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1. Full Text Intracellular angiotensin II activates rat myometrium
by Deliu, Elena and Tica, Andrei A and Motoc, Dana and Brailoiu, G. Cristina and Brailoiu, Eugen
American Journal of Physiology: Cell Physiology, ISSN 0363-6143, 09/2011, Volume 301, Issue 3, pp. C559 - C565
Calcium imaging | Microinjection | Cytosolic calcium concentration | Endoplasmic reticulum | Physiology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Myometrium - drug effects | Type C Phospholipases - metabolism | Brefeldin A - pharmacology | Angiotensin II Type 1 Receptor Blockers - pharmacology | Autophagy - drug effects | Endosomes - metabolism | Angiotensin II Type 2 Receptor Blockers - pharmacology | Macrocyclic Compounds - pharmacology | Saralasin - pharmacology | Endoplasmic Reticulum - drug effects | Estrenes - pharmacology | Myometrium - metabolism | Inositol 1,4,5-Trisphosphate Receptors - antagonists & inhibitors | Ryanodine - pharmacology | Angiotensin II - pharmacology | Pyridines - administration & dosage | Endocytosis - drug effects | Enzyme Inhibitors - pharmacology | Losartan - pharmacology | Saralasin - administration & dosage | Rats | Imidazoles - pharmacology | Piperazines - pharmacology | Rats, Sprague-Dawley | Receptor, Angiotensin, Type 2 - metabolism | Signal Transduction - drug effects | Calcium Signaling - drug effects | Models, Biological | Receptor, Angiotensin, Type 1 - metabolism | Oxazoles - pharmacology | Losartan - administration & dosage | Angiotensin II - administration & dosage | Calcium Signaling - physiology | Endoplasmic Reticulum - metabolism | Imidazoles - administration & dosage | Type C Phospholipases - antagonists & inhibitors | Lysosomes - metabolism | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Pyrrolidinones - pharmacology | Macrolides - pharmacology | NADP - analogs & derivatives | Female | NADP - metabolism | Heparin - pharmacology | Angiotensin II - metabolism | Arsenicals - pharmacology | Cells, Cultured | Sirolimus - pharmacology | Myometrium - cytology | Animals | Egtazic Acid - pharmacology | Uterus - cytology | Signal Transduction - physiology | Pyridines - pharmacology | Carbolines - pharmacology | Myometrium | Cell receptors | Calcium channels | Genetic aspects | Properties | Angiotensin | T cell receptors | Calcium | ACE inhibitors | Autophagy | Rodents | Index Medicus | microinjection | calcium imaging | cytosolic calcium concentration | endoplasmic reticulum | Receptors and Signal Transduction
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2. Comparative evaluation of HERG currents and QT intervals following challenge with suspected torsadogenic and nontorsadogenic drugs
by Katchman, Alexander N and Koerner, John and Tosaka, Toshimasa and Woosley, Raymond L and Ebert, Steven N
The Journal of pharmacology and experimental therapeutics, ISSN 0022-3565, 03/2006, Volume 316, Issue 3, pp. 1098 - 1106
Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Terfenadine - pharmacology | Rabbits | Lovastatin - pharmacology | Arsenicals - pharmacology | Humans | Cells, Cultured | Torsades de Pointes - chemically induced | Electrocardiography - drug effects | ERG1 Potassium Channel | Ether-A-Go-Go Potassium Channels - antagonists & inhibitors | Oxides - pharmacology | Animals | Ether-A-Go-Go Potassium Channels - physiology | Haloperidol - pharmacology | Potassium Channel Blockers - pharmacology | Loratadine - pharmacology | Methadone - pharmacology | Pentamidine - pharmacology | Index Medicus
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3. Full Text Itraconazole and Arsenic Trioxide Inhibit Hedgehog Pathway Activation and Tumor Growth Associated with Acquired Resistance to Smoothened Antagonists
by Kim, James and Aftab, Blake T and Tang, Jean Y and Kim, Daniel and Lee, Alex H and Rezaee, Melika and Kim, Jynho and Chen, Baozhi and King, Emily M and Borodovsky, Alexandra and Riggins, Gregory J and Epstein, Ervin H and Beachy, Philip A and Rudin, Charles M
