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1. Full Text New ex vivo approaches distinguish effective and ineffective single agents for reversing HIV-1 latency in vivo
by Bullen, C Korin and Laird, Gregory M and Durand, Christine M and Siliciano, Janet D and Siliciano, Robert F
Nature Medicine, ISSN 1078-8956, 2014, Volume 20, Issue 4, pp. 425 - 429
HIV-1 persists in a latent reservoir despite antiretroviral therapy (ART)(1-5). This reservoir is the major barrier to HIV-1 eradication(6,7). Current... 
MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | RESERVOIR | PROSTRATIN | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CD4(+) T-CELLS | CELL BIOLOGY | REPLICATION | REACTIVATION | ACTIVE ANTIRETROVIRAL THERAPY | HISTONE DEACETYLASE INHIBITORS | EXPRESSION | Anti-HIV Agents - pharmacology | Bryostatins - pharmacology | Tetradecanoylphorbol Acetate - pharmacology | HIV-1 - drug effects | Lymphocyte Activation | Humans | Transcription Factors - antagonists & inhibitors | Depsipeptides - pharmacology | Virus Latency - drug effects | Azepines - pharmacology | Triazoles - pharmacology | HIV-1 - physiology | Nuclear Proteins - antagonists & inhibitors | Ionomycin - pharmacology | HIV Infections - drug therapy | Histone Deacetylase Inhibitors - pharmacology | Indoles - pharmacology | Virus Latency - immunology | Disulfiram - pharmacology | Hydroxamic Acids - pharmacology | CD4-Positive T-Lymphocytes - drug effects | Highly active antiretroviral therapy | Physiological aspects | Development and progression | Genetic aspects | Research | Drug therapy | HIV infection | Antiretroviral drugs | T cell receptors | Pharmacology | Human immunodeficiency virus--HIV | Index Medicus
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2. Full Text Activity-dependent cleavage of the K-Cl cotransporter KCC2 mediated by calcium-activated protease calpain
by Puskarjov, Martin and Ahmad, Faraz and Kaila, Kai and Blaesse, Peter
Journal of Neuroscience, ISSN 0270-6474, 08/2012, Volume 32, Issue 33, pp. 11356 - 11364
The K-Cl cotransporter KCC2 plays a crucial role in neuronal chloride regulation. In mature central neurons, KCC2 is responsible for the low intracellular Cl-... 
PROTEOLYTIC CLEAVAGE | NMDA RECEPTOR | SYNAPTIC FUNCTION | GABAERGIC TRANSMISSION | AXON INITIAL SEGMENT | DOWN-REGULATION | DEVELOPMENTAL-CHANGES | RAT HIPPOCAMPUS | MEMBRANE TRAFFICKING | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | Calpain - metabolism | Rats, Wistar | Calcium - metabolism | Emetine - pharmacology | Male | N-Methylaspartate - pharmacology | Dose-Response Relationship, Drug | Pyramidal Cells - physiology | Statistics, Nonparametric | Calcium Ionophores - pharmacology | Pyramidal Cells - drug effects | Protein Synthesis Inhibitors - pharmacology | Action Potentials - drug effects | Animals, Newborn | Membrane Potentials - drug effects | Dipeptides - pharmacology | Valine - analogs & derivatives | Gene Expression Regulation - physiology | Rats | Magnesium - metabolism | Excitatory Amino Acid Antagonists - pharmacology | Hippocampus - cytology | Cycloheximide - pharmacology | Symporters - metabolism | Gene Expression Regulation - drug effects | Leupeptins - pharmacology | Patch-Clamp Techniques | Animals | Analysis of Variance | Cysteine Proteinase Inhibitors - pharmacology | Calpain - pharmacology | Ionomycin - pharmacology | Valine - pharmacology | Dizocilpine Maleate - pharmacology | In Vitro Techniques | Index Medicus
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3. Full Text Sulforaphane rescues amyloid-β Peptide-mediated decrease in MerTK expression through its anti-inflammatory effect in human THP-1 macrophages
by Jhang, Kyoung A and Park, Jin-Sun and Kim, Hee-Sun and Chong, Young Hae
Journal of Neuroinflammation, ISSN 1742-2094, 03/2018, Volume 15, Issue 1, pp. 75 - 75
Background: Mer tyrosine kinase (MerTK) activity necessary for amyloid-stimulated phagocytosis strongly implicates that MerTK dysregulation might contribute to... 
