Correction to Synthesis and SAR of 5-Amino- and 5-(Aminomethyl)benzofuran Histamine H3 Receptor Antagonists with Improved Potency (Unknown)
- New search for: Sun, Minghua
- New search for: Zhao, Chen
- New search for: Gfesser, Gregory A.
- New search for: Thiffault, Christine
- New search for: Miller, Thomas R.
- New search for: Marsh, Kennan
- New search for: Wetter, Jill
- New search for: Curtis, Michael
- New search for: Faghih, Ramin
- New search for: Esbenshade, Timothy A.
- New search for: Hancock, Arthur A.
- New search for: Cowart, Marlon
- New search for: Sun, Minghua
- New search for: Zhao, Chen
- New search for: Gfesser, Gregory A.
- New search for: Thiffault, Christine
- New search for: Miller, Thomas R.
- New search for: Marsh, Kennan
- New search for: Wetter, Jill
- New search for: Curtis, Michael
- New search for: Faghih, Ramin
- New search for: Esbenshade, Timothy A.
- New search for: Hancock, Arthur A.
- New search for: Cowart, Marlon
In:
Journal of Medicinal Chemistry
;
55
, 1
;
563
;
2012
- Article (Journal) / Electronic Resource
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Title:Correction to Synthesis and SAR of 5-Amino- and 5-(Aminomethyl)benzofuran Histamine H3 Receptor Antagonists with Improved Potency
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Additional title:J. Med. Chem.
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Contributors:Sun, Minghua ( author ) / Zhao, Chen ( author ) / Gfesser, Gregory A. ( author ) / Thiffault, Christine ( author ) / Miller, Thomas R. ( author ) / Marsh, Kennan ( author ) / Wetter, Jill ( author ) / Curtis, Michael ( author ) / Faghih, Ramin ( author ) / Esbenshade, Timothy A. ( author )
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Published in:Journal of Medicinal Chemistry ; 55, 1 ; 563
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Publisher:
- New search for: American Chemical Society
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Publication date:2012-01-12
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ISSN:
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Coden:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:Unknown
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Source:
Table of contents – Volume 55, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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Transition in Leadership: Opportunities and ChallengesWang, Shaomeng / Georg, Gunda I. et al. | 2012
- 2
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Low Molecular Weight Phosphotyrosine Protein Phosphatases as Emerging Targets for the Design of Novel Therapeutic AgentsMaccari, Rosanna / Ottanà, Rosaria et al. | 2012
- 23
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Synthesis, Biological Evaluation, and Docking Studies of Tetrahydrofuran- Cyclopentanone- and Cyclopentanol-Based Ligands Acting at Adrenergic α1- and Serotonine 5-HT1A ReceptorsPrandi, Adolfo / Franchini, Silvia / Manasieva, Leda Ivanova / Fossa, Paola / Cichero, Elena / Marucci, Gabriella / Buccioni, Michela / Cilia, Antonio / Pirona, Lorenza / Brasili, Livio et al. | 2012
- 23
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Synthesis, Biological Evaluation, and Docking Studies of Tetrahydrofuran- Cyclopentanone- and Cyclopentanol-Based Ligands Acting at Adrenergic alpha ~1- and Serotonine 5-HT~1~A ReceptorsPrandi, A. / Franchini, S. / Manasieva, L.I. / Fossa, P. / Cichero, E. / Marucci, G. / Buccioni, M. / Cilia, A. / Pirona, L. / Brasili, L. et al. | 2012
- 37
