نتایج جستجو برای: ژن cftr

تعداد نتایج: 21533  

Journal: :The European respiratory journal 2015
Victoria Viart Anne Bergougnoux Jennifer Bonini Jessica Varilh Raphaël Chiron Olivier Tabary Nicolas Molinari Mireille Claustres Magali Taulan-Cadars

The CFTR gene displays a tightly regulated tissue-specific and temporal expression. Mutations in this gene cause cystic fibrosis (CF). In this study we wanted to identify trans-regulatory elements responsible for CFTR differential expression in fetal and adult lung, and to determine the importance of inhibitory motifs in the CFTR-3'UTR with the aim of developing new tools for the correction of ...

Journal: :The American journal of physiology 1998
L L Clarke M C Harline

The role of the cystic fibrosis transmembrane conductance regulator (CFTR) in cAMP-stimulated HCO3- secretion across the murine duodenum was investigated. Serosal-to-mucosal flux of HCO3- (Js-->m, in mu eq.cm-2.h-1) and short-circuit current (Isc; in mu eq.cm-2.h-1) were measured by the pH stat method in duodenum from CFTR knockout [CFTR(-)] and normal [CFTR(+)] mice. Under control conditions, ...

2015
Naomi L. Pollock Oscar Moran Debora Baroni Olga Zegarra-Moran Robert C. Ford

The cystic fibrosis transmembrane conductance regulator protein (CFTR) is a chloride channel highly expressed in the gills of Salmo salar, with a role in osmoregulation. It shares 60% identity with the human CFTR channel, mutations to which can cause the common genetic disorder cystic fibrosis CF. The expression and localisation of salmon CFTR have been investigated, but the isolated protein ha...

Journal: :Respiratory Research 2001
Thomas F Scanlin Mary Catherine Glick

The cystic fibrosis transmembrane conductance regulator (CFTR) has been known for the past 11 years to be a membrane glycoprotein with chloride channel activity. Only recently has the glycosylation of CFTR been examined in detail, by O'Riordan et al in Glycobiology. Using cells that overexpress wild-type (wt)CFTR, the presence of polylactosamine was noted on the fully glycosylated form of CFTR....

Journal: :The FASEB Journal 2021

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the development of bilateral renal cysts which enlarge continuously, leading to compression adjacent intact nephrons. The growing lead a progressive decline in function. Cyst growth driven enhanced cell proliferation and chloride secretion into cyst lumen. Chloride believed occur mainly cAMP-activated cystic fibrosis trans...

Journal: :Molecular pharmacology 2004
Makoto Sugita Hiroyasu Kongo Yoshiki Shiba

Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which belongs to the superfamily of ATP-binding cassette transporters and uniquely possesses an additional large cytoplasmic domain [regulatory (R) domain]. CFTR inefficiently folds by means of co- and post-translational interactions with the cytosolic chaperones as well as luminal cha...

2014
Jessica LaRusch Jinsei Jung Ignacio J. General Michele D. Lewis Hyun Woo Park Randall E. Brand Andres Gelrud Michelle A. Anderson Peter A. Banks Darwin Conwell Christopher Lawrence Joseph Romagnuolo John Baillie Samer Alkaade Gregory Cote Timothy B. Gardner Stephen T. Amann Adam Slivka Bimaljit Sandhu Amy Aloe Michelle L. Kienholz Dhiraj Yadav M. Michael Barmada Ivet Bahar Min Goo Lee David C. Whitcomb

CFTR is a dynamically regulated anion channel. Intracellular WNK1-SPAK activation causes CFTR to change permeability and conductance characteristics from a chloride-preferring to bicarbonate-preferring channel through unknown mechanisms. Two severe CFTR mutations (CFTRsev) cause complete loss of CFTR function and result in cystic fibrosis (CF), a severe genetic disorder affecting sweat glands, ...

Journal: :The Journal of General Physiology 2003
Zhiwei Cai Toby S. Scott-Ward David N. Sheppard

When excised inside-out membrane patches are bathed in symmetrical Cl--rich solutions, the current-voltage (I-V) relationship of macroscopic cystic fibrosis transmembrane conductance regulator (CFTR) Cl- currents inwardly rectifies at large positive voltages. To investigate the mechanism of inward rectification, we studied CFTR Cl- channels in excised inside-out membrane patches from cells expr...

2017
Xi Yang Tianyou Yan Yuping Gong Xuehua Liu Huaqin Sun Wenming Xu Chunsen Wang Duolan Naren Yuhuan Zheng

Cystic fibrosis transmembrane conductance regulator (CFTR) is classified as an anion channel transporter of Cl- and HCO3-. Through interactions with its PDZ domain, CFTR is capable of regulating other proteins, such as protein phosphatase 2A (PP2A). The aberrant expression and mutation of CFTR have been observed in several tumor, but not in philadelphia chromosome-positive(Ph+) acute leukemia, ...

Journal: :Circulation 2012
Douglas L Mann

Sphingosine 1-phosphate (S1P) is a naturally occurring bioactive lysophospholipid that regulates immune responses and inflammatory processes in a variety of different organ systems, including the cardiovascular system. Within the cardiovascular system, S1P mediates cardioprotection following ischemia/reperfusion injury, cardiac remodeling, vascular tone, angiogenesis, and fibroblast migration, ...

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