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1. Full Text Structural determinants in phycotoxins and AChBP conferring high affinity binding and nicotinic AChR antagonism
by Yves Bourne and Zoran Radić and Rómulo Aráoz and Todd T. Talley and Evelyne Benoit and Denis Servent and Palmer Taylor and Jordi Molgó and Pascale Marchot and William A. Catterall
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2010, Volume 107, Issue 13, pp. 6076 - 6081
Spirolide and gymnodimine macrocyclic imine phycotoxins belong to an emerging class of chemical agents associated with marine algal blooms and shelfish... 
Receptors | Imines | Shellfish | Ligands | Agonists | Toxins | Pharmacology | Nicotinic receptors | Nitrogen | Oocytes | Pharmacological and structural analyses | Seafood poisoning | Acetylcholine binding protein | Nicotinic acetylcholine receptor | Marine phycotoxins | PLANKTON | acetylcholine binding protein | seafood poisoning | DINOFLAGELLATE ALEXANDRIUM-OSTENFELDII | SHELLFISH TOXINS | SPIROLIDE-C | PROTEIN | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | marine phycotoxins | AGONISTS | ACETYLCHOLINE-RECEPTOR | GYMNODIMINE | pharmacological and structural analyses | nicotinic acetylcholine receptor | REVEALS | Heterocyclic Compounds, 3-Ring - metabolism | Heterocyclic Compounds, 3-Ring - pharmacology | Nicotinic Antagonists - metabolism | Humans | Aplysia - metabolism | Crystallography, X-Ray | Acetylcholine - metabolism | Nicotinic Antagonists - pharmacology | Hydrocarbons, Cyclic - pharmacology | Imines - chemistry | Oocytes - drug effects | Carrier Proteins - chemistry | Female | Molecular Structure | Spiro Compounds - chemistry | Receptors, Nicotinic - metabolism | Marine Toxins - metabolism | Oocytes - metabolism | Imines - metabolism | Models, Molecular | Electric Organ - metabolism | Marine Toxins - pharmacology | Imines - pharmacology | Macromolecular Substances | Animals | Carrier Proteins - metabolism | Xenopus - metabolism | Marine Toxins - chemistry | Nicotinic Antagonists - chemistry | Heterocyclic Compounds, 3-Ring - chemistry | Torpedo - metabolism | Kinetics | In Vitro Techniques | Hydrocarbons, Cyclic - chemistry | Spiro Compounds - pharmacology | Hydrocarbons, Cyclic - metabolism | Spiro Compounds - metabolism | Marine toxins | Crystals | Physiological aspects | Acetylcholine | Structure | Properties | Protein binding | Index Medicus | Life Sciences | Neurons and Cognition | Biological Sciences
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2. Full Text Arabidopsis and Maize RidA Proteins Preempt Reactive Enamine/Imine Damage to Branched-Chain Amino Acid Biosynthesis in Plastids
by Thomas D. Niehaus and Thuy N.D. Nguyen and Satinder K. Gidda and Mona ElBadawi-Sidhu and Jennifer A. Lambrecht and Donald R. McCarty and Diana M. Downs and Arthur J.L. Cooper and Oliver Fiehn and Robert T. Mullen and Andrew D. Hanson
The Plant Cell, ISSN 1040-4651, 7/2014, Volume 26, Issue 7, pp. 3010 - 3022
RidA (for Reactive Intermediate Deaminase A) proteins are ubiquitous, yet their function in eukaryotes is unclear. It is known that deleting Salmonella... 
