Efficient gene transfer into the mouse lung by fetal intratracheal injection of rAAV2/6.2.

[1]  T. Flotte,et al.  Dual reporter comparative indexing of rAAV pseudotyped vectors in chimpanzee airway. , 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

[2]  James M. Wilson,et al.  Naturally occurring singleton residues in AAV capsid impact vector performance and illustrate structural constraints , 2009, Gene Therapy.

[3]  D. Aubert,et al.  Transient expression of genes delivered to newborn rat liver using recombinant adeno‐associated virus 2/8 vectors , 2009, The journal of gene medicine.

[4]  G. Bormans,et al.  Highly efficient multicistronic lentiviral vectors with peptide 2A sequences. , 2009, Human gene therapy.

[5]  James M. Wilson,et al.  Transduction efficiencies of novel AAV vectors in mouse airway epithelium in vivo and human ciliated airway epithelium in vitro. , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

[6]  L. Davies,et al.  Adenovirus-mediated in utero expression of CFTR does not improve survival of CFTR knockout mice. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

[7]  W. Colledge,et al.  Intra-amniotic delivery of CFTR-expressing adenovirus does not reverse cystic fibrosis phenotype in inbred CFTR-knockout mice. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

[8]  D. Geddes,et al.  In vivo imaging of gene transfer to the respiratory tract. , 2008, Biomaterials.

[9]  C. Férec,et al.  Prenatal diagnosis of cystic fibrosis: the 18‐year experience of Brittany (western France) , 2008, Prenatal diagnosis.

[10]  James M. Wilson,et al.  AAV as an immunogen. , 2007, Current gene therapy.

[11]  L. Mortelmans,et al.  Fetal gene transfer with lentiviral vectors: long-term in vivo follow-up evaluation in a rat model. , 2007, American journal of obstetrics and gynecology.

[12]  A. Leite-Moreira,et al.  Targeted gene transfer to fetal rat lung interstitium by ultrasound-guided intrapulmonary injection. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

[13]  S. Kügler,et al.  Long-term rescue of a lethal inherited disease by adeno-associated virus-mediated gene transfer in a mouse model of molybdenum-cofactor deficiency. , 2007, American journal of human genetics.

[14]  D. Warburton,et al.  Lung development and susceptibility to chronic obstructive pulmonary disease. , 2006, Proceedings of the American Thoracic Society.

[15]  James M. Wilson,et al.  Adeno-associated virus serotype 9 vectors transduce murine alveolar and nasal epithelia and can be readministered , 2006, Proceedings of the National Academy of Sciences.

[16]  B. Hogan,et al.  Epithelial stem cells of the lung: privileged few or opportunities for many? , 2006, Development.

[17]  M. Haskins,et al.  Large animal models and gene therapy , 2006, European Journal of Human Genetics.

[18]  B. Byrne,et al.  Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer , 2006, Gene Therapy.

[19]  C Coutelle,et al.  Gene Therapy Progress and Prospects: Fetal gene therapy – first proofs of concept – some adverse effects , 2005, Gene Therapy.

[20]  C. Delacourt,et al.  Comparative efficacy of intratracheal adeno-associated virus administration to newborn rats. , 2005, Human gene therapy.

[21]  S. Jezzard,et al.  Factors influencing adenovirus-mediated airway transduction in fetal mice. , 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

[22]  V. Choi,et al.  AAV hybrid serotypes: improved vectors for gene delivery. , 2005, Current gene therapy.

[23]  Bing Wang,et al.  Adeno-associated virus serotype 8 efficiently delivers genes to muscle and heart , 2005, Nature Biotechnology.

[24]  R. Samulski,et al.  Integration of adeno-associated virus (AAV) and recombinant AAV vectors. , 2004, Annual review of genetics.

[25]  M. Wilke,et al.  Animal models of cystic fibrosis. , 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[26]  Jan Deprest,et al.  Fetoscopic tracheal occlusion (FETO) for severe congenital diaphragmatic hernia: evolution of a technique and preliminary results , 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[27]  M. R. Delgado Alvira,et al.  Clades of Adeno-Associated Viruses Are Widely Disseminated in Human Tissues , 2004, Journal of Virology.

[28]  M. Brittan,et al.  Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy. , 2004, Blood.

[29]  S. Chanock,et al.  Performance of high-throughput DNA quantification methods , 2003, BMC biotechnology.

[30]  C. Coutelle,et al.  Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice , 2003, Gene Therapy.

[31]  Lili Wang,et al.  Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Lili Wang,et al.  Noninvasive gene transfer to the lung for systemic delivery of therapeutic proteins. , 2002, The Journal of clinical investigation.

[33]  James M. Allen,et al.  Adeno-Associated Virus Type 6 (AAV6) Vectors Mediate Efficient Transduction of Airway Epithelial Cells in Mouse Lungs Compared to That of AAV2 Vectors , 2001, Journal of Virology.

[34]  M. Mitchell,et al.  Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors , 2000, Gene Therapy.

[35]  M. Hiratsuka,et al.  Adenovirus-mediated in utero gene transfer in mice and guinea pigs: tissue distribution of recombinant adenovirus determined by quantitative TaqMan-polymerase chain reaction assay. , 2000, Molecular genetics and metabolism.

[36]  A. Douar,et al.  Foetal gene delivery in mice by intra-amniotic administration of retroviral producer cells and adenovirus , 1997, Gene Therapy.

[37]  J. Mullins,et al.  Photonic detection of bacterial pathogens in living hosts , 1995, Molecular microbiology.

[38]  James M. Wilson,et al.  Detection of reporter gene expression in murine airways. , 2007, Methods in molecular biology.

[39]  C. Rodeck,et al.  Widespread and efficient marker gene expression in the airway epithelia of fetal sheep after minimally invasive tracheal application of recombinant adenovirus in utero , 2004, Gene therapy.

[40]  Matthew H. Kaufman,et al.  The Atlas of Mouse Development , 1992 .