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1. Full Text Protein Tyrosine Phosphatase 1B Inhibitors: A Molecular Level Legitimate Approach for the Management of Diabetes Mellitus
by Thareja, Suresh and Aggarwal, Saurabh and Bhardwaj, T. R and Kumar, Manoj
Medicinal Research Reviews, ISSN 0198-6325, 05/2012, Volume 32, Issue 3, pp. 459 - 517
Diabetes mellitus is a systemic disease responsible for morbidity in the western world and is gradually becoming prevalent in developing countries too. The... 
metabolism | insulin | diabetes | protein tyrosine phosphatase 1B (PTP 1B) | obesity | Obesity | Diabetes | Metabolism | Insulin | Protein Tyrosine Phosphatase 1B (PTP 1B) | PTP1B INHIBITORS | CHEMISTRY, MEDICINAL | ANTIHYPERGLYCEMIC ACTIVITY | GLUCOSE-TRANSPORT | ENDOPLASMIC-RETICULUM STRESS | DIET-INDUCED OBESITY | FORMYLCHROMONE DERIVATIVES | SIGNAL-TRANSDUCTION | IN-VITRO | PHARMACOLOGY & PHARMACY | INCREASED INSULIN SENSITIVITY | STRUCTURE-BASED DESIGN | Catalytic Domain - drug effects | Humans | Benzofurans - pharmacology | Pyridazines - pharmacology | Biphenyl Compounds - pharmacology | Insulin Resistance - physiology | Janus Kinase 2 - metabolism | Acetophenones - pharmacology | Vanadium Compounds - pharmacology | Catechols - pharmacology | Chromones - pharmacology | Thiazolidinediones - pharmacology | Insulin Secretion | Phosphates - pharmacology | Amino Acid Sequence | Peptidomimetics - pharmacology | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - antagonists & inhibitors | Models, Molecular | Thiophenes - pharmacology | Naphthoquinones - pharmacology | Enzyme Inhibitors - therapeutic use | Fluorides - pharmacology | Insulin - metabolism | Animals | STAT3 Transcription Factor - drug effects | Benzoates - pharmacology | Receptor, Insulin - drug effects | Receptor, Insulin - metabolism | Signal Transduction - physiology | Thiazoles - pharmacology | Blood Glucose - metabolism | Diabetes Mellitus, Type 2 - drug therapy
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2. Full Text The cannabinoid agonist WIN55,212-2 increases intracellular calcium via CB1 receptor coupling to Gq/11 G proteins
by Jane E. Lauckner and Bertil Hille and Ken Mackie
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2005, Volume 102, Issue 52, pp. 19144 - 19149
Central nervous system responses to cannabis are primarily mediated by CB 1 receptors, which couple preferentially to G i/o G proteins. Here, we used calcium... 
Aminoalkylindole | Inositol phosphate | Neurons | Phospholipase C | Analgesics - pharmacology | Calcium - metabolism | Humans | Endoplasmic Reticulum - metabolism | Type C Phospholipases - metabolism | Cytoplasm - metabolism | Benzoxazines | Arachidonic Acids - chemistry | Calcium - chemistry | GTP-Binding Protein alpha Subunits, Gq-G11 - chemistry | Piperidines - pharmacology | Time Factors | Dronabinol - analogs & derivatives | Fluorescent Dyes - pharmacology | Receptor, Cannabinoid, CB1 - chemistry | Neurons - metabolism | Cyclohexanols - pharmacology | Dronabinol - pharmacology | Immunosuppressive Agents - pharmacology | Endocannabinoids | Ryanodine - pharmacology | Pertussis Toxin - pharmacology | Pyrazoles - pharmacology | Cell Line | Glycerides - chemistry | Cannabinoids - chemistry | Morpholines - pharmacology | Rats | Excitatory Amino Acid Antagonists - pharmacology | GTP-Binding Protein alpha Subunits, Gq-G11 - physiology | Fura-2 - analogs & derivatives | Naphthalenes - pharmacology | Hippocampus - metabolism | Receptor, Cannabinoid, CB1 - metabolism | Animals | Fura-2 - pharmacology | Protein Binding | Protein Conformation | DNA, Complementary - metabolism | phospholipase C | Biological Sciences | aminoalkylindole | neurons | inositol phosphate
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3. Full Text 2-Deoxy-d-glucose enhances tonic inhibition through the neurosteroid-mediated activation of extrasynaptic GABA(A) receptors
by Forte, N and Medrihan, L and Cappetti, B and Baldelli, P and Benfenati, F
EPILEPSIA, ISSN 0013-9580, 12/2016, Volume 57, Issue 12, pp. 1987 - 2000
ObjectiveThe inhibition of glycolysis exerts potent antiseizure effects, as demonstrated by the efficacy of ketogenic and low-glucose/nonketogenic diets in the... 