Proteins | Enzymes | Imines | Chloroplasts | Branched chain amino acids | RESEARCH ARTICLES | Root growth | Corn | Biosynthesis | Plants | Plant cells | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SACCHAROMYCES-CEREVISIAE | MEMBER | PLANT SCIENCES | CELL BIOLOGY | SALMONELLA-ENTERICA | IN-VITRO | YJGF/YER057C/UK114 FAMILY | METABOLISM | PATHWAY | ISOLEUCINE BIOSYNTHESIS | THREONINE DEHYDRATASE | L-Serine Dehydratase - genetics | Zea mays - chemistry | Metabolomics | Butyrates - metabolism | Amino Acids, Branched-Chain - metabolism | Molecular Sequence Data | Plant Roots - genetics | Aminohydrolases - genetics | Plant Shoots - chemistry | Arabidopsis Proteins - metabolism | Threonine Dehydratase - genetics | Transaminases - metabolism | Plant Proteins - metabolism | Plant Shoots - genetics | Zea mays - metabolism | Threonine Dehydratase - metabolism | Amino Acid Sequence | Zea mays - genetics | Arabidopsis Proteins - genetics | L-Serine Dehydratase - metabolism | Arabidopsis - chemistry | Plant Roots - metabolism | Transaminases - genetics | Arabidopsis - cytology | Imines - metabolism | Plant Roots - cytology | Plant Shoots - cytology | Arabidopsis - metabolism | Arabidopsis - genetics | Hydrolysis | Plant Proteins - genetics | Plastids - enzymology | Sequence Alignment | Animals | Plant Shoots - metabolism | Plant Roots - chemistry | Aminohydrolases - metabolism | Arabidopsis thaliana | Physiological aspects | Instrument industry | International economic relations
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3. Full Text Modulation of Acetaminophen-Induced Hepatotoxicity by the Xenobiotic Receptor CAR
by Jun Zhang and Wendong Huang and Steven S. Chua and Ping Wei and David D. Moore
Science, ISSN 0036-8075, 10/2002, Volume 298, Issue 5592, pp. 422 - 424
We have identified the xenobiotic receptor CAR (constitutive androstane receptor) as a key regulator of acetaminophen metabolism and hepatotoxicity. Known CAR... 
Receptors | Animals | Liver | Agonists | Reports | Mice | Automobiles | Dosage | Xenobiotics | Hepatotoxicity | Necrosis | MEDIATED INCREASES | ACTIVATION | POTENTIATION | GLUTATHIONE | MULTIDISCIPLINARY SCIENCES | CYP2B GENE | MOUSE-LIVER | MICE | TOXICITY | INDUCTION | NUCLEAR TRANSLOCATION | Phenobarbital - pharmacology | Acetaminophen - metabolism | Liver - pathology | Oxidoreductases, N-Demethylating - genetics | Cytochrome P-450 CYP3A | Glutathione - metabolism | Humans | Aryl Hydrocarbon Hydroxylases - genetics | Cytochrome P-450 Enzyme System - metabolism | Alanine Transaminase - blood | Cytochrome P-450 CYP2E1 - genetics | Cytochrome P-450 CYP2E1 - metabolism | RNA, Messenger - metabolism | Glutathione Transferase - genetics | Analgesics, Non-Narcotic - toxicity | Liver - drug effects | Time Factors | Isoenzymes - metabolism | Cytochrome P-450 CYP1A2 - genetics | Oxidoreductases, N-Demethylating - metabolism | Benzoquinones - metabolism | Acetaminophen - toxicity | Isoenzymes - genetics | Imines - metabolism | Liver - metabolism | RNA, Messenger - genetics | Glutathione Transferase - metabolism | Mice, Transgenic | Transcription Factors - antagonists & inhibitors | Androstanols - pharmacology | Receptors, Cytoplasmic and Nuclear - agonists | Receptors, Cytoplasmic and Nuclear - genetics | Analgesics, Non-Narcotic - metabolism | Transcription Factors - genetics | Cytochrome P-450 CYP1A2 - metabolism | Aryl Hydrocarbon Hydroxylases - metabolism | Mice, Knockout | Transcription Factors - metabolism | Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors | Acetylcysteine - pharmacology | Cytochrome P-450 Enzyme System - genetics | Glutathione S-Transferase pi | Pyridines - pharmacology | Transcription Factors - agonists | Receptors, Cytoplasmic and Nuclear - metabolism | Liver failure | Dosage and administration | Analgesics | Drug therapy | Acetaminophen | Drug overdose
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4. Full Text Neutral Cysteine Protease Bleomycin Hydrolase Is Essential for the Breakdown of Deiminated Filaggrin into Amino Acids
by Yayoi Kamata and Aya Taniguchi and Mami Yamamoto and Junko Nomura and Kazuhiko Ishihara and Hidenari Takahara and Toshihiko Hibino and Atsushi Takeda
Journal of Biological Chemistry, ISSN 0021-9258, 05/2009, Volume 284, Issue 19, pp. 12829 - 12836
Filaggrin is a component of the cornified cell envelope and the precursor of free amino acids acting as a natural moisturizing factor in the stratum corneum.... 
