Patterns of GI disease in adulthood associated with mutations in the CFTR gene - Test2 - elhamkhani - TriplyDB

Patterns of GI disease in adulthood associated with mutations in the CFTR gene

Patterns of GI disease in adulthood associated with mutations in the CFTR gene

http://www.wikidata.org/entity/Q24673570

about

Pass the bicarb: the importance of HCO3– for mucin release Chloride channels as drug targets.Molecular mechanism of pancreatic and salivary gland fluid and HCO3 secretion Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice Current and Emerging Therapies for the Treatment of Cystic Fibrosis or Mitigation of Its Symptoms Cystic fibrosis related liver disease--another black box in hepatology.Cirrhosis and other liver disease in cystic fibrosis.Liver transplantation in patients with cystic fibrosis: analysis of United Network for Organ Sharing data.Functional vacuolar ATPase (V-ATPase) proton pumps traffic to the enterocyte brush border membrane and require CFTR.Enzyme replacement therapy for pancreatic insufficiency: present and future Naturally occurring mutations in the canine CFTR gene.Physiology of epithelial chloride and fluid secretion Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine.The NF-kappaB signaling in cystic fibrosis lung disease: pathophysiology and therapeutic potential Ion transport mechanisms linked to bicarbonate secretion in the esophageal submucosal glands.Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.Association of CFTR gene polymorphisms with papillary thyroid cancer.Cell-specific effects of luminal acid, bicarbonate, cAMP, and carbachol on transporter trafficking in the intestine Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport.Diagnostic Accuracy of a Short Endoscopic Secretin Test in Patients With Cystic Fibrosis New ways of thinking about (and teaching about) intestinal epithelial function.Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Ganglia of Human Gastrointestinal Tract Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets.Innovative approach for self-management and social welfare of children with cystic fibrosis in Europe: development, validation and implementation of an mHealth tool (MyCyFAPP).Challenges and advances in the development of inhalable drug formulations for cystic fibrosis lung disease.Subject review: pancreatic ductal adenocarcinoma in the setting of mutations in the cystic fibrosis transmembrane conductance regulator gene: case report and review of the literature.The cystic fibrosis of exocrine pancreas Malnutrition in cystic fibrosis: a review.Cystic fibrosis: An update for clinicians. Part 1: Nutrition and gastrointestinal complications.Cystic Fibrosis from Laboratory to Bedside: The Role of A20 in NF-κB-Mediated Inflammation.Cystic fibrosis from the gastroenterologist's perspective.Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders.Pancreatic Disorders.Cystic fibrosis: a new target for 4-Imidazo[2,1-b]thiazole-1,4-dihydropyridines.Gastrointestinal surgery in adult patients with cystic fibrosis.Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis.The role of rectal chloride secretion in childhood constipation.Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.

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P2860

Patterns of GI disease in adulthood associated with mutations in the CFTR gene

http://www.wikidata.org/entity/Q24673570

description

2007 nî lūn-bûn

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2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2007 թվականի օգոստոսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年论文

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

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Michael Wilschanski

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Peter R Durie

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P2860

Identification of the cystic fibrosis gene: chromosome walking and jumping

'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel

Identification of the cystic fibrosis gene: genetic analysis

Hepatocellular carcinoma in association with cirrhosis in a patient with cystic fibrosis.

Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report.

Genotype and phenotype in cystic fibrosis.

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR).

Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis.

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