X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (70) 70
humans (50) 50
animals (46) 46
gastroenterology and hepatology (37) 37
mice (33) 33
male (32) 32
liver (23) 23
dementia (21) 21
bile acids (20) 20
receptors, cytoplasmic and nuclear - metabolism (20) 20
multidisciplinary sciences (18) 18
inflammation (17) 17
mice, inbred c57bl (15) 15
activation (14) 14
bile (14) 14
colitis (14) 14
liver diseases (14) 14
research article (14) 14
gene expression (13) 13
medicine (13) 13
rodents (13) 13
science (13) 13
disease models, animal (12) 12
expression (12) 12
gastroenterology & hepatology (12) 12
nuclear receptors (12) 12
pharmacology & pharmacy (12) 12
acids (11) 11
female (11) 11
geriatrics & gerontology (11) 11
hep g2 cells (11) 11
ligands (11) 11
physiological aspects (11) 11
receptors, cytoplasmic and nuclear - genetics (11) 11
aged (10) 10
alzheimers-disease (10) 10
animal models (10) 10
biology (10) 10
deoxycholic acid (10) 10
farnesoid x receptor (10) 10
farnesoid-x-receptor (10) 10
intestine (10) 10
mice, knockout (10) 10
signal transduction (10) 10
bile acids and salts - metabolism (9) 9
clinical neurology (9) 9
hydrogen sulfide (9) 9
immunology (9) 9
infectious diseases (9) 9
inflammatory bowel disease (9) 9
rats (9) 9
receptors (9) 9
tgr5 (9) 9
article (8) 8
cell line (8) 8
dementia - psychology (8) 8
disease (8) 8
fxr (8) 8
genes (8) 8
health aspects (8) 8
liver - metabolism (8) 8
neurosciences (8) 8
receptors, g-protein-coupled - metabolism (8) 8
alzheimer's disease (7) 7
cells, cultured (7) 7
cholesterol (7) 7
colon (7) 7
frontotemporal dementia (7) 7
gene-expression (7) 7
homeostasis (7) 7
immunity (7) 7
metabolism (7) 7
nitric oxide (7) 7
nuclear receptor (7) 7
probiotics (7) 7
proteins (7) 7
psychiatry (7) 7
receptors, g-protein-coupled - agonists (7) 7
research (7) 7
signal transduction - drug effects (7) 7
abridged index medicus (6) 6
atherosclerosis (6) 6
biochemistry & molecular biology (6) 6
colitis - chemically induced (6) 6
diabetes (6) 6
genetic aspects (6) 6
inflammatory bowel diseases (6) 6
intestinal mucosa - metabolism (6) 6
lipids (6) 6
macrophages (6) 6
microbiota (6) 6
molecular cell biology (6) 6
monocytes (6) 6
rats, wistar (6) 6
adult (5) 5
care and treatment (5) 5
cell activation (5) 5
chemistry, medicinal (5) 5
cholestasis (5) 5
cognitive impairment (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Lipid Research, ISSN 0022-2275, 04/2010, Volume 51, Issue 4, pp. 771 - 784
The farnesoid X receptor (FXR) is a bile acid activated nuclear receptor. Zucker (fa/fa) rats, harboring a loss of function mutation of the leptin receptor,... 
RESPONSE ELEMENT | TYROSINE PHOSPHORYLATION | METABOLISM | LINKING OBESITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | ANIMAL-MODELS | FARNESOID-X-RECEPTOR | NONALCOHOLIC STEATOHEPATITIS | MECHANISMS | AGONISTS | Liver - pathology | Fatty Liver - pathology | Male | Muscle, Skeletal - metabolism | Insulin Receptor Substrate Proteins - metabolism | RNA, Messenger - metabolism | Thiazolidinediones - administration & dosage | Obesity - blood | Thiazolidinediones - therapeutic use | Hypoglycemic Agents - administration & dosage | Liver - drug effects | Time Factors | Lipids - blood | Muscle, Skeletal - drug effects | Chenodeoxycholic Acid - therapeutic use | Lipid Metabolism - genetics | Phosphorylation - drug effects | Drug Therapy, Combination | Disease Models, Animal | Hypoglycemic Agents - therapeutic use | Fatty Liver - blood | Obesity - complications | Liver - metabolism | Fatty Liver - prevention & control | Insulin Resistance | Rats | Chenodeoxycholic Acid - administration & dosage | Receptors, Cytoplasmic and Nuclear - agonists | Receptors, Cytoplasmic and Nuclear - genetics | Random Allocation | Chenodeoxycholic Acid - analogs & derivatives | Gene Expression Regulation - drug effects | Rats, Zucker | Animals | Hypolipidemic Agents - administration & dosage | Lipid Metabolism - drug effects | Hypolipidemic Agents - therapeutic use | Receptors, Cytoplasmic and Nuclear - metabolism | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 9, pp. e106503 - e106503
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 10, pp. e25637 - e25637
Journal Article
Journal Article
Journal of Immunology, ISSN 0022-1767, 07/2017, Volume 199, Issue 2, pp. 718 - 733
GPBAR1 (TGR5 or M-BAR) is a G protein-coupled receptor for secondary bile acids that is highly expressed in monocytes/ macrophages. In this study, we aimed to... 