PROTEOLYTIC CLEAVAGE | EPIDERMAL DIFFERENTIATION | HUMAN SKIN | HUMAN PROFILAGGRIN | RECOMBINANT ENZYME | CORNIFIED CELL-ENVELOPE | IMMUNOHISTOCHEMICAL LOCALIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PEPTIDYLARGININE DEIMINASE | STRATUM-CORNEUM | FILAMENT-ASSOCIATED PROTEIN | Calpain - metabolism | Humans | Citrulline - metabolism | Immunoenzyme Techniques | Amino Acids - metabolism | Cysteine Endopeptidases - metabolism | Imines - chemistry | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Aminopeptidases - metabolism | Animals, Newborn | Hydrolases - metabolism | Recombinant Proteins - metabolism | Caspase 14 - metabolism | Peptide Fragments - metabolism | Imines - metabolism | Rats | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Skin - enzymology | Rats, Sprague-Dawley | Peptide Fragments - chemistry | Animals | Hydrolases - chemistry | Mice | Intermediate Filament Proteins - metabolism
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5. Full Text Bromine Is an Essential Trace Element for Assembly of Collagen IV Scaffolds in Tissue Development and Architecture
by McCall, A. Scott and Cummings, Christopher F and Bhave, Gautam and Vanacore, Roberto and Page-McCaw, Andrea and Hudson, Billy G
Cell, ISSN 0092-8674, 06/2014, Volume 157, Issue 6, pp. 1380 - 1392
Bromine is ubiquitously present in animals as ionic bromide (Br ) yet has no known essential function. Herein, we demonstrate that Br is a required cofactor... 
OXIDATION | ACIDS | ELEGANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | REACTIVITY | THIOCYANATE | INTERMEDIATE | EXTRACELLULAR-MATRIX | MUTATIONS | DROSOPHILA | BASEMENT-MEMBRANE | CELL BIOLOGY | Cell Line | Trace Elements - metabolism | Basement Membrane - ultrastructure | Bromine - metabolism | Extracellular Matrix Proteins - genetics | Humans | Imines - metabolism | Basement Membrane - metabolism | Larva - ultrastructure | Collagen - metabolism | Animals | Peroxidase - genetics | Drosophila - growth & development | Mice | Drosophila - metabolism | Bromine - deficiency | Extracellular Matrix Proteins - metabolism | Peroxidase - metabolism | Post-translational modification | Medical colleges | Architecture | Collagen | Resveratrol | Hypertension | Developmental biology
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6. Full Text The Genetic and Molecular Basis for Sunscreen Biosynthesis in Cyanobacteria
by Emily P. Balskus and Christopher T. Walsh
Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1653 - 1656
Ultraviolet UV-A and UV-B radiation is harmful to living systems, causing damage to biological macromolecules. An important strategy for dealing with UV... 
