Transduction of human MCP-3 by a parvoviral vector induces leukocyte infiltration and reduces growth of human cervical carcinoma cell xenografts.
about
The NS2 proteins of parvovirus minute virus of mice are required for efficient nuclear egress of progeny virions in mouse cells.Structural Characterization of H-1 Parvovirus: Comparison of Infectious Virions to Empty CapsidsSynergistic up-regulation of MCP-2/CCL8 activity is counteracted by chemokine cleavage, limiting its inflammatory and anti-tumoral effectsOncolytic virotherapy as emerging immunotherapeutic modality: potential of parvovirus h-1B1 lymphocytes and myeloid dendritic cells in lymphoid organs are preferential extratumoral sites of parvovirus minute virus of mice prototype strain expression.Activation of the human immune system by chemotherapeutic or targeted agents combined with the oncolytic parvovirus H-1.Chemokines and antitumor immunity: walking the tightrope.Secretion of functional monocyte chemotactic protein 3 by recombinant Mycobacterium bovis BCG attenuates vaccine virulence and maintains protective efficacy against M. tuberculosis infectionAssociation of serum cytokines with colorectal polyp number and type in adult males.Transfection of colorectal cancer cells with chemokine MCP-3 (monocyte chemotactic protein-3) gene retards tumor growth and inhibits tumor metastasis.Modulation of minute virus of mice cytotoxic activities through site-directed mutagenesis within the NS coding region.Chemokine-based immunotherapy: delivery systems and combination therapies.LuIII parvovirus selectively and efficiently targets, replicates in, and kills human glioma cells.Chimeric and pseudotyped parvoviruses minimize the contamination of recombinant stocks with replication-competent viruses and identify a DNA sequence that restricts parvovirus H-1 in mouse cells.Novel adenovirus-based helper system to support production of recombinant parvovirus.The infectivity and lytic activity of minute virus of mice wild-type and derived vector particles are strikingly different.In vivo anti-tumour activity of recombinant MVM parvoviral vectors carrying the human interleukin-2 cDNA.Suppression of metastatic hemangiosarcoma by a parvovirus MVMp vector transducing the IP-10 chemokine into immunocompetent mice.Applications of chemokines as adjuvants for vaccine immunotherapy.Investigation of the sensitivities of distinct gastric cancer cells to parvovirus H-1 induced cytotoxicity.Crucial biological functions of CCL7 in cancer.The expression and correlation between chemokine CCL7 and ABCE1 in non-small cell lung cancer
P2860
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P2860
Transduction of human MCP-3 by a parvoviral vector induces leukocyte infiltration and reduces growth of human cervical carcinoma cell xenografts.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@en
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@nl
type
label
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@en
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@nl
prefLabel
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@en
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@nl
P2093
P2860
P356
P1476
Transduction of human MCP-3 by ...... cal carcinoma cell xenografts.
@en
P2093
Cornelis JJ
Rommelaere J
Van Damme J
P2860
P304
P356
10.1002/JGM.191
P577
2001-07-01T00:00:00Z