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「Hum Gene Ther[Journal]」の検索結果

4190件中 81件~100件表示    検索結果をPubMedで見る PubMedで見る

Aberrantly Expressed Timeless Regulates Cell Proliferation and Cisplatin Efficacy in Cervical Cancer.

Exosome-mediated transfer of anti-miR-33a-5p from transduced endothelial cells enhances macrophage and vascular smooth muscle cell cholesterol efflux.

Sexually Divergent Mortality and Partial Phenotypic Rescue after Gene Therapy in a Mouse Model of Dravet Syndrome.

Period 2-Induced Activation of Autophagy Improves Cardiac Remodeling After Myocardial Infarction.

Public acceptability of gene therapy and gene editing for human use: A systematic review.

Specific overexpression of Mitofusin-2 in hepatic stellate cells ameliorates liver fibrosis in mice model.

Restoration of functional full-length dystrophin after intramuscular transplantation of Foamy Virus-transduced myoblasts.

AAV-mediated Gene Therapy for Aldehyde Dehydrogenase 2 Deficiency Reduces Esophageal DNA Damage and Adducts Associated with Chronic Ethanol Ingestion.

Differential transgene silencing of myeloid-specific promoters in the AAVS1 safe harbor locus of iPSC-derived myeloid cells.

Sustained interleukin-10 transgene expression following intraarticular AAV5-IL-10 administration to horses.

Conditional immortalization of lymphoid progenitors via tetracycline-regulated LMO2 expression.

Ly6a differential expression in BBB is responsible for strain specific CNS transduction profile of AAV-PHP.B.

A Common Outer Retina Change in Retinal Degeneration by Optical Coherence Tomography Can Be Used to Assess Outcomes of Gene Therapy.

Long-term correction of copper metabolism in WD mice with AAV8 vector delivering truncated ATP7b.

Systemic Safety of a Recombinant AAV8 Vector for Human Cocaine Hydrolase Gene Therapy: A Good Laboratory Practice Preclinical Study in Mice.

Rational engineering and pre-clinical evaluation of Neddylation and SUMOylation site modified AAV vectors in murine models of hemophilia B and Leber congenital amarousis.

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