about
Mechanisms of viral entry: sneaking in the front doorAdenoviral transduction of enterocytes and M-cells using in vitro models based on Caco-2 cells: the coxsackievirus and adenovirus receptor (CAR) mediates both apical and basolateral transductionEfficient adenovirus-mediated gene transfer into primary T cells and thymocytes in a new coxsackie/adenovirus receptor transgenic modelExpression of coxsackie adenovirus receptor and alphav-integrin does not correlate with adenovector targeting in vivo indicating anatomical vector barriersReceptor for the group B coxsackieviruses and adenoviruses: CARThe PYRIN domain-only protein POP3 inhibits ALR inflammasomes and regulates responses to infection with DNA virusesA system for the propagation of adenoviral vectors with genetically modified receptor specificities.Expression of Herpes Simplex Virus Thymidine Kinase/Ganciclovir by RNA Trans-Splicing Induces Selective Killing of HIV-Producing Cells.Ectodomain of coxsackievirus and adenovirus receptor genetically fused to epidermal growth factor mediates adenovirus targeting to epidermal growth factor receptor-positive cells.Chimeric adenoviral vectors incorporating a fiber of human adenovirus 3 efficiently mediate gene transfer into prostate cancer cells.CAR-dependent and CAR-independent pathways of adenovirus vector-mediated gene transfer and expression in human fibroblasts.Reducing the native tropism of adenovirus vectors requires removal of both CAR and integrin interactionsEnhancement of adenovirus vector entry into CD70-positive B-cell Lines by using a bispecific CD70-adenovirus fiber antibodyEngineering HIV-resistant human CD4+ T cells with CXCR4-specific zinc-finger nucleases.Synergistic suppression of apoptosis in salivary acinar cells by IGF1 and EGFA novel approach for detecting viable and tissue-specific circulating tumor cells through an adenovirus-based reporter vector.Modeling adenovirus latency in human lymphocyte cell lines.Locally-delivered T-cell-derived cellular vehicles efficiently track and deliver adenovirus delta24-RGD to infiltrating glioma.Use of adenovirus vectors expressing Epstein-Barr virus (EBV) immediate-early protein BZLF1 or BRLF1 to treat EBV-positive tumors.Modulation of adenovirus vector tropism via incorporation of polypeptide ligands into the fiber protein.Postinternalization inhibition of adenovirus gene expression and infectious virus production in human T-cell linesRecombinant adenoviral vectors can induce expression of p73 via the E4-orf6/7 proteinAdenovirus mediated gene transfer to skeletal muscle.Recombinant adenovirus-mediated cytotoxic gene therapy of lymphoproliferative disorders: is CAR important for the vector to ride?Gene transfer approaches for the treatment of inflammatory bowel disease.The transduction of Coxsackie and Adenovirus Receptor-negative cells and protection against neutralizing antibodies by HPMA-co-oligolysine copolymer-coated adenovirusTransgenic expression of the coxsackie/adenovirus receptor enables adenoviral-mediated gene delivery in naive T cells.Zinc-finger nuclease editing of human cxcr4 promotes HIV-1 CD4(+) T cell resistance and enrichment.Mesenchymal stromal cells inhibit murine syngeneic anti-tumor immune responses by attenuating inflammation and reorganizing the tumor microenvironment.Inflammation, apoptosis, and necrosis induced by neoadjuvant fas ligand gene therapy improves survival of dogs with spontaneous bone cancerA mouse model for adenovirus gene delivery.Efficient detection of human circulating tumor cells without significant production of false-positive cells by a novel conditionally replicating adenovirus.Coxsackievirus and adenovirus receptor expression in human endometrial adenocarcinoma: possible clinical implicationsMHC-dependent desensitization of intrinsic anti-self reactivity.Rapid estrogen receptor signaling is essential for the protective effects of estrogen against vascular injury.Adenovirus vector pseudotyping in fiber-expressing cell lines: improved transduction of Epstein-Barr virus-transformed B cells.Protein transduction domains fused to virus receptors improve cellular virus uptake and enhance oncolysis by tumor-specific replicating vectors.Autoregulated expression of p53 from an adenoviral vector confers superior tumor inhibition in a model of prostate carcinoma gene therapy.Surmounting limited gene delivery into primary immune cell populations: Efficient cell type-specific adenoviral transduction by CAR.Combined p19Arf and interferon-beta gene transfer enhances cell death of B16 melanoma in vitro and in vivo.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Adenoviral-mediated gene transfer in lymphocytes.
@ast
Adenoviral-mediated gene transfer in lymphocytes.
@en
type
label
Adenoviral-mediated gene transfer in lymphocytes.
@ast
Adenoviral-mediated gene transfer in lymphocytes.
@en
prefLabel
Adenoviral-mediated gene transfer in lymphocytes.
@ast
Adenoviral-mediated gene transfer in lymphocytes.
@en
P2093
P2860
P356
P1476
Adenoviral-mediated gene transfer in lymphocytes
@en
P2093
S P Hunger
P2860
P304
13159-13164
P356
10.1073/PNAS.95.22.13159
P407
P50
P577
1998-10-01T00:00:00Z