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1. Full Text Stabilizing Alginate Confinement and Polymer Coating of CO-Releasing Molecules Supported on Iron Oxide Nanoparticles to Trigger the CO Release by Magnetic Heating
by Meyer, Hajo and Winkler, Felix and Kunz, Peter and Schmidt, Annette M and Hamacher, Alexandra and Kassack, Matthias U and Janiak, Christoph
Inorganic Chemistry, ISSN 0020-1669, 11/2015, Volume 54, Issue 23, pp. 11236 - 11246
Maghemite (Fe2O3) iron oxide nanoparticles (IONPs) were synthesized, modified with covalent surface-bound CO-releasing molecules of a... 
MACROMOLECULAR THERAPEUTICS | METAL-CARBONYLS | DESIGN | GASTRONOMY | HEME | CARBON-MONOXIDE | DEXTRAN | NITRIC-OXIDE | CHEMISTRY | DELIVERY | CHEMISTRY, INORGANIC & NUCLEAR | Phenylalanine - analogs & derivatives | Humans | Half-Life | Myoglobin - chemistry | Dextrans - chemistry | Ferric Compounds - chemistry | Polyethylene Glycols - chemistry | Carbon Monoxide - chemistry | Quaternary Ammonium Compounds - chemistry | Ruthenium - chemistry | Magnetic Phenomena | Phenylalanine - chemistry | HEK293 Cells | Water - chemistry | Antineoplastic Agents - pharmacology | Glucuronic Acid - chemistry | Polyethylenes - chemistry | Metal Nanoparticles - chemistry | Solubility | Cisplatin - pharmacology | Hexuronic Acids - chemistry | Hot Temperature | Coordination Complexes - chemistry | Dihydroxyphenylalanine - chemistry | Animals | Alginates - chemistry | Cell Line, Tumor | Horses | Carbon Monoxide - analysis | Energy Transfer | Kinetics | Nanoparticles | Research | Chemical properties | Polymers | Iron oxides | Myoglobin | Optical paths | Heating | Coating | Alginates | Assaying
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2. Full Text Characterisation and drug release performance of biodegradable chitosan–graphene oxide nanocomposites
by Justin, Richard and Chen, Biqiong
Carbohydrate Polymers, ISSN 0144-8617, 03/2014, Volume 103, Issue 1, pp. 70 - 80
Biodegradable chitosan–graphene oxide (GO) nanocomposites possess improved mechanical properties and drug delivery performance over chitosan and could prove to... 
nanocomposite | Graphene oxide | Chitosan | transdermal drug delivery | POLYMER SCIENCE | MICROSPHERES | CRYSTALLINITY | IN-VIVO DEGRADATION | CHEMISTRY, ORGANIC | LYSOZYME | MECHANICAL-PROPERTIES | DELIVERY | FILMS | N-ACETYLATED CHITOSANS | CONDUCTIVITY | CHITIN | CHEMISTRY, APPLIED | Nanocomposites - chemistry | Oxides - chemistry | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Propranolol - chemistry | Antineoplastic Agents - chemistry | Timolol - chemistry | Drug Delivery Systems | Cisplatin - chemistry | Chitosan - chemistry | Adrenergic beta-Antagonists - chemistry | Surface Properties | Hydrophobic and Hydrophilic Interactions | Indomethacin - chemistry | Graphite - chemistry | Hydrogen-Ion Concentration | Drugs | Drug delivery systems | Graphene | Graphite | Vehicles
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3. Full Text NO Releasing and Anticancer Properties of Octahedral Ruthenium-Nitrosyl Complexes with Equatorial 1 H-Indazole Ligands
by Orlowska, Ewelina and Babak, Maria V and Dömötör, Orsolya and Enyedy, Eva A and Rapta, Peter and Zalibera, Michal and Bučinský, Lukáš and Malček, Michal and Govind, Chinju and Karunakaran, Venugopal and Farid, Yusuf Chouthury Shaik and McDonnell, Tara E and Luneau, Dominique and Schaniel, Dominik and Ang, Wee Han and Arion, Vladimir B
Inorganic Chemistry, ISSN 0020-1669, 09/2018, Volume 57, Issue 17, pp. 10702 - 10717
With the aim of enhancing the biological activity of ruthenium-nitrosyl complexes, new compounds with four equatorially bound indazole ligands, namely,... 
