Journal of Clinical Investigation, ISSN 0021-9738, 2008, Volume 118, Issue 1, pp. 205 - 216
TLRs may contribute to the progression of rheumatoid arthritis through recognition of microbial or host-derived ligands found in arthritic joints. Here, we...
RHEUMATOID-ARTHRITIS | MEDICINE, RESEARCH & EXPERIMENTAL | TOLL-LIKE RECEPTOR-2 | COLLAGEN-INDUCED ARTHRITIS | ANTAGONIST-DEFICIENT MICE | ACTIVATED PROTEIN-KINASE | HUMAN DENDRITIC CELLS | SYNOVIAL TISSUE | TRANSCRIPTION FACTOR FOXP3 | MEDIATES HEPATIC-INJURY | BACTERIAL-DNA | Germ-Free Life - immunology | Interleukin 1 Receptor Antagonist Protein - immunology | Toll-Like Receptor 2 - genetics | Germ-Free Life - genetics | Humans | Interleukin-17 - immunology | Toll-Like Receptor 9 - genetics | Toll-Like Receptor 4 - genetics | Interleukin 1 Receptor Antagonist Protein - genetics | Toll-Like Receptor 4 - immunology | Arthritis, Rheumatoid - microbiology | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Toll-Like Receptor 9 - immunology | Arthritis, Rheumatoid - genetics | Lymphocyte Activation - genetics | Lymphocyte Activation - immunology | Animals | Toll-Like Receptor 2 - immunology | Mice | Mice, Inbred BALB C | Arthritis, Rheumatoid - immunology | Disease Models, Animal | Polymerase chain reaction | Receptor antibodies | Prognosis | Rheumatoid arthritis | Research | Diagnosis | Health aspects
RHEUMATOID-ARTHRITIS | MEDICINE, RESEARCH & EXPERIMENTAL | TOLL-LIKE RECEPTOR-2 | COLLAGEN-INDUCED ARTHRITIS | ANTAGONIST-DEFICIENT MICE | ACTIVATED PROTEIN-KINASE | HUMAN DENDRITIC CELLS | SYNOVIAL TISSUE | TRANSCRIPTION FACTOR FOXP3 | MEDIATES HEPATIC-INJURY | BACTERIAL-DNA | Germ-Free Life - immunology | Interleukin 1 Receptor Antagonist Protein - immunology | Toll-Like Receptor 2 - genetics | Germ-Free Life - genetics | Humans | Interleukin-17 - immunology | Toll-Like Receptor 9 - genetics | Toll-Like Receptor 4 - genetics | Interleukin 1 Receptor Antagonist Protein - genetics | Toll-Like Receptor 4 - immunology | Arthritis, Rheumatoid - microbiology | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Toll-Like Receptor 9 - immunology | Arthritis, Rheumatoid - genetics | Lymphocyte Activation - genetics | Lymphocyte Activation - immunology | Animals | Toll-Like Receptor 2 - immunology | Mice | Mice, Inbred BALB C | Arthritis, Rheumatoid - immunology | Disease Models, Animal | Polymerase chain reaction | Receptor antibodies | Prognosis | Rheumatoid arthritis | Research | Diagnosis | Health aspects
Journal Article
Science, ISSN 0036-8075, 8/2013, Volume 341, Issue 6146, pp. 667 - 669
Although the gut microbiome influences numerous aspects of organismal fitness, its role in animal evolution and the origin of new species is largely unknown....
Pupae | Biological taxonomies | Microbiota | Insect larvae | REPORTS | Germ free state | Bacteria | Genomes | Hybridity | Larval development | Species | INCOMPATIBILITIES | MULTIDISCIPLINARY SCIENCES | Symbiosis | Species Specificity | Chimera - microbiology | Germ-Free Life - genetics | Chimera - physiology | Gastrointestinal Tract - microbiology | Hymenoptera - microbiology | Phylogeny | Bacteria - genetics | Animals | Bacteria - classification | Hymenoptera - physiology | Germ-Free Life - physiology | Hymenoptera - genetics | Metagenome | Lethal mutation | Origin of species | Genetic aspects | Wasps | Microbiota (Symbiotic organisms) | Somatic hybrids | Hybridization | Microbiology | Insects | Bacteriology
Pupae | Biological taxonomies | Microbiota | Insect larvae | REPORTS | Germ free state | Bacteria | Genomes | Hybridity | Larval development | Species | INCOMPATIBILITIES | MULTIDISCIPLINARY SCIENCES | Symbiosis | Species Specificity | Chimera - microbiology | Germ-Free Life - genetics | Chimera - physiology | Gastrointestinal Tract - microbiology | Hymenoptera - microbiology | Phylogeny | Bacteria - genetics | Animals | Bacteria - classification | Hymenoptera - physiology | Germ-Free Life - physiology | Hymenoptera - genetics | Metagenome | Lethal mutation | Origin of species | Genetic aspects | Wasps | Microbiota (Symbiotic organisms) | Somatic hybrids | Hybridization | Microbiology | Insects | Bacteriology
Journal Article
3.