Fungi | Phosphates | Enzymes | Imines | REPORTS | Cyanobacteria | Amino acids | Multigene family | Biosynthesis | Biochemistry | Open reading frames | ORGANISMS | PATHWAY | AMINO-ACIDS | ENZYMES | MULTIDISCIPLINARY SCIENCES | SUPERFAMILY | MYCOSPORINES | GENOME | Glycine - analogs & derivatives | Multigene Family | Cyclohexanols | Ligases - genetics | Methyltransferases - metabolism | Open Reading Frames | Methyltransferases - genetics | Anabaena variabilis - genetics | Sunscreening Agents - metabolism | Anabaena variabilis - metabolism | Ultraviolet Rays | Glycine - chemistry | Adenosine Triphosphate - metabolism | Cloning, Molecular | Escherichia coli - metabolism | Nostoc - genetics | Genes, Bacterial | Nostoc - enzymology | Biocatalysis | Imines - metabolism | Anabaena variabilis - enzymology | Bacterial Proteins - genetics | Cyclohexylamines - chemistry | Glycine - biosynthesis | Ligases - metabolism | Escherichia coli - genetics | Nostoc - metabolism | Bacterial Proteins - metabolism | Physiological aspects | Research | Properties | Sunscreens (Cosmetics) | Bacteria | Sunscreen | Molecular biology | Gene expression | Macromolecules | Clusters | Strategy | Ultraviolet
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7. Full Text An Investigation of the Bioactivation Potential and Metabolism Profile of Zebrafish versus Human
by Chng, Hui Ting and Ho, Han Kiat and Yap, Chun Wei and Lam, Siew Hong and Chan, Eric Chun Yong
Journal of Biomolecular Screening, ISSN 1087-0571, 8/2012, Volume 17, Issue 7, pp. 974 - 986
The zebrafish model has been increasingly explored as an alternative model for toxicity screening of pharmaceutical drugs. However, little is understood about... 
acetaminophen | testosterone | bioactivation | reactive metabolites | zebrafish | phase II drug metabolism | fish cytochrome P450 | liver microsomes | DANIO-RERIO | CYTOCHROME-P450 | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | TOXICITY | GENE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | MICROSOMES | IN-VIVO | LARVAE | EXPRESSION | Acetaminophen - metabolism | Glutathione - metabolism | Zebrafish Proteins - metabolism | Humans | Imines - metabolism | Microsomes, Liver - metabolism | Metabolome | Aryl Hydrocarbon Hydroxylases - metabolism | Testosterone - metabolism | Animals | Glucuronosyltransferase - metabolism | Cytochrome P-450 CYP3A - metabolism | Biotransformation | Zebrafish - metabolism | Drug Evaluation, Preclinical | Oxidoreductases, N-Demethylating - metabolism | Benzoquinones - metabolism | Index Medicus
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8. Full Text Monoamine oxidase B oxidizes a novel multikinase inhibitor KW-2449 to its iminium ion and aldehyde oxidase further converts it to the oxo-piperazine form in human
by Hosogi, Jun and Ohashi, Rui and Maeda, Hiroshi and Tashiro, Satoshi and Fuse, Eiichi and Yamamoto, Yorihiro and Kuwabara, Takashi
Drug Metabolism and Pharmacokinetics, ISSN 1347-4367, 10/2017, Volume 32, Issue 5, pp. 255 - 264
(E)-1-{4-[2-(1H-Indazol-3-yl)vinyl]benzoyl}piperazine (KW-2449) is a novel multikinase inhibitor. During our clinical study, we found that KW-2449 is mainly... 
