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PLoS pathogens, ISSN 1553-7374, 03/2018, Volume 14, Issue 3, pp. e1006940 - e1006940
Clostridium difficile is the primary cause of nosocomial diarrhea and pseudomembranous colitis. It produces dormant spores, which serve as an infectious... 
Parasitology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Virology | Clostridium difficile - genetics | Cecum - microbiology | Cell Movement - physiology | Bacillus subtilis - genetics | Regulon | Sequence Homology | Clostridium Infections - microbiology | Bacillus subtilis - growth & development | Cecum - metabolism | Mesocricetus | Clostridium Infections - genetics | Amino Acid Sequence | Clostridium Infections - metabolism | Rabbits | Operon | Bacterial Proteins - genetics | Bacterial Toxins - metabolism | Animals | Spores, Bacterial - physiology | Bacterial Proteins - metabolism | Clostridium difficile - growth & development | Mice | Clostridium difficile - metabolism | Gene Expression Regulation, Bacterial | Bacillus subtilis - metabolism | Pleiotropy | Genetic aspects | Research | Genetic transcription | Analysis | Clostridium difficile | Nosocomial infection | Regulators | Dehydrogenases | Motility | Transcription | Pathogenesis | Genomics | Gram-positive bacteria | Homology | Genomes | Spores | Pathways | Sporulation | Bacteria | Diarrhea | RNA polymerase | Gene expression | Loci | Mutants | Autolysis | Inflammatory bowel disease | Biofilms | Hospitals | Disease transmission | Software | Toxins | Mutation | Pseudomembranous colitis | Colitis | Index Medicus | Clostridium Infections/genetics | Life Sciences | Bacillus subtilis/growth & development | Clostridium difficile/metabolism | Bacterial Toxins/metabolism | Clostridium Infections/metabolism | Bacillus subtilis/metabolism | Clostridium difficile/genetics | Biochemistry, Molecular Biology | Cecum/metabolism | Bacillus subtilis/genetics | Clostridium difficile/growth & development | Bacterial Proteins/metabolism | Clostridium Infections/microbiology | Bacterial Proteins/genetics | Cell Movement/physiology | Cecum/microbiology | Spores, Bacterial/physiology
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2009, Volume 137, Issue 4, pp. 1425 - 1434
Journal Article
PloS one, ISSN 1932-6203, 07/2017, Volume 12, Issue 7, pp. e0181863 - e0181863
Background We evaluated the effect of Saccharomyces boulardii CNCM I-745 on intestinal neuromuscular anomalies in an IBS-type mouse model of gastrointestinal... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Tumor Necrosis Factor-alpha - metabolism | Muscles - microbiology | Irritable Bowel Syndrome - therapy | Muscles - virology | Gastrointestinal Motility - drug effects | Ileum - metabolism | Male | Myenteric Plexus - metabolism | Myenteric Plexus - microbiology | Diarrhea - microbiology | Inflammation - metabolism | Interleukin-1beta - metabolism | Herpes Simplex - microbiology | Interleukin-10 - metabolism | Colon - virology | Saccharomyces boulardii - growth & development | Irritable Bowel Syndrome - virology | Muscles - metabolism | Disease Models, Animal | Inflammation - microbiology | Irritable Bowel Syndrome - metabolism | Cytokines - metabolism | Enteric Nervous System - metabolism | Interleukin-4 - metabolism | Mice, Inbred C57BL | Diarrhea - virology | Inflammation - virology | Probiotics - pharmacology | Colon - metabolism | Enteric Nervous System - microbiology | Herpes Simplex - metabolism | Irritable Bowel Syndrome - microbiology | Myenteric Plexus - virology | Herpes Simplex - virology | Ileum - virology | Animals | Enteric Nervous System - virology | Diarrhea - metabolism | Colon - microbiology | Mice | Ileum - microbiology | Herpesvirus 1, Human - pathogenicity | Care and treatment | Saccharomyces boulardii | Usage | Gastrointestinal diseases | Analysis | Irritable bowel syndrome | Research | Health aspects | Herpes simplex virus | Quality of life | Immunohistochemistry | Gastrointestinal tract diseases | Nervous system | Segments | Colony-forming cells | Expulsion | Neuronal-glial interactions | Alterations | Enteric nervous system | Microorganisms | Water content | Tension | Feces | Constipation | Medical research | Immunoglobulins | Cytokines | Dietary supplements | Gene expression | Transit | Studies | Probiotics | Nitric oxide | Interleukin 10 | Peripherin | Beads | Anomalies | Neurosciences | Yeast | Interleukin | Viruses | Stimulation | Infections | Intestinal motility | Kinases | Fibers | Lysates | Interleukin 4 | Glass beads | Moisture content | Intestine | Colon | Digestive tract | Gastric motility | Inflammation | Pharmacology | Muscle contraction | Medicine | Dextran | Carbachol | Fluorescein | Viral infections | Inoculum | Integrity | Index Medicus
Journal Article
American journal of physiology: Gastrointestinal and liver physiology, ISSN 1522-1547, 07/2016, Volume 311, Issue 1, pp. G142 - G155
Loss of function mutations in the actin motor myosin Vb (Myo5b) lead to microvillus inclusion disease (MVID) and death in newborns and children. MVID results... 
MVID | MVI | CONGENITAL CHLORIDE DIARRHEA | MYOSIN VB | Myo5b | EPITHELIAL-CELL POLARITY | brush border | NHE3 | PROTRACTED DIARRHEA | MEMBRANE TRAFFICKING | TRANSMEMBRANE CONDUCTANCE REGULATOR | RECYCLING ENDOSOMES | MYO5B MUTATIONS | BRUSH-BORDER CYTOSKELETON | SYNTAXIN 3 | CFTR | Brush border | Gastroenterology & Hepatology | Physiology | Life Sciences & Biomedicine | Science & Technology | Jejunum - pathology | Enterocytes - metabolism | Humans | Myosin Heavy Chains - genetics | Malabsorption Syndromes - metabolism | Phosphoproteins - metabolism | Myosin Heavy Chains - metabolism | Jejunum - metabolism | Sodium-Hydrogen Exchangers - metabolism | Jejunum - ultrastructure | Transfection | RNA Interference | Membrane Transport Proteins - genetics | Mucolipidoses - metabolism | Membrane Transport Proteins - metabolism | Ion Transport | Caco-2 Cells | Microvilli - pathology | Myosin Type V - metabolism | Signal Transduction | Gene Expression Regulation | Mucolipidoses - genetics | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Malabsorption Syndromes - genetics | Microvilli - genetics | Chloride-Bicarbonate Antiporters - metabolism | Mucolipidoses - pathology | Phenotype | Myosin Type V - genetics | Microvilli - metabolism | Microvilli - ultrastructure | Adaptor Proteins, Signal Transducing - metabolism | Enterocytes - ultrastructure | Malabsorption Syndromes - pathology | Sodium-Hydrogen Exchanger 3 | Ion transport | Genetic aspects | Health aspects | Gastrointestinal diseases | Mutation (Biology) | Index Medicus | Epithelial Biology and Secretion
Journal Article
European Journal of Cancer, ISSN 0959-8049, 2016, Volume 68, pp. 1 - 10
Abstract Purpose We performed a multi-centre phase I study to assess the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of the orally available small... 