Full Text
Impact of the resident microbiota on the nutritional phenotype of drosophila melanogaster
PLoS ONE, ISSN 1932-6203, 05/2012, Volume 7, Issue 5, p. e36765
Background: Animals are chronically infected by benign and beneficial microorganisms that generally promote animal health through their effects on the...
INSULIN | LIFE-SPAN | LACTOBACILLUS-PLANTARUM | BACTERIA | HOMEOSTASIS | GUT-MICROBIOTA | HEALTHY-SUBJECTS | BLOOD-GLUCOSE | BIOLOGY | COLONIZATION | MECHANISMS | Germ-Free Life - genetics | Metagenome - physiology | Drosophila melanogaster - metabolism | Drosophila melanogaster - microbiology | Fertility - genetics | Metagenome - genetics | Phenotype | Animals | Acetobacter - metabolism | Larva - growth & development | RNA, Ribosomal, 16S - genetics | Female | Larva - genetics | Germ-Free Life - physiology | Host-Pathogen Interactions - physiology | Type 2 diabetes | Microbiota (Symbiotic organisms) | RNA | Drosophila | Physiological aspects | Genetic aspects | Glucose | Health aspects | Dextrose | Metabolic rate | Physiological effects | Senescence | rRNA 16S | Growth rate | Genes | Homeostasis | Eggs | Microorganisms | Microbiota | Bacteria | Physiology | Carbohydrates | Immune response | Nutrition | Metabolism | Insulin | Studies | Energy balance | Nutrition research | Musculoskeletal system | Insects | Animal health | Protein synthesis | Stem cells | Flies | Fecundity | Larval development
INSULIN | LIFE-SPAN | LACTOBACILLUS-PLANTARUM | BACTERIA | HOMEOSTASIS | GUT-MICROBIOTA | HEALTHY-SUBJECTS | BLOOD-GLUCOSE | BIOLOGY | COLONIZATION | MECHANISMS | Germ-Free Life - genetics | Metagenome - physiology | Drosophila melanogaster - metabolism | Drosophila melanogaster - microbiology | Fertility - genetics | Metagenome - genetics | Phenotype | Animals | Acetobacter - metabolism | Larva - growth & development | RNA, Ribosomal, 16S - genetics | Female | Larva - genetics | Germ-Free Life - physiology | Host-Pathogen Interactions - physiology | Type 2 diabetes | Microbiota (Symbiotic organisms) | RNA | Drosophila | Physiological aspects | Genetic aspects | Glucose | Health aspects | Dextrose | Metabolic rate | Physiological effects | Senescence | rRNA 16S | Growth rate | Genes | Homeostasis | Eggs | Microorganisms | Microbiota | Bacteria | Physiology | Carbohydrates | Immune response | Nutrition | Metabolism | Insulin | Studies | Energy balance | Nutrition research | Musculoskeletal system | Insects | Animal health | Protein synthesis | Stem cells | Flies | Fecundity | Larval development
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 09/2012, Volume 109, Issue 39, pp. E2605 - E2614
How fish larvae are protected from infection before the maturation of adaptive immunity, a process which may take up to several weeks in most species, has long...
