| scholarly article | Q13442814 |
| P50 | author | Ivana Novak | Q38322982 |
| P2093 | author name string | Michael Wilschanski | |
| P2860 | cites work | Pass the bicarb: the importance of HCO3– for mucin release | Q22306298 |
| Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger | Q24290545 | ||
| IRBIT, an inositol 1,4,5-trisphosphate receptor-binding protein, specifically binds to and activates pancreas-type Na+/HCO3- cotransporter 1 (pNBC1) | Q24293420 | ||
| Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis | Q78582128 | ||
| DeltaF508 mutation results in impaired gastric acid secretion | Q79441368 | ||
| The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis | Q81281959 | ||
| Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis | Q85159970 | ||
| Distribution of aquaporin water channels AQP1 and AQP5 in the ductal system of the human pancreas | Q24304463 | ||
| Patterns of GI disease in adulthood associated with mutations in the CFTR gene | Q24673570 | ||
| Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA | Q28119124 | ||
| Molecular cloning, chromosomal localization, tissue distribution, and functional expression of the human pancreatic sodium bicarbonate cotransporter | Q28275417 | ||
| Bicarbonate and fluid secretion evoked by cholecystokinin, bombesin and acetylcholine in isolated guinea-pig pancreatic ducts | Q28354110 | ||
| IRBIT coordinates epithelial fluid and HCO3- secretion by stimulating the transporters pNBC1 and CFTR in the murine pancreatic duct | Q28504720 | ||
| IRBIT governs epithelial secretion in mice by antagonizing the WNK/SPAK kinase pathway | Q28512680 | ||
| TMEM16A confers receptor-activated calcium-dependent chloride conductance | Q28590097 | ||
| Mechanism of direct bicarbonate transport by the CFTR anion channel | Q28941788 | ||
| Identification of the cystic fibrosis gene: genetic analysis | Q29614402 | ||
| The solute carrier 26 family of proteins in epithelial ion transport | Q31152083 | ||
| Dynamic regulation of CFTR bicarbonate permeability by [Cl-]i and its role in pancreatic bicarbonate secretion | Q33348947 | ||
| Expression cloning of TMEM16A as a calcium-activated chloride channel subunit | Q33370813 | ||
| Pathology of gastrointestinal organs in a porcine model of cystic fibrosis | Q33703755 | ||
| New horizons in the treatment of cystic fibrosis | Q33756002 | ||
| Chloride channels: often enigmatic, rarely predictable | Q33775731 | ||
| Cyclic AMP potentiates Ca2+-dependent exocytosis in pancreatic duct epithelial cells | Q33814299 | ||
| Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth | Q33929671 | ||
| An animal model for cystic fibrosis made by gene targeting | Q33970549 | ||
| Purinergic receptors in airway epithelia | Q34016545 | ||
| Emerging treatments in cystic fibrosis | Q34019357 | ||
| Inhibition of acinar apoptosis occurs during acute pancreatitis in the human homologue DeltaF508 cystic fibrosis mouse | Q34085307 | ||
| Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis. | Q34090196 | ||
| Neural hormonal regulation of exocrine pancreatic secretion | Q34139137 | ||
| Localization of the cystic fibrosis transmembrane conductance regulator in pancreas | Q34195125 | ||
| Secretin causes H+/HCO3- secretion from pig pancreatic ductules by vacuolar-type H(+)-adenosine triphosphatase | Q34319825 | ||
| The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). | Q34635892 | ||
| TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity | Q34821709 | ||
| Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice | Q34978226 | ||
| Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model | Q35097413 | ||
| Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosis | Q35121200 | ||
| Genetic determination of exocrine pancreatic function in cystic fibrosis | Q35195369 | ||
| Combined bicarbonate conductance-impairing variants in CFTR and SPINK1 variants are associated with chronic pancreatitis in patients without cystic fibrosis | Q35209665 | ||
| A mouse model for the delta F508 allele of cystic fibrosis. | Q35765143 | ||
| Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials | Q43173791 | ||
| Ducts isolated from the pancreas of CFTR-null mice secrete fluid | Q43298556 | ||
| Visualization of ATP release in pancreatic acini in response to cholinergic stimulus. Use of fluorescent probes and confocal microscopy | Q43626724 | ||
