cytokine SDF1 and its receptor, CXC chemokine receptor 4, to regions of necrosis and angiogenesis in human glioblastoma. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.
[4] 白水 倫生. Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene , 1995 .
[5] Kouji Matsushima,et al. The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract , 1998, Nature.
[6] M. Kagnoff,et al. Chemokine receptor expression by human intestinal epithelial cells. , 1999, Gastroenterology.
[7] H. Kleinman,et al. Vascular endothelial growth factor and basic fibroblast growth factor induce expression of CXCR4 on human endothelial cells: In vivo neovascularization induced by stromal-derived factor-1alpha. , 1999, The American journal of pathology.
[8] G. Murphy,et al. CXCR‐4, a chemokine receptor, is overexpressed in and required for proliferation of glioblastoma tumor cells , 1998, Journal of surgical oncology.
[9] G. Stein,et al. Interferon regulatory factors: growth control and histone gene regulation – it’s not just interferon anymore , 1997, Journal of Molecular Medicine.
[10] S. Namkoong,et al. Antiproliferative effects of retinoic acid/interferon in cervical carcinoma cell lines: Cooperative growth suppression of IRF‐1 and p53 , 2000, International journal of cancer.
[11] M. Mori,et al. Reduced expression of the CXCR4 receptor mRNA in hepatocellular carcinoma and lack of inducibility of its ligand alpha-chemokine hIRH/SDF1alpha/PBSF in vitro. , 1999, International journal of oncology.
[12] R. Strieter,et al. CXC chemokine modulation of angiogenesis: the importance of balance between angiogenic and angiostatic members of the family. , 1998, Journal of investigative medicine : the official publication of the American Federation for Clinical Research.
[13] E. Odintsova,et al. Attenuation of EGF receptor signaling by a metastasis suppressor, the tetraspanin CD82/KAI-1 , 2000, Current Biology.
[14] W. Gong,et al. Chemokines and their role in tumor growth and metastasis. , 1998, Journal of immunological methods.
[15] M. Karin,et al. Antitumor promotion by phenolic antioxidants: inhibition of AP-1 activity through induction of Fra expression. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[16] L. Kirshenbaum,et al. A direct requirement of nuclear factor-κB for suppression of apoptosis in ventricular myocytes , 2000 .
[17] H. Kleinman,et al. Vascular endothelial growth factor and basic fibroblast growth factor induce expression of CXCR4 on human endothelial cells: In vivo neovascularization induced by stromal-derived factor-1alpha. , 1999, The American journal of pathology.
[18] P. Brown,et al. DNA arrays for analysis of gene expression. , 1999, Methods in enzymology.
[19] Jianbin Wang,et al. Chemokine receptors and virus entry in the central nervous system. , 1999, Journal of neurovirology.
[20] T. Mcclanahan,et al. Involvement of chemokine receptors in breast cancer metastasis , 2001, Nature.
[21] H. Friess,et al. KAI1 expression is up-regulated in early pancreatic cancer and decreased in the presence of metastases. , 1996, Cancer research.
[22] M. Mori,et al. CXCR4 mRNA expression in colon, esophageal and gastric cancers and hepatitis C infected liver. , 1999, International journal of oncology.
[23] D. Fradelizi,et al. CD82, member of the tetra-span-transmembrane protein family, is a costimulatory protein for T cell activation. , 1995, Journal of immunology.
[24] J. Barrett,et al. KAI1, a metastasis suppressor gene for prostate cancer on human chromosome 11p11.2. , 1995, Science.
[25] C Murdoch,et al. Cxc chemokine receptor expression on human endothelial cells. , 1999, Cytokine.
[26] S. Rafii,et al. Chemotaxis of primitive hematopoietic cells in response to stromal cell-derived factor-1. , 2000, The Journal of clinical investigation.
[27] I. Weinstein,et al. Molecular cloning of TPAR1, a gene whose expression is repressed by the tumor promoter 12-O-tetradecanoylphorbol 13-acetate (TPA). , 1994, Experimental cell research.
[28] J. Westwick,et al. Expression of functional CXCR4 chemokine receptors on human colonic epithelial cells. , 1999, The Journal of clinical investigation.
[29] M. Mori,et al. Reduced expression of the CXC chemokine hIRH/SDF‐1α mRNA in hepatoma and digestive tract cancer , 1997, International journal of cancer.
[30] L. Kirshenbaum,et al. A direct requirement of nuclear factor-kappa B for suppression of apoptosis in ventricular myocytes. , 2000, American journal of physiology. Heart and circulatory physiology.
[31] Mark A. Watson,et al. EGR1 Target Genes in Prostate Carcinoma Cells Identified by Microarray Analysis* , 2000, The Journal of Biological Chemistry.
[32] J. Inazawa,et al. Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene. , 1995, Genomics.
[33] G. Murphy,et al. Molecular characterization of CXCR–4: A potential brain tumor‐associated gene , 1998, Journal of surgical oncology.
[34] Masahiko Kuroda,et al. Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development , 1998, Nature.