Alzheimer's disease | Innate immune response | MerTK | Sulforaphane | Aβ1-42 | CLEARANCE | PHAGOCYTOSIS | ACTIVATION | ALZHEIMERS-DISEASE | TAM RECEPTORS | IMMUNOLOGY | MYELOID CELLS | NEUROSCIENCES | A beta 1-42 | PATHWAY | INFLAMMATION | APOPTOTIC CELLS | RECEPTOR TYROSINE KINASE | Tumor Necrosis Factor-alpha - metabolism | RNA, Small Interfering - genetics | Cell Fractionation | Nitriles - pharmacology | Calcium - metabolism | Amyloid beta-Peptides - pharmacology | Humans | Peptide Fragments - pharmacology | Sulfones - pharmacology | THP-1 Cells - drug effects | Interleukin-1beta - metabolism | Tumor Necrosis Factor-alpha - immunology | Calcium Ionophores - pharmacology | Protein Synthesis Inhibitors - pharmacology | Isothiocyanates - pharmacology | Anti-Inflammatory Agents - pharmacology | c-Mer Tyrosine Kinase - metabolism | Interleukin-1beta - immunology | Cycloheximide - pharmacology | Antibodies - pharmacology | Gene Expression Regulation - drug effects | Signal Transduction - drug effects | Ionomycin - pharmacology | Thapsigargin - pharmacology | RNA, Small Interfering - metabolism | Index Medicus | Alzheimer’s disease
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4. Full Text Activation of GPCRs modulates quantal size in chromaffin cells through G(beta gamma) and PKC
by Chen, XK and Wang, LC and Zhou, Y and Cai, Q and Prakriya, M and Duan, KL and Sheng, ZH and Lingle, C and Zhou, Z
NATURE NEUROSCIENCE, ISSN 1097-6256, 09/2005, Volume 8, Issue 9, pp. 1160 - 1168
Exocytosis proceeds by either full fusion or 'kiss-and-run' between vesicle and plasma membrane. Switching between these two modes permits the cell to regulate... 
TRANSMITTER RELEASE | VESICLE FUSION | PROTEIN-KINASE-C | PRESYNAPTIC INHIBITION | EXOCYTOSIS | NEUROTRANSMITTER RELEASE | RECEPTOR | BETA-GAMMA-SUBUNITS | NEUROSCIENCES | FUSION PORE KINETICS | SECRETORY GRANULES | GTP-Binding Protein beta Subunits - pharmacology | Receptors, G-Protein-Coupled - metabolism | Recombinant Fusion Proteins - pharmacology | Calcium - metabolism | Analgesics, Opioid - pharmacology | Membrane Potentials - radiation effects | Patch-Clamp Techniques - methods | Somatostatin - pharmacology | Dynamins - pharmacology | Adenosine Triphosphate - pharmacology | Neural Inhibition - physiology | Drug Interactions | Protein Kinase C - metabolism | Potassium Chloride - pharmacology | Action Potentials - radiation effects | GTP-Binding Protein beta Subunits - metabolism | Chromaffin Cells - drug effects | Electric Stimulation - methods | Action Potentials - drug effects | Ionophores - pharmacology | Pertussis Toxin - pharmacology | Membrane Potentials - drug effects | Protein Kinases - pharmacology | GTP-Binding Protein gamma Subunits - metabolism | Enkephalin, Ala-MePhe-Gly- - pharmacology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Thionucleotides - pharmacology | Enzyme Activation - drug effects | Adenosine Triphosphate - analogs & derivatives | Adrenal Medulla - cytology | Action Potentials - physiology | Chromaffin Cells - metabolism | Animals | Ionomycin - pharmacology | Muscarine - pharmacology | Electrochemistry - methods | Dose-Response Relationship, Radiation | Enzyme Activation - physiology | Neural Inhibition - drug effects | Chromaffin cells | Physiological aspects | Cell receptors | Research | G proteins | Protein kinases | Index Medicus
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5. Full Text Calcium signaling stimulates translation of HIF-α during hypoxia
by Hui, Anna S and Bauer, Amy L and Striet, Justin B and Schnell, Phillip O and Czyzyk-Krzeska, Maria F
FASEB Journal, ISSN 0892-6638, 03/2006, Volume 20, Issue 3, pp. 466 - 475
Hypoxia-inducible factors (HIFs) are ubiquitous transcription factors that mediate adaptation to hypoxia by inducing specific sets of target genes. It is well... 