Cancer cell, ISSN 1535-6108, 01/2013, Volume 23, Issue 1, pp. 23 - 34
Oncology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Anilides - therapeutic use | Hedgehog Proteins - metabolism | Drug Resistance, Neoplasm | Antineoplastic Agents - therapeutic use | Hedgehog Proteins - physiology | Itraconazole - pharmacology | Arsenicals - therapeutic use | Medulloblastoma - pathology | Smoothened Receptor | Antineoplastic Agents - pharmacology | Pyridines - therapeutic use | Oxides - therapeutic use | Arsenicals - pharmacology | Carcinoma, Basal Cell - pathology | Medulloblastoma - metabolism | Carcinoma, Basal Cell - metabolism | Itraconazole - therapeutic use | Oxides - pharmacology | Animals | Signal Transduction - drug effects | Anilides - pharmacology | Receptors, G-Protein-Coupled - antagonists & inhibitors | Carcinoma, Basal Cell - drug therapy | Mice | Pyridines - pharmacology | Medulloblastoma - drug therapy | Arsenic | Itraconazole | Index Medicus
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4. Full Text Characterization of Ovalbumin Absorption Pathways in the Rat Intestine, Including the Effects of Aspirin
by Yokooji, Tomoharu and Nouma, Hitomi and Matsuo, Hiroaki and Institute of Biomedical and Health Sciences and bFaculty of Pharmaceutical Sciences and aDepartment of Pathophysiology and Therapeutics and Hiroshima University
Biological & pharmaceutical bulletin, ISSN 0918-6158, 2014, Volume 37, Issue 8, pp. 1359 - 1365
paracellular pathway | aspirin | absorption | clathrin-dependent endocytosis | ovalbumin | Ovalbumin | Aspirin | Absorption | Paracellular pathway | Clathrin-dependent endocytosis | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Colchicine - pharmacology | Serum Albumin, Bovine - pharmacology | Fluorescein-5-isothiocyanate - pharmacology | Arsenicals - pharmacology | Endocytosis - drug effects | Intestinal Absorption - drug effects | Fluorescein-5-isothiocyanate - analogs & derivatives | Male | Ovalbumin - pharmacology | Rats, Sprague-Dawley | beta-Cyclodextrins - pharmacology | Animals | Ovalbumin - pharmacokinetics | Dextrans - pharmacology | Intestine, Small - drug effects | Macrolides - pharmacology | Ovalbumin - blood | Allergens - pharmacology | Aspirin - pharmacology | Intestine, Small - metabolism | Allergens - blood | Index Medicus
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5. Full Text Protein kinase- and lipase inhibitors of inositide metabolism deplete IP 7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity
by Rajasekaran, Subu Surendran and Illies, Christopher and Shears, Stephen B and Wang, Huanchen and Ayala, Thais S and Martins, Joilson O and Daré, Elisabetta and Berggren, Per-Olof and Barker, Christopher J
Cellular signalling, ISSN 0898-6568, 01/2018, Volume 42, pp. 127 - 133
Cricetulus | Inositol Phosphates - antagonists & inhibitors | Humans | Phosphotransferases (Phosphate Group Acceptor) - genetics | Succinimides - pharmacology | Insulin - biosynthesis | Insulin-Secreting Cells - metabolism | Adenosine Triphosphate - antagonists & inhibitors | Adenosine Triphosphate - metabolism | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Insulin-Secreting Cells - cytology | Phosphotransferases (Phosphate Group Acceptor) - metabolism | Chromones - pharmacology | Inositol Phosphates - metabolism | Insulin Secretion | Recombinant Proteins - metabolism | Cell Line | Gene Expression | Phosphotransferases (Phosphate Group Acceptor) - antagonists & inhibitors | Arsenicals - pharmacology | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Recombinant Proteins - genetics | Triazoles - pharmacology | Insulin - metabolism | Animals | Androstadienes - pharmacology | Insulin-Secreting Cells - drug effects | Receptor, Insulin - pharmacology | Wortmannin | Adenosine Diphosphate - metabolism