Evolution | Epigenetic | Live imaging | Cytokines | Gene regulation | GNOTOBIOTIC ZEBRAFISH | epigenetic | MULTIDISCIPLINARY SCIENCES | evolution | GUT MICROBIOTA | GERM-FREE | T-CELL | MODEL | live imaging | UNSEEN MAJORITY | gene regulation | INFLAMMATION | TOLL-LIKE RECEPTORS | cytokines | HISTONE MODIFICATIONS | NF-KAPPA-B | Chromatin - metabolism | Germ-Free Life - immunology | Zebrafish - immunology | Zebrafish - embryology | Bacteria - immunology | Inflammation - metabolism | Zebrafish - classification | Chromatin - immunology | Myeloid Differentiation Factor 88 - immunology | Zebrafish Proteins - immunology | Toll-Like Receptors - metabolism | Inflammation - microbiology | Histones - immunology | Zebrafish Proteins - metabolism | Germ-Free Life - genetics | Toll-Like Receptors - immunology | Myeloid Differentiation Factor 88 - genetics | Inflammation - immunology | Animals | Histones - genetics | Toll-Like Receptors - genetics | Zebrafish - metabolism | Inflammation - genetics | Histones - metabolism | Zebrafish Proteins - genetics | Chromatin - genetics | Myeloid Differentiation Factor 88 - metabolism | Biological Sciences | PNAS Plus
Evolution | Epigenetic | Live imaging | Cytokines | Gene regulation | GNOTOBIOTIC ZEBRAFISH | epigenetic | MULTIDISCIPLINARY SCIENCES | evolution | GUT MICROBIOTA | GERM-FREE | T-CELL | MODEL | live imaging | UNSEEN MAJORITY | gene regulation | INFLAMMATION | TOLL-LIKE RECEPTORS | cytokines | HISTONE MODIFICATIONS | NF-KAPPA-B | Chromatin - metabolism | Germ-Free Life - immunology | Zebrafish - immunology | Zebrafish - embryology | Bacteria - immunology | Inflammation - metabolism | Zebrafish - classification | Chromatin - immunology | Myeloid Differentiation Factor 88 - immunology | Zebrafish Proteins - immunology | Toll-Like Receptors - metabolism | Inflammation - microbiology | Histones - immunology | Zebrafish Proteins - metabolism | Germ-Free Life - genetics | Toll-Like Receptors - immunology | Myeloid Differentiation Factor 88 - genetics | Inflammation - immunology | Animals | Histones - genetics | Toll-Like Receptors - genetics | Zebrafish - metabolism | Inflammation - genetics | Histones - metabolism | Zebrafish Proteins - genetics | Chromatin - genetics | Myeloid Differentiation Factor 88 - metabolism | Biological Sciences | PNAS Plus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2016, Volume 113, Issue 50, pp. E8141 - E8150
Th17 cells accrue in the intestine in response to particular microbes. In rodents, segmented filamentous bacteria (SFB) induce intestinal Th17 cells, but...
Probiotic | Microbiota | Intestine | Mucosal immunology | Th17 cells | microbiota | RHEUMATOID-ARTHRITIS | mucosal immunology | intestine | DENDRITIC CELLS | MULTIDISCIPLINARY SCIENCES | HELPER-CELLS | INNATE | SEGMENTED FILAMENTOUS BACTERIA | probiotic | T(H)17 CELLS | INTERLEUKIN-17 | TYPE-2 IMMUNITY | GENOME-WIDE ASSOCIATION | Germ-Free Life - immunology | Humans | Inflammatory Bowel Diseases - immunology | Immunity, Mucosal | Symbiosis - immunology | Male | Arthritis, Experimental - microbiology | Gene Expression Profiling | Symbiosis - genetics | Intestinal Mucosa - cytology | Intestinal Mucosa - immunology | Arthritis, Experimental - etiology | Inflammatory Bowel Diseases - pathology | Female | Th17 Cells - cytology | Bifidobacterium adolescentis - isolation & purification | Germ-Free Life - genetics | Mice, Inbred C57BL | Arthritis, Experimental - immunology | Bifidobacterium adolescentis - immunology | Intestinal Mucosa - microbiology | Probiotics | Animals | Th17 Cells - immunology | Inflammatory Bowel Diseases - microbiology | Mice | Gastrointestinal Microbiome - immunology | Biological Sciences | PNAS Plus
Probiotic | Microbiota | Intestine | Mucosal immunology | Th17 cells | microbiota | RHEUMATOID-ARTHRITIS | mucosal immunology | intestine | DENDRITIC CELLS | MULTIDISCIPLINARY SCIENCES | HELPER-CELLS | INNATE | SEGMENTED FILAMENTOUS BACTERIA | probiotic | T(H)17 CELLS | INTERLEUKIN-17 | TYPE-2 IMMUNITY | GENOME-WIDE ASSOCIATION | Germ-Free Life - immunology | Humans | Inflammatory Bowel Diseases - immunology | Immunity, Mucosal | Symbiosis - immunology | Male | Arthritis, Experimental - microbiology | Gene Expression Profiling | Symbiosis - genetics | Intestinal Mucosa - cytology | Intestinal Mucosa - immunology | Arthritis, Experimental - etiology | Inflammatory Bowel Diseases - pathology | Female | Th17 Cells - cytology | Bifidobacterium adolescentis - isolation & purification | Germ-Free Life - genetics | Mice, Inbred C57BL | Arthritis, Experimental - immunology | Bifidobacterium adolescentis - immunology | Intestinal Mucosa - microbiology | Probiotics | Animals | Th17 Cells - immunology | Inflammatory Bowel Diseases - microbiology | Mice | Gastrointestinal Microbiome - immunology | Biological Sciences | PNAS Plus
Journal Article
Journal of Immunology, ISSN 0022-1767, 02/2011, Volume 186, Issue 3, pp. 1531 - 1537
Retinoic acid-related orphan receptor (ROR)gamma t(+) TCR alpha beta(+) cells expressing IL-17, termed Th17 cells, are most abundant in the intestinal lamina...