Oxygen-sensitive cells | Protein kinase C | Carotid body | Protein translation | PC12 cells | MAMMALIAN TARGET | protein translation | INDUCIBLE FACTOR-1-ALPHA | oxygen-sensitive cells | BIOCHEMISTRY & MOLECULAR BIOLOGY | carotid body | KIDNEY HEK293 CELLS | CELL BIOLOGY | HEK-293 CELLS | MESSENGER-RNA | TYROSINE-HYDROXYLASE GENE | BIOLOGY | TUMOR-SUPPRESSOR PROTEIN | CHANNEL ACTIVITY | protein kinase C | Cell Hypoxia - physiology | Protein Biosynthesis | Nitriles - pharmacology | Protein Kinase C-alpha - metabolism | Humans | RNA, Messenger - metabolism | Kidney | Cell Line - drug effects | Isoquinolines - pharmacology | Basic Helix-Loop-Helix Transcription Factors - biosynthesis | Indoles - pharmacology | Flavonoids - pharmacology | Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis | Protein Synthesis Inhibitors - pharmacology | Calcium Signaling | Cell Line - metabolism | Protein Kinase C-alpha - antagonists & inhibitors | Butadienes - pharmacology | Aryl Hydrocarbon Receptor Nuclear Translocator - analysis | Basic Helix-Loop-Helix Transcription Factors - genetics | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | RNA, Small Interfering - pharmacology | Rats | Sulfonamides - pharmacology | Sirolimus - pharmacology | Cycloheximide - pharmacology | PC12 Cells - drug effects | Animals | PC12 Cells - metabolism | Protein Kinases - physiology | Ionomycin - pharmacology | Polyribosomes - metabolism | RNA Caps - physiology | TOR Serine-Threonine Kinases | Carbazoles - pharmacology | Benzylamines - pharmacology | Index Medicus
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6. Full Text Characterisation of (R)-2-(2-fluorobiphenyl-4-yl)-N-(3-methylpyridin-2-yl)propanamide as a dual fatty acid amide hydrolase: Cyclooxygenase inhibitor
by Gouveia-Figueira, Sandra and Karlsson, Jessica and Deplano, Alessandro and Hashemian, Sanaz and Svensson, Mona and Sundbom, Marcus Fredriksson and Congiu, Cenzo and Onnis, Valentina and Fowler, Christopher J and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Farmakologi and Kemiska institutionen and Umeå universitet and Teknisk-naturvetenskapliga fakulteten
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, pp. e0139212 - e0139212
Background Increased endocannabinoid tonus by dual-action fatty acid amide hydrolase (FAAH) and substrate selective cyclooxygenase (COX-2) inhibitors is a... 
