scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00018-018-2755-6 |
P698 | PubMed publication ID | 29411041 |
P50 | author | Xiaohua Jiang | Q79346056 |
P2093 | author name string | Yan Wang | |
Hsiao Chang Chan | |||
Jieting Zhang | |||
P2860 | cites work | Identification of the cystic fibrosis gene: chromosome walking and jumping | Q22299423 |
Longevity of Patients With Cystic Fibrosis in 2000 to 2010 and Beyond: Survival Analysis of the Cystic Fibrosis Foundation Patient Registry | Q22305306 | ||
Regulation of the polarity protein Par6 by TGFbeta receptors controls epithelial cell plasticity | Q24297858 | ||
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP | Q24307520 | ||
Hsp90 cochaperone Aha1 downregulation rescues misfolding of CFTR in cystic fibrosis | Q24316177 | ||
Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome | Q24533430 | ||
Patterns of GI disease in adulthood associated with mutations in the CFTR gene | Q24673570 | ||
Emerging role of cystic fibrosis transmembrane conductance regulator - an epithelial chloride channel in gastrointestinal cancers | Q26753851 | ||
Hypoxia, Epithelial-Mesenchymal Transition, and TET-Mediated Epigenetic Changes | Q26767183 | ||
Integrated analysis of residue coevolution and protein structure in ABC transporters | Q27303593 | ||
The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): THREE-DIMENSIONAL STRUCTURE AND LOCALIZATION OF A CHANNEL GATE | Q27674253 | ||
Inflammation and cancer: back to Virchow? | Q28036756 | ||
Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA | Q28119124 | ||
Loss of human Scribble cooperates with H-Ras to promote cell invasion through deregulation of MAPK signalling | Q28287899 | ||
Cystic fibrosis transmembrane regulator (CFTR) DeltaF508 mutation and 5T allele in patients with chronic pancreatitis and exocrine pancreatic cancer. PANKRAS II Study Group | Q28345126 | ||
Ischemia-induced enhancement of CFTR expression on the plasma membrane in neonatal rat ventricular myocytes | Q28566635 | ||
Down-regulated CFTR During Aging Contributes to Benign Prostatic Hyperplasia | Q28575323 | ||
Cryptorchidism-induced CFTR down-regulation results in disruption of testicular tight junctions through up-regulation of NF-κB/COX-2/PGE2 | Q28578305 | ||
Cadmium regulates the expression of the CFTR chloride channel in human airway epithelial cells | Q28751514 | ||
Identification of the cystic fibrosis gene: genetic analysis | Q29614402 | ||
A role for the TGFbeta-Par6 polarity pathway in breast cancer progression | Q30489618 | ||
TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patients | Q80551100 | ||
Cystic fibrosis transmembrane conductance regulator (CFTR) gene 5T allele may protect against prostate cancer: a case-control study in Chinese Han population | Q80969525 | ||
Transforming growth factor-beta signaling in stem cells and cancer | Q81322178 | ||
Volume-activated chloride currents in fetal human nasopharyngeal epithelial cells | Q83474717 | ||
CFTR, SPINK1, PRSS1, and CTRC mutations are not associated with pancreatic cancer in German patients | Q87365078 | ||
Predictive value of cystic fibrosis transmembrane conductance regulator (CFTR) in the diagnosis of gastric cancer | Q87497581 | ||
A DNA hypermethylation profile reveals new potential biomarkers for prostate cancer diagnosis and prognosis | Q88147924 | ||
Cystic fibrosis | Q89219005 | ||
CFTR is a tumor suppressor gene in murine and human intestinal cancer | Q89262168 | ||
Ion channels/transporters as epigenetic regulators? -a microRNA perspective | Q38046769 | ||
Role of pHi, and proton transporters in oncogene-driven neoplastic transformation | Q38184984 | ||
Cystic fibrosis transmembrane conductance regulator protein (CFTR) expression in the developing human brain: comparative immunohistochemical study between patients with normal and mutated CFTR. | Q38234056 | ||
Localization of cystic fibrosis transmembrane conductance regulator to lipid rafts of epithelial cells is required for Pseudomonas aeruginosa-induced cellular activation | Q38346649 | ||
A pharmacogenetic study of docetaxel and thalidomide in patients with castration-resistant prostate cancer using the DMET genotyping platform. | Q38347610 | ||
Targeting the PI3K/Akt/mTOR signalling pathway in Cystic Fibrosis | Q38631561 | ||
Hydrogen sulfide stimulates CFTR in Xenopus oocytes by activation of the cAMP/PKA signalling axis | Q38725246 | ||
