نتایج جستجو برای: ژن cftr

تعداد نتایج: 21533  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
R E Ellsworth D C Jamison J W Touchman S L Chissoe V V Braden Maduro G G Bouffard N L Dietrich S M Beckstrom-Sternberg L M Iyer L A Weintraub M Cotton L Courtney J Edwards R Maupin P Ozersky T Rohlfing P Wohldmann T Miner K Kemp J Kramer I Korf K Pepin L Antonacci-Fulton R S Fulton P Minx L W Hillier R K Wilson R H Waterston W Miller E D Green

The identification of the cystic fibrosis transmembrane conductance regulator gene (CFTR) in 1989 represents a landmark accomplishment in human genetics. Since that time, there have been numerous advances in elucidating the function of the encoded protein and the physiological basis of cystic fibrosis. However, numerous areas of cystic fibrosis biology require additional investigation, some of ...

Journal: :International journal of oncology 2015
Jin Li Jie Ting Zhang Xiaohua Jiang Xiaoshun Shi Jianfei Shen Fenglan Feng Jingyi Chen Guihong Liu Ping He Juhong Jiang Lai Ling Tsang Yan Wang Rafael Rosell Long Jiang Jianxing He Hsiao Chang Chan

An increased risk of non-small cell lung cancer (NSCLC) in cystic fibrosis (CF) patients and carriers of CF transmembrane conductance regulator (CFTR) mutations has been proposed. However, the role of CFTR in lung cancer remains controversial. In the present study, CFTR expression was assessed in 165 NSCLC tumors and 22 normal lung samples with validation in an independent series of 131 samples...

Journal: :The Journal of biological chemistry 2000
B D Moyer M Duhaime C Shaw J Denton D Reynolds K H Karlson J Pfeiffer S Wang J E Mickle M Milewski G R Cutting W B Guggino M Li B A Stanton

Polarization of cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel to the apical plasma membrane in epithelial cells is critical for vectorial chloride transport. Previously, we reported that the C terminus of CFTR constitutes a PDZ-interacting domain that is required for CFTR polarization to the apical plasma membrane and interaction with the PDZ doma...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Sabrina Noel Christelle Faveau Caroline Norez Christian Rogier Yvette Mettey Frédéric Becq

The cystic fibrosis transmembrane conductance regulator (CFTR) represents the main Cl(-) channel in the apical membrane of epithelial cells for cAMP-dependent Cl(-) secretion. Here we report on the synthesis and screening of a small library of 6-phenylpyrrolo[2,3-b]pyrazines (named RP derivatives) evaluated as activators of wild-type CFTR, G551D-CFTR, and F508del-CFTR Cl(-) channels. Iodide eff...

Journal: :Genesis 2008
Craig A Hodges Calvin U Cotton Mark R Palmert Mitchell L Drumm

The cystic fibrosis transmembrane conductance regulator (CFTR) gene encodes a cAMP-regulated chloride channel that is important in controlling the exchange of fluid and electrolytes across epithelial cells. Mutation of CFTR can lead to cystic fibrosis (CF), the most common lethal genetic disease in Caucasians. CF is a systemic illness with multiple organ systems affected including pulmonary, ga...

2015
Firhan A. Malik Anja Meissner Illya Semenkov Steven Molinski Stan Pasyk Saumel Ahmadi Hai H. Bui Christine E. Bear Darcy Lidington Steffen-Sebastian Bolz Michael B. Butterworth

The cystic fibrosis transmembrane conductance regulator (CFTR) attenuates sphingosine-1-phosphate (S1P) signaling in resistance arteries and has emerged as a prominent regulator of myogenic vasoconstriction. This investigation demonstrates that S1P inhibits CFTR activity via adenosine monophosphate-activated kinase (AMPK), establishing a potential feedback link. In Baby Hamster Kidney (BHK) cel...

2016
Jinhong Park Poonam Khloya Yohan Seo Satish Kumar Ho K. Lee Dong-Kyu Jeon Sungwoo Jo Pawan K. Sharma Wan Namkung Jeffrey M. Beekman

The most common mutation of CFTR, affecting approximately 90% of CF patients, is a deletion of phenylalanine at position 508 (F508del, ΔF508). Misfolding of ΔF508-CFTR impairs both its trafficking to the plasma membrane and its chloride channel activity. To identify small molecules that can restore channel activity of ΔF508-CFTR, we synthesized and evaluated eighteen novel hydroxypyrazoline ana...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2007
J Denry Sato M Christine Chapline Renee Thibodeau Raymond A Frizzell Bruce A Stanton

BACKGROUND Serum- and glucocorticoid-inducible kinase-1 (SGK1) increases CFTR Cl currents in Xenopus oocytes by an unknown mechanism. Because SGK increases the plasma membrane expression of other ion channels, the goal of this paper was to test the hypothesis that SGK1 stimulates CFTR Cl currents by increasing the number of CFTR Cl channels in the plasma membrane. METHODS CFTR Cl currents wer...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
G B Pier M Grout T S Zaidi

The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride ion channel, but its relationship to the primary clinical manifestation of CF, chronic Pseudomonas aeruginosa pulmonary infection, is unclear. We report that CFTR is a cellular receptor for binding, endocytosing, and clearing P. aeruginosa from the normal lung. Murine cells expressing recombinant human wild-type CFTR i...

2011
Loïc Drévillon Gaëlle Tanguy Alexandre Hinzpeter Nicole Arous Alix de Becdelièvre Abdel Aissat Agathe Tarze Michel Goossens Pascale Fanen

The CFTR (cystic fibrosis transmembrane conductance regulator) protein is a large polytopic protein whose biogenesis is inefficient. To better understand the regulation of CFTR processing and trafficking, we conducted a genetic screen that identified COMMD1 as a new CFTR partner. COMMD1 is a protein associated with multiple cellular pathways, including the regulation of hepatic copper excretion...

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