IBUPROFEN | ENZYME | COX-2 | OXYGENATION | ENDOCANNABINOIDS | MULTIDISCIPLINARY SCIENCES | ANANDAMIDE | INDOMETHACIN | FLURBIPROFEN | LINEAR-MODELS | ANTIINFLAMMATORY DRUGS | Endocannabinoids - metabolism | Stereoisomerism | Humans | Brain - enzymology | Male | Arachidonic Acids - metabolism | Isoenzymes - metabolism | Benzamides - pharmacology | Carbamates - pharmacology | Amides - pharmacology | Amidohydrolases - metabolism | Amidohydrolases - antagonists & inhibitors | Polyunsaturated Alkamides - metabolism | Cyclooxygenase Inhibitors - pharmacology | Hydrolysis | Animals | Arachidonic Acid - pharmacology | Cyclooxygenase 2 - metabolism | Lipid Metabolism - drug effects | Lipopolysaccharides - pharmacology | Amides - chemistry | Ionomycin - pharmacology | RAW 264.7 Cells | Mice | Cyclooxygenase 1 - metabolism | Flurbiprofen - pharmacology | Interferon-gamma - pharmacology | Prostaglandins - metabolism | Brain | COX-2 inhibitors | Neurosciences | Lipids | Enantiomers | Arachidonic acid | Macrophages | Prostaglandin endoperoxide synthase | Pain | 2-Arachidonylglycerol | Rodents | Inhibition | Nonsteroidal anti-inflammatory drugs | Flurbiprofen | Functional foods & nutraceuticals | Fatty-acid amide hydrolase | Enzymes | Hydrolase | Substrate inhibition | Pharmacology | Prostaglandin D2 | Fatty acids | Substrates | Anandamide | Environmental science | Inhibitors | Cyclooxygenase-1 | Interferon | Cyclooxygenase-2 | Oxygenation | Pharmaceuticals | Index Medicus | Basic Medicine | Farmakologi och toxikologi | Medical and Health Sciences | Pharmacology and Toxicology | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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7. Full Text Sphingomyelinase-induced adhesion of eryptotic erythrocytes to endothelial cells
by Abed, Majed and Towhid, Syeda T and Mia, Sobuj and Pakladok, Tatsiana and Alesutan, Ioana and Borst, Oliver and Gawaz, Meinrad and Gulbins, Erich and Lang, Florian
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 11/2012, Volume 303, Issue 9, pp. C991 - C999
Abed M, Towhid ST, Mia S, Pakladok T, Alesutan I, Borst O, Gawaz M, Gulbins E, Lang F. Sphingomyelinase-induced adhesion of eryptotic erythrocytes to... 
Eryptosis | Adhesion | Phosphatidylserine | CXCL16 | Endothelium | endothelium | PHYSIOLOGY | SR-PSOX | BERGHEI-INFECTED MICE | adhesion | VASCULAR ENDOTHELIUM | CELL BIOLOGY | phosphatidylserine | eryptosis | SCAVENGER RECEPTOR | DISEASE | RED-BLOOD-CELLS | PHOSPHATIDYLSERINE EXPOSURE | SUICIDAL DEATH | EXPRESSION | CXC CHEMOKINE LIGAND-16 | Apoptosis - drug effects | Humans | Phosphatidylserines - physiology | Receptors, Scavenger - antagonists & inhibitors | Human Umbilical Vein Endothelial Cells - physiology | Receptors, Scavenger - physiology | Calcium Ionophores - pharmacology | Annexin A5 - physiology | Chemokines, CXC - antagonists & inhibitors | Calcium - pharmacology | Human Umbilical Vein Endothelial Cells - drug effects | Chemokine CXCL16 | Sphingomyelin Phosphodiesterase - pharmacology | Cells, Cultured | Gene Silencing | Antibodies, Neutralizing - pharmacology | Cell Size | Glucose - pharmacology | Cell Adhesion - drug effects | Chemokines, CXC - genetics | Ceramides - pharmacology | Erythrocytes - drug effects | Receptors, Scavenger - genetics | Cell Adhesion - physiology | Ionomycin - pharmacology | Chemokines, CXC - physiology | Erythrocytes - physiology | Apoptosis - physiology | Proteins | Glucose | Calcium | Erythrocytes | Cell adhesion & migration | Index Medicus
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8. Full Text Nitric oxide plays a critical role in suppression of T-cell proliferation by mesenchymal stem cells
by Sato, Kazuya and Ozaki, Katsutoshi and Oh, Iekuni and Meguro, Akiko and Hatanaka, Keiko and Nagai, Tadashi and Muroi, Kazuo and Ozawa, Keiya
Blood, ISSN 0006-4971, 01/2007, Volume 109, Issue 1, pp. 228 - 234
The molecular mechanisms by which mesenchymal stem cells (MSCs) suppress T-cell proliferation are poorly understood, and whether a soluble factor plays a major... 