CFTR Controls the Activity of NF-κB by Enhancing the Degradation of TRADD. | Q38726388 | ||
Design, Synthesis, and Evaluation of Heat Shock Protein 90 Inhibitors in Human Breast Cancer and Its Metastasis. | Q38734171 | ||
miR-146a, miR-155, miR-370, and miR-708 Are CFTR-Dependent, Predicted FOXO1 Regulators and Change at Onset of CFRDs. | Q38743042 | ||
Adenovirus‑mediated overexpression of cystic fibrosis transmembrane conductance regulator enhances invasiveness and motility of serous ovarian cancer cells. | Q38820930 | ||
The mechanism between epithelial mesenchymal transition in breast cancer and hypoxia microenvironment | Q38822202 | ||
Cystic fibrosis transmembrane conductance regulator is involved in polyphenol-induced swelling of the endothelial glycocalyx | Q38886186 | ||
Technological advances shed light on left ventricular cardiac disturbances in cystic fibrosis | Q38897168 | ||
High level of CFTR expression is associated with tumor aggression and knockdown of CFTR suppresses proliferation of ovarian cancer in vitro and in vivo. | Q38903612 | ||
Structural Basis of Intracellular TGF-β Signaling: Receptors and Smads | Q38934096 | ||
Membrane-initiated estradiol signaling of epithelial-mesenchymal transition-associated mechanisms through regulation of tight junctions in human breast cancer cells. | Q39000905 | ||
Emerging relationship between CFTR, actin and tight junction organization in cystic fibrosis airway epithelium | Q39005103 | ||
Disrupted interaction between CFTR and AF-6/afadin aggravates malignant phenotypes of colon cancer | Q39039014 | ||
Augmentation of S-Nitrosoglutathione Controls Cigarette Smoke-Induced Inflammatory-Oxidative Stress and Chronic Obstructive Pulmonary Disease-Emphysema Pathogenesis by Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function | Q39071592 | ||
Downregulation of CFTR promotes epithelial-to-mesenchymal transition and is associated with poor prognosis of breast cancer | Q39115171 | ||
HSP90 as a novel molecular target in non-small-cell lung cancer | Q39139943 | ||
Amplification of FSH signaling by CFTR and nuclear soluble adenylyl cyclase in the ovary | Q39201838 | ||
Update on hypoxia-inducible factors and hydroxylases in oxygen regulatory pathways: from physiology to therapeutics | Q39205984 | ||
CFTR suppresses tumor progression through miR-193b targeting urokinase plasminogen activator (uPA) in prostate cancer | Q39314424 | ||
Stressor-driven extracellular acidosis as tumor inducer via aberrant enzyme activation: A review on the mechanisms and possible prophylaxis | Q39331202 | ||
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities | Q39346514 | ||
Overexpression of cystic fibrosis transmembrane conductance regulator (CFTR) is associated with human cervical cancer malignancy, progression and prognosis | Q39390028 | ||
CFTR negatively regulates cyclooxygenase-2-PGE(2) positive feedback loop in inflammation | Q39474714 | ||
Promoter hypermethylation of the CFTR gene and clinical/pathological features associated with non-small cell lung cancer. | Q39541029 | ||
Expression of wild-type CFTR suppresses NF-kappaB-driven inflammatory signalling | Q39678214 | ||
CFTR and tight junctions in cultured bronchial epithelial cells. | Q39789180 | ||
∆F508 CFTR interactome remodelling promotes rescue of cystic fibrosis | Q40006173 | ||
Frequency of carriers of cystic fibrosis gene among patients with myeloid malignancy and melanoma | Q40096774 | ||
Lower Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Promotes the Proliferation and Migration of Endometrial Carcinoma. | Q37677195 | ||
TGF-β1 promotes colorectal cancer immune escape by elevating B7-H3 and B7-H4 via the miR-155/miR-143 axis | Q37687142 | ||
CFTR is a potential marker for nasopharyngeal carcinoma prognosis and metastasis | Q37718318 | ||
Regulation and roles of bicarbonate transporters in cancer | Q37719006 | ||
MicroRNAs and their target gene networks in renal cell carcinoma | Q37828237 | ||
MicroRNAs and cystic fibrosis--an epigenetic perspective. | Q37863190 | ||
Estrogen dependent signaling in reproductive tissues - a role for estrogen receptors and estrogen related receptors | Q37941428 | ||
Cell polarity proteins and cancer. | Q37998815 | ||
MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms | Q40262856 | ||
Cadmium, Lead, and Depressive Symptoms: Analysis of National Health and Nutrition Examination Survey 2011-2012. | Q40435846 | ||