| Pancreatic acinar cell dysfunction in CFTR(-/-) mice is associated with impairments in luminal pH and endocytosis | Q43770471 | ||
| Two types of chloride channel on duct cells cultured from human fetal pancreas | Q43995113 | ||
| Secretion of electrolytes by the pancreas of the anaestetized rat | Q44203166 | ||
| Where have all the Na+ channels gone? In search of functional ENaC in exocrine pancreas | Q44209009 | ||
| Omeprazole, a proton pump inhibitor, improves residual steatorrhoea in cystic fibrosis patients treated with high dose pancreatic enzymes | Q44589197 | ||
| Acidic duodenal pH alters gene expression in the cystic fibrosis mouse pancreas | Q44830083 | ||
| Production of a severe cystic fibrosis mutation in mice by gene targeting | Q45868497 | ||
| Fluid secretion in interlobular ducts isolated from guinea-pig pancreas | Q46292509 | ||
| P2Y2 and P2Y4 receptors regulate pancreatic Ca(2+)-activated K+ channels differently | Q46630784 | ||
| A proinflammatory, antiapoptotic phenotype underlies the susceptibility to acute pancreatitis in cystic fibrosis transmembrane regulator (-/-) mice | Q46637437 | ||
| Cystic fibrosis transmembrane conductance regulator currents in guinea pig pancreatic duct cells: inhibition by bicarbonate ions | Q46702578 | ||
| Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype. | Q47831516 | ||
| Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type Cftr gene expression | Q48080544 | ||
| The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectrics | Q48869835 | ||
| WNK1 and WNK4 modulate CFTR activity. | Q50640928 | ||
| Phase 2 randomized safety and efficacy trial of nebulized denufosol tetrasodium in cystic fibrosis. | Q51021959 | ||
| Twenty-four hour ambulatory gastric and duodenal pH profiles in cystic fibrosis: effect of duodenal hyperacidity on pancreatic enzyme function and fat absorption. | Q51580760 | ||
| Gastric acid hypersecretion in cystic fibrosis. | Q51652242 | ||
| A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus. | Q52507286 | ||
| Renal function and renotropic effects of secretin in cystic fibrosis. | Q52997543 | ||
| Purinoceptors evoke different electrophysiological responses in pancreatic ducts. P2Y inhibits K(+) conductance, and P2X stimulates cation conductance. | Q53922809 | ||
| Effect of bicarbonate on potassium conductance of isolated perfused rat pancreatic ducts. | Q54290847 | ||
| Modification of pancreatic lipase properties by directed molecular evolution. | Q54390616 | ||
| Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis. | Q55067851 | ||
| Successful targeting of the mouse cystic fibrosis transmembrane conductance regulator gene in embryonal stem cells | Q57557425 | ||
| Duodenal pH in cystic fibrosis and its relationship to fat malabsorption | Q58385527 | ||
| An intermediate-conductance Ca2+-activated K+ channel is important for secretion in pancreatic duct cells | Q61640378 | ||
| Effect of vasoactive intestinal peptide, carbachol and other agonists on the membrane voltage of pancreatic duct cells | Q61640418 | ||
| Electrophysiological study of transport systems in isolated perfused pancreatic ducts: properties of the basolateral membrane | Q61640427 | ||
| Properties of the luminal membrane of isolated perfused rat pancreatic ducts | Q61640430 | ||
| Changes in the exocrine pancreas secondary to altered small intestinal function in the CF mouse. | Q64892494 | ||
| Recurrent acute pancreatitis in patients with cystic fibrosis with normal pancreatic enzymes | Q66907681 | ||
| Potentiation effect of cholecystokinin-octapeptide on pancreatic bicarbonate secretion stimulated by a physiologic dose of secretin in humans | Q67294747 | ||
| Regulation of maxi-K+ channels on pancreatic duct cells by cyclic AMP-dependent phosphorylation | Q67665178 | ||
| Pancreatic, hepatic, and duodenal mucosal bicarbonate secretion during infusion of secretin and cholecystokinin. Evidence of the importance of hepatic bicarbonate in the neutralization of acid in the duodenum of anaesthetized pigs | Q68053197 | ||
| Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas | Q68434984 | ||
| Secretin-regulated chloride channel on the apical plasma membrane of pancreatic duct cells | Q69051907 | ||
| Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis | Q70053115 | ||
| Immunohistochemical localization of carbonic anhydrase isoenzymes in the human pancreas | Q71538117 | ||
| Exocrine pancreatic alterations in long-lived surviving cystic fibrosis mice | Q71581608 | ||