LINEAGE COMMITMENT | ADAPTIVE IMMUNITY | RETINOIC ACID | ROR-GAMMA-T | HELPER-CELLS | REGULATORY T-CELLS | INTESTINAL IMMUNE-RESPONSES | PROINFLAMMATORY IL-17(+) | NKP46(+) CELLS | IMMUNOLOGY | FILAMENTOUS BACTERIA | T-Lymphocytes, Helper-Inducer - microbiology | Gram-Positive Bacterial Infections - immunology | Cell Proliferation | Germ-Free Life - immunology | Molecular Sequence Data | Male | Green Fluorescent Proteins - genetics | Cell Differentiation - genetics | Lymphocyte Activation - genetics | Lymphocyte Activation - immunology | Intestinal Mucosa - immunology | T-Lymphocytes, Helper-Inducer - immunology | Female | Nuclear Receptor Subfamily 1, Group F, Member 3 - deficiency | T-Lymphocytes, Helper-Inducer - pathology | Forkhead Transcription Factors - deficiency | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Amino Acid Sequence | Forkhead Transcription Factors - biosynthesis | Germ-Free Life - genetics | Interleukin-17 - genetics | Mice, Transgenic | CD4 Lymphocyte Count | Interleukin-17 - biosynthesis | Intestinal Mucosa - microbiology | Forkhead Transcription Factors - genetics | Receptors, Antigen, T-Cell - physiology | Mice, Knockout | Gram-Positive Bacterial Infections - pathology | Cell Differentiation - immunology | Animals | Green Fluorescent Proteins - biosynthesis | Nuclear Receptor Subfamily 1, Group F, Member 3 - biosynthesis | Mice | Receptors, Antigen, T-Cell - genetics | Receptors, Antigen, T-Cell - deficiency | Intestinal Mucosa - pathology | Life Sciences | Immunology
LINEAGE COMMITMENT | ADAPTIVE IMMUNITY | RETINOIC ACID | ROR-GAMMA-T | HELPER-CELLS | REGULATORY T-CELLS | INTESTINAL IMMUNE-RESPONSES | PROINFLAMMATORY IL-17(+) | NKP46(+) CELLS | IMMUNOLOGY | FILAMENTOUS BACTERIA | T-Lymphocytes, Helper-Inducer - microbiology | Gram-Positive Bacterial Infections - immunology | Cell Proliferation | Germ-Free Life - immunology | Molecular Sequence Data | Male | Green Fluorescent Proteins - genetics | Cell Differentiation - genetics | Lymphocyte Activation - genetics | Lymphocyte Activation - immunology | Intestinal Mucosa - immunology | T-Lymphocytes, Helper-Inducer - immunology | Female | Nuclear Receptor Subfamily 1, Group F, Member 3 - deficiency | T-Lymphocytes, Helper-Inducer - pathology | Forkhead Transcription Factors - deficiency | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Amino Acid Sequence | Forkhead Transcription Factors - biosynthesis | Germ-Free Life - genetics | Interleukin-17 - genetics | Mice, Transgenic | CD4 Lymphocyte Count | Interleukin-17 - biosynthesis | Intestinal Mucosa - microbiology | Forkhead Transcription Factors - genetics | Receptors, Antigen, T-Cell - physiology | Mice, Knockout | Gram-Positive Bacterial Infections - pathology | Cell Differentiation - immunology | Animals | Green Fluorescent Proteins - biosynthesis | Nuclear Receptor Subfamily 1, Group F, Member 3 - biosynthesis | Mice | Receptors, Antigen, T-Cell - genetics | Receptors, Antigen, T-Cell - deficiency | Intestinal Mucosa - pathology | Life Sciences | Immunology
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 10/2010, Volume 207, Issue 11, pp. 2323 - 2330
Suppression mediated by regulatory T cells (T reg cells) represents a unique, cell-extrinsic mechanism of in-trans negative regulation that restrains multiple...
MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNITY | HOMEOSTASIS | BACTERIA | NOD MICE | PROTEIN | AUTOIMMUNITY | TRANSCRIPTION FACTOR FOXP3 | IMMUNOLOGY | MATURATION | Inflammation - microbiology | Germ-Free Life - immunology | Germ-Free Life - genetics | Intestine, Small - microbiology | Enteritis - genetics | Immunity, Innate - genetics | Inflammation - immunology | Lymphocyte Depletion | Adaptive Immunity - genetics | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Immunity, Innate - immunology | Pancreatitis - genetics | Bacteria - immunology | Animals | Enteritis - microbiology | Enteritis - immunology | Inflammation - genetics | Pancreatitis - immunology | Mice | Adaptive Immunity - immunology | Pancreatitis - microbiology | Intestine, Small - immunology | Brief Definitive Report
MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNITY | HOMEOSTASIS | BACTERIA | NOD MICE | PROTEIN | AUTOIMMUNITY | TRANSCRIPTION FACTOR FOXP3 | IMMUNOLOGY | MATURATION | Inflammation - microbiology | Germ-Free Life - immunology | Germ-Free Life - genetics | Intestine, Small - microbiology | Enteritis - genetics | Immunity, Innate - genetics | Inflammation - immunology | Lymphocyte Depletion | Adaptive Immunity - genetics | Mice, Knockout | T-Lymphocytes, Regulatory - immunology | Immunity, Innate - immunology | Pancreatitis - genetics | Bacteria - immunology | Animals | Enteritis - microbiology | Enteritis - immunology | Inflammation - genetics | Pancreatitis - immunology | Mice | Adaptive Immunity - immunology | Pancreatitis - microbiology | Intestine, Small - immunology | Brief Definitive Report
Journal Article
Blood, ISSN 0006-4971, 02/2017, Volume 129, Issue 6, pp. 729 - 739
Bone marrow suppression is an adverse effect associated with many antibiotics, especially when administered for prolonged treatment courses. Recent advances in...
GRANULOPOIESIS | STEM-CELLS | HEMATOLOGY | NEUTROPENIA | T-CELLS | DISEASE | CD8-Positive T-Lymphocytes - pathology | STAT1 Transcription Factor - deficiency | Hematopoietic Stem Cells - pathology | Anemia - pathology | Gastrointestinal Microbiome - physiology | Leukopenia - therapy | Hematopoiesis - drug effects | Granulocytes - drug effects | Leukopenia - chemically induced | CD8-Positive T-Lymphocytes - metabolism | Thrombocytosis - microbiology | Bone Marrow Cells - drug effects | Granulocytes - pathology | Anti-Bacterial Agents - adverse effects | B-Lymphocytes - pathology | Granulocytes - metabolism | Thrombocytosis - pathology | B-Lymphocytes - metabolism | Hematopoietic Stem Cells - drug effects | Gene Expression | Leukopenia - microbiology | Macrophages - pathology | Signal Transduction | Germ-Free Life - genetics | Mice, Inbred C57BL | Bone Marrow Cells - pathology | Anemia - chemically induced | Anemia - therapy | Hematopoiesis - genetics | Hematopoietic Stem Cells - metabolism | Germ-Free Life - drug effects | STAT1 Transcription Factor - genetics | Leukopenia - pathology | Fecal Microbiota Transplantation | Thrombocytosis - chemically induced | Mice, Knockout | B-Lymphocytes - drug effects | Macrophages - metabolism | Animals | Gastrointestinal Microbiome - drug effects | CD8-Positive T-Lymphocytes - drug effects | Macrophages - drug effects | Mice | Anemia - microbiology | Thrombocytosis - therapy | Bone Marrow Cells - metabolism | Hematopoiesis and Stem Cells