IMMUNITY | HOMEOSTASIS | DENDRITIC CELLS | INTEGRINS | FARNESOID X RECEPTOR | INFLAMMATION | CHEMOKINES | MONOCYTE CHEMOATTRACTANT PROTEIN-1 | THERAPEUTIC TARGETS | MICROBIOTA | IMMUNOLOGY | Receptors, G-Protein-Coupled - metabolism | Chemokine CCL2 - immunology | Tumor Necrosis Factor-alpha - genetics | Antigens, Ly - genetics | Interleukin-1beta - genetics | Receptors, G-Protein-Coupled - agonists | T-Lymphocytes, Regulatory - immunology | Intestinal Mucosa - immunology | Colitis - chemically induced | Tumor Necrosis Factor-alpha - immunology | Colitis - immunology | Macrophages - immunology | Cell Line | Promoter Regions, Genetic | Interleukin-10 - deficiency | Interleukin-6 - genetics | Gene Expression Regulation - immunology | Trinitrobenzenesulfonic Acid - administration & dosage | Interleukin-1beta - immunology | Chemokine CCL2 - genetics | Inflammation - immunology | Macrophage Activation | Cholestanols - pharmacology | Phenotype | T-Lymphocytes, Regulatory - drug effects | Animals | Receptors, G-Protein-Coupled - deficiency | Antigens, Ly - immunology | Mucous Membrane - immunology | Interleukin-10 - genetics | Colitis - metabolism | Interleukin-6 - immunology | Macrophages - drug effects | Mice | Oxazolone - administration & dosage | Receptors, G-Protein-Coupled - genetics | Interleukin-10 - immunology | Cell Movement | Cholestanols - administration & dosage | CC chemokine receptors | Oxazolone | Animal models | Inflammatory bowel diseases | Trafficking | Mucosa | Activation | Regulatory sequences | Macrophages | Recruitment | Interleukin 6 | Genotype & phenotype | Cell activation | Intestine | Foxp3 protein | Colon | CD11b antigen | Bile acids | CCR7 protein | Lamina propria | Exposure | Cyclic AMP response element-binding protein | Gene expression | Ablation | CD4 antigen | Inflammatory bowel disease | White blood cells | Monocytes | Acids | Tumor necrosis factor | γ-Interferon | Interleukin 10 | Interferon | Colitis | Monocyte chemoattractant protein 1 | Bile | Index Medicus | Abridged Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2015, Volume 10, Issue 11, pp. e0141082 - e0141082
Background GPBAR1 is a bile acids activated receptor expressed in entero-hepatic tissues. In the liver expression of GPBAR1 is restricted to sinusoidal and... 
MOLECULAR TARGETS | HOMOCYSTEINE | HEPATIC STELLATE CELLS | CIRRHOSIS | MULTIDISCIPLINARY SCIENCES | NITRIC-OXIDE | FARNESOID-X-RECEPTOR | MICROCIRCULATION | HYDROGEN-SULFIDE | NORMAL RAT-LIVER | BILE-ACIDS | Hydrogen Sulfide - metabolism | Hypertension, Portal - physiopathology | Rats, Wistar | Ursodeoxycholic Acid - analogs & derivatives | Humans | Oncogene Protein v-akt - physiology | Endothelium, Vascular - drug effects | Male | Forkhead Transcription Factors - physiology | Receptors, G-Protein-Coupled - agonists | Endothelin-1 - physiology | Real-Time Polymerase Chain Reaction | Receptors, G-Protein-Coupled - physiology | Liver - metabolism | Mice, Inbred C57BL | Endothelium, Vascular - physiopathology | Rats | Bile Acids and Salts - metabolism | Hypertension, Portal - drug therapy | Cholestanols - pharmacology | Animals | Signal Transduction - drug effects | Signal Transduction - physiology | Forkhead Box Protein O1 | Mice | Sulfide | Animal models | Transcription | Liver | Carbon tetrachloride | AKT protein | Kinases | Vasodilation | Recruitment | Hydrogen sulfide | FOXO1 protein | Animal tissues | Hypertension | Bile acids | Liver diseases | Vasoconstriction | Methionine | Endothelin 1 | Cyclic AMP response element-binding protein | Gene expression | Cirrhosis | Acids | Hepatocytes | Perfusion | Nitric oxide | Norepinephrine | Bile | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 02/2017, Volume 7, Issue 1, pp. 42801 - 42801
Journal Article
02/2019
JHEP 05 (2019) 088 This paper presents the combinations of single-top-quark production cross-section measurements by the ATLAS and CMS Collaborations, using... 
Physics - High Energy Physics - Experiment
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, pp. e45425 - e45425
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, pp. e54472 - e54472
Background: Toll like receptors (TLRs) sense the intestinal microbiota and regulate the innate immune response. A dysregulation of TLRs function participates... 