Indazoles - chemistry | Nitric Oxide - chemistry | Cell Survival | Drug Stability | HCT116 Cells | Humans | Nitrogen Oxides - chemistry | Models, Molecular | Cisplatin - pharmacology | Antineoplastic Agents - chemistry | Ruthenium - chemistry | Blotting, Western | Ruthenium - pharmacology | Quantum Theory | Organometallic Compounds - chemical synthesis | X-Ray Diffraction | Nitrogen Oxides - pharmacology | Water - chemistry | Electrochemistry | Inhibitory Concentration 50 | Ligands | Organometallic Compounds - chemistry | Antineoplastic Agents - pharmacology | Organometallic Compounds - pharmacology | Analytical chemistry | or physical chemistry | Medicinal Chemistry | Inorganic chemistry | Chemical Sciences | Theoretical and
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4. Full Text Hesperidin attenuates cisplatin-induced acute renal injury by decreasing oxidative stress, inflammation and DNA damage
by Sahu, Bidya Dhar and Kuncha, Madhusudana and Sindhura, G. Jeevana and Sistla, Ramakrishna
Phytomedicine, ISSN 0944-7113, 03/2013, Volume 20, Issue 5, pp. 453 - 460
Nephrotoxicity is an important complication in cancer patients undergoing cisplatin therapy. Oxidative stress, inflammation and apoptosis/necrosis are the... 
Oxidative stress | Inflammation | Nephrotoxicity | Hesperidin | Cisplatin | Apoptosis | CHEMISTRY, MEDICINAL | ACID | RATS | MECHANISMS | TOXICITY | PLANT SCIENCES | INTEGRATIVE & COMPLEMENTARY MEDICINE | ANTIOXIDANT | PHARMACOLOGY & PHARMACY | Hesperidin - therapeutic use | Kidney - pathology | Rats, Wistar | Apoptosis - drug effects | Blood Urea Nitrogen | Caspase 3 - chemistry | Kidney - enzymology | Malondialdehyde - chemistry | Male | Peroxidase - chemistry | Glutathione Reductase - chemistry | Reactive Oxygen Species - chemistry | Glutathione Peroxidase - chemistry | Inflammation - drug therapy | Acute Kidney Injury - chemically induced | Cytoprotection | Kidney - drug effects | Nitric Oxide - chemistry | Rats | Superoxide Dismutase - chemistry | Animals | Tumor Necrosis Factor-alpha - chemistry | Hesperidin - chemistry | Cisplatin - adverse effects | Creatinine - blood | Kidney - chemistry | Glutathione - chemistry | DNA Damage | Oxidative Stress - drug effects | Lipid Peroxidation | Antioxidants | Complications and side effects | Care and treatment | Medicine, Botanic | Medicine, Herbal | Kidney diseases | Research | Control | DNA damage
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5. Full Text Polymer-cisplatin conjugate nanoparticles for acid-responsive drug delivery
by Aryal, Santosh and Hu, Che-Ming Jack and Zhang, Liangfang
ACS Nano, ISSN 1936-0851, 01/2010, Volume 4, Issue 1, pp. 251 - 258
We report the synthesis of novel acid-responsive therapeutic nanoparticles (NPs) with sub-100 nm size consisting of polymer-cisplatin conjugates. The... 
Polymeric nanoparticle | Stimuli-responsive | Drug delivery | Cisplatin | Controlled release | CELLS | polymeric nanoparticle | MATERIALS SCIENCE, MULTIDISCIPLINARY | COMPLEXES | DOXORUBICIN | NANOCARRIERS | NANOSCIENCE & NANOTECHNOLOGY | drug delivery | PLGA-PEG NANOPARTICLES | stimuli-responsive | CANCER | CHEMISTRY, MULTIDISCIPLINARY | controlled release | PRODRUG | EFFICACIES | RESISTANCE | ANTICANCER DRUGS | cisplatin | Cell Survival - drug effects | Nanoparticles - chemistry | Humans | Polyethylene Glycols - chemistry | Prodrugs - chemistry | Cisplatin - pharmacology | Antineoplastic Agents - chemistry | Drug Carriers - chemistry | Prodrugs - metabolism | Antineoplastic Agents - metabolism | Cisplatin - metabolism | Hydrazines - chemistry | Levulinic Acids - chemistry | Polyesters - chemistry | Cisplatin - chemistry | Endocytosis | Intracellular Space - metabolism | Antineoplastic Agents - blood | Cell Line, Tumor | Cisplatin - blood | Polymers - chemistry | Antineoplastic Agents - pharmacology | Kinetics | Hydrogen-Ion Concentration
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6. Full Text Charge-Convertible Carbon Dots for Imaging-Guided Drug Delivery with Enhanced in Vivo Cancer Therapeutic Efficiency
by Feng, Tao and Ai, Xiangzhao and An, Guanghui and Yang, Piaoping and Zhao, Yanli
ACS Nano, ISSN 1936-0851, 04/2016, Volume 10, Issue 4, pp. 4410 - 4420
Carbon dots (CDs) are remarkable nanocarriers due to their promising optical and biocompatible capabilities. However, their practical applicability in cancer... 