Functional and molecular characterization of a volume-activated chloride channel in rabbit corneal epithelial cells. | Q40474037 | ||
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis | Q40488178 | ||
TGFbeta down-regulation of the CFTR: a means to limit epithelial chloride secretion | Q40533318 | ||
Hypoxia-induced inhibition of whole cell membrane currents and ion transport of A549 cells | Q40598336 | ||
Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP | Q40794305 | ||
CFTR deltaF508 carrier status, risk of breast cancer before the age of 40 and histological grading in a population-based case-control study | Q41004860 | ||
CFTR is a mechanosensitive anion channel: a real stretch? | Q41118255 | ||
Loss of cystic fibrosis transmembrane conductance regulator impairs lung endothelial cell barrier function and increases susceptibility to microvascular damage from cigarette smoke | Q41178546 | ||
CFTR as a cAMP-dependent regulator of sodium channels | Q41312779 | ||
Estrogen-dependent expression of the cystic fibrosis transmembrane regulator gene in a novel uterine epithelial cell line. | Q41446679 | ||
Molecular Structure of the Human CFTR Ion Channel. | Q41598483 | ||
Atomic Structure of the Cystic Fibrosis Transmembrane Conductance Regulator | Q41599873 | ||
Upregulation of CFTR in patients with endometriosis and its involvement in NFκB-uPAR dependent cell migration | Q42130797 | ||
Defective CFTR-regulated granulosa cell proliferation in polycystic ovarian syndrome | Q42472394 | ||
CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship | Q42809539 | ||
Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinoma | Q43004128 | ||
Cancer risk in cystic fibrosis: a 20-year nationwide study from the United States | Q43684856 | ||
Effect of phenol red and steroid hormones on cystic fibrosis transmembrane conductance regulator in mouse endometrial epithelial cells | Q43758615 | ||
Hypoxia decreases active Na transport across primary rat alveolar epithelial cell monolayers | Q43906839 | ||
Involvement of CFTR in uterine bicarbonate secretion and the fertilizing capacity of sperm | Q44600125 | ||
Cancer risk and PCOS. | Q44771365 | ||
Bicarbonate secretion: it takes two to tango | Q44824846 | ||
Constitutive activation of nuclear factor κB contributes to cystic fibrosis transmembrane conductance regulator expression and promotes human cervical cancer progression and poor prognosis | Q45239383 | ||
Elevated levels of miR-145 correlate with SMAD3 down-regulation in cystic fibrosis patients. | Q45803588 | ||
A novel set of DNA methylation markers in urine sediments for sensitive/specific detection of bladder cancer | Q45873847 | ||
The cystic fibrosis transmembrane conductance regulator controls biliary epithelial inflammation and permeability by regulating Src tyrosine kinase activity. | Q45923491 | ||
Physiological basis of cystic fibrosis: a historical perspective | Q46380953 | ||
miR-155 regulates high glucose-induced cardiac fibrosis via the TGF-β signaling pathway | Q48177139 | ||
CFTR-β-catenin interaction regulates mouse embryonic stem cell differentiation and embryonic development | Q48232238 | ||
Bacterial overgrowth, dysbiosis, inflammation, and dysmotility in the Cystic Fibrosis intestine | Q49551226 | ||
Polymorphisms of SPINK1 N34S and CFTR in patients with sporadic and familial pancreatic cancer | Q50171485 | ||
Clinical and morphological characteristics of sporadic genetically determined pancreatitis as compared to idiopathic pancreatitis: higher risk of pancreatic cancer in CFTR variants. | Q50921436 | ||
Cancer risk in patients with cystic fibrosis: the European data. CF/CSG Group. | Q51013790 | ||
Exaggerated apoptosis and NF-kappaB activation in pancreatic and tracheal cystic fibrosis cells. | Q51022821 | ||
Mouse microRNA-23b regulates expression of Hes1 gene in P19 cells. | Q51097380 | ||
Early colon screening of adult patients with cystic fibrosis reveals high incidence of adenomatous colon polyps. | Q51182247 | ||
[Whole Genome Expression Profiling Analysis of Metastasis and Drug-resistance-related Genes in Epithelial Ovarian Cancer Cells]. | Q51472916 | ||
The cystic fibrosis transmembrane conductance regulator as a biomarker in non-small cell lung cancer. | Q51650974 | ||
CFTR expression is regulated during both the cycle of the seminiferous epithelium and the oestrous cycle of rodents. | Q52227548 | ||