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Synthesis, Characterization and Biological Evaluation of Ureidofibrate-Like Derivatives Endowed with Peroxisome Proliferator-Activated Receptor ActivityPorcelli, L. / Gilardi, F. / Laghezza, A. / Piemontese, L. / Mitro, N. / Azzariti, A. / Altieri, F. / Cervoni, L. / Fracchiolla, G. / Giudici, M. et al. | 2012
- 55
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Studies toward Novel Peptidomimetic Inhibitors of Thioredoxin–Thioredoxin Reductase SystemKłossowski, Szymon / Muchowicz, Angelika / Firczuk, Małgorzata / Świech, Marta / Redzej, Adam / Golab, Jakub / Ostaszewski, Ryszard et al. | 2012
- 68
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Ethionamide Boosters. 2. Combining Bioisosteric Replacement and Structure-Based Drug Design To Solve Pharmacokinetic Issues in a Series of Potent 1,2,4-Oxadiazole EthR InhibitorsFlipo, Marion / Desroses, Matthieu / Lecat-Guillet, Nathalie / Villemagne, Baptiste / Blondiaux, Nicolas / Leroux, Florence / Piveteau, Catherine / Mathys, Vanessa / Flament, Marie-Pierre / Siepmann, Juergen et al. | 2012
- 84
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Conicasterol E, a Small Heterodimer Partner Sparing Farnesoid X Receptor Modulator Endowed with a Pregnane X Receptor Agonistic Activity, from the Marine Sponge Theonella swinhoeiSepe, Valentina / Ummarino, Raffaella / D’Auria, Maria Valeria / Chini, Maria Giovanna / Bifulco, Giuseppe / Renga, Barbara / D’Amore, Claudio / Debitus, Cécile / Fiorucci, Stefano / Zampella, Angela et al. | 2012
- 94
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Myelin Imaging Compound (MIC) Enhanced Magnetic Resonance Imaging of MyelinationFrullano, Luca / Zhu, Junqing / Wang, Changning / Wu, Chunying / Miller, Robert H. / Wang, Yanming et al. | 2012
- 106
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Bivalent Smac Mimetics with a Diazabicyclic Core as Highly Potent Antagonists of XIAP and cIAP1/2 and Novel Anticancer AgentsPeng, Yuefeng / Sun, Haiying / Lu, Jianfeng / Liu, Liu / Cai, Qian / Shen, Rong / Yang, Chao-Yie / Yi, Han / Wang, Shaomeng et al. | 2012
- 115
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Strategies to Mitigate the Bioactivation of 2-Anilino-7-Aryl-Pyrrolo[2,1-f][1,2,4]triazines: Identification of Orally Bioavailable, Efficacious ALK InhibitorsMesaros, Eugen F. / Thieu, Tho V. / Wells, Gregory J. / Zificsak, Craig A. / Wagner, Jason C. / Breslin, Henry J. / Tripathy, Rabindranath / Diebold, James L. / McHugh, Robert J. / Wohler, Ashley T. et al. | 2012
- 126
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In Silico Assay for Assessing Phospholipidosis Potential of Small Druglike Molecules: Training, Validation, and Refinement Using Several Data SetsFischer, Holger / Atzpodien, Elke-Astrid / Csato, Miklos / Doessegger, Lucette / Lenz, Barbara / Schmitt, Georg / Singer, Thomas et al. | 2012
- 140
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Discovery of a Novel Class of Orally Active Trypanocidal N-Myristoyltransferase InhibitorsBrand, Stephen / Cleghorn, Laura A. T. / McElroy, Stuart P. / Robinson, David A. / Smith, Victoria C. / Hallyburton, Irene / Harrison, Justin R. / Norcross, Neil R. / Spinks, Daniel / Bayliss, Tracy et al. | 2012
- 153
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α-Aryl-N-alkyl Nitrones, as Potential Agents for Stroke Treatment: Synthesis, Theoretical Calculations, Antioxidant, Anti-inflammatory, Neuroprotective, and Brain–Blood Barrier Permeability PropertiesChioua, Mourad / Sucunza, David / Soriano, Elena / Hadjipavlou-Litina, Dimitra / Alcázar, Alberto / Ayuso, Irene / Oset-Gasque, María Jesús / González, María Pilar / Monjas, Leticia / Rodríguez-Franco, María Isabel et al. | 2012
