AAV vector integration sites in mouse hepatocellular carcinoma. - Wikidata - awgldk - TriplyDB

AAV vector integration sites in mouse hepatocellular carcinoma.

AAV vector integration sites in mouse hepatocellular carcinoma.

http://www.wikidata.org/entity/Q45869780

about

Small nucleolar RNA signatures as biomarkers for non-small-cell lung cancer Adeno-associated virus vector integration A transposon and transposase system for human application Gene therapy for mucopolysaccharidosis Preferential delivery of the Sleeping Beauty transposon system to livers of mice by hydrodynamic injection Ku70, an essential gene, modulates the frequency of rAAV-mediated gene targeting in human somatic cells Targeting adeno-associated virus and adenoviral gene therapy for hepatocellular carcinoma The gene therapy journey for hemophilia: are we there yet?A short perspective on gene therapy: Clinical experience on gene therapy of gliomablastoma multiforme Animal models of hemophilia Long-term correction of Sandhoff disease following intravenous delivery of rAAV9 to mouse neonates Comparative analysis of DNA nanoparticles and AAVs for ocular gene delivery Changing channels in pain and epilepsy: Exploiting ion channel gene therapy for disorders of neuronal hyperexcitability A universal system to select gene-modified hepatocytes in vivo MeCP2-dependent repression of an imprinted miR-184 released by depolarization Epstein-Barr virus nuclear antigen 1 does not cause lymphoma in C57BL/6J mice Gene Therapy for Metabolic Diseases Impact of hydrodynamic injection and phiC31 integrase on tumor latency in a mouse model of MYC-induced hepatocellular carcinoma Analysis of small nucleolar RNAs in sputum for lung cancer diagnosis.Lessons Learned from Animal Models of Inherited Bleeding Disorders.Somatic Therapy of a Mouse SMA Model with a U7 snRNA Gene Correcting SMN2 Splicing Translational data from adeno-associated virus-mediated gene therapy of hemophilia B in dogs Group II intron-based gene targeting reactions in eukaryotes.Long-term tracking of segmental bone healing mediated by genetically engineered adipose-derived stem cells: focuses on bone remodeling and potential side effects.Mechanisms of nucleotide trafficking during siRNA delivery to endothelial cells using perfluorocarbon nanoemulsions.Gene expression in lung and liver after intravenous infusion of polyethylenimine complexes of Sleeping Beauty transposons.Development of a hybrid baculoviral vector for sustained transgene expression Baculovirus transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.Cell penetrating peptide POD mediates delivery of recombinant proteins to retina, cornea and skin.AAV provides an alternative for gene therapy of the peripheral sensory nervous system.Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects.Gene correction in human embryonic and induced pluripotent stem cells: promises and challenges ahead.AAV-mediated liver-directed gene therapy.SnoRNA U50 is a candidate tumor-suppressor gene at 6q14.3 with a mutation associated with clinically significant prostate cancer Incorporation of pseudouridine into mRNA enhances translation by diminishing PKR activation.Delivery of molecules into cells using localized single cell electroporation on ITO micro-electrode based transparent chip.rAAV-mediated tumorigenesis: still unresolved after an AAV assault Adeno-associated virus-mediated gene transfer Gene therapy of mdx mice with large truncated dystrophins generated by recombination using rAAV6.Mesenchymal stem cells for the treatment of neurodegenerative disease.

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P2860

AAV vector integration sites in mouse hepatocellular carcinoma.

http://www.wikidata.org/entity/Q45869780

description

2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh-hant

name

AAV vector integration sites in mouse hepatocellular carcinoma.

@en

AAV vector integration sites in mouse hepatocellular carcinoma.

@nl

type

label

AAV vector integration sites in mouse hepatocellular carcinoma.

@en

AAV vector integration sites in mouse hepatocellular carcinoma.

@nl

prefLabel

AAV vector integration sites in mouse hepatocellular carcinoma.

@en

AAV vector integration sites in mouse hepatocellular carcinoma.

@nl

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SCIENCE.1142658

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AAV vector integration sites in mouse hepatocellular carcinoma

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Carole Vogler

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Elizabeth M Brunt

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Yi Li

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P2860

Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

Large-scale analysis of adeno-associated virus vector integration sites in normal human cells.

Imprinted DLK1 is a putative tumor suppressor gene and inactivated by epimutation at the region upstream of GTL2 in human renal cell carcinoma.

Observed incidence of tumorigenesis in long-term rodent studies of rAAV vectors.

Analysis of tumors arising in male B6C3F1 mice with and without AAV vector delivery to liver.

Nuclear Ploidy in Mammalian Parenchymal Liver Cells

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477

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scholarly article

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10.1126/SCIENCE.1142658

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P433

5837

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317

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Daniel G. Miller

Anthony Donsante

David W Russell

P577

2007-07-01T00:00:00Z

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P698

17656716

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