GRANULOPOIESIS | STEM-CELLS | HEMATOLOGY | NEUTROPENIA | T-CELLS | DISEASE | CD8-Positive T-Lymphocytes - pathology | STAT1 Transcription Factor - deficiency | Hematopoietic Stem Cells - pathology | Anemia - pathology | Gastrointestinal Microbiome - physiology | Leukopenia - therapy | Hematopoiesis - drug effects | Granulocytes - drug effects | Leukopenia - chemically induced | CD8-Positive T-Lymphocytes - metabolism | Thrombocytosis - microbiology | Bone Marrow Cells - drug effects | Granulocytes - pathology | Anti-Bacterial Agents - adverse effects | B-Lymphocytes - pathology | Granulocytes - metabolism | Thrombocytosis - pathology | B-Lymphocytes - metabolism | Hematopoietic Stem Cells - drug effects | Gene Expression | Leukopenia - microbiology | Macrophages - pathology | Signal Transduction | Germ-Free Life - genetics | Mice, Inbred C57BL | Bone Marrow Cells - pathology | Anemia - chemically induced | Anemia - therapy | Hematopoiesis - genetics | Hematopoietic Stem Cells - metabolism | Germ-Free Life - drug effects | STAT1 Transcription Factor - genetics | Leukopenia - pathology | Fecal Microbiota Transplantation | Thrombocytosis - chemically induced | Mice, Knockout | B-Lymphocytes - drug effects | Macrophages - metabolism | Animals | Gastrointestinal Microbiome - drug effects | CD8-Positive T-Lymphocytes - drug effects | Macrophages - drug effects | Mice | Anemia - microbiology | Thrombocytosis - therapy | Bone Marrow Cells - metabolism | Hematopoiesis and Stem Cells
Journal Article
DRUG METABOLISM AND DISPOSITION, ISSN 0090-9556, 10/2015, Volume 43, Issue 10, pp. 1572 - 1580
Intestinal bacteria have been shown to be important in regulating host intermediary metabolism and contributing to obesity. However, relatively less is known...
CYTOCHROME-P450 | PHARMACOLOGY & PHARMACY | BIOTRANSFORMATION | MICROBIOTA | GUT FLORA | EXPRESSION | Germ-Free Life - genetics | Liver - metabolism | Mice, Inbred C57BL | Cytochrome P-450 Enzyme System - metabolism | Male | RNA - genetics | Sequence Analysis, RNA - methods | Pharmaceutical Preparations - metabolism | Animals | Liver - drug effects | Cytochrome P-450 Enzyme System - genetics | Mice | Pharmaceutical Preparations - administration & dosage | Special Section on Drug Metabolism and the Microbiome
CYTOCHROME-P450 | PHARMACOLOGY & PHARMACY | BIOTRANSFORMATION | MICROBIOTA | GUT FLORA | EXPRESSION | Germ-Free Life - genetics | Liver - metabolism | Mice, Inbred C57BL | Cytochrome P-450 Enzyme System - metabolism | Male | RNA - genetics | Sequence Analysis, RNA - methods | Pharmaceutical Preparations - metabolism | Animals | Liver - drug effects | Cytochrome P-450 Enzyme System - genetics | Mice | Pharmaceutical Preparations - administration & dosage | Special Section on Drug Metabolism and the Microbiome
Journal Article
BMC Research Notes, ISSN 1756-0500, 2012, Volume 5, Issue 1, pp. 402 - 402
Postnatal regulation of the small intestinal mucus layer is potentially important in the development of adult gut functionality. We hypothesized that the...
