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Item Metadata only The CFTR-Based high-throughput screening assay for GPCR modulators(Mahidol University. Mahidol University Library and Knowledge Center, 2023) Buranee Yangthara; Varanuj ChatsudthipongItem Metadata only Identification and characterization of cftr inhibitors for cholera therapy(Mahidol University. Mahidol University Library and Knowledge Center, 2023) Chatchai Muanprasat; Varanuj ChatsudthipongItem Metadata only The study of parathyroid hormone action and signaling pathways in the regulation of Ion transport in Caco-2 monolayer using alternating current and direct current electrophysiological techniques(Mahidol University. Mahidol University Library and Knowledge Center, 2023) Suparerk Laohapitakworn; Narattaphol Charoenphandhu; Nateetip Krishnamra; Sutthasinee PoonyachotiItem Metadata only Vitamin D and prebiotics for intestinal health in cystic fibrosis: Rationale and design for a randomized, placebo-controlled, double-blind, 2 x 2 trial of administration of prebiotics and cholecalciferol (vitamin D3) (Pre-D trial) in adults with cystic fibrosis(2024-04-01) Sivapiromrat A.K.; Suppakitjanusant P.; Wang Y.; Hu C.; Binongo J.; Hunt W.R.; Weinstein S.; Jathal I.; Alvarez J.A.; Chassaing B.; Ziegler T.R.; Gewirtz A.T.; Tangpricha V.; Sivapiromrat A.K.; Mahidol UniversityIndividuals with cystic fibrosis (CF) have dysfunctional intestinal microbiota and increased gastrointestinal (GI) inflammation also known as GI dysbiosis. It is hypothesized that administration of high-dose cholecalciferol (vitamin D3) togetherItem Metadata only Predicting glycemic control status and high blood glucose levels through voice characteristic analysis in patients with cystic fibrosis-related diabetes (CFRD)(2023-12-01) Suppakitjanusant P.; Kasemkosin N.; Sivapiromrat A.K.; Weinsein S.; Ongphiphadhanakul B.; Hunt W.R.; Sueblinvong V.; Tangpricha V.; Mahidol UniversityCystic fibrosis-related diabetes (CFRD) is associated with reduced life expectancy in adults with cystic fibrosis (CF). Voice analysis may be a convenient method for diagnosing and monitoring CFRD. This study aims to determine the relationshipPublication Metadata only Partial rescue of F508del-cystic fibrosis transmembrane conductance regulator channel gating with modest improvement of protein processing, but not stability, by a dual-acting small molecule(2018-04-01) Jia Liu; Hermann Bihler; Carlos M. Farinha; Nikhil T. Awatade; Ana M. Romão; Dayna Mercadante; Yi Cheng; Isaac Musisi; Walailak Jantarajit; Yiting Wang; Zhiwei Cai; Margarida D. Amaral; Martin Mense; David N. Sheppard; University of Bristol; Mahidol University; Faculdade de Ciências, Universidade de Lisboa; Cystic Fibrosis Foundation Therapeutics© 2018 The British Pharmacological Society Background and Purpose: Rescue of F508del-cystic fibrosis (CF) transmembrane conductance regulator (CFTR), the most common CF mutation, requires small molecules that overcome protein processing, stabilityItem Metadata only Chronic and acute modulator treatment restore wild-type-like activity and stability to the primary cystic fibrosis-causing CFTR variant(2026-02-03) Rodrat M.; Charlick J.N.; Sheppard D.N.; Rodrat M.; Mahidol UniversityElexacaftor-tezacaftor-ivacaftor has transformed the treatment of people with cystic fibrosis (CF) and the predominant cystic fibrosis transmembrane conductance regulator (CFTR) variant F508del by delivering the faulty channel to the plasma membranePublication Metadata only Simultaneous overexpression of multidrug efflux pumps in Pseudomonas aeruginosa non-cystic fibrosis clinical isolates(2014-01-01) Kanchana Poonsuk; Chanwit Tribuddharat; Rungtip Chuanchuen; Chulalongkorn University; Mahidol UniversityThe purpose of this study was to examine expression and regulation of 6 multidrug efflux systems, including MexAB-OprM, MexCD-OprJ, MexEF-OprN, MexXY, MexJK, and MexVW, in 13 non-cystic fibrosis (CF) clinical isolates of Pseudomonas aeruginosaPublication Metadata only Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis [3](2005-02-15) Iris Schrijver; Wikrom Karnsakul; Chanin Limwongse; Sudha Ramalingam; Ramalingam Sankaran; Phyllis Gardner; Richard Moss; Stanford University Medical Center; Mahidol UniversityPublication Metadata only Case report of a Thai male cystic fibrosis patinet with the 1898+ 1G-->T splicing mutation in the CFTR gene: a review of East Asian cases. Mutations in brief no. 196. Online.(1998-12-01) S. Suwanjutha; N. N. Huang; D. Wattanasirichaigoon; T. Sura; A. Harris; M. Macek; Mahidol UniversityCystic fibrosis (CF) is the most common fatal autosomal recessive multisystem disorder, which occurs mainly in European-derived populations. The incidence of CF varies between 1 in 2000 to 3000 live-births in various ethnic groups. The disease