X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (8171) 8171
Publication (1614) 1614
Book Review (67) 67
Book Chapter (32) 32
Conference Proceeding (12) 12
Book / eBook (1) 1
Dissertation (1) 1
Government Document (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (4553) 4553
humans (4095) 4095
index medicus (2056) 2056
mice (1886) 1886
enterotoxins - metabolism (1758) 1758
enterotoxins - biosynthesis (1600) 1600
immunology (1558) 1558
microbiology (1491) 1491
female (1347) 1347
enterotoxins - pharmacology (1251) 1251
male (1218) 1218
enterotoxins - genetics (1063) 1063
bacterial toxins - metabolism (980) 980
escherichia coli - metabolism (918) 918
research article (898) 898
enterotoxins - immunology (894) 894
escherichia coli proteins (887) 887
molecular sequence data (858) 858
biochemistry & molecular biology (779) 779
enterotoxins (772) 772
infectious diseases (728) 728
staphylococcus aureus - metabolism (684) 684
amino acid sequence (664) 664
escherichia-coli (644) 644
bacterial toxins - genetics (643) 643
escherichia coli (639) 639
bacterial toxins (618) 618
expression (614) 614
rats (608) 608
cell line (593) 593
cells, cultured (593) 593
rabbits (593) 593
enterotoxins - toxicity (590) 590
superantigens (588) 588
staphylococcus aureus (583) 583
proteins (568) 568
research (525) 525
toxins (515) 515
adult (509) 509
diarrhea - microbiology (508) 508
diarrhea (500) 500
enterotoxin (494) 494
mice, inbred balb c (480) 480
virulence (479) 479
heat-labile enterotoxin (472) 472
enterotoxins - analysis (458) 458
bacterial toxins - biosynthesis (452) 452
analysis (449) 449
bacteria (438) 438
t-lymphocytes - immunology (431) 431
enterotoxins - chemistry (430) 430
biotechnology & applied microbiology (426) 426
cell biology (418) 418
identification (415) 415
escherichia coli - genetics (413) 413
bacterial toxins - pharmacology (400) 400
base sequence (390) 390
heat-stable enterotoxin (389) 389
bacterial proteins - metabolism (380) 380
strains (371) 371
food microbiology (367) 367
cholera-toxin (366) 366
mice, inbred c57bl (364) 364
bacterial proteins - genetics (358) 358
protein binding (355) 355
binding sites (353) 353
enzyme-linked immunosorbent assay (352) 352
genes (351) 351
staphylococcus aureus - immunology (351) 351
activation (350) 350
superantigens - immunology (349) 349
toxin (344) 344
bacterial toxins - toxicity (341) 341
physiological aspects (340) 340
time factors (339) 339
cells (333) 333
intestinal mucosa - metabolism (332) 332
feces - microbiology (328) 328
receptors, enterotoxin (327) 327
lymphocyte activation (325) 325
middle aged (324) 324
multidisciplinary sciences (324) 324
polymerase chain reaction (322) 322
in vitro techniques (317) 317
gene expression (309) 309
pharmacology & pharmacy (308) 308
escherichia coli infections - microbiology (305) 305
kinetics (305) 305
infection (303) 303
medicine (301) 301
binding (300) 300
bacterial toxins - immunology (299) 299
food science & technology (298) 298
medicine, research & experimental (292) 292
cattle (290) 290
receptor (287) 287
swine (287) 287
guanylate cyclase - metabolism (282) 282
hot temperature (281) 281
staphylococcus aureus - isolation & purification (280) 280
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (7744) 7744
Japanese (102) 102
Russian (97) 97
Chinese (53) 53
German (51) 51
Polish (37) 37
Spanish (31) 31
French (25) 25
Czech (9) 9
Slovak (7) 7
Italian (6) 6
Dutch (4) 4
Ukrainian (4) 4
Serbian (3) 3
Hebrew (2) 2
Korean (2) 2
Romanian (2) 2
Arabic (1) 1
Bulgarian (1) 1
Hungarian (1) 1
Portuguese (1) 1
Swedish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


CELL, ISSN 0092-8674, 10/2003, Volume 115, Issue 1, pp. 25 - 35
The ClyA protein is a pore-forming cytotoxin expressed by Escherichia coli and some other enterobacteria. It confers cytotoxic activity toward mammalian cells,... 