COLITIS | METABOLISM | MACROPHAGES | MULTIDISCIPLINARY SCIENCES | LIVER | TOLL-LIKE RECEPTORS | PPAR-GAMMA | FARNESOID-X RECEPTOR | IRF-7 | NUCLEAR HORMONE-RECEPTORS | INNATE IMMUNITY | Monocytes - cytology | Colitis - genetics | Humans | Immunity, Innate - genetics | Toll-Like Receptor 9 - genetics | Male | Monocytes - metabolism | Interferon Regulatory Factor-7 - genetics | Trinitrobenzenesulfonic Acid | Intestines - immunology | Toll-Like Receptor 9 - immunology | Receptors, Cytoplasmic and Nuclear - immunology | Colitis - chemically induced | Myeloid Differentiation Factor 88 - immunology | Tumor Necrosis Factor-alpha - immunology | Signal Transduction - radiation effects | Colitis - immunology | Promoter Regions, Genetic | Toll-Like Receptor 9 - deficiency | Cells, Cultured | Myeloid Differentiation Factor 88 - genetics | Inflammation | Interferon Regulatory Factor-7 - immunology | Receptors, Cytoplasmic and Nuclear - genetics | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Myeloid Differentiation Factor 88 - deficiency | Signal Transduction - drug effects | Signal Transduction - physiology | Mice | Oligodeoxyribonucleotides - pharmacology | Receptors, Cytoplasmic and Nuclear - metabolism | Microbiota (Symbiotic organisms) | Genes | Genetic research | Physiological aspects | Interferon | Colitis | Deoxycholic acid | Transcription factors | Liver | Homeostasis | Lipids | Innate immunity | Activation | Immunity | Proteins | Receptors | Cell activation | Microbiota | Microorganisms | Intestine | Rodents | Animal tissues | Gastroenterology | Toll-like receptors | Lipid metabolism | Intestinal microflora | Localization | CpG islands | Immune response | Tumor necrosis factor-α | Metabolism | Gene expression | TLR9 protein | TLR3 protein | Immune systems | Inflammatory bowel disease | Interferon regulatory factor 7 | Probiotics | Signaling | Monocytes | Acids | TLR2 protein | MyD88 protein | Ligands | Bile | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e94798 - e94798
Background: The human immunodeficiency virus type 1 (HIV-1) p17 is a matrix protein involved in virus life's cycle. CXCR2 and Syndecan-2, the two major... 
FIBROSIS | PROTEOGLYCANS | CONTRACTILITY | MULTIDISCIPLINARY SCIENCES | LIVER | RECEPTOR | HEPARAN-SULFATE | GP120 | HUMAN-IMMUNODEFICIENCY-VIRUS | PORTAL PRESSURE | EXPRESSION | HIV Antigens - pharmacology | Humans | Middle Aged | Vaccination | Actins - metabolism | Hepatic Stellate Cells - metabolism | HIV Antigens - metabolism | Male | Hepatic Stellate Cells - cytology | gag Gene Products, Human Immunodeficiency Virus - pharmacology | gag Gene Products, Human Immunodeficiency Virus - metabolism | HIV-1 - physiology | rho-Associated Kinases - metabolism | Adult | Female | Hepatic Stellate Cells - drug effects | Syndecan-2 - metabolism | Cell Line | HIV-1 - metabolism | Receptors, Interleukin-8 - metabolism | Collagen Type I - metabolism | Endothelin-1 - metabolism | Disease Progression | Protein Transport | Gene Expression Regulation - drug effects | HIV-1 - immunology | Liver Cirrhosis - virology | Signal Transduction - drug effects | Receptors, Interleukin-8B - metabolism | rho GTP-Binding Proteins - metabolism | Cytoskeleton - metabolism | Liver Cirrhosis - pathology | Protein Binding | Antibodies, Viral - immunology | Aged | Cytoskeleton - drug effects | Physiological aspects | Research | Viral proteins | HIV (Viruses) | Health aspects | Liver cells | Endothelin | Liver | Intracellular signalling | Viruses | Smooth muscle | Activation | Confocal | Kinases | Cell adhesion & migration | Fibers | Proteins | Genotype & phenotype | Signal transduction | Hepatitis | Receptors | Pathways | Rodents | Human immunodeficiency virus--HIV | Extracellular matrix | p17 Protein | Life sciences | Pretreatment | Matrix protein | Heparan sulfate | Stellate cells | Liver diseases | CXCR2 protein | Markers | Contractility | Histology | Endothelin 1 | Exposure | Gene expression | Laser microscopy | Medicine | Pathology | Microscopy | Collagen | Fibrosis | Cytoskeleton | Clinical medicine | Syndecan | Index Medicus | HIV | Human immunodeficiency virus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 13689 - 13
Gpbar1 is a bile acid activated receptor for secondary bile acids. Here we have investigated the mechanistic role of Gpbar1 in the regulation of adipose... 
BEIGE ADIPOCYTES | STEATOSIS | FATTY LIVER-DISEASE | MULTIDISCIPLINARY SCIENCES | MOUSE | EXPRESSION | CELL | Animal models | Adipose tissue | Bile acids | Liver | Energy expenditure | Cyclic AMP response element-binding protein | Insulin | Fructose | Bile | High fat diet
Journal Article