VITAMIN-C | 2-Deoxy-d-glucose | Ascorbic acid | ACID | ANTICONVULSANT | KETOGENIC DIET | K-ATP | CLINICAL NEUROLOGY | SEIZURES | EXCITABILITY | METABOLISM | GABA tonic inhibition | Glycolysis | Pentose phosphate pathway | NEURONS | Neurosteroid metabolism | MODULATION | gamma-Aminobutyric Acid - metabolism | Male | Isoquinolines - pharmacology | Finasteride - pharmacology | Glyburide - pharmacology | Deoxyglucose - pharmacology | Statistics, Nonparametric | Female | Antineoplastic Agents - pharmacology | Neurons - drug effects | 4-Aminopyridine - pharmacology | Potassium Channel Blockers - pharmacology | Antimetabolites - pharmacology | GABA-A Receptor Antagonists - pharmacology | Membrane Potentials - drug effects | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Bicuculline - pharmacology | Hippocampus - cytology | Hypoglycemic Agents - pharmacology | Iodoacetates - pharmacology | Animals | Receptors, GABA - metabolism | Mice | In Vitro Techniques | Neural Inhibition - drug effects
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4. Full Text Sub-normothermic preservation of donor hearts for transplantation using a novel solution, Somah: A comparative pre-clinical study
by Lowalekar, Samar K., MD and Cao, Haiyan, MD, PhD and Lu, Xiu-Gui, MD and Treanor, Patrick R., CCP, LCP and Thatte, Hemant S., MSc, PhD
Journal of Heart and Lung Transplantation, ISSN 1053-2498, 2014, Volume 33, Issue 9, pp. 963 - 970
Background Hearts preserved ex vivo at extreme hypothermia (4°C) undergo time-dependent irreversible injury. Our studies using a novel solution, Somah, suggest... 
Surgery | 2D echo | organ edema | transplantation | ex vivo cardiac function | organ preservation solutions | in vitro cardiac animation | high energy phosphates | SURGERY | CARDIAC & CARDIOVASCULAR SYSTEMS | INJURY | CARDIOMYOCYTES | FLOW | COLD-STORAGE | ORGAN PRESERVATION | RESPIRATORY SYSTEM | PERFUSION PRESERVATION | ISCHEMIA-REPERFUSION | Tissue Survival - physiology | Histidine - pharmacology | Temperature | Sodium Chloride - pharmacology | Organ Preservation - methods | Tissue Survival - drug effects | Mannitol - pharmacology | Disaccharides - pharmacology | Glutathione - pharmacology | Time Factors | Carnitine - pharmacology | Swine | Female | Insulin - pharmacology | Oxygen Consumption | Raffinose - pharmacology | Heart Transplantation | Glucose - pharmacology | Organ Preservation Solutions - pharmacology | Adenosine - pharmacology | Carnosine - pharmacology | Cryopreservation - methods | Lactates | Animals | Glutamates - pharmacology | Heart - drug effects | Allopurinol - pharmacology | Electrolytes - pharmacology | Clinical trials | Comparative analysis
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5. Full Text Secretion of ATP from Schwann cells in response to uridine triphosphate
by Liu, Guo Jun and Werry, Eryn L and Bennett, Max R
European Journal of Neuroscience, ISSN 0953-816X, 01/2005, Volume 21, Issue 1, pp. 151 - 160
The mechanisms by which uridine triphosphate (UTP) stimulates ATP release from Schwann cells cultured from the sciatic nerve were investigated using online... 