- 153
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alpha -Aryl-N-alkyl Nitrones, as Potential Agents for Stroke Treatment: Synthesis, Theoretical Calculations, Antioxidant, Antiinflammatory, Neuroprotective, and Brain-Blood Barrier Permeability PropertiesChioua, M. / Sucunza, D. / Soriano, E. / Hadjipavlou-Litina, D. / Alcazar, A. / Ayuso, I. / Oset-Gasque, M.J. / Gonzalez, M.P. / Monjas, L. / Rodriguez-Franco, M.I. et al. | 2012
- 169
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Discovery of Kinase Spectrum Selective Macrocycle (16E)-14-Methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene (SB1317/TG02), a Potent Inhibitor of Cyclin Dependent Kinases (CDKs), Janus Kinase 2 (JAK2), and Fms-like Tyrosine Kinase-3 (FLT3) for the Treatment of CancerWilliam, Anthony D. / Lee, Angeline C.-H. / Goh, Kee Chuan / Blanchard, Stéphanie / Poulsen, Anders / Teo, Ee Ling / Nagaraj, Harish / Lee, Chai Ping / Wang, Haishan / Williams, Meredith et al. | 2012
- 197
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Discovery of a Potent and Orally Bioavailable Benzolactam-Derived Inhibitor of Polo-Like Kinase 1 (MLN0905)Duffey, Matthew O. / Vos, Tricia J. / Adams, Ruth / Alley, Jennifer / Anthony, Justin / Barrett, Cynthia / Bharathan, Indu / Bowman, Douglas / Bump, Nancy J. / Chau, Ryan et al. | 2012
- 209
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Molecular Basis of Structure–Activity Relationships between Salphen Metal Complexes and Human Telomeric DNA QuadruplexesCampbell, Nancy H. / Karim, Nurul H. Abd / Parkinson, Gary N. / Gunaratnam, Mekala / Petrucci, Vanessa / Todd, Alan K. / Vilar, Ramon / Neidle, Stephen et al. | 2012
- 223
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A New Generation of Radiofluorinated Pyrimidine-2,4,6-triones as MMP-Targeted Radiotracers for Positron Emission TomographySchrigten, Daniela / Breyholz, Hans-Jörg / Wagner, Stefan / Hermann, Sven / Schober, Otmar / Schäfers, Michael / Haufe, Günter / Kopka, Klaus et al. | 2012
- 233
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Analogues of Orphan Nuclear Receptor Small Heterodimer Partner Ligand and Apoptosis Inducer (E)-4-[3-(1-Adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic Acid. 2. Impact of 3-Chloro Group Replacement on Inhibition of Proliferation and Induction of Apoptosis of Leukemia and Cancer Cell LinesXia, Zebin / Correa, Ricardo G. / Das, Jayanta K. / Farhana, Lulu / Castro, David J. / Yu, Jinghua / Oshima, Robert G. / Fontana, Joseph A. / Reed, John C. / Dawson, Marcia I. et al. | 2012
- 250
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Cyclobutane Derivatives As Novel Nonpeptidic Small Molecule Agonists of Glucagon-Like Peptide-1 ReceptorLiu, Qing / Li, Na / Yuan, Yunyun / Lu, Huili / Wu, Xiaoyan / Zhou, Caihong / He, Min / Su, Haoran / Zhang, Meng / Wang, Jia et al. | 2012
- 268
-
Discovery of a Novel and Potent Class of F. tularensis Enoyl-Reductase (FabI) Inhibitors by Molecular Shape and Electrostatic MatchingHevener, Kirk E. / Mehboob, Shahila / Su, Pin-Chih / Truong, Kent / Boci, Teuta / Deng, Jiangping / Ghassemi, Mahmood / Cook, James L. / Johnson, Michael E. et al. | 2012
- 268
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Discovery of a Novel and Potent Class of F. tularensis Enoyl-Reductase (Fabl) Inhibitors by Molecular Shape and Electrostatic MatchingHevener, K.E. / Mehboob, S. / Su, P.-C. / Truong, K. / Boci, T. / Deng, J. / Ghassemi, M. / Cook, J.L. / Johnson, M.E. et al. | 2012
- 280
-