in vivo studies | cancer therapy | carbon dots | charge convertibility | imaging guiding | VITRO | ACID | PRO-DRUG | MATERIALS SCIENCE, MULTIDISCIPLINARY | TUMOR | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | BIODISTRIBUTION | CHEMISTRY, MULTIDISCIPLINARY | QUANTUM DOTS | PHARMACOKINETICS | POLY(ETHYLENE GLYCOL) | UP-CONVERSION NANOPARTICLES | RATIONAL DESIGN | Neoplasm Transplantation | Optical Imaging | Nanoparticles - chemistry | Humans | Polyethylene Glycols - chemistry | Carbon - chemistry | Drug Carriers - chemistry | Neoplasms, Experimental - diagnostic imaging | Tissue Distribution | Cisplatin - chemistry | Antineoplastic Agents - adverse effects | Surface Properties | Female | Antineoplastic Agents - pharmacology | Polyamines - chemistry | Cell Survival | Drug Stability | Cisplatin - pharmacology | Antineoplastic Agents - chemistry | Particle Size | Animals | Cell Line, Tumor | Cisplatin - adverse effects | Drug Liberation | Mice | Neoplasms, Experimental - drug therapy | Hydrogen-Ion Concentration
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7. Full Text Diazido Mixed‐Amine Platinum(IV) Anticancer Complexes Activatable by Visible‐Light Form Novel DNA Adducts
by Zhao, Yao and Woods, Julie A and Farrer, Nicola J and Robinson, Kim S and Pracharova, Jitka and Kasparkova, Jana and Novakova, Olga and Li, Huilin and Salassa, Luca and Pizarro, Ana M and Clarkson, Guy J and Song, Lijiang and Brabec, Viktor and Sadler, Peter J
Chemistry – A European Journal, ISSN 0947-6539, 07/2013, Volume 19, Issue 29, pp. 9578 - 9591
Platinum diam(m)ine complexes, such as cisplatin, are successful anticancer drugs, but suffer from problems of resistance and side‐effects. Photoactivatable... 
platinum | DNA binding | medicinal chemistry | photoactivity | antitumor agents | ANTITUMOR PLATINUM | RECOGNITION | TRANS-DIAMMINEDICHLOROPLATINUM(II) | CIS | CIS-DIAMMINEDICHLOROPLATINUM(II) | TRANS | CHEMISTRY, MULTIDISCIPLINARY | CISPLATIN | INTERSTRAND CROSS-LINKS | PT-195 NMR | BINDING | Pyridines - chemistry | Humans | DNA Adducts - chemistry | Crystallography, X-Ray | Prodrugs - chemistry | Cisplatin - pharmacology | Antineoplastic Agents - chemistry | Azides - chemistry | Platinum - chemistry | Chemistry, Pharmaceutical | Organoplatinum Compounds - pharmacology | Cisplatin - chemistry | DNA - chemistry | Light | Antineoplastic Agents - pharmacology | Azides - pharmacology | Organoplatinum Compounds - chemistry | Care and treatment | Amines | Chromosomal proteins | Pyridine | Analysis | DNA | Genetic research | Nucleotides | DNA-ligand interactions | Ovarian cancer | Cancer | Platinum | Deoxyribonucleic acid--DNA | Drugs | Activated | Biotechnology | Deoxyribonucleic acid | Crosslinking | Lesions | Chemical compounds | Full Papers
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8. Full Text Pt(IV) complexes as prodrugs for cisplatin
by Shi, Yi and Liu, Shu-An and Kerwood, Deborah J and Goodisman, Jerry and Dabrowiak, James C
Journal of Inorganic Biochemistry, ISSN 0162-0134, 2012, Volume 107, Issue 1, pp. 6 - 14
The antitumor effects of platinum(IV) complexes, considered prodrugs for cisplatin, are believed to be due to biological reduction of Pt(IV) to Pt(II), with... 
