Search Results - "Yendluri, Satya"
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Dose-dependent effects of siRNA-mediated inhibition of SCAP on PCSK9, LDLR, and plasma lipids in mouse and rhesus monkey[S]
Published in Journal of lipid research (01-12-2016)“…SREBP cleavage-activating protein (SCAP) is a key protein in the regulation of lipid metabolism and a potential target for treatment of dyslipidemia. SCAP is…”
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2
Novel Immunocompetent Murine Tumor Model for Evaluation of Conditionally Replication-Competent (Oncolytic) Murine Adenoviral Vectors
Published in Journal of Virology (01-04-2009)“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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3
Enhanced gene transfer efficiency in the murine striatum and an orthotopic glioblastoma tumor model, using AAV-7- and AAV-8-pseudotyped vectors
Published in Human gene therapy (01-08-2006)“…In this study, recombinant AAV vectors pseudotyped with viral capsids derived from AAV serotypes 7 and 8 were evaluated for gene transfer in the murine…”
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4
Antiviral Nucleotide Incorporation by Recombinant Human Mitochondrial RNA Polymerase Is Predictive of Increased In Vivo Mitochondrial Toxicity Risk
Published in Antimicrobial agents and chemotherapy (01-12-2016)“…Nucleoside or nucleotide inhibitors are a highly successful class of antivirals due to selectivity, potency, broad coverage, and high barrier to resistance…”
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5
Development of Lipoprotein(a) siRNAs for Mechanism of Action Studies in Non-Human Primate Models of Atherosclerosis
Published in Journal of cardiovascular translational research (01-02-2015)“…Lipoprotein(a) [Lp(a)] has recently been recognized as an independent risk factor for coronary heart disease. While plasma Lp(a) levels are correlated with…”
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Abstract B261: Characterization of FASN-selective small-molecule inhibitors in preclinical tumor models
Published in Molecular cancer therapeutics (01-11-2013)“…Abstract The purpose of this study is to characterize the activity of small-molecule FASN inhibitors in preclinical models of human cancer to evaluate their…”
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130. Insertion of Transgenes into the E3 or L3 Region To Allow Tumor Selective Expression from Armed Oncolytic Adenoviruses
Published in Molecular therapy (01-05-2006)“…The ability to arm oncolytic vectors with transgenes gives researchers a mechanism for potential improvements in the vector potency. However, depending on the…”
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AAV Serotype 8-Mediated Gene Delivery of a Soluble VEGF Receptor to the CNS for the Treatment of Glioblastoma
Published in Molecular therapy (01-05-2006)“…The presence of the blood–brain barrier complicates drug delivery in the development of therapeutic agents for the treatment of glioblastoma multiforme (GBM)…”
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Third-generation lentivirus vectors efficiently transduce and phenotypically modify vascular cells: implications for gene therapy
Published in Journal of molecular and cellular cardiology (01-07-2003)“…Grafting of saphenous vein (SV) conduits into the arterial circulation triggers a number of adaptive pathological changes characterized by progressive medial…”
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974. Adeno-Associated Viral (AAV)-Mediated Gene Transfer of Soluble Vascular Endothelial Growth Factor Receptor 3 (sVEGFR3) Inhibits Development of Lymph Node Metastases
Published in Molecular therapy (01-05-2004)“…The metastatic spread of tumor cells represents a critical point in tumor progression. The presence of metastases in regional lymph nodes is a strong indicator…”
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