purinergic receptors | exocytosis | bioluminescence | protein kinase C | Bioluminescence | Protein kinase C | Purinergic receptors | Exocytosis | NERVE | MECHANISMS | RELEASE | ASTROCYTES | NEUROSCIENCES | UTP | NUCLEOTIDE RECEPTORS | GLUTAMATE | CALCIUM | NEURONS | SMOOTH-MUSCLE-CELLS | Guanosine Triphosphate - pharmacology | Nucleic Acid Synthesis Inhibitors - pharmacology | Calcium - metabolism | Adenosine Triphosphate - secretion | Brefeldin A - pharmacology | Phorbol 12,13-Dibutyrate - pharmacology | Receptors, Purinergic P2Y2 | Cytochalasin D - pharmacology | Phenanthridines - pharmacology | Type C Phospholipases - antagonists & inhibitors | Diagnostic Imaging - methods | Dose-Response Relationship, Drug | Alkaloids | Botulinum Toxins - pharmacology | Glycyrrhetinic Acid - pharmacology | Drug Interactions | Isoquinolines - pharmacology | Glyburide - pharmacology | Time Factors | Botulinum Toxins, Type A | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Sciatic Nerve - cytology | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Protein Synthesis Inhibitors - pharmacology | Pyridoxal Phosphate - analogs & derivatives | Schwann Cells - secretion | Suramin - pharmacology | Schwann Cells - drug effects | Animals, Newborn | Pyridoxal Phosphate - pharmacology | Uridine Triphosphate - pharmacology | Purinergic P2 Receptor Antagonists | Rats | Protein Kinase C - antagonists & inhibitors | Purinergic P2 Receptor Agonists | Sulfonamides - pharmacology | Microscopy, Confocal - methods | Rats, Sprague-Dawley | Immunohistochemistry - methods | Animals | Benzophenanthridines | Receptors, Purinergic P2 - metabolism | Thapsigargin - pharmacology | Furosemide - pharmacology
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6. Full Text Luminescence-Based Assay to Screen Preservation Solutions for Optimal Ability to Maintain Viability of Rat Intestinal Grafts
by Kasahara, N and Kikuchi, T and Doi, J and Teratani, T and Fujimoto, Y and Uemoto, S and Yasuda, Y and Kobayashi, E
Transplantation Proceedings, ISSN 0041-1345, 2013, Volume 45, Issue 6, pp. 2486 - 2490
Abstract Background Segmental intestinal transplantations from living, genetically related donors provide advantages compared with those from cadaveric... 
Surgery | AGENT | SURGERY | SMALL-BOWEL TRANSPLANTATION | UW SOLUTION | GLUTAMINE | LIVER | IMMUNOLOGY | COLD-STORAGE | TRANSPLANTATION | Isotonic Solutions - pharmacology | Intestine, Small - pathology | Sodium Chloride - pharmacology | Organ Preservation - methods | Hypertonic Solutions - pharmacology | Cold Ischemia - adverse effects | Gluconates - pharmacology | Luminescent Measurements | Intestine, Small - transplantation | Mannitol - pharmacology | Luciferases - genetics | Glutathione - pharmacology | Time Factors | Adenosine Triphosphate - metabolism | Potassium Chloride - pharmacology | Phosphates - pharmacology | High-Throughput Screening Assays - methods | Cell Survival - drug effects | Insulin - pharmacology | Procaine - pharmacology | Rats, Transgenic | Tissue Culture Techniques | Raffinose - pharmacology | Rats | Spectrometry, Fluorescence | Glucose - pharmacology | Organ Preservation Solutions - pharmacology | Adenosine - pharmacology | Hydroxyethyl Starch Derivatives - pharmacology | Animals | Intestine, Small - drug effects | Allopurinol - pharmacology | Intestine, Small - metabolism | Luciferases - biosynthesis | Trehalose - pharmacology
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7. Full Text Statins inhibit cyclooxygenase-2 and matrix metalloproteinase-9 in human endothelial cells: Anti-angiogenic actions possibly contributing to plaque stability
by Massaro, Marika and Zampolli, Antonella and Scoditti, Egeria and Carluccio, Maria Annunziata and Storelli, Carlo and Distante, Alessandro and De Caterina, Raffaele
Cardiovascular Research, ISSN 0008-6363, 05/2010, Volume 86, Issue 2, pp. 311 - 320
Cyclooxygenase (COX)-2 expression is increased in inflammation and angiogenesis and also in atherosclerotic plaques, where it co-localizes with... 
