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1. Full Text The P-Glycoprotein Transport System and Cardiovascular Drugs
by Wessler, Jeffrey D., MD, MPhil and Grip, Laura T., BS and Mendell, Jeanne, PhD, MPH and Giugliano, Robert P., MD, SM
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2013, Volume 61, Issue 25, pp. 2495 - 2502
Permeability glycoprotein (P-gp) mediates the export of drugs from cells located in the small intestine, blood-brain barrier, hepatocytes, and kidney proximal... 
Cardiovascular | Internal Medicine | adverse drug event(s) | P-glycoprotein | drug-drug interaction | pharmacology | adverse drug event(s) drug-drug interaction P-glycoprotein pharmacology | CARDIAC & CARDIOVASCULAR SYSTEMS | HEALTHY-SUBJECTS | ATRIAL-FIBRILLATION | CLINICAL-RELEVANCE | IN-VITRO | CLOPIDOGREL | ORAL ANTICOAGULANTS | CARDIAC GLYCOSIDE | DIGOXIN | MULTIDRUG-RESISTANCE | FACTOR XA INHIBITOR | Protein Structure, Tertiary | Cardiovascular Agents - therapeutic use | Animals | Cardiovascular Diseases - metabolism | Cardiovascular Diseases - drug therapy | Humans | ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism | Cardiovascular Agents - metabolism | Protein Transport - physiology | ATP-Binding Cassette, Sub-Family B, Member 1 - chemistry | Protein Transport - drug effects | Cardiovascular Agents - pharmacology | Medical colleges | Anticoagulants (Medicine) | Permeability | Anti-arrhythmia drugs | Anticoagulants | Membranes | Blood-brain barrier | Human immunodeficiency virus--HIV | Rodents | Nervous system | Drug therapy | Binding sites | Cancer | Index Medicus | Abridged Index Medicus
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2. Full Text Amphiregulin Enhances Regulatory T Cell-Suppressive Function via the Epidermal Growth Factor Receptor
by Zaiss, Dietmar M.W and van Loosdregt, Jorg and Gorlani, Andrea and Bekker, Cornelis P.J and Gröne, Andrea and Sibilia, Maria and van Bergen en Henegouwen, Paul M.P and Roovers, Rob C and Coffer, Paul J and Sijts, Alice J.A.M
Immunity, ISSN 1074-7613, 02/2013, Volume 38, Issue 2, pp. 275 - 284
Epidermal growth factor receptor (EGFR) is known to be critically involved in tissue development and homeostasis as well as in the pathogenesis of cancer. Here... 
CETUXIMAB | RESPONSES | TOLERANCE | MAST-CELLS | DISEASE | MODEL | IMMUNOLOGY | CARCINOMA | EXPRESSION | METASTATIC COLORECTAL-CANCER | EGF RECEPTOR | Forkhead Transcription Factors - immunology | Cell Communication - immunology | Receptor, Epidermal Growth Factor - genetics | T-Lymphocytes, Regulatory - metabolism | Humans | Colitis - pathology | Homeodomain Proteins - immunology | Amphiregulin | Glycoproteins - pharmacology | T-Lymphocytes, Regulatory - immunology | Signal Transduction - immunology | Melanoma, Experimental - immunology | EGF Family of Proteins | Colitis - chemically induced | Peptide Fragments - immunology | Mast Cells - metabolism | Colitis - immunology | Glycoproteins - genetics | Mast Cells - immunology | Receptor, Epidermal Growth Factor - immunology | Peptide Fragments - administration & dosage | Glycoproteins - antagonists & inhibitors | Intercellular Signaling Peptides and Proteins - genetics | Melanoma, Experimental - pathology | Antibodies, Neutralizing - pharmacology | Membrane Proteins - immunology | Mice, Transgenic | Forkhead Transcription Factors - genetics | Mast Cells - drug effects | Homeodomain Proteins - genetics | Gene Expression Regulation - drug effects | Membrane Proteins - administration & dosage | Glycoproteins - immunology | T-Lymphocytes, Regulatory - drug effects | Animals | Melanoma, Experimental - genetics | Signal Transduction - drug effects | Intercellular Signaling Peptides and Proteins - pharmacology | Lymphocyte Activation - drug effects | Colitis - metabolism | Mice | Intercellular Signaling Peptides and Proteins - immunology | Epidermal growth factor | Universities and colleges | T cells | Analysis | Vaccination | Cells | Flow cytometry | Cytokines | Cloning | Melanoma | Kinases | Experiments | Cancer therapies | Rodents | Bone marrow | Software | Tumors | Cancer
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3. Full Text Interaction and uptake of exosomes by ovarian cancer cells
by Escrevente, Cristina and Keller, Sascha and Altevogt, Peter and Costa, Júlia
BMC Cancer, ISSN 1471-2407, 03/2011, Volume 11, Issue 1, pp. 108 - 108
Background: Exosomes consist of membrane vesicles that are secreted by several cell types, including tumors and have been found in biological fluids. Exosomes... 