OUTER-MEMBRANE VESICLES | HOST-CELLS | IN-VITRO | HEAT-LABILE ENTEROTOXIN | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI K-12 | GENERAL SECRETORY PATHWAY | SHEA | PROTEIN SECRETION | HEMOLYSIN-E | CELL BIOLOGY | Oxidation-Reduction | Protein Disulfide-Isomerases - metabolism | Humans | Bacterial Proteins - chemistry | Hemolysin Proteins - chemistry | Bacterial Toxins - chemistry | Cell Membrane - chemistry | Bacterial Toxins - metabolism | Animals | Transport Vesicles - metabolism | Cytotoxins - chemistry | Escherichia coli - metabolism | Cytotoxins - metabolism | Bacterial Proteins - metabolism | Polymers - chemistry | Cell Membrane - metabolism | Membrane Proteins - metabolism | HeLa Cells | Escherichia coli - ultrastructure | Hemolysin Proteins - metabolism | Polymers - metabolism | Salmonella - metabolism | Transport Vesicles - ultrastructure | Bacterial toxins | Physiological aspects | Gram-negative bacteria | Secretion | Biological transport | Bacterial Toxins/chemistry/metabolism | Cytotoxins/chemistry/metabolism | Salmonella/metabolism | Cell Membrane/chemistry/metabolism | Escherichia coli/metabolism/ultrastructure | Bacterial Proteins/chemistry/metabolism | Transport Vesicles/metabolism/ultrastructure | Membrane Proteins/metabolism | Hemolysin Proteins/chemistry/metabolism | Polymers/chemistry/metabolism | Hela Cells | Protein Disulfide-Isomerase/metabolism
Journal Article
Science, ISSN 0036-8075, 9/2011, Volume 333, Issue 6049, pp. 1642 - 1646
Midbrain dopamine neurons regulate many important behavioral processes, and their dysfunctions are associated with several human neuropsychiatric disorders... 
Locomotion | Brain | Receptors | Neurons | Attention deficit hyperactivity disorder | REPORTS | Midbrain | Mice | T tests | Behavioral neuroscience | Habituation | RESISTANT | PATHWAY | MULTIDISCIPLINARY SCIENCES | DOPAMINE | NEURONS | DEPENDENT PROTEIN-KINASE | AMPHETAMINE | UROGUANYLIN | MICE LACKING | DEFICIT/HYPERACTIVITY DISORDER | Receptors, Glutamate - metabolism | Glycine - analogs & derivatives | Glycine - metabolism | Amphetamine - administration & dosage | Motor Activity - drug effects | Gastrointestinal Hormones - pharmacology | Receptors, Muscarinic - metabolism | Ventral Tegmental Area - cytology | Substantia Nigra - metabolism | Cyclic GMP-Dependent Protein Kinases - metabolism | Receptors, Guanylate Cyclase-Coupled - metabolism | Substantia Nigra - cytology | Receptors, Peptide - genetics | Resorcinols - pharmacology | Attention Deficit Disorder with Hyperactivity - metabolism | Gastrointestinal Hormones - metabolism | Behavior, Animal - drug effects | Neurons - metabolism | Receptors, Guanylate Cyclase-Coupled - genetics | Dopamine - metabolism | Resorcinols - metabolism | Disease Models, Animal | Impulsive Behavior | Natriuretic Peptides - metabolism | Signal Transduction | Mice, Inbred C57BL | Attention | Receptors, Enterotoxin | Natriuretic Peptides - pharmacology | Mice, Knockout | Patch-Clamp Techniques | Animals | Attention Deficit Disorder with Hyperactivity - genetics | Cyclic GMP - metabolism | Glycine - pharmacology | Ventral Tegmental Area - metabolism | Ligands | Enzyme Activation | Receptors, Peptide - metabolism | Physiological aspects | Development and progression | Guanylate cyclase | Health aspects | Attention-deficit hyperactivity disorder | Attention deficit disorder | Proteins | Signal transduction | Neurotransmitters | Hyperactivity
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 2016, Volume 213, Issue 1, pp. 53 - 73
Protective immunoglobulin A (IgA) responses to oral antigens are usually orchestrated by gut dendritic cells (DCs). Here, we show that lung CD103(+) and... 
