Widespread long-term gene transfer to mouse skeletal muscles and heart.
about
GATA-6 induces p21(Cip1) expression and G1 cell cycle arrestReflecting on 80 years of excellenceA simplified system for generating recombinant adenovirusesCRISPR-Cas9 as a Powerful Tool for Efficient Creation of Oncolytic VirusesLong-chain fatty acids regulate liver carnitine palmitoyltransferase I gene (L-CPT I) expression through a peroxisome-proliferator-activated receptor alpha (PPARalpha)-independent pathwayProtection against Fas-mediated and tumor necrosis factor receptor 1-mediated liver injury by blockade of FADD without loss of nuclear factor-kappaB activationGene therapy delivery systems for enhancing viral and nonviral vectors for cardiac diseases: current concepts and future applications.Noninvasive measurement of gene expression in skeletal muscle.Cytotoxic T-lymphocyte target proteins and their major histocompatibility complex class I restriction in response to adenovirus vectors delivered to mouse liver.In vitro and in vivo biology of recombinant adenovirus vectors with E1, E1/E2A, or E1/E4 deleted.Immune response to recombinant capsid proteins of adenovirus in humans: antifiber and anti-penton base antibodies have a synergistic effect on neutralizing activity.Transient inhibition of CD28 and CD40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administrationAdenoviral cardiotrophin-1 gene transfer protects pmn mice from progressive motor neuronopathy.Bax-mediated cell death by the Gax homeoprotein requires mitogen activation but is independent of cell cycle activityRegulation of smooth muscle cell migration and integrin expression by the Gax transcription factor.Efficient adenoviral-mediated ornithine transcarbamylase expression in deficient mouse and human hepatocytes.Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disordersPhenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer.Gene therapy for Parkinson's disease: review and update.Tetracycline-regulated cardiac gene expression in vivo.Catheter-based antegrade intracoronary viral gene delivery with coronary venous blockade.Targeted expression of transforming growth factor-beta 1 in intracardiac grafts promotes vascular endothelial cell DNA synthesis.Adenovirus-mediated urokinase gene transfer induces liver regeneration and allows for efficient retrovirus transduction of hepatocytes in vivo.Noninvasive imaging of lipid nanoparticle-mediated systemic delivery of small-interfering RNA to the liver.Adenoviral-mediated gene transfer to fetal pulmonary epithelia in vitro and in vivo.Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbitReversal of the phenotype by K-rasval12 silencing mediated by adenovirus-delivered siRNA in human pancreatic cancer cell line Panc-1The Himar1 mariner transposase cloned in a recombinant adenovirus vector is functional in mammalian cellsProlonged and effective blockade of tumor necrosis factor activity through adenovirus-mediated gene transferIn vivo and in vitro analysis of electrical activity-dependent expression of muscle acetylcholine receptor genes using adenovirus.Duchenne muscular dystrophy gene therapy: Lost in translation?In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs.Gene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo.Selective depletion of heat shock protein 70 (Hsp70) activates a tumor-specific death program that is independent of caspases and bypasses Bcl-2.Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-alpha-glucosidaseCoronary restenosis and gene therapy.Adenovirus-mediated expression of a voltage-gated potassium channel in vitro (rat cardiac myocytes) and in vivo (rat liver). A novel strategy for modifying excitabilityNf2 gene inactivation in arachnoidal cells is rate-limiting for meningioma development in the mouse.The evolution of heart gene delivery vectorsCystic fibrosis transmembrane conductance regulator does not affect neutrophil migration across cystic fibrosis airway epithelial monolayers
P2860
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P2860
Widespread long-term gene transfer to mouse skeletal muscles and heart.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@ast
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@en
type
label
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@ast
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@en
prefLabel
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@ast
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@en
P2093
P2860
P356
P1476
Widespread long-term gene transfer to mouse skeletal muscles and heart.
@en
P2093
Stratford-Perricaudet LD
P2860
P304
P356
10.1172/JCI115902
P407
P577
1992-08-01T00:00:00Z