Increased intestinal hydration by activation of the epithelial enzyme linked receptor guanylate cyclase C (GC-C) is a pharmacological principle for treating constipation. Activating mutations in the GUCY2C gene encoding GC-C cause Familial GUCY2C diarrhea syndrome (FGDS) which has been diagnosed with severe dysmotility.To investigate gut motility and hormones before and after a meal in FGDS patients and compare with healthy controls (HC).Bristol stool chart and stool frequency was assessed. Before and after a meal occlusive and non-occlusive contractions were obtained using ultrasound. A wireless motility capsule (WMC) recorded gut transit time, pH, contractions and pressure. Plasma levels of selected gut hormones were measured at different...
The gut-brain axis is a multi-modal bi-directional communication system integrating gastrointestinal...
Background: Changes in intestinal motility are likely to contribute to irritable bowel syndrome (IBS...
Meconium ileus, intestinal obstruction in the newborn, is caused in most cases by CFTR mutations mod...
<div><p>Introduction</p><p>Increased intestinal hydration by activation of the epithelial enzyme lin...
Introduction: Increased intestinal hydration by activation of the epithelial enzyme linked receptor ...
Guanylate cyclase-C (GC-C) is a transmembrane receptor activated by bacterial heat-stable enterotoxi...
BACKGROUND Familial diarrhea disorders are, in most cases, severe and caused by recessive mutations....
Background: With 25% prevalence of Crohn's disease, Familial GUCY2C diarrhea syndrome (FGDS) is a mo...
INTRODUCTION: Gain-of-function mutations in guanylyl cyclase C (GCC) result in persistent diarrhea w...
Guanylyl cyclase C (GC-C) is predominantly expressed in intestinal epithelial cells and serves as th...
AbstractGuanylyl cyclase C (GC-C) is predominantly expressed in intestinal epithelial cells and serv...
Objective: Activating mutations in the GUCY2C gene, which encodes the epithelial receptor guanylate ...
Contains fulltext : 70215.pdf (publisher's version ) (Closed access)The phenotype ...
Background Diabetic constipation is traditionally attributed to slow colonic transit, despite limit...
Gut dysmotility is associated with constipation, diarrhea, and functional gastrointestinal disorders...
The gut-brain axis is a multi-modal bi-directional communication system integrating gastrointestinal...
Background: Changes in intestinal motility are likely to contribute to irritable bowel syndrome (IBS...
Meconium ileus, intestinal obstruction in the newborn, is caused in most cases by CFTR mutations mod...
<div><p>Introduction</p><p>Increased intestinal hydration by activation of the epithelial enzyme lin...
Introduction: Increased intestinal hydration by activation of the epithelial enzyme linked receptor ...
Guanylate cyclase-C (GC-C) is a transmembrane receptor activated by bacterial heat-stable enterotoxi...
BACKGROUND Familial diarrhea disorders are, in most cases, severe and caused by recessive mutations....
Background: With 25% prevalence of Crohn's disease, Familial GUCY2C diarrhea syndrome (FGDS) is a mo...
INTRODUCTION: Gain-of-function mutations in guanylyl cyclase C (GCC) result in persistent diarrhea w...
Guanylyl cyclase C (GC-C) is predominantly expressed in intestinal epithelial cells and serves as th...
AbstractGuanylyl cyclase C (GC-C) is predominantly expressed in intestinal epithelial cells and serv...
Objective: Activating mutations in the GUCY2C gene, which encodes the epithelial receptor guanylate ...
Contains fulltext : 70215.pdf (publisher's version ) (Closed access)The phenotype ...
Background Diabetic constipation is traditionally attributed to slow colonic transit, despite limit...
Gut dysmotility is associated with constipation, diarrhea, and functional gastrointestinal disorders...
The gut-brain axis is a multi-modal bi-directional communication system integrating gastrointestinal...
Background: Changes in intestinal motility are likely to contribute to irritable bowel syndrome (IBS...
Meconium ileus, intestinal obstruction in the newborn, is caused in most cases by CFTR mutations mod...