Weighted gene co-expression network analysis of pneumocytes under exposure to a carcinogenic dose of chloroprene. | Q52883103 | ||
Cystic fibrosis of the pancreas. A generalised disturbance of water and electrolyte movement in exocrine tissues. | Q54377227 | ||
Methylation of multiple genes as molecular markers for diagnosis of a small, well-differentiated hepatocellular carcinoma. | Q54485840 | ||
Cancer Risk in Nontransplanted and Transplanted Cystic Fibrosis Patients: A 10-Year Study | Q56779668 | ||
The Risk of Cancer among Patients with Cystic Fibrosis | Q56779992 | ||
Cancer risk among patients with cystic fibrosis and their first-degree relatives | Q57697731 | ||
Blockers of volume-activated Cl? currents inhibit endothelial cell proliferation | Q62661291 | ||
Cystic fibrosis hetero- and homozygosity is associated with inhibition of breast cancer growth | Q71046595 | ||
Stimulation of the cystic fibrosis transmembrane regulator expression by estrogen in vivo | Q72089887 | ||
The cystic fibrosis delta F508 gene mutation and cancer | Q73509772 | ||
F508 amino acid deletion mutation of CFTR gene in Korean lung cancer patients | Q73806208 | ||
Impairment of cation transport in A549 cells and rat alveolar epithelial cells by hypoxia | Q73847876 | ||
Distribution and regulation of ENaC subunit and CFTR mRNA expression in murine female reproductive tract | Q77759146 | ||
Glibenclamide induces apoptosis through inhibition of cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channels and intracellular Ca(2+) release in HepG2 human hepatoblastoma cells | Q78109574 | ||
The phenotypic consequences of CFTR mutations | Q35206694 | ||
Analysis of CFTR interactome in the macromolecular complexes | Q35228705 | ||
Cigarette smoke exposure reveals a novel role for the MEK/ERK1/2 MAPK pathway in regulation of CFTR | Q35434553 | ||
Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator | Q35438966 | ||
Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility. | Q35834494 | ||
Association of CFTR gene polymorphisms with papillary thyroid cancer | Q35995455 | ||
Mechanisms of bicarbonate secretion in the pancreatic duct | Q36041035 | ||
Methylation profile of the promoter CpG islands of 14 "drug-resistance" genes in hepatocellular carcinoma | Q36076351 | ||
Overexpression of Plasminogen Activator Inhibitor-1 in Advanced Gastric Cancer with Aggressive Lymph Node Metastasis | Q36186928 | ||
The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis. | Q36263013 | ||
The Enigmatic Gut in Cystic Fibrosis: Linking Inflammation, Dysbiosis, and the Increased Risk of Malignancy | Q36268539 | ||
CFTR mediates bicarbonate-dependent activation of miR-125b in preimplantation embryo development | Q36294566 | ||
Inhibition of αENaC expression and ENaC activity following blockade of the circadian clock-regulatory kinases CK1δ/ε. | Q36312671 | ||
CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants. | Q36398902 | ||
Cellular chloride and bicarbonate retention alters intracellular pH regulation in Cftr KO crypt epithelium | Q36480411 | ||
The CFTR ion channel: gating, regulation, and anion permeation | Q36488258 | ||
The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment | Q36594740 | ||
Contribution of α7 nicotinic receptor to airway epithelium dysfunction under nicotine exposure | Q36673189 | ||
Testicular cancer and cryptorchidism | Q36700205 | ||
Genomic landscape of non-small cell lung cancer in smokers and never-smokers | Q36851245 | ||
Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities | Q36865792 | ||
Role of oxygen availability in CFTR expression and function | Q36951832 | ||
Hypoxia inducible factor-1 (HIF-1)-mediated repression of cystic fibrosis transmembrane conductance regulator (CFTR) in the intestinal epithelium | Q37061658 | ||
Cigarette smoke and CFTR: implications in the pathogenesis of COPD | Q37234904 | ||
Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion | Q37328491 | ||
Transcriptional regulation of cell polarity in EMT and cancer | Q37333606 | ||
Polarity proteins in migration and invasion | Q37333610 | ||
MARCH2 regulates autophagy by promoting CFTR ubiquitination and degradation and PIK3CA-AKT-MTOR signaling | Q37371610 | ||
EMT, the cytoskeleton, and cancer cell invasion | Q37377630 | ||
Role of CFTR in epithelial physiology. | Q37553595 | ||
Cigarette smoke induces systemic defects in cystic fibrosis transmembrane conductance regulator function | Q37572359 | ||