Angiogenesis | Cyclooxygenase-2 | Metalloproteinases | Statins | Atherosclerosis | CARDIAC & CARDIOVASCULAR SYSTEMS | COA REDUCTASE INHIBITORS | PROTEIN | COX-2 | ANTIANGIOGENIC THERAPY | IN-VITRO | EPITHELIAL-CELLS | MESSENGER-RNA | INFLAMMATION | GROWTH-FACTOR | EXPRESSION | Tumor Necrosis Factor-alpha - metabolism | Neovascularization, Physiologic - drug effects | Tetradecanoylphorbol Acetate - pharmacology | rho GTP-Binding Proteins - antagonists & inhibitors | Humans | Nitrobenzenes - pharmacology | RNA, Messenger - metabolism | Simvastatin - pharmacology | Dose-Response Relationship, Drug | Botulinum Toxins - pharmacology | Matrix Metalloproteinase 9 - metabolism | Cyclooxygenase 2 - genetics | Matrix Metalloproteinase 9 - genetics | Heptanoic Acids - pharmacology | Cyclooxygenase 2 Inhibitors - pharmacology | Down-Regulation | Cells, Cultured | Enzyme Inhibitors - pharmacology | Angiogenesis Inhibitors - pharmacology | Mevalonic Acid - metabolism | Sulfonamides - pharmacology | Polyisoprenyl Phosphates - metabolism | Atorvastatin Calcium | Pyrroles - pharmacology | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology | ADP Ribose Transferases - pharmacology | rho GTP-Binding Proteins - metabolism | Cyclooxygenase 2 - metabolism | Endothelial Cells - enzymology | Endothelial Cells - drug effects
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8. Full Text Inhibitory effects of children's toothpastes on Streptococcus mutans, Streptococcus sanguinis and Lactobacillus acidophilus
by Evans, A and Leishman, S J and Walsh, L J and Seow, W K
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry, ISSN 1818-6300, 04/2015, Volume 16, Issue 2, p. 219
As suppression of Streptococcus mutans in young children may prevent or delay colonisation of the oral cavity, toothbrushing with dentifrices containing... 
Diphosphates - pharmacology | Sweetening Agents - pharmacology | Anti-Infective Agents, Local - pharmacology | Humans | Tin Fluorides - pharmacology | Lactobacillus acidophilus - drug effects | Sodium Fluoride - pharmacology | Streptococcus mutans - drug effects | Triclosan - pharmacology | Dentifrices - pharmacology | Fluorides - pharmacology | Surface-Active Agents - pharmacology | Xylitol - pharmacology | Streptococcus sanguis - drug effects | Toothpastes - pharmacology | Sodium Dodecyl Sulfate - pharmacology | Cariostatic Agents - pharmacology | Anti-Bacterial Agents - pharmacology | Child | Phosphates - pharmacology | Sorbitol - pharmacology | Polyethylene Glycols - pharmacology
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9. Full Text Zoledronate and Ion-releasing Resins Impair Dentin Collagen Degradation
by Tezvergil-Mutluay, A and Seseogullari-Dirihan, R and Feitosa, V.P and Tay, F.R and Watson, T.F and Pashley, D.H and Sauro, S
Journal of Dental Research, ISSN 0022-0345, 10/2014, Volume 93, Issue 10, pp. 999 - 1004
This study analyzed the amounts of solubilized telopeptides cross-linked carboxyterminal telopeptide of type I collagen (ICTP) and C-terminal crosslinked... 