Hematology, Oncology and Palliative Medicine | Pharmacodynamics | MEK inhibitor | Phase I | Optimal biological dose | Pharmacokinetics | Life Sciences & Biomedicine | Oncology | Science & Technology | Lung Neoplasms - drug therapy | Pancreatic Neoplasms - metabolism | Nausea - chemically induced | Allosteric Regulation | Humans | Lung Neoplasms - metabolism | Middle Aged | Male | Fatigue - chemically induced | Ribosomal Protein S6 Kinases, 70-kDa - drug effects | Protein Kinase Inhibitors - adverse effects | Colorectal Neoplasms - drug therapy | Chromatography, Liquid | Proto-Oncogene Proteins c-akt - metabolism | MAP Kinase Kinase 1 - antagonists & inhibitors | Bile Duct Neoplasms - metabolism | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Administration, Oral | Carcinoma, Non-Small-Cell Lung - metabolism | Neoplasms - drug therapy | Maximum Tolerated Dose | Mesothelioma - metabolism | Mitogen-Activated Protein Kinase 3 - metabolism | Anorexia - chemically induced | Glycogen Synthase Kinase 3 beta - drug effects | Mitogen-Activated Protein Kinase 1 - metabolism | Neoplasms - metabolism | Phosphoproteins - drug effects | Mitogen-Activated Protein Kinase 1 - drug effects | Cholangiocarcinoma - metabolism | Chromatography, High Pressure Liquid | Diarrhea - chemically induced | Mitogen-Activated Protein Kinase 3 - drug effects | Pancreatic Neoplasms - drug therapy | Tandem Mass Spectrometry | Uterine Cervical Neoplasms - metabolism | Esophageal Neoplasms - metabolism | Adult | Female | Colorectal Neoplasms - metabolism | Bile Duct Neoplasms - drug therapy | Drug Eruptions - etiology | Abdominal Pain - chemically induced | Uterine Cervical Neoplasms - drug therapy | Glycogen Synthase Kinase 3 beta - metabolism | Mesothelioma - drug therapy | Cholangiocarcinoma - drug therapy | MAP Kinase Kinase 2 - antagonists & inhibitors | Protein Kinase Inhibitors - therapeutic use | Aged | Protein Kinase Inhibitors - pharmacology | Carcinoma, Non-Small-Cell Lung - drug therapy | Esophageal Neoplasms - drug therapy | Proto-Oncogene Proteins c-akt - drug effects | Care and treatment | Protein kinases | Mitogens | Cells | Tumors | Index Medicus
Journal Article
Cellular microbiology, ISSN 1462-5814, 11/2017, Volume 19, Issue 11, pp. e12757 - n/a
Summary Enteropathogenic Escherichia coli (EPEC) uses a type III secretion system to inject effector proteins into host intestinal epithelial cells causing... 
enteropathogenic Escherichia coli | tight junctions | Crumbs3 | polarity | Life Sciences & Biomedicine | Microbiology | Science & Technology | Cell Biology | Membrane Glycoproteins - metabolism | Humans | Intestines - metabolism | Diarrhea - pathology | Epithelial Cells - physiology | Diarrhea - microbiology | Enteropathogenic Escherichia coli - pathogenicity | Madin Darby Canine Kidney Cells | Membrane Transport Proteins - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Sorting Nexins - metabolism | Tight Junctions - metabolism | Cell Line | Dynamins - antagonists & inhibitors | Chloride-Bicarbonate Antiporters - antagonists & inhibitors | Mice, Inbred C57BL | Escherichia coli Infections - microbiology | Escherichia coli Proteins - metabolism | Endocytosis - physiology | Type III Secretion Systems - metabolism | Carrier Proteins - genetics | Sodium-Potassium-Exchanging ATPase - metabolism | Animals | Carrier Proteins - metabolism | Escherichia coli Infections - pathology | Dogs | Escherichia coli Proteins - genetics | Cell Polarity - physiology | Mice | Nucleoside-Phosphate Kinase - metabolism | Analysis | Escherichia coli | Muscle proteins | Gene expression | Health aspects | Adenosine triphosphatase | Integrins | Membranes | Epithelial cells | Secretion | Diarrhea | Infections | Solutes | Na+/K+-exchanging ATPase | Ablation | Morphogenesis | Proteins | Endocytosis | E coli | Intestine | Rodents | Dynamin | Polarity | Disruption | Nexin | Cytoplasm | Index Medicus
Journal Article
Cell host & microbe, ISSN 1931-3128, 03/2012, Volume 11, Issue 3, pp. 227 - 239
Journal Article