DENDRITIC CELLS | ONCOLOGY | VESICLES | PATHWAY | RELEASED EXOSOMES | MULTIVESICULAR BODY | MICROVESICLES | ENDOCYTOSIS | GLYCOPEPTIDES | TUMOR-GROWTH | MASS-SPECTROMETRY | Exosomes - metabolism | Succinimides - pharmacokinetics | Neoplasms, Glandular and Epithelial - pathology | Fluoresceins - pharmacokinetics | Proteins - pharmacokinetics | Endocytosis - drug effects | Humans | Cells, Cultured | Ovarian Neoplasms - pathology | Neoplasms, Glandular and Epithelial - metabolism | Luminescent Measurements | Glycoproteins - pharmacology | Endocytosis - physiology | Exosomes - physiology | Carcinoma, Ovarian Epithelial | Female | Glycoproteins - pharmacokinetics | Biological Transport - drug effects | Ovarian Neoplasms - metabolism | Proteins - pharmacology | Microscopy, Fluorescence | Proteins | Care and treatment | RNA | Physiological aspects | Glycoproteins | Research | Ovarian cancer
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4. Full Text Broad-Spectrum Inhibition of Retroviral and Filoviral Particle Release by Tetherin
by Nolwenn Jouvenet and Stuart J. D. Neil and Maria Zhadina and Trinity Zang and Zerina Kratovac and Youngnam Lee and Matthew McNatt and Theodora Hatziioannou and Paul D. Bieniasz
Journal of Virology, ISSN 0022-538X, 02/2009, Volume 83, Issue 4, pp. 1837 - 1844
Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
REPLICATION | VIROLOGY | GENE | TYPE-1 VPU | VPU PROTEIN | CELL-SURFACE | ENVELOPE PROTEIN | EBOLA | IDENTIFICATION | INTERFERONS | HIV-1 VPU | Cell Line | Antiviral Agents - pharmacology | Humans | Membrane Glycoproteins - pharmacology | GPI-Linked Proteins | Antigens, CD - pharmacology | Filoviridae - drug effects | Retroviridae - drug effects | Virus-Cell Interactions
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5. Full Text Involvement of the Snake Toxin Receptor CLEC-2, in Podoplanin-mediated Platelet Activation, by Cancer Cells
by Katsue Suzuki-Inoue and Yukinari Kato and Osamu Inoue and Mika Kato Kaneko and Kazuhiko Mishima and Yutaka Yatomi and Yasuo Yamazaki and Hisashi Narimatsu and Yukio Ozaki
Journal of Biological Chemistry, ISSN 0021-9258, 09/2007, Volume 282, Issue 36, pp. 25993 - 26001
Podoplanin (aggrus), a transmembrane sialoglycoprotein, is involved in tumor cell-induced platelet aggregation, tumor metastasis, and lymphatic vessel... 