matrix metalloproteinase | bisphosphonates | calcium phosphates | phosphorylation | cathepsins | proteolysis | REMINERALIZATION | PHOSPHATE | MATRIX METALLOPROTEINASES | PHOSPHORIC-ACID | DENTISTRY, ORAL SURGERY & MEDICINE | STROMELYSIN-1 | INHIBITORS | FILLERS | EXPRESSION | BINDING | Resin Cements - pharmacology | Humans | Spectroscopy, Fourier Transform Infrared | Collagen - drug effects | Edetic Acid - pharmacology | Calcium Phosphates - pharmacology | Calcium Compounds - pharmacology | Cathepsins - antagonists & inhibitors | Matrix Metalloproteinases - pharmacology | Silicates - pharmacology | Tooth Demineralization - chemically induced | Solubility | Materials Testing | Imidazoles - pharmacology | Bone Density Conservation Agents - pharmacology | Calcium Sulfate - pharmacology | Matrix Metalloproteinase Inhibitors - pharmacology | Dentin - drug effects | Aluminum Compounds - pharmacology | Collagen Type I - analysis | Saliva, Artificial - chemistry | Cathepsins - pharmacology | Diphosphonates - pharmacology | Peptides - analysis | Hydrogen-Ion Concentration | Research Reports
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10. Full Text Melanopsin for precise optogenetic activation of astrocyte‐neuron networks
by Mederos, Sara and Hernández‐Vivanco, Alicia and Ramírez‐Franco, Jorge and Martín‐Fernández, Mario and Navarrete, Marta and Yang, Aimei and Boyden, Edward S and Perea, Gertrudis
Glia, ISSN 0894-1491, 05/2019, Volume 67, Issue 5, pp. 915 - 934
Optogenetics has been widely expanded to enhance or suppress neuronal activity and it has been recently applied to glial cells. Here, we have used a new... 
melanopsin | astrocytes | synaptic plasticity | optogenetics | neuron–glia interactions | SLEEP | GLUTAMATE RELEASE | DEPENDENT RELEASE | NEUROSCIENCES | TRANSMITTER RELEASE | neuron-glia interactions | D-SERINE | HEMICHANNELS | VESICULAR NUCLEOTIDE TRANSPORTER | LONG-TERM POTENTIATION | ATP | Glial Fibrillary Acidic Protein - genetics | Optogenetics - methods | 2-Amino-5-phosphonovalerate - pharmacology | Glial Fibrillary Acidic Protein - metabolism | Channelrhodopsins - metabolism | Alanine - analogs & derivatives | Rod Opsins - genetics | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Light | Rod Opsins - metabolism | Egtazic Acid - analogs & derivatives | Neurons - metabolism | Pyridoxal Phosphate - analogs & derivatives | Azo Compounds - pharmacology | Alanine - pharmacology | Xanthenes - pharmacology | Synaptic Potentials - physiology | Pyridoxal Phosphate - pharmacology | Mice, Inbred C57BL | Mice, Transgenic | Excitatory Amino Acid Antagonists - pharmacology | Chelating Agents - pharmacology | Pyrimidines - pharmacology | Channelrhodopsins - genetics | Hippocampus - cytology | Triazoles - pharmacology | Adenosine A2 Receptor Antagonists - pharmacology | Animals | Egtazic Acid - pharmacology | Nerve Net - metabolism | Mice | Inositol 1,4,5-Trisphosphate Receptors - genetics | Astrocytes - metabolism | Neurons | Analysis | Adenosine | Astrocytes | Calcium imaging | Optics | Activation | Glial cells | Neuronal-glial interactions | Melanopsin | Proteins | Calcium signalling | Genetic code | Synaptic transmission | Neural networks | Coding | Information processing | Signal processing | Genetics | Hippocampus | Inositol 1,4,5-trisphosphate | Calcium ions
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11. Pharmacology of GABA and glycine neurotransmission
by Alger, B. E and Möhler, Hanns
2001, Handbook of experimental pharmacology, ISBN 3540676163, Volume 150., xxi, 413
GABA | Amino acid neurotransmitters | Receptors | Glycine | Physiological effect
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12. Full Text Enhanced steatosis by nuclear receptor ligands: A study in cultured human hepatocytes and hepatoma cells with a characterized nuclear receptor expression profile
by Moya, Marta and José Gómez-Lechón, M and Castell, José V and Jover, Ramiro
Chemico-Biological Interactions, ISSN 0009-2797, 2010, Volume 184, Issue 3, pp. 376 - 387
Steatosis is the first step in the development of non-alcoholic fatty liver disease (NAFLD). However, the mechanisms involved in its pathogenesis are not fully... 
