相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Development of lentiviral vectors with regulated respiratory epithelial expression in vivo
Benjamin Hendrickson et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2007)
Repeated aerosolized AAV-CFTR for treatment of cystic fibrosis: A Randomized placebo-controlled phase 2B trial
Richard B. Moss et al.
HUMAN GENE THERAPY (2007)
Gene delivery to airway epithetiat cells in vivo:: a direct comparison of apicat and basotateral transduction strategies using pseudotyped lentivirus vectors
Karlea L. Kremer et al.
JOURNAL OF GENE MEDICINE (2007)
Targeted Gene Transfer to Fetal Rat Lung Interstitium by Ultrasound-guided Intrapulmonary Injection
Tiago Henriques-Coelho et al.
MOLECULAR THERAPY (2007)
Long-term persistence of gene expression from adeno-associated virus serotype 5 in the mouse airways
S. G. Sumner-Jones et al.
GENE THERAPY (2006)
Readministration of helper-dependent adenovirus to mouse lung
DR Koehler et al.
GENE THERAPY (2006)
Influenza M2 envelope protein augments avian influenza hemagglutinin pseudotyping of lentiviral vectors
T McKay et al.
GENE THERAPY (2006)
Prevalence of neutralizing antibodies against adeno-associated virus (AAV) types 2, 5, and 6 in cystic fibrosis and normal populations: Implications for gene therapy using AAV vectors
CL Halbert et al.
HUMAN GENE THERAPY (2006)
Pathogenesis of early lung disease in cystic fibrosis: A window of opportunity to eradicate bacteria
TD Starner et al.
ANNALS OF INTERNAL MEDICINE (2005)
Persistent gene expression in mouse nasal epithelia following feline immunodeficiency virus-based vector gene transfer
PL Sinn et al.
JOURNAL OF VIROLOGY (2005)
Factors influencing adenovirus-mediated airway transduction in fetal mice
SMK Buckley et al.
MOLECULAR THERAPY (2005)
Detection of plasmid DNA vectors following gene transfer to the murine airways
IA Pringle et al.
GENE THERAPY (2005)
Intrapulmonary and intramyocardial gene transfer in rhesus monkeys (Macaca mulatta):: Safety and efficiency of HIV-1-derived lentiviral vectors for fetal gene delivery
AF Tarantal et al.
MOLECULAR THERAPY (2005)
Recent developments in recombinant AAV-mediated gene therapy for lung diseases
TR Flotte
CURRENT GENE THERAPY (2005)
Gene transfer to respiratory epithelia with lentivirus pseudotyped with jaagsiekte sheep retrovirus envelope glycoprotein
PL Sinn et al.
HUMAN GENE THERAPY (2005)
Delivery of CFTR by adenoviral vector to cystic fibrosis mouse lung in a model of chronic Pseudomonas aeruginosa lung infection
AM van Heeckeren et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2004)
Glycocalyx restricts adenoviral vector access to apical receptors expressed on respiratory epithelium in vitro and in vivo: Role for tethered mucins as barriers to lumenal infection
JR Stonebraker et al.
JOURNAL OF VIROLOGY (2004)
Widespread and efficient marker gene expression in the airway epithelia of fetal sheep after minimally invasive tracheal application of recombinant adenovirus in utero
D Peebles et al.
GENE THERAPY (2004)
Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy
SN Waddington et al.
BLOOD (2004)
Effect of Pseudomonas-induced chronic lung inflammation on specific cytotoxic T-cell responses to adenoviral vectors in mice
MF Tosi et al.
GENE THERAPY (2004)
Factors influencing the titer and infectivity of lentiviral vectors
AC Logan et al.
HUMAN GENE THERAPY (2004)
Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice
SN Waddington et al.
GENE THERAPY (2003)
Human fetal trachea-scid mouse xenografts: Efficacy of vesicular stomatitis virus-G pseudotyped lentiviral-mediated gene transfer
FY Lim et al.
JOURNAL OF PEDIATRIC SURGERY (2003)
Lentivirus vectors pseudotyped with filoviral envelope glycoproteins transduce airway epithelia from the apical surface independently of folate receptor alpha
PL Sinn et al.
JOURNAL OF VIROLOGY (2003)
Analysis of gene transfer and expression in skeletal muscle using enhanced EIAV lentivirus vectors
JP O'Rourke et al.
MOLECULAR THERAPY (2003)
Pseudotyped lentivirus vectors derived from simian immunodeficiency virus SIVagm with envelope glycoproteins from paramyxovirus
M Kobayashi et al.
JOURNAL OF VIROLOGY (2003)
Enhancement of adenovirus-mediated gene transfer to the airways by DEAE dextran and sodium caprate in vivo
LG Gregory et al.
MOLECULAR THERAPY (2003)
Covering the limb - formation of the integument
C Byrne et al.
JOURNAL OF ANATOMY (2003)
Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer
M Limberis et al.
HUMAN GENE THERAPY (2002)
Lung edema clearance:: 20 years of progress -: Invited review:: Clearance of lung liquid during the perinatal period
PM Barker et al.
JOURNAL OF APPLIED PHYSIOLOGY (2002)
High-level transduction and gene expression in hematopoietic repopulating cells using a human imunodeficiency virus type 1-based lentiviral vector containing an internal spleen focus forming virus promoter
C Demaison et al.
HUMAN GENE THERAPY (2002)
Lentiviral vectors for efficient transduction of isolated primary quiescent hepatocytes
J Seppen et al.
JOURNAL OF HEPATOLOGY (2002)
High levels of transduction of human dendritic cells with optimized SIV vectors
PE Mangeot et al.
MOLECULAR THERAPY (2002)
Lentiviral vector gene transfer into fetal rhesus monkeys (Macaca mulatta):: Lung-targeting approaches
AF Tarantal et al.
MOLECULAR THERAPY (2001)
Filovirus-pseudotyped lentiviral vector can efficiently and stably transduce airway epithelia in vivo
GP Kobinger et al.
NATURE BIOTECHNOLOGY (2001)
Host responses and persistence of vector genome following intrabronchial administration of an E1-E3- adenovirus gene transfer vector to normal individuals
BG Harvey et al.
MOLECULAR THERAPY (2001)
Gene transfer into the fetal primate: Evidence for the secretion of transgene product
JE Larson et al.
MOLECULAR THERAPY (2000)
Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis
SC Hyde et al.
GENE THERAPY (2000)
分享论文