| CFTR and calcium-activated chloride currents in pancreatic duct cells of a transgenic CF mouse | Q71609179 | ||
| Accumulation of intracellular HCO3- by Na(+)-HCO3- cotransport in interlobular ducts from guinea-pig pancreas | Q71673993 | ||
| Increased expression of sulfated gp300 and acinar tissue pathology in pancreas of CFTR(-/-) mice | Q71690764 | ||
| Calcium-activated chloride conductance is not increased in pancreatic duct cells of CF mice | Q71709185 | ||
| Interactions between secretin and acetylcholine in the regulation of fluid secretion by isolated rat pancreatic ducts | Q71762759 | ||
| The cystic fibrosis transmembrane conductance regulator as a marker of human pancreatic duct development | Q73676025 | ||
| Significant cholinergic role in secretin-stimulated exocrine secretion in isolated rat pancreas | Q74255007 | ||
| Synergistic effects of cAMP- and calcium-mediated amylase secretion in isolated pancreatic acini from cystic fibrosis mice | Q77324279 | ||
| Luminal ATP stimulates fluid and HCO3- secretion in guinea-pig pancreatic duct | Q78157388 | ||
| Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations. | Q35844736 | ||
| Processing and function of CFTR-DeltaF508 are species-dependent | Q35991100 | ||
| Membrane localization of H+ and HCO3- transporters in the rat pancreatic duct | Q36435278 | ||
| Dynamics intrinsic to cystic fibrosis transmembrane conductance regulator function and stability | Q36629079 | ||
| Review article: duodenal bicarbonate - mucosal protection, luminal chemosensing and acid-base balance | Q36702146 | ||
| Confocal microscopic analysis of intracellular pH regulation in isolated guinea pig pancreatic ducts | Q36847208 | ||
| Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs | Q36944556 | ||
| No potassium, no acid: K+ channels and gastric acid secretion | Q36967648 | ||
| Sodium channels and cystic fibrosis | Q36999398 | ||
| Purinergic receptors in the endocrine and exocrine pancreas. | Q37119875 | ||
| CFTR functions as a bicarbonate channel in pancreatic duct cells | Q37124268 | ||
| Cystic fibrosis and nutrition: linking phospholipids and essential fatty acids with thiol metabolism | Q37170937 | ||
| Functional coupling of apical Cl-/HCO3- exchange with CFTR in stimulated HCO3- secretion by guinea pig interlobular pancreatic duct | Q37231297 | ||
| Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis | Q37233641 | ||
| Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion | Q37328491 | ||
| Update on the Mechanisms of Gastric Acid Secretion | Q37785842 | ||
| Purinergic signalling in epithelial ion transport: regulation of secretion and absorption | Q37809120 | ||
| Cystic fibrosis transmembrane regulator correctors and potentiators | Q38118742 | ||
| Mutations of the cystic fibrosis gene in patients with chronic pancreatitis | Q38502091 | ||
| Purinergic regulation of CFTR and Ca(2+)-activated Cl(-) channels and K(+) channels in human pancreatic duct epithelium | Q39201947 | ||
| Effect of duramycin on chloride transport and intracellular calcium concentration in cystic fibrosis and non‐cystic fibrosis epithelia | Q39629752 | ||
| Pattern of Ca2+ increase determines the type of secretory mechanism activated in dog pancreatic duct epithelial cells | Q40253019 | ||
| Characterization of vectorial chloride transport pathways in the human pancreatic duct adenocarcinoma cell line HPAF | Q40652671 | ||
| Ca2+ activates cystic fibrosis transmembrane conductance regulator- and Cl- -dependent HCO3 transport in pancreatic duct cells | Q40693281 | ||
| Downregulated in adenoma and putative anion transporter are regulated by CFTR in cultured pancreatic duct cells | Q40773534 | ||
| A mouse model for the cystic fibrosis delta F508 mutation. | Q40789334 | ||
| Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct | Q40816480 | ||
| Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis | Q40821697 | ||
| Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts | Q40954140 | ||
| Concurrent and independent HCO3- and Cl- secretion in a human pancreatic duct cell line (CAPAN-1). | Q41025755 | ||
| Calcium-activated chloride conductance in a pancreatic adenocarcinoma cell line of ductal origin (HPAF) and in freshly isolated human pancreatic duct cells | Q41035207 | ||
| Phosphorylation-regulated low-conductance Cl- channels in a human pancreatic duct cell line | Q41525891 | ||
| Pancreatic bicarbonate secretion involves two proton pumps. | Q41556981 | ||