Weighted gene co-expression network analysis in identification of metastasis-related genes of lung squamous cell carcinoma based on the Cancer Genome Atlas database | Q37636947 | ||
Defective CFTR- β-catenin interaction promotes NF-κB nuclear translocation and intestinal inflammation in cystic fibrosis | Q37665560 | ||
Carbonic Anhydrase Activity Monitored In Vivo by Hyperpolarized 13C-Magnetic Resonance Spectroscopy Demonstrates Its Importance for pH Regulation in Tumors | Q30985593 | ||
Methylcap-seq reveals novel DNA methylation markers for the diagnosis and recurrence prediction of bladder cancer in a Chinese population | Q31058055 | ||
Role of pertussis toxin-sensitive G-proteins in intracellular Ca2+ release and apoptosis induced by inhibiting cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channels in HepG2 human hepatoblastoma cells | Q31948359 | ||
Hypoxia increases corneal cell expression of CFTR leading to increased Pseudomonas aeruginosa binding, internalization, and initiation of inflammation | Q33208286 | ||
Dynamic regulation of CFTR bicarbonate permeability by [Cl-]i and its role in pancreatic bicarbonate secretion | Q33348947 | ||
Impact of CFTR Modulation on Intestinal pH, Motility, and Clinical Outcomes in Patients With Cystic Fibrosis and the G551D Mutation | Q33551857 | ||
Tissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTR | Q33586056 | ||
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and risk for pancreatic adenocarcinoma | Q33596314 | ||
Elevated miR-155 promotes inflammation in cystic fibrosis by driving hyperexpression of interleukin-8 | Q33808094 | ||
Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines. | Q33818738 | ||
Tobacco carcinogen NNK transporter MRP2 regulates CFTR function in lung epithelia: implications for lung cancer | Q33844906 | ||
Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients | Q33869132 | ||
Defective CFTR leads to aberrant β-catenin activation and kidney fibrosis. | Q33899411 | ||
A PDZ-interacting domain in CFTR is an apical membrane polarization signal | Q33902133 | ||
Hypoxia regulates gene expression of alveolar epithelial transport proteins | Q33910362 | ||
Cystic fibrosis transmembrane conductance regulator gene mutation and lung cancer risk | Q33952622 | ||
Cystic fibrosis transmembrane conductance regulator protein repair as a therapeutic strategy in cystic fibrosis | Q34023921 | ||
Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion. | Q34162541 | ||
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis | Q34206913 | ||
Factors associated with Type I and Type II endometrial cancer | Q34233057 | ||
Regulation of male fertility by CFTR and implications in male infertility. | Q34282487 | ||
Use of kinase inhibitors to correct ΔF508-CFTR function | Q34304720 | ||
CFTR: interacting with everything? | Q34322998 | ||
CFTR interacts with ZO-1 to regulate tight junction assembly and epithelial differentiation through the ZONAB pathway. | Q34339107 | ||
Epithelial ovarian cancer risk among women with polycystic ovary syndrome | Q34400660 | ||
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis | Q34537405 | ||
Differential Gene Expression Landscape of Co-Existing Cervical Pre-Cancer Lesions Using RNA-seq | Q34574451 | ||
A cytokine-mediated link between innate immunity, inflammation, and cancer | Q34625152 | ||
Tight Junction–Associated Signaling Pathways Modulate Cell Proliferation in Uveal Melanoma | Q34646857 | ||
Plasma membrane CFTR regulates RANTES expression via its C-terminal PDZ-interacting motif | Q34811102 | ||
The NF-kappaB signaling in cystic fibrosis lung disease: pathophysiology and therapeutic potential | Q35043484 | ||
Pharmacological modulation of the AKT/microRNA-199a-5p/CAV1 pathway ameliorates cystic fibrosis lung hyper-inflammation | Q35073075 | ||
Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosis | Q35121200 | ||
Regulation of TGF-beta signaling and its roles in progression of tumors | Q35161752 | ||
P433 | issue | 10 | |
P921 | main subject | cystic fibrosis | Q178194 |
transmembrane protein | Q424204 | ||
P304 | page(s) | 1737-1756 | |
P577 | publication date | 2018-02-06 | |
P1433 | published in | Cellular and Molecular Life Sciences | Q5058352 |
P1476 | title | Cystic fibrosis transmembrane conductance regulator-emerging regulator of cancer | |
P478 | volume | 75 |
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