SYNTHASE | RESPONSES | ENGRAFTMENT | ACTIVATION | PATHWAY | IMMUNOSUPPRESSION | GROWTH | HEMATOLOGY | MARROW STROMAL CELLS | INHIBIT | TRANSPLANTATION | CD8-Positive T-Lymphocytes - cytology | Dinoprostone - physiology | Humans | B-Lymphocyte Subsets - cytology | T-Lymphocyte Subsets - drug effects | CD8-Positive T-Lymphocytes - metabolism | Phosphorylation - drug effects | Macrophages - physiology | B-Lymphocyte Subsets - drug effects | Nitric Oxide - biosynthesis | Signal Transduction | CD4-Positive T-Lymphocytes - metabolism | Cell Division - drug effects | Receptors, Antigen, T-Cell - physiology | Mice, Knockout | B-Lymphocyte Subsets - metabolism | Mice | Tryptophan - pharmacology | HeLa Cells | Interleukin-2 - biosynthesis | Indoleamine-Pyrrole 2,3,-Dioxygenase - physiology | Nitric Oxide Synthase Type II - metabolism | Tetradecanoylphorbol Acetate - pharmacology | T-Lymphocyte Subsets - cytology | Concanavalin A - pharmacology | Nitric Oxide - pharmacology | STAT5 Transcription Factor - metabolism | Protein Processing, Post-Translational - drug effects | Nitric Oxide Synthase Type II - antagonists & inhibitors | Tryptophan - analogs & derivatives | Enzyme Induction - drug effects | Transforming Growth Factor beta - antagonists & inhibitors | Mesenchymal Stromal Cells - physiology | NG-Nitroarginine Methyl Ester - pharmacology | Transforming Growth Factor beta - immunology | Cell Line | Antigens, CD19 - analysis | CD4-Positive T-Lymphocytes - cytology | Mice, Inbred C57BL | Nitric Oxide Synthase Type II - deficiency | Nitric Oxide - physiology | Cyclooxygenase Inhibitors - pharmacology | Animals | Lymphocyte Activation - drug effects | CD8-Positive T-Lymphocytes - drug effects | Ionomycin - pharmacology | CD4-Positive T-Lymphocytes - drug effects | Indoleamine-Pyrrole 2,3,-Dioxygenase - antagonists & inhibitors | Interferon-gamma - biosynthesis | Prostaglandin-Endoperoxide Synthases - physiology | Index Medicus | Abridged Index Medicus
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9. Full Text Activation state of the M3 muscarinic acetylcholine receptor modulates mammalian odorant receptor signaling
by Li, Yun Rose and Matsunami, Hiroaki
Science Signaling, ISSN 1945-0877, 01/2011, Volume 4, Issue 155, pp. ra1 - ra1
A diverse repertoire of heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors (GPCRs) enables cells to sense their environment.... 