| High intracellular pH in CFPAC: A pancreas cell line from a patient with cystic fibrosis is lowered by retrovirus-mediated CFTR gene transfer | Q41661082 | ||
| Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene | Q41669744 | ||
| Apoptosis participates in the remodeling of the endocrine pancreas in the neonatal rat. | Q42436119 | ||
| Cystic fibrosis gene mutation reduces epithelial cell acidification and injury in acid-perfused mouse duodenum | Q42469051 | ||
| Effect of ATP, carbachol and other agonists on intracellular calcium activity and membrane voltage of pancreatic ducts | Q42476129 | ||
| cAMP-regulated whole cell chloride currents in pancreatic duct cells | Q42482968 | ||
| Effect of Slc26a6 deletion on apical Cl-/HCO3- exchanger activity and cAMP-stimulated bicarbonate secretion in pancreatic duct | Q42499589 | ||
| Loss of TMEM16A causes a defect in epithelial Ca2+-dependent chloride transport | Q42660614 | ||
| Protons released during pancreatic acinar cell secretion acidify the lumen and contribute to pancreatitis in mice | Q42944148 | ||
| Effect of P2X(7) receptor knockout on exocrine secretion of pancreas, salivary glands and lacrimal glands | Q42965444 | ||
| ATP storage and uptake by isolated pancreatic zymogen granules | Q43074659 | ||
| P433 | issue | 5 | |
| P921 | main subject | cystic fibrosis | Q178194 |
| pancreas | Q9618 | ||
| P304 | page(s) | a009746 | |
| P577 | publication date | 2013-05-01 | |
| P1433 | published in | Cold Spring Harbor Perspectives in Medicine | Q21042440 |
| P1476 | title | The cystic fibrosis of exocrine pancreas | |
| P478 | volume | 3 |
| Q26998861 | Acid-base transport in pancreas-new challenges |
| Q38265305 | Acid-base transport in pancreatic cancer: molecular mechanisms and clinical potential. |
| Q99551734 | Advances in Ca2+ modulation of gastrointestinal anion secretion and its dysregulation in digestive disorders (Review) |
| Q39261074 | Alternating pH landscapes shape epithelial cancer initiation and progression: Focus on pancreatic cancer. |
| Q60920753 | Animal Models in the Pathophysiology of Cystic Fibrosis |
| Q49958195 | CFTR mutation enhances Dishevelled degradation and results in impairment of Wnt-dependent hematopoiesis. |
| Q38134726 | Cell volume regulation in epithelial physiology and cancer |
| Q64980440 | Contribution of pancreatic enzyme replacement therapy to survival and quality of life in patients with pancreatic exocrine insufficiency. |
| Q55376866 | Cystic Fibrosis-Related Diabetes. |
| Q92697837 | Cystic Fibrosis-Related Diabetes: Pathophysiology and Therapeutic Challenges |
| Q64941190 | Deconstructing the principles of ductal network formation in the pancreas. |
| Q48108670 | Electrophysiological properties of anion exchangers in the luminal membrane of guinea pig pancreatic duct cells. |
| Q26744381 | Epithelial Anion Transport as Modulator of Chemokine Signaling |
| Q52739000 | Evolving Mechanistic Views and Emerging Therapeutic Strategies for Cystic Fibrosis-Related Diabetes. |
| Q38832770 | Genophenotypic Analysis of Pediatric Patients With Acute Recurrent and Chronic Pancreatitis |
| Q48342582 | In silico analysis of the transportome in human pancreatic ductal adenocarcinoma |
| Q51710619 | Ivacaftor: from bench to bedside... and back again. |
| Q58722211 | KRAS and TP53 Cooperate to Induce Pancreatic Ductal Adenocarcinoma in Sus scrofa Pigs |
| Q27302962 | Loss of cftr function leads to pancreatic destruction in larval zebrafish. |
| Q38130386 | Molecular basis of potassium channels in pancreatic duct epithelial cells |
| Q49795312 | Pancreatic and Islet Remodeling in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Knockout Ferrets |
| Q36424575 | Pancreatic pathophysiology in cystic fibrosis |
| Q38317614 | Pancreatitis in dogs and cats: definitions and pathophysiology. |
| Q91936416 | Patient-derived pancreas-on-a-chip to model cystic fibrosis-related disorders |
| Q35636415 | Proton Pump Inhibitors Inhibit Pancreatic Secretion: Role of Gastric and Non-Gastric H+/K+-ATPases. |
| Q41302801 | Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis |
| Q37092681 | The adenosine A2B receptor is involved in anion secretion in human pancreatic duct Capan-1 epithelial cells |
| Q37122355 | The cystic fibrosis intestine |
| Q47318866 | The long and winding road: stem cells for cystic fibrosis |
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