B-LYMPHOCYTE STIMULATOR | MEDICINE, RESEARCH & EXPERIMENTAL | SYSTEMIC-LUPUS-ERYTHEMATOSUS | PEYERS PATCH | IMMUNOGLOBULIN-A | RETINOIC ACID | INFLUENZA-VIRUS INFECTION | HEAT-LABILE ENTEROTOXIN | NECROSIS-FACTOR FAMILY | ESCHERICHIA-COLI | IMMUNOLOGY | T-CELLS | Receptors, CCR - metabolism | CD24 Antigen - metabolism | Dendritic Cells - immunology | Adaptor Proteins, Vesicular Transport - genetics | Immunoglobulin A - genetics | Integrins - genetics | Adaptor Proteins, Vesicular Transport - metabolism | Integrins - metabolism | Cell Movement - genetics | Antigens, CD - metabolism | Gastrointestinal Tract - immunology | Microbiota | Immunoglobulin Class Switching - drug effects | B-Lymphocytes - metabolism | Dendritic Cells - metabolism | Macrophages, Alveolar - immunology | Tretinoin - pharmacology | Gene Expression | Receptors, CCR - genetics | Myeloid Differentiation Factor 88 - genetics | Gastrointestinal Tract - microbiology | Integrin alpha Chains - metabolism | Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism | Gastrointestinal Tract - metabolism | B-Lymphocytes - drug effects | Transforming Growth Factor beta - pharmacology | Animals | B-Cell Activating Factor - metabolism | B-Lymphocytes - immunology | B-Cell Activating Factor - genetics | Immunoglobulin A - immunology | Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics | Mice | Macrophages, Alveolar - metabolism | Immunoglobulin Class Switching - genetics | Myeloid Differentiation Factor 88 - metabolism | Lung - immunology
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2012, Volume 287, Issue 39, pp. 32578 - 32587
Staphylococcal superantigens (SAgs), such as toxic shock syndrome toxin-1 (TSST-1), are the main cause of toxic shock syndrome (TSS). SAgs deregulate the host... 
CELLS | ACTIVATION | ALPHA-CONVERTING ENZYME | INFLAMMATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENTEROTOXINS | PENETRATION | NECROSIS-FACTOR-ALPHA | CLEAVAGE | EXPRESSION | SYNDECANS | ADAM17 Protein | Interleukin-8 - genetics | Human Umbilical Vein Endothelial Cells - metabolism | Humans | Syndecan-1 - genetics | ErbB Receptors - genetics | Glycoproteins - metabolism | Receptors, Tumor Necrosis Factor, Type I - metabolism | Amphiregulin | Superantigens - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | EGF Family of Proteins | Bacterial Toxins - genetics | Dipeptides - metabolism | Interleukin-8 - metabolism | Transforming Growth Factor alpha - metabolism | Staphylococcus aureus - metabolism | Glycoproteins - genetics | Staphylococcus aureus - genetics | ErbB Receptors - metabolism | Syndecan-1 - metabolism | Signal Transduction | Intercellular Signaling Peptides and Proteins - genetics | Receptors, Tumor Necrosis Factor, Type I - genetics | Transforming Growth Factor alpha - genetics | Hydroxamic Acids - metabolism | ADAM Proteins - metabolism | Bacterial Toxins - metabolism | Enterotoxins - genetics | Models, Biological | Superantigens - genetics | Enterotoxins - metabolism | Human Umbilical Vein Endothelial Cells - pathology | ADAM Proteins - genetics | Dipeptides - genetics | Molecular Bases of Disease | Shedding | Toxic Shock Syndrome | ADAM ADAMTS | Epidermal Growth Factor Receptor (EGFR) | Epithelial Cell | Mucosal Immunology | Superantigen | Staphylococcus aureus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2012, Volume 90, Issue 5, pp. 893 - 899
Meconium ileus, intestinal obstruction in the newborn, is caused in most cases by mutations modulated by yet-unidentified modifier genes. We now show that in... 
