Search Results - "MONIA, B. P"
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Knockdown of the gene encoding Drosophila tribbles homologue 3 (Trib3) improves insulin sensitivity through peroxisome proliferator-activated receptor-γ (PPAR-γ) activation in a rat model of insulin resistance
Published in Diabetologia (01-04-2011)“…Aims/hypothesis Insulin action is purportedly modulated by Drosophila tribbles homologue 3 (TRIB3), which in vitro prevents thymoma viral proto-oncogene (AKT)…”
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Evaluation of 2'-modified oligonucleotides containing 2'-deoxy gaps as antisense inhibitors of gene expression
Published in The Journal of biological chemistry (05-07-1993)“…We have used a previously described 17-mer phosphorothioate (Monia, B.P., Johnston, J.F., Ecker, D. J., Zounes, M.A., Lima, W.F., and Freier, S.M. (1992) J…”
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Association of c-Raf expression with survival and its targeting with antisense oligonucleotides in ovarian cancer
Published in British journal of cancer (30-11-2001)“…c-Raf is an essential component of the extracellular related kinase (ERK) signal transduction pathway. Immunohistochemical staining indicated that c-Raf was…”
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Bcl-xL antisense oligonucleotides radiosensitise colon cancer cells
Published in British journal of cancer (06-10-2003)“…Advanced colon cancer is a malignancy with poor response to various treatment modalities including ionising radiation (IR) and chemotherapy. Both IR and…”
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Kinetic characteristics of Escherichia coli RNase H1: cleavage of various antisense oligonucleotide-RNA duplexes
Published in Biochemical journal (01-12-1995)“…1. The effects of variations in substrates on the kinetic properties of Escherichia coli RNase H were studied using antisense oligonucleotides of various types…”
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Targeted delivery of antisense oligonucleotides to pancreatic β-cells
Published in Science advances (01-10-2018)“…Antisense oligonucleotide (ASO) silencing of the expression of disease-associated genes is an attractive novel therapeutic approach, but treatments are limited…”
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Polyethyleneimine grafted with pluronic P85 enhances Ku86 antisense delivery and the ionizing radiation treatment efficacy in vivo
Published in Gene therapy (01-11-2004)“…In an effort to improve the efficacy of antisense delivery, we evaluated polyethyleneimine (PEI, 2 kDa) alone or grafted with nonionic amphiphilic block…”
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Destabilization of Raf-1 by geldanamycin leads to disruption of the Raf-1-MEK-mitogen-activated protein kinase signalling pathway
Published in Molecular and Cellular Biology (01-10-1996)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Inhibition of proteolysis and cell cycle progression in a multiubiquitination-deficient yeast mutant
Published in Molecular and Cellular Biology (01-08-1994)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Antitumor activity of a C-raf antisense oligonucleotide in combination with standard chemotherapeutic agents against various human tumors transplanted subcutaneously into nude mice
Published in Clinical cancer research (01-07-1997)“…A 20-mer phosphorothioate oligodeoxynucleotide (ODN) directed against human C-raf kinase (CGP 69846A or ISIS 5132) was analyzed for its antitumor activity…”
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Coagulation factor XI as a novel target for antithrombotic treatment
Published in Journal of thrombosis and haemostasis (01-11-2010)“…Coagulation factor (F)XI was first described as a member of the contact pathway of coagulation. However, the ‘classic’ theory of the extrinsic and intrinsic…”
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Selective inhibition of mutant Ha-ras mRNA expression by antisense oligonucleotides
Published in The Journal of biological chemistry (05-10-1992)“…A biological reporter gene assay was employed to determine the crucial parameters for maximizing selective targeting of a Ha-ras codon 12 point mutation…”
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c-raf-1 Depletion and Tumor Responses in Patients Treated with the c-raf-1 Antisense Oligodeoxynucleotide ISIS 5132 (CGP 69846A)
Published in Clinical cancer research (01-12-1999)“…Abnormally regulated signaling through proliferative signal transduction pathways characterizes many of the common solid tumors. The best described of these…”
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PKC-ε Is Required for Mechano-sensitive Activation of ERK1/2 in Endothelial Cells
Published in The Journal of biological chemistry (12-12-1997)“…Mechano-sensitive regulation of endothelial cells (EC) function by shear stress is critical for flow-induced vasodilation and gene expression. Previous studies…”
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PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts trastuzumab resistance in patients
Published in Cancer cell (01-08-2004)“…The ErbB2-targeting antibody, trastuzumab (Herceptin), has remarkable therapeutic efficacy in certain patients with ErbB2-overexpressing tumors. The overall…”
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Biophysical and antisense properties of oligodeoxynucleotides containing 7-propynyl-, 7-iodo- and 7-cyano-7-deaza-2-amino-2′-deoxyadenosines
Published in Nucleic acids research (15-07-1998)“…The synthesis of 7-propynyl-, 7-iodo- and 7-cyano-7-deaza-2-amino-2′-deoxyadenosines is described. The nucleosides were synthesized, functionalized into the…”
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Implication of RNA structure on antisense oligonucleotide hybridization kinetics
Published in Biochemistry (Easton) (08-12-1992)“…A 47-nucleotide transcript of the activated Ha-ras gene was prepared and determined, by enzymatic structure mapping, to form a stable hairpin structure. Six…”
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2‘-O-Aminopropyl Ribonucleotides: A Zwitterionic Modification That Enhances the Exonuclease Resistance and Biological Activity of Antisense Oligonucleotides
Published in Journal of medicinal chemistry (20-12-1996)“…Oligonucleotides containing 2‘-O-aminopropyl-substituted RNA have been synthesized. The 2‘-O-(aminopropyl)adenosine (APA), 2‘-O-(aminopropyl)cytidine (APC),…”
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Preclinical Evaluation of the Effects of a Novel Antisense Compound Targeting C-raf Kinase in Mice and Monkeys
Published in Toxicological sciences (01-12-1998)“…CGP 69846A (ISIS 5132) is an antisense phosphorothioate oligodeoxynucleotide which targets human C-raf kinase and is currently being developed as an…”
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