about
Creation of non-human primate neurogenetic disease models by gene targeting and nuclear transferIn utero recombinant adeno-associated virus gene transfer in mice, rats, and primatesFactors determining the risk of inadvertent retroviral transduction of male germ cells after in utero gene transfer in sheep.Current status of gene therapy for cystic fibrosis pulmonary disease.Rescue of ATPa3-deficient murine malignant osteopetrosis by hematopoietic stem cell transplantation in utero.From gene transfer to gene therapy in lysosomal storage diseases affecting the central nervous system.Enhancing polyethylenimine's delivery of plasmid DNA into mammalian cells.In utero stem cell transplantation: two steps forward but one step back?N-isopropylacrylamide-modified polyethylenimines as effective gene carriers.Gene repair in the new age of gene therapy.Multiorgan engraftment and differentiation of human cord blood CD34+ Lin- cells in goats assessed by gene expression profiling.Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transductionSelf-assembled BolA-like amphiphilic peptides as viral-mimetic gene vectors for cancer cell targeted gene delivery.Transabdominal first trimester embryofetoscopy as a potential approach to early in utero stem cell transplantation and gene therapy.A study to determine if human umbilical cord hematopoietic stem cells can survive in baboon extra-embryonic celomic fluid: a prerequisite for determining the feasibility of in-utero stem cell xeno-transplantation via celocentesis.Intracellular plasmid DNA delivery by self-assembled nanoparticles of amphiphilic PHML-b-PLLA-b-PHML copolymers and the endocytosis pathway analysis.Newborn liver gene transfer by an HIV-2-based lentiviral vector.Summary report of a symposium: genes and gene delivery for diseases of alcoholism.HIV-1-derived lentiviral vectors and fetal route of administration on transgene biodistribution and expression in rhesus monkeys.Evaluation of prenatal intra-amniotic LAMB3 gene delivery in a mouse model of Herlitz disease.Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa.Efficient engraftment of in utero transplanted mice with retrovirally transduced hematopoietic stem cells.Sustained delivery of therapeutic concentrations of human clotting factor IX--a comparison of adenoviral and AAV vectors administered in utero.Immune response to lentiviral bilirubin UDP-glucuronosyltransferase gene transfer in fetal and neonatal rats.Efficient gene transfer into neonatal mouse brain using electroporation.
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Prospects for in utero human gene therapy.
@ast
Prospects for in utero human gene therapy.
@en
type
label
Prospects for in utero human gene therapy.
@ast
Prospects for in utero human gene therapy.
@en
prefLabel
Prospects for in utero human gene therapy.
@ast
Prospects for in utero human gene therapy.
@en
P1433
P1476
Prospects for in utero human gene therapy.
@en
P2093
Anderson WF
P304
P356
10.1126/SCIENCE.285.5436.2084
P407
P577
1999-09-01T00:00:00Z