AGGREGATION-INDUCING FACTOR | MARKER | DC-SIGN | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANE-PROTEIN | AGGRUS | MURINE COLON ADENOCARCINOMA-26 | GLYCOPROTEIN | MONOCLONAL-ANTIBODIES | TUMORS | EXPRESSION | Neoplasms - metabolism | Cricetinae | Phospholipase C gamma - metabolism | Cricetulus | Membrane Glycoproteins - metabolism | Endothelial Cells - metabolism | Humans | Membrane Glycoproteins - pharmacology | Mice, Transgenic | Viper Venoms - pharmacology | Recombinant Proteins | Enzyme Activation - drug effects | N-Acetylneuraminic Acid - metabolism | Polysaccharides - metabolism | Lectins, C-Type - metabolism | Neoplasm Metastasis | Animals | Viper Venoms - metabolism | src-Family Kinases - metabolism | Cell Line, Tumor | Mice | Platelet Aggregation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | CHO Cells
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6. Full Text Targeting Apoptosis Pathways in Cancer Therapy
by Ghobrial, Irene M and Witzig, Thomas E and Adjei, Alex A
CA: A Cancer Journal for Clinicians, ISSN 0007-9235, 05/2005, Volume 55, Issue 3, pp. 178 - 194
Apoptosis, or programmed cell death, is a mechanism by which cells undergo death to control cell proliferation or in response to DNA damage. The understanding... 
PROGRAMMED CELL-DEATH | MULTIPLE-MYELOMA | PHASE-II TRIAL | SURVIVIN EXPRESSION | ONCOLOGY | PROTEASOME INHIBITION | PROSTATE-CANCER | BCL-2 FAMILY-MEMBERS | NF-KAPPA-B | ACUTE PROMYELOCYTIC LEUKEMIA | ARSENIC TRIOXIDE | Apoptosis - drug effects | Antibodies, Monoclonal - pharmacology | Humans | Membrane Glycoproteins - pharmacology | Neoplasms - enzymology | Antibodies, Monoclonal - therapeutic use | Drug Delivery Systems | Neoplasms - drug therapy | Tumor Necrosis Factor-alpha - pharmacology | Tumor Necrosis Factor-alpha - therapeutic use | Apoptosis Regulatory Proteins | Membrane Glycoproteins - therapeutic use | TNF-Related Apoptosis-Inducing Ligand | Signal Transduction - drug effects | Phosphatidylinositol 3-Kinases - drug effects | Apoptosis - physiology | Neoplasms - physiopathology | Research | Cancer | Apoptosis | Proteins | Medical treatment | Cells
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7. Full Text NADPH oxidase-derived reactive oxygen species mediate the cerebrovascular dysfunction induced by the amyloid β peptide
by Park, Laibaik and Anrather, Josef and Zhou, Ping and Frys, Kelly and Pitstick, Rose and Younkin, Steven and Carlson, George A and Iadecola, Costantino
Journal of Neuroscience, ISSN 0270-6474, 02/2005, Volume 25, Issue 7, pp. 1769 - 1777
Overproduction of the amyloid beta (Abeta) peptide is a key factor in the pathogenesis of Alzheimer's disease (AD), but the mechanisms of its pathogenic... 
gp91 | Reactive oxygen species | Hydroethidine | Cerebral blood flow | Alzheimer's disease | Tg2576 | OXIDATIVE STRESS | ENDOTHELIAL DYSFUNCTION | SUPEROXIDE-PRODUCTION | ALZHEIMERS-DISEASE BRAINS | SOMATOSENSORY ACTIVATION | NEUROSCIENCES | gp91(phox) | reactive oxygen species | NITRIC-OXIDE | A-BETA | cerebral blood flow | PRECURSOR PROTEIN | hydroethidine | CEREBRAL-BLOOD-FLOW | TRANSGENIC MOUSE MODEL | Reactive Oxygen Species - metabolism | Oxidative Stress | Peptide Fragments - toxicity | Humans | Molecular Sequence Data | Male | Glycoproteins - pharmacology | Phenanthridines - pharmacology | NADPH Oxidases - deficiency | Membrane Glycoproteins - physiology | NADPH Oxidases - genetics | Female | Nitric Oxide Donors - pharmacology | Peptide Fragments - genetics | X Chromosome - genetics | Bradykinin - pharmacology | Amino Acid Sequence | Alzheimer Disease - physiopathology | Nerve Tissue Proteins - physiology | Acetylcholine - pharmacology | Amyloid beta-Peptides - toxicity | Amyloid beta-Peptides - biosynthesis | Mice, Inbred C57BL | Hyperemia - etiology | Mice, Transgenic | Cerebrovascular Circulation | Adenosine - pharmacology | Laser-Doppler Flowmetry | Calcimycin - pharmacology | NADPH Oxidase 2 | Peptide Fragments - biosynthesis | Membrane Glycoproteins - genetics | Amyloid beta-Protein Precursor - genetics | Animals | Vibrissae - physiology | Alzheimer Disease - metabolism | Mice | NADPH Oxidases - physiology | S-Nitroso-N-Acetylpenicillamine - pharmacology | Membrane Glycoproteins - deficiency | Amyloid beta-Protein Precursor - biosynthesis | Neurobiology of Disease | gp91phox
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8. Full Text Regulation of Vascular Calcification by Osteoclast Regulatory Factors RANKL and Osteoprotegerin
by Collin-Osdoby, Patricia
Circulation Research, ISSN 0009-7330, 11/2004, Volume 95, Issue 11, pp. 1046 - 1057
Vascular calcification often occurs with advancing age, atherosclerosis, various metabolic disorders such as diabetes mellitus and end-stage renal disease, or... 