TRANSMEMBRANE CONDUCTANCE REGULATOR | HEAT-STABLE ENTEROTOXIN | HCO3-SECRETION | MODIFIER LOCUS | GENETICS & HEREDITY | DEPENDENT PROTEIN-KINASE | CYSTIC-FIBROSIS | GENETIC COMPARISONS | INTESTINAL-OBSTRUCTION | PUTATIVE RECEPTOR | MICE LACKING | Intestinal Obstruction - physiopathology | Enterotoxins - toxicity | Cystic Fibrosis - physiopathology | Diarrhea - physiopathology | Humans | Bacterial Toxins - toxicity | Molecular Sequence Data | Male | Meconium - metabolism | Intestines - metabolism | Receptors, Guanylate Cyclase-Coupled - metabolism | Receptors, Peptide - genetics | Gastrointestinal Hormones - metabolism | HEK293 Cells | Female | Genes, Modifier | Receptors, Guanylate Cyclase-Coupled - genetics | Amino Acid Sequence | Natriuretic Peptides - metabolism | Down-Regulation | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Receptors, Enterotoxin | Bacterial Toxins - metabolism | Phenotype | Animals | Escherichia coli Proteins | Cyclic GMP - metabolism | Pedigree | Cystic Fibrosis - genetics | Enterotoxins - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Diarrhea - etiology | Diarrhea - metabolism | Heterozygote | Mice | Mutation | Intestinal Obstruction - genetics | Intestinal Obstruction - metabolism | Receptors, Peptide - metabolism | Gene mutations | Causes of | Protein biosynthesis | Genetic aspects | Research | Nucleotide sequencing | Meconium aspiration syndrome | DNA sequencing | Enzymes | Intestines | Obstructions | Peptides | Cystic fibrosis | Beer | uroguanylin | Neonates | Enterotoxins | Diarrhea | Guanylate cyclase | Thermal stability | Enzymatic activity | Intestine | Cyclic GMP | Meconium | Cystic fibrosis transmembrane conductance regulator | Report
Journal Article
Journal Article
Naunyn-Schmiedeberg's Archives of Pharmacology, ISSN 0028-1298, 3/2011, Volume 383, Issue 3, pp. 253 - 262
Toxin A and toxin B from Clostridium difficile are the causative agents of the antibiotic-associated pseudomembranous colitis. They are of an A/B structure... 
Neurosciences | Endocytosis | Biomedicine | Rho GTPases | Bacterial toxin | Clostridium difficile | Autoproteolysis | Pharmacology/Toxicology | CELLS | APOPTOSIS | DOMAIN | DEPENDS | INOSITOL HEXAKISPHOSPHATE | DISEASE | PHARMACOLOGY & PHARMACY | GLUCOSYLATION | RHO-GTPASES | PROTEINS | EXPRESSION | Phytic Acid - chemistry | NIH 3T3 Cells | Apoptosis - drug effects | Humans | Bacterial Proteins - chemistry | Caspase 3 - metabolism | Caspase 8 - metabolism | Cysteine Proteases - metabolism | cdc42 GTP-Binding Protein - metabolism | rhoA GTP-Binding Protein - metabolism | Dose-Response Relationship, Drug | Glucosyltransferases - metabolism | Cytotoxins - pharmacology | Cytotoxins - metabolism | Cell Membrane - metabolism | Dithiothreitol - chemistry | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Glycosylation | Bacterial Toxins - chemistry | Cell Shape - drug effects | HT29 Cells | Bacterial Proteins - pharmacology | Bacterial Toxins - metabolism | Animals | Amino Acid Substitution - physiology | Bacterial Toxins - pharmacology | Cytotoxins - chemistry | Enterotoxins - metabolism | Bacterial Proteins - metabolism | Cytosol - metabolism | Mice | Enterotoxins - chemistry | Enterotoxins - pharmacology | rac1 GTP-Binding Protein - metabolism | Protein Structure, Tertiary - physiology | Inositol | G proteins
Journal Article
Toxins, ISSN 2072-6651, 02/2017, Volume 9, Issue 2, pp. 50 - 50
Some Staphylococcus aureus isolates produced toxic shock syndrome toxin-1 (TSST-1) which is a pyrogenic toxin superantigen (PTSAg). The toxin activates a large... 
