Search Results - "Chiba, P."
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Classification of arm swing as a clinical marker of advancing spinal deformity among community-dwelling female volunteers 60 years or older
Published in Scientific reports (20-05-2019)“…The clinical characteristics of adult spinal deformity (ASD) include worsening of deformity during gait, which leads to unstable posture and propensity to…”
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First results of a national external quality assessment scheme for the detection of SARS-CoV-2 genome sequences
Published in Journal of clinical virology (01-08-2020)“…•Implementation of SARS-CoV-2 genome testing by numerous laboratories in Austria.•Broad range of combinations of nucleic acid extraction and RT-PCR…”
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Pharmacoinformatic approaches to design natural product type ligands of ABC-transporters
Published in Current pharmaceutical design (01-05-2010)“…ABC-transporter have been recognized as being responsible for multiple drug resistance in tumor therapy, for decreased brain uptake and low oral…”
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O083 : Absence of BSEP/ABCB11 protects from cholestatic liver and bile duct injury in a mouse model of sclerosing cholangitis
Published in Journal of hepatology (01-04-2015)Get full text
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Multidrug-resistant cancer cells are preferential targets of the new antineoplastic lanthanum compound KP772 (FFC24)
Published in Biochemical pharmacology (15-06-2007)“…Recently, we have introduced [tris(1,10-phenanthroline)lanthanum(III)] trithiocyanate (KP772, FFC24) as a new lanthanum compound which has promising anticancer…”
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Future directions for drug transporter modelling
Published in Xenobiotica (01-10-2007)“…Since the late 1980s computational methods such as quantitative structure-activity relationship (QSAR) and pharmacophore approaches have become more widely…”
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Intrinsic and acquired forms of resistance against the anticancer ruthenium compound KP1019 [indazolium trans-[tetrachlorobis(1H-indazole)ruthenate (III)] (FFC14A)
Published in The Journal of pharmacology and experimental therapeutics (01-01-2005)“…KP1019 [indazolium trans-[tetrachlorobis(1H-indazole)ruthenate (III)] (FFC14A) is a metal complex with promising anticancer activity. Since chemoresistance is…”
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The importance of a nitrogen atom in modulators of multidrug resistance
Published in Molecular pharmacology (01-10-1999)“…The presence of a nitrogen atom, charged at physiological pH, has frequently been considered to be a hallmark of P-glycoprotein (PGP) inhibitors, although…”
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Structural requirements for activity of propafenone-type modulators in P-glycoprotein-mediated multidrug resistance
Published in Molecular pharmacology (01-06-1996)“…The sodium channel blocker propafenone and a series of analogs have been identified as effective modulators of P-glyco-protein-mediated multidrug resistance in…”
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Structure–activity relationship studies of propafenone analogs based on P-glycoprotein ATPase activity measurements
Published in Biochemical pharmacology (01-11-1999)“…Propafenone analogs (PAs) were previously identified as potent inhibitors of P-glycoprotein (Pgp)-mediated toxin efflux. For this as well as other classes of…”
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Interaction field based and hologram based QSAR analysis of propafenone-type modulators of multidrug resistance
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-09-2005)“…Overexpression of membrane bound, ATP-dependent transport proteins is one of the predominant mechanisms leading to multiple drug resistance in tumor therapy as…”
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Structure-activity-relationship studies on modulators of the multidrug transporter P-glycoprotein--an overview
Published in Wiener Klinische Wochenschrift (1995)“…Resistance of tumor cells to a wide variety of cytotoxic agents represents a major problem in cancer therapy. In most cases, the cross resistance profile has…”
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Psoralen-loaded lipid-polymer hybrid nanoparticles enhance doxorubicin efficacy in multidrug-resistant HepG2 cells
Published in International journal of nanomedicine (01-01-2019)“…Psoralen (PSO), a major active component of Psoralea corylifolia, has been shown to overcome multidrug resistance in cancer. A drug carrier comprising a…”
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Flagging Drugs That Inhibit the Bile Salt Export Pump
Published in Molecular pharmaceutics (04-01-2016)“…The bile salt export pump (BSEP) is an ABC-transporter expressed at the canalicular membrane of hepatocytes. Its physiological role is to expel bile salts into…”
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Computational models for prediction of interactions with ABC-transporters
Published in Drug discovery today (01-04-2008)“…The polyspecific ligand recognition pattern of ATB-binding cassette (ABC)-transporters, combined with the limited knowledge on the molecular basis of their…”
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Artificial neural networks as versatile tools for prediction of MDR-modulatory activity
Published in Advances in experimental medicine and biology (1999)“…Following our ongoing studies on structure-activity relationship studies of propafenone-type modulators of multidrug resistance, we performed both a…”
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P-glycoprotein substrate binding domains are located at the transmembrane domain/transmembrane domain interfaces: a combined photoaffinity labeling-protein homology modeling approach
Published in Molecular pharmacology (01-02-2005)“…P-glycoprotein (P-gp) is an energy-dependent multidrug efflux pump conferring resistance to cancer chemotherapy. Characterization of the mechanism of drug…”
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Investigation of cytotoxic effects of 8 norbornane derivatives on 4 human cancer cell lines using the MTT assay
Published in Pharmazie (01-09-1995)“…A group of 8 structurally modified norbornane analogs, selected on basis of water solubility, was tested for its potential cytotoxic effects using a modified…”
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Self-Organizing Maps for Identification of New Inhibitors of P-Glycoprotein
Published in Journal of medicinal chemistry (05-04-2007)“…Self-organizing maps were trained to separate high- and low-active propafenone-type inhibitors of P-glycoprotein. The trained maps were subsequently used to…”
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P-glycoprotein, multidrug resistance-associated proteins and human organic anion transporting polypeptide influence the intracellular accumulation of atazanavir
Published in Antiviral therapy (01-01-2009)“…Drug efflux (for example, P-glycoprotein [P-gp], multidrug resistance-associated proteins [MRPs] and breast cancer resistance protein [BCRP]) and influx (for…”
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