Blood vessels | Calcification | RANKL | OPG | Artherosclerosis | CARDIAC & CARDIOVASCULAR SYSTEMS | BONE METABOLISM | blood vessels | DEFICIENT MICE | RESPONSE FACTOR-I | APOPTOSIS-INDUCING LIGAND | ARTERIAL CALCIFICATION | RECEPTOR ACTIVATOR | GENE-EXPRESSION | PERIPHERAL VASCULAR DISEASE | SMOOTH-MUSCLE-CELLS | calcification | artherosclerosis | HEMATOLOGY | NF-KAPPA-B | ENDOTHELIAL GROWTH-FACTOR | Calcinosis - complications | Immune System - physiology | Receptor Activator of Nuclear Factor-kappa B | Vascular Diseases - complications | Humans | Endothelium, Vascular - drug effects | RANK Ligand | Glycoproteins - pharmacology | Osteoprotegerin | Membrane Glycoproteins - physiology | Carrier Proteins - pharmacology | Osteoclasts - physiology | Osteoporosis - physiopathology | Muscle, Smooth, Vascular - drug effects | Carrier Proteins - physiology | Bone and Bones - physiology | Membrane Glycoproteins - pharmacology | Arteriosclerosis - physiopathology | Receptors, Cytoplasmic and Nuclear - physiology | Vascular Diseases - physiopathology | Glycoproteins - physiology | Mice, Knockout | Animals | Receptors, Tumor Necrosis Factor | Osteoporosis - complications | Mice | Calcinosis - physiopathology
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9. Full Text The role of osteoprotegerin and tumor necrosis factor-related apoptosis-inducing ligand in human microvascular endothelial cell survival
by Pritzker, L.B and Scatena, M and Giachelli, C.M
Molecular Biology of the Cell, ISSN 1059-1524, 06/2004, Volume 15, Issue 6, pp. 2834 - 2841
Endothelial cell survival and antiapoptotic pathways, including those stimulated by extracellular matrix, are critical regulators of vasculogenesis,... 