Superantigen | Direct acting anti-TSST-1 | Human scFv | Toxic shock syndrome (TSS) | Staphylococcus aureus | DOMAIN | BACTERIAL SUPERANTIGENS | CRYSTAL-STRUCTURE | PROTEIN-STRUCTURE | FOOD SCIENCE & TECHNOLOGY | superantigen | PREDICTION | direct acting anti-TSST-1 | 3-DIMENSIONAL STRUCTURE | IN-VITRO | human scFv | STRUCTURAL BASIS | T-CELL-ACTIVATION | TOXIC-SHOCK-SYNDROME | TOXICOLOGY | Humans | Antibodies, Neutralizing - metabolism | Shock, Septic - immunology | Bacterial Toxins - antagonists & inhibitors | Single-Chain Antibodies - metabolism | T-Lymphocytes - metabolism | T-Lymphocytes - drug effects | Bacterial Toxins - genetics | T-Lymphocytes - microbiology | Staphylococcal Infections - immunology | Bacterial Toxins - immunology | Antibodies, Neutralizing - genetics | Host-Pathogen Interactions | Enterotoxins - genetics | Escherichia coli - genetics | Staphylococcus aureus - immunology | T-Lymphocytes - immunology | Mutation | Shock, Septic - prevention & control | Antibodies, Monoclonal, Humanized - genetics | Shock, Septic - metabolism | Superantigens - metabolism | Single-Chain Antibodies - genetics | Enterotoxins - immunology | Antibodies, Monoclonal, Humanized - pharmacology | Escherichia coli - metabolism | Inflammation Mediators - metabolism | Histocompatibility Antigens Class II - metabolism | Staphylococcal Infections - microbiology | Staphylococcal Infections - metabolism | Staphylococcus aureus - metabolism | Staphylococcus aureus - genetics | Cytokines - metabolism | Single-Chain Antibodies - pharmacology | Cells, Cultured | Antibodies, Monoclonal, Humanized - metabolism | Antibodies, Neutralizing - pharmacology | Superantigens - immunology | Shock, Septic - microbiology | Bacterial Toxins - metabolism | Lymphocyte Activation - drug effects | Cell Surface Display Techniques | Superantigens - genetics | Enterotoxins - antagonists & inhibitors | Enterotoxins - metabolism | Protein Binding | Staphylococcal Infections - prevention & control | Receptors, Antigen, T-Cell, alpha-beta - metabolism | Staphylococcus aureus - drug effects | Inflammation | Lymphocytes T | Immunology | Phages | Immune system
Journal Article
Nature, ISSN 0028-0836, 12/2017, Volume 552, Issue 7684, pp. 248 - 252
Diabetic retinopathy is an important cause of blindness in adults(1,2), and is characterized by progressive loss of vascular cells and slow dissolution of... 
BLOOD-RETINAL BARRIER | ACID | ANGIOGENESIS | CHOLESTEROL | STABILITY | MULTIDISCIPLINARY SCIENCES | ENDOTHELIAL-CELLS | DEPENDENT ENDOCYTOSIS | MEMBRANES | VE-CADHERIN | ASSOCIATION | Retina - drug effects | Retina - metabolism | Cadherins - metabolism | Pericytes - drug effects | Humans | Capillary Permeability - drug effects | Male | Diabetic Retinopathy - pathology | Antigens, CD - metabolism | Vitreous Body - metabolism | Pericytes - pathology | Retina - enzymology | Intercellular Junctions - pathology | Female | Cell Membrane - drug effects | Disease Models, Animal | Ependymoglial Cells | Cell Survival - drug effects | Endothelial Cells - metabolism | Mice, Inbred C57BL | Solubility | Pancreatic Elastase - metabolism | Fatty Acids, Unsaturated - metabolism | Diabetic Retinopathy - metabolism | Disease Progression | Cell Movement - drug effects | Diabetic Retinopathy - prevention & control | Animals | Carrier Proteins - metabolism | Diabetic Retinopathy - enzymology | Intercellular Junctions - drug effects | Presenilin-1 - metabolism | Mice | Endothelial Cells - pathology | Epoxide Hydrolases - antagonists & inhibitors | Retina - pathology | Docosahexaenoic Acids - metabolism | Endothelial Cells - drug effects | Prevention | Physiological aspects | Enzymes | Diabetic retinopathy | Hydrolases | Epoxy compounds | Retinopathy | Pathogenesis | Cell junctions | Retina | Glial cells | Cell interactions | Kinases | Docosahexaenoic acid | Epoxide hydrolase | Vascularization | Proteins | Signal transduction | Hyperglycemia | N-Cadherin | Rodents | Inhibition | Growth factors | Edema | Abnormalities | Diabetes mellitus | Permeability | Cadherin | Cholesterol | Endothelial cells | Acids | Presenilin 1 | Nitric oxide | Blindness | Vitreous humour | Adults | Infiltration | Diabetes | Staphylococcal enterotoxin H
Journal Article
Scientific Reports, ISSN 2045-2322, 04/2014, Volume 4, Issue 1, p. 5820
Journal Article
Metabolism, ISSN 0026-0495, 2014, Volume 63, Issue 6, pp. 831 - 840
Abstract Objective The bacteria Staphylococcus aureus is part of the normal bacterial flora and produces a repertoire of enterotoxins which can cause food... 