Monoamine oxidase B | Iminium ion | Hepatocyte | Piperazine | In vitro in vivo extrapolation | Aldehyde oxidase | Liver microsomes | Metabolism | In vitro in vivo extrapolation | CLEARANCE | CYTOCHROME-P450 | RAT | CATALYZED OXIDATION | GUINEA-PIG | BIOTRANSFORMATION | PHARMACOKINETICS | LIVER | PHARMACOLOGY & PHARMACY | DERIVATIVES | DRUG-METABOLISM | Humans | Microsomes, Liver - metabolism | Cytochrome P-450 Enzyme System - metabolism | Macaca fascicularis | Piperazines - metabolism | Piperazines - chemistry | Hepatocytes - metabolism | Monoamine Oxidase - chemistry | Imines - chemistry | Mitochondria - chemistry | Ions - chemistry | Indazoles - chemistry | Oxidation-Reduction | Imines - metabolism | Rats | Indazoles - metabolism | Mitochondria - metabolism | Ions - metabolism | Microsomes, Liver - chemistry | Cytochrome P-450 Enzyme System - chemistry | Animals | Aldehyde Oxidase - metabolism | Dogs | Hepatocytes - chemistry | Monoamine Oxidase - metabolism | Oxidases | Health aspects | Phosphotransferases | Drug metabolism | Enzymes | Dosage and administration | Research | Analysis
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9. Full Text Occurrence of marine algal toxins in oyster and phytoplankton samples in Daya Bay, South China Sea
by Jiang, Tianjiu and Jiang, Tao and Liu, Lei and Li, Yang and Zhang, Jing and Tan, Zhijun and Wu, Haiyan and Lu, Songhui
Chemosphere, ISSN 0045-6535, 09/2017, Volume 183, pp. 80 - 88
The occurrence and seasonal variations of marine algal toxins in phytoplankton and oyster samples in Daya Bay (DYB), South China Sea were investigated. Two... 
Okadaic acid | Shellfish toxins | Dinophysis | Domoic acid | Pectenotoxin | Pseudo-nitzschia | ACUMINATA | PSEUDO-NITZSCHIA BACILLARIOPHYCEAE | SP-NOV BACILLARIOPHYCEAE | ALEXANDRIUM-OSTENFELDII DINOPHYCEAE | PECTENOTOXIN-2 SECO ACID | GYMNODIMINE | ENVIRONMENTAL SCIENCES | DINOPHYSISTOXIN-1 | LIPOPHILIC SHELLFISH TOXINS | Bays - chemistry | Heterocyclic Compounds, 3-Ring - metabolism | Ostreidae - chemistry | Kainic Acid - analogs & derivatives | Okadaic Acid - metabolism | Imines - analysis | Pyrans - analysis | Marine Toxins - analysis | Tandem Mass Spectrometry | Pyrans - metabolism | China | Dinoflagellida - metabolism | Phytoplankton - metabolism | Phytoplankton - chemistry | Marine Toxins - metabolism | Okadaic Acid - analysis | Imines - metabolism | Environmental Monitoring - methods | Heterocyclic Compounds, 3-Ring - analysis | Water Pollutants, Chemical - analysis | Kainic Acid - metabolism | Kainic Acid - analysis | Water Pollutants, Chemical - metabolism | Animals | Hydrocarbons, Cyclic - analysis | Ostreidae - metabolism | Chromatography, Liquid - methods | Hydrocarbons, Cyclic - metabolism | Marine biology | Liquid chromatography | Marine toxins | Mass spectrometry | Amphibians | Analysis
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10. Full Text Metabolism and bioactivation of famitinib, a novel inhibitor of receptor tyrosine kinase, in cancer patients
by Xie, Cen and Zhou, Jialan and Guo, Zitao and Diao, Xingxing and Gao, Zhiwei and Zhong, Dafang and Jiang, Haoyuan and Zhang, Lijia and Chen, Xiaoyan
British Journal of Pharmacology, ISSN 0007-1188, 04/2013, Volume 168, Issue 7, pp. 1687 - 1706
Background and Purpose Famitinib is a novel multi‐targeted receptor tyrosine kinase inhibitor under development for cancer treatment. This study aims to... 