ANTITUMOR AGENTS | CARBOPLATIN | REDUCTION | CARBONATE | GLUTATHIONE | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTICANCER DRUG | PLATINUM(IV) COMPLEXES | ASCORBIC-ACID | BINDING | CHEMISTRY, INORGANIC & NUCLEAR | Cisplatin - analogs & derivatives | Oxidation-Reduction | DNA, Circular - chemistry | Prodrugs - chemistry | Coordination Complexes - chemistry | Platinum - chemistry | Cisplatin - chemistry | Electrophoresis, Agar Gel | Plasmids - chemistry | Ascorbic Acid - chemistry | Carbonates - chemistry | Electrophoretic Mobility Shift Assay | Glutathione - chemistry | Molecular Structure | Reducing Agents - chemistry | Antimitotic agents | Circular DNA | Carbonates | Antineoplastic agents
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9. Full Text Biocompatible Zr-based nanoscale MOFs coated with modified poly(ε-caprolactone) as anticancer drug carriers
by Filippousi, Maria and Turner, Stuart and Leus, Karen and Siafaka, Panoraia I and Tseligka, Eirini D and Vandichel, Matthias and Nanaki, Stavroula G and Vizirianakis, Ioannis S and Bikiaris, Dimitrios N and Van Der Voort, Pascal and Van Tendeloo, Gustaaf
International Journal of Pharmaceutics, ISSN 0378-5173, 07/2016, Volume 509, Issue 1-2, pp. 208 - 218
Nanoscale Zr-based metal organic frameworks (MOFs) UiO-66 and UiO-67 were studied as potential anticancer drug delivery vehicles. Two model drugs were used,... 
Polymer | Drug delivery | SEM | UiO-67 | ADF-STEM | Metal-organic frameworks/UiO-66 | MICROSPHERES | STABILITY | ENCAPSULATION | RELEASE | DELIVERY | NANOPARTICLES | IN-VITRO | METAL-ORGANIC FRAMEWORKS | CISPLATIN | DEGRADATION | PHARMACOLOGY & PHARMACY | Nanoparticles - chemistry | Humans | Coated Materials, Biocompatible - chemistry | Delayed-Action Preparations - chemistry | Polyethylene Glycols - chemistry | Caproates - chemistry | Antineoplastic Agents - administration & dosage | Antineoplastic Agents - chemistry | Drug Carriers - chemistry | Cisplatin - administration & dosage | Delayed-Action Preparations - administration & dosage | Particle Size | Paclitaxel - chemistry | Cisplatin - chemistry | Zirconium - chemistry | Cell Line, Tumor | Hydrophobic and Hydrophilic Interactions | Polymers - chemistry | Vitamin E - chemistry | Paclitaxel - administration & dosage | Drug Delivery Systems - methods | Lactones - chemistry | Antimitotic agents | Drugs | Drug delivery systems | Analysis | Catalysis | Antineoplastic agents | Vehicles | Squamous cell carcinoma | Gliomas | Polyethylene glycol | Polymer industry | Polyols | Index Medicus
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10. Full Text Regulating the anticancer properties of organometallic dendrimers using pyridylferrocene entities: Synthesis, cytotoxicity and DNA binding studies
by Govender, Preshendren and Riedel, Tina and Dyson, Paul J and Smith, Gregory S
Dalton Transactions, ISSN 1477-9226, 2016, Volume 45, Issue 23, pp. 9529 - 9539
A new series of eight first- and second-generation heterometallic ferrocenyl-derived metal-arene metallodendrimers, containing ruthenium(II) p-cymene,... 
