Parvovirus-mediated gene transfer for the haemophilias

scientific article

Parvovirus-mediated gene transfer for the haemophilias is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1046/J.1351-8216.2001.00121.X
P698PubMed publication ID11966856

P2093author name stringChao H
Walsh CE
P2860cites workrAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophyQ28144597
Advances toward gene therapy for hemophilia at the millenniumQ33739072
Repeat transduction in the mouse lung by using adeno-associated virus vectors with different serotypesQ33793801
Adeno-associated virus type 5 (AAV5) but not AAV2 binds to the apical surfaces of airway epithelia and facilitates gene transferQ33802811
Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivoQ33811409
Immune responses to adenovirus and adeno-associated virus in humans.Q33874473
Building a better vector: the manipulation of AAV virionsQ33928283
Molecular biology of adeno-associated virusesQ34002311
Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient miceQ35621550
Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virusQ36159178
Cloning of adeno-associated virus into pBR322: rescue of intact virus from the recombinant plasmid in human cellsQ36288360
Sustained correction of bleeding disorder in hemophilia B mice by gene therapyQ36454880
Infectious entry pathway of adeno-associated virus and adeno-associated virus vectorsQ39589898
Efficient lentiviral transduction of liver requires cell cycling in vivoQ40909303
High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap.Q40933793
Defective adenoassociated viral-mediated transfection of insulin gene by direct injection into liver parenchyma decreases blood glucose of diabetic miceQ41060258
Adeno-associated virus type 2 binds to a 150-kilodalton cell membrane glycoproteinQ41226028
Analysis of the Cell and Erythrocyte Binding Activities of the Dimple and Canyon Regions of the Canine Parvovirus CapsidQ41317029
In vivo gene therapy of hemophilia B: sustained partial correction in factor IX-deficient dogsQ41524708
New developments in the generation of Ad-free, high-titer rAAV gene therapy vectorsQ41634721
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brainQ42280576
The use of adeno-associated virus to circumvent the maturation-dependent viral transduction of muscle fibersQ42485226
Effects of gamma irradiation on the transduction of dividing and nondividing cells in brain and muscle of rats by adeno-associated virus vectorsQ42525047
Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophiliaQ45060641
Adeno-associated virus (AAV)-3-based vectors transduce haematopoietic cells not susceptible to transduction with AAV-2-based vectorsQ45741486
Recombinant adeno-associated virus for muscle directed gene therapyQ45764433
Quantitative analysis of the packaging capacity of recombinant adeno-associated virusQ45766162
The molecular basis of haemophilia B.Q45854871
Persistent expression of canine factor IX in hemophilia B caninesQ45862802
Several log increase in therapeutic transgene delivery by distinct adeno-associated viral serotype vectorsQ45873434
Detection of adeno-associated virus type 2 in human peripheral blood cellsQ45878397
Sustained and complete phenotype correction of hemophilia B mice following intramuscular injection of AAV1 serotype vectorsQ45879602
P407language of work or nameEnglishQ1860
P921main subjecthemophiliaQ134003
P304page(s)60-67
P577publication date2002-03-01
P1433published inHaemophiliaQ15753375
P1476titleParvovirus-mediated gene transfer for the haemophilias
P478volume8 Suppl 2

Reverse relations

cites work (P2860)
Q35127766Haemophilia B: from molecular diagnosis to gene therapy.
Q45865401Pre-existing AAV capsid-specific CD8+ T cells are unable to eliminate AAV-transduced hepatocytes

Search more.