Cultured human hepatocytes | HepG2 | NAFLD | Fatty acids | Nuclear receptor ligands | Steatosis | RAT-LIVER | LIPID-METABOLISM | PROLIFERATOR-ACTIVATED RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RETINOIC ACID RECEPTORS | PREGNANE-X-RECEPTOR | PPAR GAMMA 1 | NONALCOHOLIC FATTY LIVER | CONSTITUTIVE ANDROSTANE RECEPTOR | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | TOXICOLOGY | DRUG-METABOLISM | Vitamin A - pharmacology | Farnesol - pharmacology | Humans | Hepatocytes - metabolism | PPAR gamma - metabolism | Terpenes - pharmacology | Phloroglucinol - pharmacology | Indoles - pharmacology | Hepatocytes - drug effects | Cholesterol - analogs & derivatives | Fatty Liver - metabolism | Bridged Bicyclo Compounds - pharmacology | Androstenols - pharmacology | Cells, Cultured | Receptors, Cytoplasmic and Nuclear - genetics | Calcifediol - pharmacology | Fatty Liver - drug therapy | Hep G2 Cells | Pregnenediones - pharmacology | PPAR gamma - agonists | Tamoxifen - pharmacology | Cholesterol - pharmacology | Ligands | Phloroglucinol - analogs & derivatives | Selective Estrogen Receptor Modulators - pharmacology | Receptors, Cytoplasmic and Nuclear - metabolism | Phosphates | Cell research | Corticosteroids | Liver diseases | Estrogen | Albumin | Triglycerides | Hepatoma | Retinoids | Tamoxifen | Messenger RNA | Synthesis | Choline | Physiological aspects | Progesterone | Rifampin | Protein binding
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13. Full Text Dipeptidylpeptidase 4 inhibition enhances lymphocyte trafficking, improving both naturally occurring tumor immunity and immunotherapy
by Barreira Da Silva, Rosa and Laird, Melissa E and Yatim, Nader and Fiette, Laurence and Ingersoll, Molly A and Albert, Matthew L
Nature Immunology, ISSN 1529-2908, 07/2015, Volume 16, Issue 8, pp. 850 - 858
The success of antitumor immune responses depends on the infiltration of solid tumors by effector T cells, a process guided by chemokines. Here we show that in... 
CD26 EXPRESSION | CELLS | CXCL10 | CHEMOKINE ACTIVITY | IN-VIVO | RECEPTOR | IMMUNOLOGY | CD26/DIPEPTIDYL PEPTIDASE-IV | PROTEINS | CANCER | POSTTRANSLATIONAL MODIFICATION | Dipeptidyl Peptidase 4 - metabolism | Immunotherapy - methods | Male | Adoptive Transfer | Dipeptidyl-Peptidase IV Inhibitors - pharmacology | Cell Movement - immunology | Flow Cytometry | Lymphocytes - immunology | Neoplasms, Experimental - immunology | Chemokine CXCL10 - immunology | Neoplasms, Experimental - genetics | Female | Sitagliptin Phosphate | Dipeptidyl Peptidase 4 - immunology | Chemokines - immunology | Lymphocytes - metabolism | Receptors, CXCR3 - metabolism | Mice, Inbred C57BL | Neoplasms, Experimental - therapy | Dipeptidyl Peptidase 4 - genetics | Mice, Transgenic | Mice, Knockout | Triazoles - pharmacology | Cell Movement - drug effects | Animals | Receptors, CXCR3 - immunology | Cell Line, Tumor | Chemokines - metabolism | Mice, Inbred BALB C | Pyrazines - pharmacology | Chemokine CXCL10 - metabolism | Care and treatment | Usage | Immunotherapy | Development and progression | Inflammation | Health aspects | Chemokines | Tumors | Neoplasms, Experimental/genetics | Immunotherapy/methods | Cell Movement/drug effects | Neoplasms, Experimental/therapy | Lymphocytes/metabolism | Lymphocytes/immunology | Dipeptidyl Peptidase 4/genetics | Life Sciences | Chemokine CXCL10/immunology | Immunology | Pyrazines/pharmacology | Dipeptidyl Peptidase 4/immunology | Dipeptidyl-Peptidase IV Inhibitors/pharmacology | Chemokines/metabolism | Receptors, CXCR3/immunology | Receptors, CXCR3/metabolism | Neoplasms, Experimental/immunology | Triazoles/pharmacology | Cell Movement/immunology | Chemokines/immunology | Dipeptidyl Peptidase 4/metabolism | Chemokine CXCL10/metabolism
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