16S rRNA | Postnatal transcription onset | Probiotics | Escherichia coli Nissle | Lactobacillus acidophilus NCFM | Germ free mice | LinRegPCR | qPCR | Monocolonized | Mucin-2 - genetics | Metagenome - physiology | Gene Expression Regulation, Developmental | Mucins - metabolism | Trefoil Factor-3 | Mucus - metabolism | Transcription, Genetic | Microbial Consortia - genetics | Escherichia coli - physiology | Real-Time Polymerase Chain Reaction | Mucin-3 - genetics | Animals, Newborn | Mucin-2 - metabolism | Mucin-1 - metabolism | Mucin-3 - metabolism | Lactobacillus acidophilus - physiology | Germ-Free Life - genetics | Intestine, Small - microbiology | Mucin-4 - metabolism | Mucin-4 - genetics | Mucus - microbiology | Animals | RNA, Ribosomal, 16S - genetics | Mice | Intestine, Small - metabolism | Mucins - genetics | Mucin-1 - genetics | Dams | Microbiota (Symbiotic organisms) | RNA | Genes | Escherichia coli | Mucins | Genetic transcription | Microbial colonies | Protein binding | Microbiology | E coli | Efficiency | Colleges & universities | Bacteria | Software | Life sciences | Gene expression | Experiments | Manuscripts | Food
16S rRNA | Postnatal transcription onset | Probiotics | Escherichia coli Nissle | Lactobacillus acidophilus NCFM | Germ free mice | LinRegPCR | qPCR | Monocolonized | Mucin-2 - genetics | Metagenome - physiology | Gene Expression Regulation, Developmental | Mucins - metabolism | Trefoil Factor-3 | Mucus - metabolism | Transcription, Genetic | Microbial Consortia - genetics | Escherichia coli - physiology | Real-Time Polymerase Chain Reaction | Mucin-3 - genetics | Animals, Newborn | Mucin-2 - metabolism | Mucin-1 - metabolism | Mucin-3 - metabolism | Lactobacillus acidophilus - physiology | Germ-Free Life - genetics | Intestine, Small - microbiology | Mucin-4 - metabolism | Mucin-4 - genetics | Mucus - microbiology | Animals | RNA, Ribosomal, 16S - genetics | Mice | Intestine, Small - metabolism | Mucins - genetics | Mucin-1 - genetics | Dams | Microbiota (Symbiotic organisms) | RNA | Genes | Escherichia coli | Mucins | Genetic transcription | Microbial colonies | Protein binding | Microbiology | E coli | Efficiency | Colleges & universities | Bacteria | Software | Life sciences | Gene expression | Experiments | Manuscripts | Food
Journal Article
BMC Genomics, ISSN 1471-2164, 07/2007, Volume 8, Issue 1, pp. 215 - 215
To gain insight into host-microbe interactions in a piglet model, a functional genomics approach was used to address the working hypothesis that...
Animals, Newborn | Intestinal Mucosa - metabolism | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Electron Transport - genetics | Germ-Free Life - genetics | Intestine, Small - microbiology | Gene Expression Profiling | Signal Transduction - genetics | Intestinal Mucosa - microbiology | Gene Regulatory Networks | Intestinal Mucosa - cytology | Cell Differentiation - genetics | Host-Parasite Interactions - genetics | Metabolic Networks and Pathways - genetics | Animals | Intestinal Mucosa - immunology | Swine | Transcription, Genetic | Intestine, Small - metabolism | Immunity, Mucosal - genetics | Principal Component Analysis | Intestine, Small - immunology | Messenger RNA | Intestine, Small | Physiological aspects | Genetic aspects | Genetic transcription | Research | Properties | Epithelium
Animals, Newborn | Intestinal Mucosa - metabolism | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Electron Transport - genetics | Germ-Free Life - genetics | Intestine, Small - microbiology | Gene Expression Profiling | Signal Transduction - genetics | Intestinal Mucosa - microbiology | Gene Regulatory Networks | Intestinal Mucosa - cytology | Cell Differentiation - genetics | Host-Parasite Interactions - genetics | Metabolic Networks and Pathways - genetics | Animals | Intestinal Mucosa - immunology | Swine | Transcription, Genetic | Intestine, Small - metabolism | Immunity, Mucosal - genetics | Principal Component Analysis | Intestine, Small - immunology | Messenger RNA | Intestine, Small | Physiological aspects | Genetic aspects | Genetic transcription | Research | Properties | Epithelium
Journal Article
BMC Genomics, ISSN 1471-2164, 07/2012, Volume 13, Issue 1, pp. 335 - 335
Background: Epidemiological studies have suggested that the encounter with commensal microorganisms during the neonatal period is essential for normal...