ANGIOSTATIC TREATMENT | IN-VITRO | RUTHENIUM(II)-ARENE PTA COMPLEXES | ESTROGEN-RECEPTOR MODULATORS | HALF-SANDWICH RHODIUM | COMPOUND RAPTA-C | ARENE-RUTHENIUM COMPLEXES | STRUCTURAL-CHARACTERIZATION | POLY(PROPYLENEIMINE) DENDRITIC SCAFFOLDS | POTENTIAL ANTICANCER | CHEMISTRY, INORGANIC & NUCLEAR | Pyridines - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Models, Molecular | Cyclopentanes - chemistry | Dendrimers - chemical synthesis | Antineoplastic Agents - chemistry | Coordination Complexes - chemistry | Ruthenium - chemistry | Cisplatin - chemistry | DNA - chemistry | Schiff Bases - chemistry | HEK293 Cells | Cell Line, Tumor | Coordination Complexes - chemical synthesis | Dendrimers - chemistry | Monoterpenes - chemistry | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Benzene Derivatives - chemistry | Iridium - chemistry | Rhodium - chemistry | DNA - drug effects | Binding | Biotechnology | Kidneys | Mathematical analysis | Deoxyribonucleic acid | Metalorganic compounds | Ligands | Dimers
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11. Full Text Determinants for Simultaneous Binding of Copper and Platinum to Human Chaperone Atox1: Hitchhiking not Hijacking
by Palm-Espling, Maria E and Andersson, C. David and Björn, Erik and Linusson, Anna and Wittung-Stafshede, Pernilla and Umeå universitet and Teknisk-naturvetenskapliga fakulteten and Kemiska institutionen
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e70473
Cisplatin (CisPt) is an anticancer agent that has been used for decades to treat a variety of cancers. CisPt treatment causes many side effects due to... 
PROTEIN | MULTIDISCIPLINARY SCIENCES | COMPLEXES | METAL-METAL BONDS | METALLOCHAPERONE | CHEMISTRY | CISPLATIN RESISTANCE | BASIS-SETS | ABSORPTION | TRANSPORTER ATP7B | CELLULAR PHARMACOLOGY | Platinum - metabolism | Protein Unfolding | Humans | Protein Multimerization | Models, Molecular | Platinum - chemistry | Metallochaperones - chemistry | Multiprotein Complexes - chemistry | Copper - chemistry | Copper - metabolism | Protein Binding | Protein Conformation | Metallochaperones - metabolism | Binding Sites | Proteins | Usage | Health aspects | Chromatography | Spectroscopy | Metals | Detoxification | Cisplatin | Heavy metals | Anticancer properties | Studies | Side effects | Chemistry | Platinum | Ligands | Sequestering | Transport | Copper | Coordination compounds | Cytoplasm | Binding sites | Deoxyribonucleic acid--DNA | Cancer | Naturvetenskap | Kemi | copper-transport | biologisk kemi | Natural Sciences | Annan kemi | biological chemistry | Chemical Sciences | Other Chemistry Topics | Atox1 | Deoxyribonucleic acid | DNA
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12. Full Text Biotin Decorated Gold Nanoparticles for Targeted Delivery of a Smart-Linked Anticancer Active Copper Complex: In Vitro and in Vivo Studies
by Pramanik, Anup K and Siddikuzzaman, Siddikuzzaman and Palanimuthu, Duraippandi and Somasundaram, Kumaravel and Samuelson, Ashoka G
Bioconjugate Chemistry, ISSN 1043-1802, 12/2016, Volume 27, Issue 12, pp. 2874 - 2885
The synthesis and anticancer activity of a copper(II) diacetyl-bis(N4-methylthiosemicarbazone) complex and its nanoconjugates are reported. The copper(II)... 
DRUG-DELIVERY | COMBINATION THERAPY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, ORGANIC | TUMOR-CELLS | FUNCTIONALIZED CARBON NANOTUBES | CHEMISTRY, MULTIDISCIPLINARY | CANCER-THERAPY | QUANTUM DOTS | CISPLATIN | GLUTATHIONE | BIS(THIOSEMICARBAZONE) COMPLEXES | DIHYDROLIPOIC ACID | Gold - chemistry | Chemistry Techniques, Synthetic | Nanoparticles - chemistry | Humans | Polyethylene Glycols - chemistry | Antineoplastic Agents - administration & dosage | Antineoplastic Agents - chemistry | Nanoconjugates - administration & dosage | Coordination Complexes - chemistry | Biotin - chemistry | Xenograft Model Antitumor Assays | Thiosemicarbazones - chemistry | Animals | Copper - chemistry | Mice, Nude | Coordination Complexes - chemical synthesis | Copper - administration & dosage | Female | Drug Delivery Systems - methods | Nanoconjugates - chemistry | Thioctic Acid - chemistry
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13. Full Text Folate conjugation to polymeric micelles via boronic acid ester to deliver platinum drugs to ovarian cancer cell lines
by Scarano, Wei and Duong, Hien T. T and Lu, Hongxu and De Souza, Paul L and Stenzel, Martina H
Biomacromolecules, ISSN 1525-7797, 04/2013, Volume 14, Issue 4, pp. 962 - 975
In this study, a novel technique was used for the reversible attachment of folic acid on the surface of polymeric micelles for a tumor-specific drug delivery... 