quinone‐imine | metabolism | famitinib | hepatotoxicity | bioactivation | quinone-imine | LUNG | IDENTIFICATION | RENAL-CELL CARCINOMA | STRATEGIES | IN-VITRO | ACETAMINOPHEN | LIVER | SUNITINIB | PHARMACOLOGY & PHARMACY | FULMINANT HEPATIC-FAILURE | Neoplasms - metabolism | Pyrroles - metabolism | Pyrroles - pharmacokinetics | Oxidation-Reduction | Administration, Oral | Humans | Microsomes, Liver - metabolism | Middle Aged | Cytochrome P-450 Enzyme System - metabolism | Male | Hepatocytes - metabolism | Receptor Protein-Tyrosine Kinases - metabolism | Antineoplastic Agents - metabolism | Tissue Distribution | Indoles - metabolism | Isoenzymes - metabolism | Biotransformation | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Indoles - pharmacokinetics | Antineoplastic Agents - pharmacokinetics | Hepatocytes - drug effects | Tyrosine | Cysteine | Cancer patients | Care and treatment | Metabolites | Hydroxylation | Quinone | Physiological aspects | Phenols | Liquid chromatography | Mass spectrometry | Urine | Enzymes | Metabolism | Cancer | Index Medicus | Research Papers
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11. Full Text Development of a solid-phase receptor-based assay for the detection of cyclic imines using a microsphere-flow cytometry system
by Rodríguez, Laura P and Vilariño, Natalia and Molgó, Jordi and Aráoz, Rómulo and Louzao, M. Carmen and Taylor, Palmer and Talley, Todd and Botana, Luis M
Analytical Chemistry, ISSN 0003-2700, 02/2013, Volume 85, Issue 4, pp. 2340 - 2347
Biologically active macrocycles containing a cyclic imine were isolated for the first time from aquaculture sites in Nova Scotia, Canada, during the 1990s.... 
MARINE DINOFLAGELLATE | CHEMISTRY, ANALYTICAL | DINOFLAGELLATE ALEXANDRIUM-OSTENFELDII | NEW-ZEALAND | FLUORESCENCE POLARIZATION | SHELLFISH TOXINS | STATE TRANSITIONS | BIVALVE PINNA-MURICATA | CHROMATOGRAPHY-MASS SPECTROMETRY | CHOLINERGIC RECEPTOR | ACETYLCHOLINE-BINDING-PROTEIN | Flow Cytometry - methods | Heterocyclic Compounds, 3-Ring - metabolism | Imines - analysis | Biotin - chemistry | Microspheres | Receptors, Nicotinic - chemistry | Biotin - metabolism | Carrier Proteins - chemistry | Spiro Compounds - analysis | Bungarotoxins - metabolism | Lymnaea - metabolism | Streptavidin - chemistry | Receptors, Nicotinic - metabolism | Immobilized Proteins - chemistry | Phycoerythrin - chemistry | Imines - metabolism | Bungarotoxins - analysis | Heterocyclic Compounds, 3-Ring - analysis | Animals | Carrier Proteins - metabolism | Streptavidin - metabolism | Hydrocarbons, Cyclic - analysis | Torpedo - metabolism | Immobilized Proteins - metabolism | Protein Binding | Shellfish - analysis | Hydrocarbons, Cyclic - metabolism | Spiro Compounds - metabolism | Flow cytometry | Schiff bases | Usage | Analysis | Research | Radioligand assay | Index Medicus | Life Sciences | Neurons and Cognition | spirolide | acetylcholine binding protein | gymnodimine | microsphere-based assay | α-bungarotoxin | marine phycotoxins | nicotinic acetylcholine receptor
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12. Full Text Metabolomics reveals the formation of aldehydes and iminium in gefitinib metabolism
by Liu, Xing and Lu, Yuanfu and Guan, Xinfu and Dong, Bingning and Chavan, Hemantkumar and Wang, Jin and Zhang, Yiqing and Krishnamurthy, Partha and Li, Feng
Biochemical Pharmacology, ISSN 0006-2952, 09/2015, Volume 97, Issue 1, pp. 111 - 121
Gefitinib (GEF), an inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase, is widely used for the treatment of cancers, particularly non-small... 