MATRIX | ACTIVATION | ANGIOGENESIS | RECEPTOR | TRAIL-INDUCED APOPTOSIS | INTEGRIN ALPHA(V)BETA | NF-KAPPA-B | EXPRESSION | VASCULAR SMOOTH-MUSCLE | DEATH-DOMAIN | CELL BIOLOGY | Tumor Necrosis Factor-alpha - metabolism | Immunoprecipitation | Membrane Glycoproteins - metabolism | Recombinant Fusion Proteins - pharmacology | Apoptosis - drug effects | Humans | Tumor Necrosis Factor-alpha - genetics | GPI-Linked Proteins | Glycoproteins - metabolism | Glycoproteins - pharmacology | Receptors, TNF-Related Apoptosis-Inducing Ligand | Receptors, Tumor Necrosis Factor, Member 10c | Osteoprotegerin | Polylysine - metabolism | Tumor Necrosis Factor Decoy Receptors | TNF-Related Apoptosis-Inducing Ligand | Sialoglycoproteins - pharmacology | Tumor Necrosis Factor-alpha - immunology | Cell Membrane - metabolism | Membrane Glycoproteins - immunology | Culture Media, Serum-Free - pharmacology | Antibodies, Monoclonal - immunology | Glycoproteins - genetics | Receptors, Tumor Necrosis Factor - metabolism | Cell Line | Cell Survival - drug effects | Endothelial Cells - metabolism | Membrane Glycoproteins - pharmacology | Osteopontin | Receptors, Cytoplasmic and Nuclear - genetics | Membrane Glycoproteins - genetics | Glycoproteins - secretion | Tumor Necrosis Factor-alpha - pharmacology | Apoptosis Regulatory Proteins | Signal Transduction - drug effects | Endothelial Cells - cytology | Protein Binding | Endothelial Cells - drug effects | Receptors, Cytoplasmic and Nuclear - metabolism
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10. Full Text Mechanisms underlying interferon-γ-induced priming of microglial reactive oxygen species production
by Spencer, Nicholas G and Schilling, Tom and Miralles, Francesc and Eder, Claudia
PLoS ONE, ISSN 1932-6203, 09/2016, Volume 11, Issue 9, pp. e0162497 - e0162497
Microglial priming and enhanced reactivity to secondary insults cause substantial neuronal damage and are hallmarks of brain aging, traumatic brain injury and... 
CELLS | ACTIVATION | PROTEIN | SUPEROXIDE-PRODUCTION | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | PROLIFERATION | ION CHANNELS | K+ CHANNEL | MEDIATED NEUROTOXICITY | NOX2 | Microglia - metabolism | Reactive Oxygen Species - metabolism | Membrane Glycoproteins - metabolism | NADPH Oxidases - metabolism | Peroxynitrous Acid - agonists | Glycoproteins - pharmacology | Reactive Oxygen Species - agonists | Adenosine Triphosphate - pharmacology | Glutathione - agonists | Glutathione - biosynthesis | Membrane Glycoproteins - antagonists & inhibitors | Phenanthrolines - pharmacology | Nitric Oxide Synthase Type II - antagonists & inhibitors | NADPH Oxidases - genetics | Potassium Channels, Inwardly Rectifying - antagonists & inhibitors | Peroxynitrous Acid - antagonists & inhibitors | p38 Mitogen-Activated Protein Kinases - metabolism | Microglia - cytology | NG-Nitroarginine Methyl Ester - pharmacology | Cell Line | Nitric Oxide - biosynthesis | Microglia - drug effects | Signal Transduction | Nitric Oxide - antagonists & inhibitors | NADPH Oxidases - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Gene Expression Regulation | p38 Mitogen-Activated Protein Kinases - genetics | Glutathione - antagonists & inhibitors | Potassium Channels, Inwardly Rectifying - genetics | Imidazoles - pharmacology | NADPH Oxidase 2 | Nitric Oxide - agonists | Membrane Glycoproteins - genetics | Peroxynitrous Acid - biosynthesis | Reactive Oxygen Species - antagonists & inhibitors | Animals | Nitric Oxide Synthase Type II - genetics | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Acetylcysteine - pharmacology | Mice | Pyridines - pharmacology | Potassium Channels, Inwardly Rectifying - metabolism | Interferon-gamma - pharmacology | Nitric Oxide Synthase Type II - metabolism | Brain | Cell culture | Reactive oxygen species | Traumatic brain injury | Disease | Oxidase | Infections | Experiments | Channels | NAD(P)H oxidase | Neurotoxicity | Head injuries | CYBB protein | Aging | Inhibition | Glutathione | Peroxynitrite | Oxygen | Neurodegenerative diseases | Potassium channels (inwardly-rectifying) | Research & development--R&D | Neutrophils | MAP kinase | Priming | Microglia | NG-Nitroarginine methyl ester | Neurological diseases | Pathology | Brain research | Nitric oxide | γ-Interferon | Brain damage | N-Acetyl-L-cysteine | Interferon | Intracellular | Potassium | Dementia | Index Medicus | Research & development | R&D
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11. Full Text Interaction between heptad repeat 1 and 2 regions in spike protein of SARS-associated coronavirus: implications for virus fusogenic mechanism and identification of fusion inhibitors
by Liu, Shuwen and Xiao, Gengfu and Chen, Yibang and He, Yuxian and Niu, Jinkui and Escalante, Carlos R and Xiong, Huabao and Farmar, James and Debnath, Asim K and Tien, Po and Jiang, Shibo
The Lancet, ISSN 0140-6736, 03/2004, Volume 363, Issue 9413, pp. 938 - 947
Studies on the fusion-inhibitory peptides derived from the heptad repeat 1 and 2 (HR1 and HR2) regions of the HIV-1 envelope glycoprotein gp41 provided crucial... 