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6. Full Text The Mitochondrial Phosphate Carrier Interacts with Cyclophilin D and May Play a Key Role in the Permeability Transition
by Anna W. C. Leung and Pinadda Varanyuwatana and Andrew P. Halestrap
The Journal of biological chemistry, ISSN 0021-9258, 09/2008, Volume 283, Issue 39, pp. 26312 - 26323
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Mitochondria, Heart - metabolism | Cyclosporine - pharmacology | Mitochondria, Liver - metabolism | Protein Conformation - drug effects | Phosphate Transport Proteins - metabolism | Cyclophilins - metabolism | Mitochondrial ADP, ATP Translocases - antagonists & inhibitors | Mitochondrial ADP, ATP Translocases - metabolism | Cyclophilins - antagonists & inhibitors | Mitochondrial Proteins - metabolism | Protein Binding - drug effects | Dibenzocycloheptenes - pharmacology | Ethylmaleimide - pharmacology | Ion Transport - drug effects | Arsenicals - pharmacology | Mitochondrial Proteins - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Rats | Mitochondrial Membranes - metabolism | Benzoquinones - pharmacology | Animals | Cell Membrane Permeability - physiology | Cell Membrane Permeability - drug effects | Spiro Compounds - pharmacology | Protein Binding - physiology | Index Medicus
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7. Full Text Anti-estrogen resistance in breast cancer is induced by the tumor microenvironment and can be overcome by inhibiting mitochondrial function in epithelial cancer cells
by Martinez-Outschoorn, Ubaldo E and Goldberg, Allison F and Lin, Zhao and Ko, Ying-Hui and Flomenberg, Neal and Wang, Chenguang and Pavlides, Stephanos and Pestell, Richard G and Howell, Anthony and Sotgia, Federica and Lisanti, Michael P
Cancer biology & therapy, ISSN 1538-4047, 11/2011, Volume 12, Issue 10, pp. 924 - 938
Warburg Effect | TIGAR | metformin | reactive oxygen species (ROS) | cancer associated fibroblasts | microenvironment | glucose uptake | drug resistance | tumor stroma | mitochondrial oxidative phosphorylation | aerobic glycolysis | tamoxifen | oxidative stress | Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | Oxidative stress | Reactive oxygen species (ROS) | Tumor stroma | Cancer associated fibroblasts | Microenvironment | Drug resistance | Tamoxifen | Glucose uptake | Aerobic glycolysis | Metformin | Mitochondrial oxidative phosphorylation | Warburg effect | Life Sciences & Biomedicine | Oncology | Science & Technology | Estradiol - analogs & derivatives | Apoptosis - drug effects | Coculture Techniques | Humans | Ketone Bodies - metabolism | Drug Resistance, Neoplasm | Intracellular Signaling Peptides and Proteins - metabolism | Breast Neoplasms - metabolism | Fulvestrant | Estrogen Receptor Modulators - therapeutic use | Female | Estradiol - pharmacology | Fibroblasts - metabolism | Tumor Microenvironment - drug effects | Arsenic Trioxide | Estradiol - therapeutic use | Arsenicals - pharmacology | Lactic Acid - metabolism | Metformin - pharmacology | Mitochondria - metabolism | Mitochondria - drug effects | Breast Neoplasms - drug therapy | Poly(ADP-ribose) Polymerase Inhibitors | Estrogen Receptor Modulators - pharmacology | Hypoglycemic Agents - pharmacology | Oxides - pharmacology | Apoptosis Regulatory Proteins | Fibroblasts - drug effects | Tamoxifen - therapeutic use | Tamoxifen - pharmacology | Cell Line, Tumor | Doxorubicin - pharmacology | Index Medicus | Research Paper
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8. Full Text Mechanisms of Arsenical and Diamidine Uptake and Resistance in Trypanosoma brucei
by Enock Matovu and Mhairi L. Stewart and Federico Geiser and Reto Brun and Pascal Mäser and Lynsey J. M. Wallace and Richard J. Burchmore and John C. K. Enyaru and Michael P. Barrett and Ronald Kaminsky and Thomas Seebeck and Harry P. de Koning
Eukaryotic Cell, ISSN 1535-9778, 10/2003, Volume 2, Issue 5, pp. 1003 - 1008
