New research identifies faster detection of viruses
... for present-day drug discovery programmes. The interactions between transmembrane protein receptors and their ligands are responsible for viral detection ... is challenging due to the special architecture and consistency of transmembrane proteins in liquids. For the first time, Trinity College Dublin's ...Dendreon Reports First Quarter 2009 Financial Results
... in the fourth quarter of this year. Presented preclinical data at the AUA meeting announcing that D3263, a small molecule targeting TRPM8 (a transmembrane cation channel protein), reduced the size of the prostate in an animal model of benign prostatic hyperplasia (BPH) alone or in combination with ...Dendreon Reports Fourth Quarter and 2008 Year End Financial Results
... application with the U.S. Food and Drug Administration (FDA) to evaluate D-3263, the Company's lead small molecule candidate which targets TRPM8 (a transmembrane cation channel protein), in a Phase 1 dose escalation study in cancer. The application was cleared by the FDA in January 2009. ...Chronic Lung Disease - Axentis Pharma Attracts Investment Interest
... the most common life-threatening hereditary disease amongst Caucasian populations. The disease is caused by a mutation in the CFTR (cystic fibrosis transmembrane conductance regulator) gene found on chromosome 7. This mutation causes increased secretion deposits on mucous membranes. Lung complications ...Dendreon Reports Third Quarter 2008 Financial Results
... to be completed in mid-2009. * Presented preclinical data on the Company's lead small molecule candidate, D-3263, which targets Trp-p8 (a transmembrane cation channel protein also known as Trp-M8), supporting Trp-p8 as a therapeutic cancer target. Dendreon plans to file an Investigational ...Cystic Fibrosis: License Agreement Boosts Development of Therapy Against Lung Infections
... (CF) is the most common life-threatening inherited multi-organ disease in Caucasians and is caused by a mutation in the CFTR-gene (cystic fibrosis transmembrane conductance regulator) on chromosome 7. The defective gene leads to viscous secretions and impaired mucociliary clearance. The most devastating ...Third Wave boosts numbers in latest report
... Among Third Wave's key 2004 goals was the development of a pipeline of products and capabilities for a variety of conditions cystic fibrosis transmembrane conductance regulator (CFTR), hepatitis C virus (HCV) and human papillomavirus (HPV), among others. "We met those milestones," Puisis said during a ...Gq-coupled receptor assays: a comparison of FLEXstation and FLIPR
... and pharmaceutical companies. The cell line used in these studies, M1 CHO, is stably transfected with the M1 muscarinic receptor. This transmembrane protein is a G q coupled acetylcholine receptor. It is stimulated with carbachol, which leads to the release of calcium into the cytosol, and is ...Gq-coupled receptor assays using FLEXstation: M1 muscarinic receptor
... EXCELLENT FOR ASSAY DEVELOP-MENT AS DEMONSTRATED BY Z FACTOR INTRODUCTION G q -coupled receptors are transmembrane proteins that are responsible for transmitting extracellular signals to the inside of the cell, which ultimately leads to changes in gene expression. ...The serotonin 5-HT 2C receptor is a subtype of the serotonin receptor that belongs to the rhodopsin-like seven transmembrane superfamily of G protein-coupled receptors (1). 5-HT 2C receptors are widely expressed in the brain and spinal cord and are particularly enriched in ...
The use of CypHer5E and the IN Cell Analyzer 1000 for live-cell receptor internalization studies
... automated lamp-based IN Cell Analyzer 1000, with integrated image analysis software.GPCRs are the largest family of proteins involved in transmembrane signal transduction and represent an important area for the validation of therapeutic small molecule drug targets. Agonist-induced internalization of ...
Fluorescence-Based Single-Tube Assays to Rapidly Detect Human Gene Mutations
... the most common mutation that causes cystic fibrosis (CF). This mutation, a three-base-pair deletion, within exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, accounts for approximately 70% of all mutant CF alleles. 3,4 The Factor II (G20210A) Mx4000 molecular ...