MEMBRANE-FUSION | MEDICINE, GENERAL & INTERNAL | GP41 CORE STRUCTURE | HIV-1 GP41 | ENVELOPE GLYCOPROTEIN | SYNTHETIC PEPTIDES | TYPE-1 GP41 | INFECTION IN-VITRO | COILED-COIL | ACUTE RESPIRATORY SYNDROME | POTENT INHIBITORS | Anti-HIV Agents - pharmacology | Surface Plasmon Resonance | Viral Envelope Proteins - pharmacology | Viral Fusion Proteins - metabolism | Membrane Glycoproteins - metabolism | Humans | Membrane Glycoproteins - chemistry | Protein Conformation - drug effects | HIV Envelope Protein gp41 - metabolism | Chromatography, High Pressure Liquid | HIV Envelope Protein gp41 - chemistry | SARS Virus - metabolism | HIV Envelope Protein gp41 - pharmacology | Viral Fusion Proteins - chemistry | HIV Envelope Protein gp41 - drug effects | Viral Envelope Proteins - metabolism | Severe Acute Respiratory Syndrome - metabolism | Circular Dichroism | Oligopeptides - chemistry | Membrane Fusion - drug effects | Electrophoresis, Polyacrylamide Gel | Membrane Glycoproteins - pharmacology | Cells, Cultured | SARS Virus - drug effects | Oligopeptides - metabolism | Severe Acute Respiratory Syndrome - drug therapy | SARS Virus - chemistry | Sequence Homology, Nucleic Acid | Spike Glycoprotein, Coronavirus | Anti-HIV Agents - chemistry | Severe Acute Respiratory Syndrome - prevention & control | Chemical Fractionation | Oligopeptides - drug effects | Viral Envelope Proteins - chemistry | Membrane Fusion - physiology | Reports | Usage | Diagnosis | Peptides | Severe acute respiratory syndrome | Pathology | Viruses | Membranes | Prophylaxis | Homology | Infections | Proteins | Hepatitis | Spectrum analysis | Human immunodeficiency virus--HIV | Dichroism | Docking | Electrophoresis | Inhibition | Sedimentation & deposition | Glycoprotein gp41 | Spike protein | Gel electrophoresis | Glycoprotein | Trimers | Liquid chromatography | Cell membranes | High-performance liquid chromatography | Sedimentation | Molecular chains | Helicity | Circular dichroism | Software | Surface plasmon resonance | Protein structure | High performance liquid chromatography
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12. Full Text Effects of ibrutinib treatment on murine platelet function during inflammation and in primary hemostasis
by Lee, Robert H and Piatt, Raymond and Conley, Pamela B and Bergmeier, Wolfgang
Haematologica, ISSN 0390-6078, 02/2017, Volume 102, Issue 3, pp. e89 - e92
COLLAGEN | LEUKEMIA | HEMATOLOGY | THROMBUS STABILITY | GPVI | Crotalid Venoms - pharmacology | Receptors, Purinergic P2Y12 - deficiency | Skin - metabolism | Lectins, C-Type - genetics | Lectins, C-Type - metabolism | Blood Platelets - cytology | Platelet Membrane Glycoproteins - metabolism | Platelet Membrane Glycoproteins - agonists | Collagen - pharmacology | Lung - metabolism | Platelet Aggregation - drug effects | Blood Platelets - drug effects | Receptors, Purinergic P2Y12 - metabolism | Skin - pathology | Pyrazoles - pharmacology | Receptors, Purinergic P2Y12 - genetics | Hemostasis - drug effects | Hemorrhage