SYSTEM | NASAL-MUCOSA | FUNCTIONAL EXPRESSION | ADENYLYL-CYCLASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN-COUPLED-RECEPTORS | SURFACE EXPRESSION | NEURONS | OLFACTORY RECEPTOR | MOLECULAR-BASIS | FAMILY | CELL BIOLOGY | Immunohistochemistry | Receptors, Odorant - metabolism | Receptors, G-Protein-Coupled - metabolism | Humans | Benzofurans - pharmacology | Pyrrolidines - pharmacology | Transfection | Membrane Transport Proteins - genetics | Muscarinic Antagonists - pharmacology | Protein Binding - drug effects | HEK293 Cells | Membrane Transport Proteins - metabolism | Cyclic AMP - metabolism | Cholinergic Agonists - pharmacology | Ionophores - pharmacology | Signal Transduction | Colforsin - pharmacology | Receptor, Muscarinic M3 - metabolism | Atropine - pharmacology | Receptor, Muscarinic M3 - genetics | Olfactory Receptor Neurons - metabolism | Olfactory Receptor Neurons - drug effects | Carbachol - pharmacology | Receptors, Odorant - genetics | Ionomycin - pharmacology | Receptors, G-Protein-Coupled - genetics | Index Medicus
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10. Full Text Impact of Commonly Used Transplant Immunosuppressive Drugs on Human NK Cell Function Is Dependent upon Stimulation Condition
by Meehan, Aislin C and Mifsud, Nicole A and Nguyen, Thi H. O and Levvey, Bronwyn J and Snell, Greg I and Kotsimbos, Tom C and Westall, Glen P
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, pp. e60144 - e60144
Lung transplantation is a recognised treatment for patients with end stage pulmonary disease. Transplant recipients receive life-long administration of... 
SOLID-ORGAN TRANSPLANTATION | NATURAL-KILLER-CELLS | LUNG TRANSPLANTATION | IN-VITRO | ACTIVATION | INHIBITION | MULTIDISCIPLINARY SCIENCES | PERIPHERAL-BLOOD | CYTOTOXICITY | MYCOPHENOLATE-MOFETIL | CYCLOSPORINE | Cyclosporine - pharmacology | Humans | Cells, Cultured | Morpholines - pharmacology | Male | Interferon-gamma - metabolism | Prednisolone - pharmacology | Lung Transplantation | Mycophenolic Acid - pharmacology | Acetophenones - pharmacology | Adult | Female | Lysosomal-Associated Membrane Protein 1 - metabolism | Flavonoids - pharmacology | Killer Cells, Natural - drug effects | Killer Cells, Natural - metabolism | Benzopyrans - pharmacology | Chromones - pharmacology | Immunosuppressive Agents - pharmacology | Killer cells | Corticosteroids | Analysis | Lung diseases | Immunotherapy | Transplantation of organs, tissues, etc | Organ transplant recipients | Mycophenolate mofetil | Drug therapy | T cells | Prednisolone | Mycophenolic acid | Lung | Cytotoxicity | Drug screening | Cell activation | Natural killer cells | Active control | Antigens | Cytokines | Medical treatment | Interleukin 12 | Rapamycin | T cell receptors | Patients | Immunosuppression | Major histocompatibility complex | Surveillance | γ-Interferon | Ligands | Drugs | Ionomycin | Transplants & implants | Toxicity | Cyclosporins | Medical services | Lung transplantation | Stimulation | Lymphocytes T | Transplantation | Activation | Kinases | Clinical outcomes | Immunosuppressive agents | Immunology | Pathways | Interleukin 2 | Lymphocytes | Xenografts | Immune system | Cytomegalovirus | Immune response | Cell survival | Graft rejection | Immune systems | Medicine | Rejection | Biopsy | Cell lines | Histocompatibility antigen HLA | Viral infections | Index Medicus
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11. Full Text SOST is a target gene for PTH in bone
by Keller, Hansjoerg and Kneissel, Michaela
Bone, ISSN 8756-3282, 2005, Volume 37, Issue 2, pp. 148 - 158
Intermittent parathyroid hormone (PTH) application is an established pharmacological principle to stimulate bone formation. Yet, the molecular mechanisms... 