Metabolomics | Iminium | Gefitinib | Aldehyde | Bioactivation | DNA-ADDUCTS | CYTOCHROME-P450 | DRUG-INTERACTIONS | TOXICITY | MECHANISMS | PREGNANE-X-RECEPTOR | CELL LUNG-CANCER | IN-VITRO | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | Cytochrome P-450 CYP3A Inhibitors - pharmacology | Humans | Microsomes, Liver - metabolism | Aldehydes - metabolism | Antineoplastic Agents - metabolism | Protein Kinase Inhibitors - chemistry | Cytochrome P-450 CYP3A - genetics | Quinazolines - metabolism | Isoenzymes - metabolism | Microsomes, Liver - drug effects | Cytochrome P-450 CYP3A - chemistry | Imines - chemistry | Membrane Proteins - metabolism | Microsomes, Liver - enzymology | Molecular Structure | Quinazolines - chemistry | Recombinant Proteins - metabolism | Metabolic Detoxication, Phase II | Isoenzymes - genetics | Membrane Proteins - genetics | Imines - metabolism | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Antineoplastic Agents - chemistry | Metabolomics - methods | Mice, Knockout | Animals | Membrane Proteins - antagonists & inhibitors | Cytochrome P-450 CYP3A - metabolism | Metabolic Detoxication, Phase I | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Mice | Isoenzymes - antagonists & inhibitors | Aldehydes - chemistry | Protein Kinase Inhibitors - metabolism | Antimitotic agents | Physiological aspects | Antineoplastic agents | Index Medicus
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13. Full Text Controlled Cell Adhesion on Poly(dopamine) Interfaces Photopatterned with Non‐Fouling Brushes
by Rodriguez‐Emmenegger, Cesar and Preuss, Corinna M and Yameen, Basit and Pop‐Georgievski, Ognen and Bachmann, Michael and Mueller, Jan O and Bruns, Michael and Goldmann, Anja S and Bastmeyer, Martin and Barner‐Kowollik, Christopher
Advanced Materials, ISSN 0935-9648, 11/2013, Volume 25, Issue 42, pp. 6123 - 6127
Bioinspired poly(dopamine) (PDA) films are merged with antifouling poly(MeOEGMA) brushes utilizing a nitrile imine‐mediated tetrazole‐ene cycloaddition... 
nitrile imine‐mediated tetrazole‐ene cycloaddition (NITEC) | micropatterning | photoligation | poly(dopamine) | antifouling polymer brushes | nitrile imine-mediated tetrazole-ene cycloaddition (NITEC) | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | CLICK CHEMISTRY | BLOOD-PLASMA | MATERIALS SCIENCE, MULTIDISCIPLINARY | PROTEIN RESISTANCE | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | ION MASS-SPECTROMETRY | PHOTOCLICK CHEMISTRY | 1,3-DIPOLAR CYCLOADDITION | POLYMER BRUSHES | COATINGS | SURFACE-CHEMISTRY | Polyethylene Glycols - metabolism | Recombinant Fusion Proteins - biosynthesis | Cell Line | Green Fluorescent Proteins - metabolism | Cell Adhesion Molecules - genetics | Acrylates - chemistry | Rats | Polyethylene Glycols - chemistry | Green Fluorescent Proteins - genetics | Phosphoproteins - genetics | Phosphoproteins - metabolism | Cell Adhesion | Cell Adhesion Molecules - metabolism | Indoles - metabolism | Animals | Acrylates - metabolism | Recombinant Fusion Proteins - genetics | Polymers - chemistry | Microfilament Proteins - metabolism | Indoles - chemistry | Microfilament Proteins - genetics | Silicon - chemistry | Polymers - metabolism | Phenols | Polymers | Adhesion
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