POLYMER SCIENCE | BLOCK-COPOLYMERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPLEXES | CHEMISTRY, ORGANIC | CROSS-LINKED MICELLES | CARBON NANOTUBES | ANTITUMOR DRUGS | IN-VITRO | PENTAFLUOROPHENYL ESTERS | CISPLATIN | BINDING CONSTANTS | ANTICANCER DRUGS | Dopamine - chemistry | Cell Survival - drug effects | Cell Proliferation | Acrylates - chemistry | Boronic Acids - metabolism | Cisplatin - analogs & derivatives | Polymers - chemical synthesis | Humans | Folic Acid - chemistry | Boronic Acids - chemistry | Antineoplastic Agents - administration & dosage | Antineoplastic Agents - chemistry | Drug Carriers - chemistry | Cisplatin - administration & dosage | Cisplatin - chemistry | Micelles | Methyl Ethers - chemistry | Cell Line, Tumor | Female | Polymers - chemistry | Ovarian Neoplasms - drug therapy | Dopamine - metabolism | Index Medicus
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14. Full Text Identification of Cisplatin-Binding Proteins Using Agarose Conjugates of Platinum Compounds
by Karasawa, Takatoshi and Sibrian-Vazquez, Martha and Strongin, Robert M and Steyger, Peter S
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, p. e66220
Cisplatin is widely used as an antineoplastic drug, but its ototoxic and nephrotoxic side-effects, as well as the inherent or acquired resistance of some... 
HAIR-CELLS | CARBOPLATIN | CHAPERONE-ACTIVITY | CRYSTAL-STRUCTURE | DNA | MULTIDISCIPLINARY SCIENCES | INDUCED OTOTOXICITY | CANCER | MASS-SPECTROMETRY | STATISTICAL-MODEL | CHILDREN | Ribosomal Proteins - chemistry | Adenosine Triphosphatases - isolation & purification | Epithelial Cells - chemistry | Glycoconjugates - chemistry | Antineoplastic Agents - chemical synthesis | Calreticulin - isolation & purification | Membrane Glycoproteins - chemistry | Valosin Containing Protein | Kidney Tubules, Proximal - chemistry | Cell Cycle Proteins - chemistry | Cisplatin - chemistry | HSP90 Heat-Shock Proteins - chemistry | HSP90 Heat-Shock Proteins - isolation & purification | Nonmuscle Myosin Type IIA - chemistry | Epithelial Cells - cytology | Cell Line | Kidney Tubules, Proximal - cytology | Cell Cycle Proteins - isolation & purification | Membrane Glycoproteins - isolation & purification | Cisplatin - analogs & derivatives | Cell Extracts - chemistry | Antineoplastic Agents - chemistry | Glycoconjugates - chemical synthesis | Organ of Corti - chemistry | Calreticulin - chemistry | Nonmuscle Myosin Type IIA - isolation & purification | Ribosomal Proteins - isolation & purification | Animals | Sepharose - chemistry | Organ of Corti - cytology | Protein Binding | Adenosine Triphosphatases - chemistry | Mice | Cisplatin - chemical synthesis | Complications and side effects | Drug interactions | Physiological aspects | Dosage and administration | Research | Binding proteins | Cisplatin | Pediatrics | Oxidative stress | Hsp90 protein | Conjugates | Toxicity | Lung cancer | Cytotoxicity | Selectivity | Proteins | Spectrometry | Calreticulin | Platinum compounds | Platinum | Chlorides | Myosin | Cell cycle | Deoxyribonucleic acid--DNA | Killing | Binding | Gel electrophoresis | Heat shock proteins | Hearing impairment | Side effects | Cochlea | Mutation | Protein interaction | Ototoxicity | Cancer | Apoptosis | Amino groups | Kidney transplantation | Heat shock | Deoxyribonucleic acid
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