PTH and PTH/RP | Gene expression | Osteoblasts | Histomorphometry-animal | INTERMITTENT TREATMENT | ANABOLIC ACTION | PARATHYROID-HORMONE 1-34 | OSTEOPROGENITOR CELLS | OSTEOCLAST DIFFERENTIATION FACTOR | histomorphometry-animal | OVARIECTOMIZED RATS | TRABECULAR BONE | CANCELLOUS BONE | BMP ANTAGONIST | ENDOCRINOLOGY & METABOLISM | osteoblasts | gene expression | GROWTH-FACTOR-I | Bone Morphogenetic Proteins - antagonists & inhibitors | Tetradecanoylphorbol Acetate - pharmacology | Rats, Wistar | Parathyroid Hormone - pharmacology | Peptide Fragments - pharmacology | RNA, Messenger - metabolism | Skull - physiology | Peptide Fragments - physiology | Bone Morphogenetic Proteins - metabolism | Female | Protein Synthesis Inhibitors - pharmacology | Bone Morphogenetic Proteins - genetics | Skull - drug effects | Parathyroid Hormone - physiology | Cell Line | Bone Density | Ovariectomy | Colforsin - pharmacology | Tissue Culture Techniques | Rats | Femur - drug effects | Parathyroid Hormone - antagonists & inhibitors | Glycoproteins | RNA Stability | Cycloheximide - pharmacology | Femur - physiology | Cyclic AMP - antagonists & inhibitors | Animals | Peptide Fragments - antagonists & inhibitors | Genetic Markers - genetics | Ionomycin - pharmacology | Mice | Osteogenesis | Messenger RNA | Parathyroid hormone | Analysis | Genetic research | Protein biosynthesis | Bones | Peptide hormones | Density | Index Medicus
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12. Full Text Regulatory action of calcium ion on cyclic AMP-Enhanced expression of implantation- related factors in human endometrial cells
by Kusama, Kazuya and Yoshie, Mikihiro and Tamura, Kazuhiro and Imakawa, Kazuhiko and Isaka, Keiichi and Tachikawa, Eiichi
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, pp. e0132017 - e0132017
Decidualization of human endometrial stroma and gland development is mediated through cyclic AMP (cAMP), but the role of intracellular calcium ion (Ca2+) on... 
MENSTRUAL-CYCLE | CA2+ ENTRY | HUMAN DECIDUAL CELLS | ADENYLYL CYCLASES | MULTIDISCIPLINARY SCIENCES | GLANDULAR CELLS | PROLACTIN | DIFFERENTIATION | STROMAL CELLS | BINDING PROTEIN | CAMP | Biomarkers - metabolism | Cell Line | Calcium - pharmacology | Embryo Implantation - drug effects | Colforsin - pharmacology | Dinoprostone - biosynthesis | Humans | Stromal Cells - metabolism | Ions | Ryanodine Receptor Calcium Release Channel - metabolism | Chelating Agents - pharmacology | Dantrolene - pharmacology | Calcium Channel Blockers - pharmacology | Decidua - metabolism | Cyclic AMP - pharmacology | Models, Biological | Cyclooxygenase 2 - metabolism | Stromal Cells - drug effects | Female | Calcium Channels, L-Type - metabolism | Decidua - drug effects | Endometrium - cytology | Alamethicin - pharmacology | Ionophores - pharmacology | Calcium channels | Pituitary hormones | Ionophores | Protein binding | Nifedipine | Ionomycin | Transcription | Calcium | Laboratories | Epithelial cells | Insulin-like growth factor-binding protein 1 | Variations | Prostaglandin E2 | Intracellular signalling | Insulin-like growth factors | Calcium ionophores | Kinases | Calcium influx | Prostaglandin endoperoxide synthase | Calcium signalling | Proteins | Signal transduction | Prolactin | Physiology | Endometrium | Medical research | Calcium (intracellular) | Menstruation | Calcium channels (voltage-gated) | Cyclic AMP | Implantation | Pharmacology | Decidua | Breeding of animals | Gene expression | Embryos | Pharmacy | Calcium channels (L-type) | Forskolin | Cyclooxygenase-2 | Intracellular | Index Medicus
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13. Full Text The Ca2+/Calmodulin-dependent Protein Kinase Kinases Are AMP-activated Protein Kinase Kinases
by Rebecca L. Hurley and Kristin A. Anderson and Jeanne M. Franzone and Bruce E. Kemp and Anthony R. Means and Lee A. Witters
Journal of Biological Chemistry, ISSN 0021-9258, 08/2005, Volume 280, Issue 32, pp. 29060 - 29066
The AMP-activated protein kinase (AMPK) is an important regulator of cellular metabolism in response to metabolic stress and to other regulatory signals. AMPK... 
