About: Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis

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About: Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 1985

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1985 (uk) article scientifique publié en 1985 (fr) artículu científicu espublizáu en febreru de 1985 (ast) im Februar 1985 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 February 1985 (en)
publication date	wds:Q70053115-BCBE05AA-2D4F-467D-AC08-90B81149E3E2
publication date	1985-02-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q70053115-06B07D66-614D-4C52-88A7-E30BC06F34C6 wds:Q70053115-1C5F8E20-83AE-4795-BA54-30BED99A029B wds:Q70053115-6C6F697D-E096-44D4-A273-6F31854FD879 wds:Q70053115-B848E761-D188-4EF0-8A03-DCD0367140A7 wds:Q70053115-E1B6B3AE-7A76-4879-B80A-9F599C10CB16
author name string	Gaskin K Weizman Z Forstner G Kopelman H Durie P
rdfs:label	Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (en) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (nl) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (sq)
skos:prefLabel	Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (en) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (nl) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (sq)
name	Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (en) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (nl) Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (sq)
title	wds:Q70053115-75D34101-96B2-4754-B65C-172886FC1A92
title	Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis (en)
page(s)	wds:Q70053115-FBA52209-54E5-4CFE-8370-A446328A6CC3
page(s)	329-334
instance of	wds:Q70053115-5F0171AF-3E3D-475C-BF4D-EAC68A71250D
instance of	scholarly article
main subject	wds:Q70053115-9BD0B0F9-3E02-41D6-B4CB-7BED505FB036
main subject	cystic fibrosis
PubMed ID	wds:Q70053115-365BA1A4-6597-4D11-849B-5C0C9DA3E5CE
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3969086
PubMed ID	3969086
published in	wds:Q70053115-EAA076C2-914E-4D14-AAC7-8BDAC5EC14CD
published in	The New England Journal of Medicine
issue	wds:Q70053115-EFF4DF94-0306-4D3B-8D9F-1C6FD7E92ACD
volume	wds:Q70053115-7DFC6BE7-458E-4A0A-840D-595A94B6AA22
issue	6
volume	312
DOI	wds:Q70053115-E1B0732C-CAE0-4A23-AE79-4A84247600D2
DOI	http://dx.doi.org/10.1056/NEJM198502073120601
DOI	10.1056/NEJM198502073120601
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70053115
is cites work of	The cystic fibrosis intestine Localization of the cystic fibrosis transmembrane conductance regulator in pancreas Bile acid secretion in cystic fibrosis: evidence for a defect unrelated to fat malabsorption Genetic determination of exocrine pancreatic function in cystic fibrosis Cystic fibrosis Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis Cystic fibrosis Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis. Expression and localization of cystic fibrosis transmembrane conductance regulator in the rat endocrine pancreas Regulation of Absorption in the Human Sweat Duct Patterns of GI disease in adulthood associated with mutations in the CFTR gene Human pancreatic exocrine response to nutrients in health and disease Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas Pathophysiology of the exocrine pancreas in cystic fibrosis Familial concordance of pancreatic function in cystic fibrosis Cyclosporin pharmacokinetics in heart-lung transplant recipients with cystic fibrosis. Effects of pancreatic enzymes and ranitidine Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways Pancreatic and biliary secretion are both altered in cystic fibrosis pigs. Pancreatic pathophysiology in cystic fibrosis The cystic fibrosis of exocrine pancreas Cystic fibrosis--a gastroenterological cornucopia Pancreatic aspects of cystic fibrosis and other inherited causes of pancreatic dysfunction Towards the ideal quantitative pancreatic function test: analysis of test variables that influence validity Pancreatitis in young children with cystic fibrosis Pathology of pancreatic and intestinal disorders in cystic fibrosis Patterns of gastrointestinal disease associated with mutations of CFTR. Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium Mechanisms of bicarbonate secretion: lessons from the airways Pancreas divisum The neglected ion: HCO3- Pseudomonas aeruginosa and Burkholderia cepacia infection in cystic fibrosis patients treated in Toronto and Copenhagen. Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis CFTR: A New Horizon in the Pathomechanism and Treatment of Pancreatitis Bioelectric properties of cystic fibrosis airways obtained at heart-lung transplantation Diagnostic Accuracy of a Short Endoscopic Secretin Test in Patients With Cystic Fibrosis Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line Cystic fibrosis mutations and genetic predisposition to idiopathic chronic pancreatitis Helicobacter pylori and Clostridium difficile in cystic fibrosis patients Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations Gastrointestinal Manifestations of Cystic Fibrosis. Role of CFTR in epithelial physiology. Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis. Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction Cystic fibrosis-related diabetes: from CFTR dysfunction to oxidative stress. Genetic and immunologic aspects of cystic fibrosis Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci MRI appearance of the pancreas in patients with cystic fibrosis: a comparison of pancreas volume in diabetic and non-diabetic patients. Newly diagnosed cystic fibrosis in middle and later life Pancreatitis and cystic fibrosis gene mutations

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