Hygiene hypothesis | Metagene profiler | Germ-free | Type 1 interferon | Toll-like receptor | ADJUVANT-INDUCED ARTHRITIS | GENE SET ENRICHMENT | COMMENSAL BACTERIA | TOLERANCE | ONTOLOGY TERMS | COLONIZATION | GUT MICROBIOTA | AUTOIMMUNE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | EXPRESSION | MetaGene Profiler | Germ-Free Life - immunology | Gene Expression Profiling | Immune System - growth & development | Liver - growth & development | Organ Specificity - genetics | Gene Expression Regulation, Developmental | Intestine, Small - growth & development | Toll-Like Receptors - metabolism | Spleen - growth & development | Animals, Newborn | Multigene Family - genetics | Bacteria - metabolism | Immune System - microbiology | Oligonucleotide Array Sequence Analysis - methods | Germ-Free Life - genetics | Liver - metabolism | Signal Transduction - genetics | Reverse Transcriptase Polymerase Chain Reaction | Animals | Spleen - metabolism | Models, Biological | Toll-Like Receptors - genetics | Mice | Intestine, Small - metabolism | Cluster Analysis | Usage | DNA microarrays | Perinatal infection | Genetic aspects | Research | Health aspects | Risk factors | Immune system | Infants (Newborn) | Analysis | Sunscreens (Cosmetics) | Liver | Genes | Interferon | B cells | Biological response modifiers | Studies | Microorganisms | Algorithms | Cytokines | Statistical methods | Gene expression | Experiments | Thermal cycling
Hygiene hypothesis | Metagene profiler | Germ-free | Type 1 interferon | Toll-like receptor | ADJUVANT-INDUCED ARTHRITIS | GENE SET ENRICHMENT | COMMENSAL BACTERIA | TOLERANCE | ONTOLOGY TERMS | COLONIZATION | GUT MICROBIOTA | AUTOIMMUNE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | EXPRESSION | MetaGene Profiler | Germ-Free Life - immunology | Gene Expression Profiling | Immune System - growth & development | Liver - growth & development | Organ Specificity - genetics | Gene Expression Regulation, Developmental | Intestine, Small - growth & development | Toll-Like Receptors - metabolism | Spleen - growth & development | Animals, Newborn | Multigene Family - genetics | Bacteria - metabolism | Immune System - microbiology | Oligonucleotide Array Sequence Analysis - methods | Germ-Free Life - genetics | Liver - metabolism | Signal Transduction - genetics | Reverse Transcriptase Polymerase Chain Reaction | Animals | Spleen - metabolism | Models, Biological | Toll-Like Receptors - genetics | Mice | Intestine, Small - metabolism | Cluster Analysis | Usage | DNA microarrays | Perinatal infection | Genetic aspects | Research | Health aspects | Risk factors | Immune system | Infants (Newborn) | Analysis | Sunscreens (Cosmetics) | Liver | Genes | Interferon | B cells | Biological response modifiers | Studies | Microorganisms | Algorithms | Cytokines | Statistical methods | Gene expression | Experiments | Thermal cycling
Journal Article
ILAR Journal, ISSN 1084-2020, 08/2015, Volume 56, Issue 2, pp. 169 - 178
The gastrointestinal (GI) microbiota forms a mutualistic relationship with the host through complex and dynamic interactions. Because of the complexity and...
ASF | Gnotobiotic | Microbiota | microbiota | OLIGONUCLEOTIDE PROBES | GERMFREE MICE | INTESTINAL MICROBIOTA | GASTROINTESTINAL-TRACT | BACTERIAL FLORA | INFLAMMATORY-BOWEL-DISEASE | T-CELL RESPONSES | gnotobiotic | VETERINARY SCIENCES | LYMPHATIC TISSUE | HELICOBACTER-HEPATICUS | IMMUNE REACTIVITY | Bacteria - metabolism | Animals | Germ-Free Life - genetics | Humans | Gastrointestinal Microbiome - physiology | Mice | Germ-Free Life - physiology | Gastrointestinal Microbiome - genetics
ASF | Gnotobiotic | Microbiota | microbiota | OLIGONUCLEOTIDE PROBES | GERMFREE MICE | INTESTINAL MICROBIOTA | GASTROINTESTINAL-TRACT | BACTERIAL FLORA | INFLAMMATORY-BOWEL-DISEASE | T-CELL RESPONSES | gnotobiotic | VETERINARY SCIENCES | LYMPHATIC TISSUE | HELICOBACTER-HEPATICUS | IMMUNE REACTIVITY | Bacteria - metabolism | Animals | Germ-Free Life - genetics | Humans | Gastrointestinal Microbiome - physiology | Mice | Germ-Free Life - physiology | Gastrointestinal Microbiome - genetics
Journal Article