SNF1 | YEAST | ENERGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPONENTS | CASCADE | UPSTREAM KINASES | MECHANISMS | LKB1 | SNF1-ACTIVATING KINASES | BETA | Deoxyglucose - metabolism | Phosphorylation | Threonine - chemistry | Calcium - metabolism | Humans | Protein Kinases - chemistry | Immunoblotting | Aminoimidazole Carboxamide - pharmacology | Ribonucleotides - pharmacology | Isoquinolines - pharmacology | RNA Interference | Culture Media, Serum-Free - pharmacology | Protein-Serine-Threonine Kinases - metabolism | Fibroblasts - metabolism | Calmodulin - metabolism | Cells, Cultured | Naphthalimides | Deoxyglucose - chemistry | Animals | Aminoimidazole Carboxamide - analogs & derivatives | Protein Isoforms | Protein Kinases - physiology | Cell Line, Tumor | Ionomycin - pharmacology | Mannitol - chemistry | Benzimidazoles - pharmacology | Mice | Enzyme Activation | HeLa Cells | COS Cells | RNA, Small Interfering - metabolism | Index Medicus
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14. Full Text Physiological effect of protein kinase C on ENaC-mediated lung liquid regulation in the adult rat lung
by Soukup, Benjamin and Benjamin, Audra and Orogo-Wenn, Maria and Walters, Dafydd
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 01/2012, Volume 302, Issue 1, pp. L133 - L139
Soukup B, Benjamin A, Orogo-Wenn M, Walters D. Physiological effect of protein kinase C on ENaC-mediated lung liquid regulation in the adult rat lung. Am J... 
Calcium-dependent protein kinase C | Phorbol 12-myristate 13-acetate | Ionomycin | ALPHA-ENAC | PHYSIOLOGY | ION-TRANSPORT | phorbol 12-myristate 13-acetate | calcium-dependent protein kinase C | EPITHELIAL SODIUM-CHANNEL | FLUID CLEARANCE | RESPIRATORY SYSTEM | ionomycin | II CELLS | NA+ TRANSPORT | ABSORPTION | PHORBOL ESTER | ANESTHETIZED SHEEP | FETAL LAMB | Isotonic Solutions - pharmacology | Epithelial Cells - metabolism | Tetradecanoylphorbol Acetate - pharmacology | Rats, Wistar | Epithelial Cells - drug effects | Maleimides - pharmacology | Tetradecanoylphorbol Acetate - analogs & derivatives | Male | Epithelial Sodium Channels - metabolism | Lung - enzymology | Epithelial Sodium Channels - drug effects | Protein Kinase C - metabolism | Indoles - pharmacology | Terbutaline - pharmacology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Sodium Channel Blockers - pharmacology | Protein Kinase C - antagonists & inhibitors | Electric Impedance | Benzophenanthridines - pharmacology | Animals | Signal Transduction - drug effects | Lung - drug effects | Amiloride - pharmacology | Ionomycin - pharmacology | Biological Transport - physiology | Physiological aspects | Research | Lungs | Protein kinases | Physiology | Pharmacology | Kinases | Rodents | Index Medicus
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