Endocrinology & Metabolism | Insulin sensitivity | SEA | Glucose- and lipid metabolism | CRYSTAL-STRUCTURE | PROTEIN-KINASE | TUMOR-NECROSIS-FACTOR | IN-VITRO | INSULIN-RESISTANCE | STAPHYLOCOCCAL-ENTEROTOXIN-A | ENDOCRINOLOGY & METABOLISM | GLUCOSE-UPTAKE | INTERLEUKIN-6 STIMULATES LIPOLYSIS | CLASS-II | ADIPOSE-TISSUE | Diabetes Mellitus, Type 2 - microbiology | Humans | Adipocytes - drug effects | Diabetes Mellitus, Type 2 - metabolism | Superantigens - metabolism | DNA-Binding Proteins - metabolism | Escherichia coli K12 | Bacterial Infections - complications | Biological Assay | Phosphorylation - drug effects | Lipogenesis | Bacterial Infections - microbiology | STAT3 Transcription Factor - metabolism | Cytokine Receptor gp130 - metabolism | Enterotoxins | Electrophoresis, Polyacrylamide Gel | Insulin Resistance | Alcohol Oxidoreductases - metabolism | Lipid Metabolism | Blotting, Western | Lipolysis | Insulin - metabolism | Animals | Signal Transduction - drug effects | Adipocytes - metabolism | STAT3 Transcription Factor - drug effects | Cytokine Receptor gp130 - drug effects | Glucose - metabolism | Superantigens - pharmacology | Bacterial Infections - metabolism | Physiological aspects | T cells | Index Medicus | Cell and Molecular Biology | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Endocrine Journal, ISSN 0918-8959, 2015, Volume 62, Issue 10, pp. 939 - 947
Guanylin (Gn), a bioactive peptide, and its receptor, guanylyl cyclase-C (GC-C), are primarily present in the intestine and maintain homeostasis in body... 
VASP | Proinflammatory factor | cGMP | PKG | High-fat diet | PEPTIDE | ADHESION | OBESITY | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | NITRIC-OXIDE | ACTIN CYTOSKELETON | UROGUANYLIN | EXPRESSION | ADIPOSE-TISSUE | ENA/VASP | Immunohistochemistry | Phosphorylation | Obesity - immunology | Receptors, Peptide - agonists | Macrophages, Peritoneal - pathology | Diet, High-Fat - adverse effects | Panniculitis, Peritoneal - pathology | Male | Panniculitis, Peritoneal - etiology | Panniculitis, Peritoneal - metabolism | Phosphoproteins - metabolism | Cyclic GMP-Dependent Protein Kinases - metabolism | Receptors, Guanylate Cyclase-Coupled - metabolism | Receptors, Peptide - genetics | Gastrointestinal Hormones - metabolism | Inflammation Mediators - metabolism | Obesity - etiology | Microfilament Proteins - metabolism | Receptors, Guanylate Cyclase-Coupled - genetics | Second Messenger Systems | Natriuretic Peptides - genetics | Intra-Abdominal Fat - immunology | Natriuretic Peptides - metabolism | Rats, Transgenic | Macrophages, Peritoneal - enzymology | Macrophages, Peritoneal - immunology | Rats | Random Allocation | Receptors, Enterotoxin | Intra-Abdominal Fat - metabolism | Cell Adhesion Molecules - metabolism | Obesity - metabolism | Obesity - pathology | Panniculitis, Peritoneal - immunology | Animals | Cyclic GMP - metabolism | Receptors, Guanylate Cyclase-Coupled - agonists | Gastrointestinal Hormones - genetics | Protein Processing, Post-Translational | Intra-Abdominal Fat - enzymology | Intra-Abdominal Fat - pathology | Macrophages, Peritoneal - metabolism | Receptors, Peptide - metabolism
Journal Article