Life Sciences & Biomedicine | Microbiology | Mycology | Science & Technology | Adenosine - pharmacokinetics | Stilbamidines - pharmacology | Pentamidine - pharmacokinetics | Inhibitory Concentration 50 | Female | Arsenicals - pharmacokinetics | Cell Death - drug effects | Inosine - pharmacology | Pentamidine - pharmacology | Diminazene - pharmacology | Hypoxanthine - pharmacology | Melarsoprol - pharmacology | Trypanosoma brucei brucei - metabolism | Arsenicals - pharmacology | Gene Silencing | Nucleoside Transport Proteins - genetics | Adenine - pharmacology | Adenosine - pharmacology | Benzamidines - pharmacology | Trypanosoma brucei brucei - drug effects | Cell Division - drug effects | Drug Resistance - genetics | Animals | Nucleoside Transport Proteins - physiology | Mice | Mutation | Index Medicus
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9. Full Text Modulation of arsenic trioxide-induced apoptosis by genistein and functionally related agents in U937 human leukaemia cells. Regulation by ROS and mitogen-activated protein kinases
by Sánchez, Yolanda and Calle, Consuelo and de Blas, Elena and Aller, Patricio
Chemico-biological interactions, ISSN 0009-2797, 2009, Volume 182, Issue 1, pp. 37 - 44
Arsenic trioxide | Genistein | Tyrosine kinase inhibitors | Apoptosis | Mitogen-activated protein kinases | U937 leukaemia cells | Pharmacology & Pharmacy | Biochemistry & Molecular Biology | Toxicology | Life Sciences & Biomedicine | Science & Technology | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Humans | Immunoblotting | Hydroquinones - pharmacology | U937 Cells | Antineoplastic Agents - pharmacology | Catechin - pharmacology | Estradiol - pharmacology | Adamantane - analogs & derivatives | Adamantane - pharmacology | Arsenicals - pharmacology | RNA, Small Interfering - pharmacology | Etoposide - pharmacology | Antioxidants - pharmacology | Drug Synergism | Oxides - pharmacology | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Genistein - pharmacology | HL-60 Cells | Catechin - analogs & derivatives | Protein Kinase Inhibitors - pharmacology | Enzyme Activation | Cell Cycle - drug effects | Microscopy, Fluorescence | Mitogen-Activated Protein Kinases - metabolism | Tyrosine | Cysteine | Catechin | Arsenic | Leukemia | Estrogen | Etoposide | Antioxidants | Analysis | Angiogenesis inhibitors | Protein kinases | Isoflavones | Index Medicus
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10. Full Text Arsenic trioxide induces Noxa-dependent apoptosis in rhabdomyosarcoma cells and synergizes with antimicrotubule drugs
by Meister, Michael Torsten and Boedicker, Cathinka and Graab, Ulrike and Hugle, Manuela and Hahn, Heidi and Klingebiel, Thomas and Fulda, Simone
Cancer letters, ISSN 0304-3835, 2016, Volume 381, Issue 2, pp. 287 - 295
Hematology, Oncology and Palliative Medicine | Arsenic trioxide | Hedgehog | Cell death | Rhabdomyosarcoma | Apoptosis | Noxa | Life Sciences & Biomedicine | Oncology | Science & Technology | Up-Regulation | Vincristine - pharmacology | Caspase Inhibitors - pharmacology | Zinc Finger Protein GLI1 - metabolism | Apoptosis - drug effects | Tubulin Modulators - pharmacology | Furans - pharmacology | Humans | Rhabdomyosarcoma - metabolism | Gene Expression Regulation, Neoplastic | Hedgehog Proteins - metabolism | Rhabdomyosarcoma - pathology | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Dose-Response Relationship, Drug | Proto-Oncogene Proteins c-bcl-2 - metabolism | Transfection | RNA Interference | Time Factors | Rhabdomyosarcoma - drug therapy | Ketones - pharmacology | Cell Survival - drug effects | Zinc Finger Protein GLI1 - genetics | Arsenicals - pharmacology | Mitochondria - metabolism | Mitochondria - drug effects | Mitochondria - pathology | Drug Synergism | Oxides - pharmacology | Signal Transduction - drug effects | Cell Line, Tumor | Rhabdomyosarcoma - genetics | Vinblastine - pharmacology | Proto-Oncogene Proteins c-bcl-2 - genetics | Arsenic | Index Medicus
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