Comparative Study of the Affinity and Metabolism of Type I and Type II Binding Quinoline Carboxamide Analogues by Cytochrome P450 3A4Dahal, Upendra P. / Joswig-Jones, Carolyn / Jones, Jeffrey P. et al. | 2012
- 291
-
Malaria-Infected Mice Are Completely Cured by One 6 mg/kg Oral Dose of a New Monomeric Trioxane Sulfide Combined with MefloquineSlack, Rachel D. / Mott, Bryan T. / Woodard, Lauren E. / Tripathi, Abhai / Sullivan, David / Nenortas, Elizabeth / Girdwood, Sonya C. T. / Shapiro, Theresa A. / Posner, Gary H. et al. | 2012
- 297
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Stilbene–Chalcone Hybrids: Design, Synthesis, and Evaluation as a New Class of Antimalarial Scaffolds That Trigger Cell Death through Stage Specific ApoptosisSharma, Naina / Mohanakrishnan, Dinesh / Shard, Amit / Sharma, Abhishek / Saima / Sinha, Arun K. / Sahal, Dinkar et al. | 2012
- 312
-
Structure–Activity Relationships for Amide-, Carbamate-, And Urea-Linked Analogues of the Tuberculosis Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)Blaser, Adrian / Palmer, Brian D. / Sutherland, Hamish S. / Kmentova, Iveta / Franzblau, Scott G. / Wan, Baojie / Wang, Yuehong / Ma, Zhenkun / Thompson, Andrew M. / Denny, William A. et al. | 2012
- 327
-
Piperazine-2,3-dicarboxylic Acid Derivatives as Dual Antagonists of NMDA and GluK1-Containing Kainate ReceptorsIrvine, Mark W. / Costa, Blaise M. / Dlaboga, Daniel / Culley, Georgia R. / Hulse, Richard / Scholefield, Caroline L. / Atlason, Palmi / Fang, Guangyu / Eaves, Richard / Morley, Richard et al. | 2012
- 342
-
Structure–Activity Relationships of Truncated C2- or C8-Substituted Adenosine Derivatives as Dual Acting A2A and A3 Adenosine Receptor LigandsHou, Xiyan / Majik, Mahesh S. / Kim, Kyunglim / Pyee, Yuna / Lee, Yoonji / Alexander, Varughese / Chung, Hwa-Jin / Lee, Hyuk Woo / Chandra, Girish / Lee, Jin Hee et al. | 2012
- 357
-
(1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent γ-Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine AddictionPan, Yue / Gerasimov, Madina R. / Kvist, Trine / Wellendorph, Petrine / Madsen, Karsten K. / Pera, Elena / Lee, Hyunbeom / Schousboe, Arne / Chebib, Mary / Bräuner-Osborne, Hans et al. | 2012
- 357
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(1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent gamma -Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine AddictionPan, Y. / Gerasimov, M.R. / Kvist, T. / Wellendorph, P. / Madsen, K.K. / Pera, E. / Lee, H. / Schousboe, A. / Chebib, M. / Brauner-Osborne, H. et al. | 2012
- 367
-
Design, Synthesis, and Biological Evaluation of Potent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2Reddy, P. V. Narasimha / Jensen, Katherine C. / Mesecar, Andrew D. / Fanwick, Phillip E. / Cushman, Mark et al. | 2012
- 378
-
Chemical Modification of the Multitarget Neuroprotective Compound FisetinChiruta, Chandramouli / Schubert, David / Dargusch, Richard / Maher, Pamela et al. | 2012
- 390
-
Synthesis, Biological Evaluation, And Molecular Modeling of Chalcone Derivatives As Potent Inhibitors of Mycobacterium tuberculosis Protein Tyrosine Phosphatases (PtpA and PtpB)Chiaradia, Louise Domeneghini / Martins, Priscila Graziela Alves / Cordeiro, Marlon Norberto Sechini / Guido, Rafael Victorio Carvalho / Ecco, Gabriela / Andricopulo, Adriano Defini / Yunes, Rosendo Augusto / Vernal, Javier / Nunes, Ricardo José / Terenzi, Hernán et al. | 2012
- 403
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7,8-Dichloro-1-oxo- beta -carbolines as a Versatile Scaffold for the Development of Potent and Selective Kinase Inhibitors with Unusual Binding ModesHuber, K. / Brault, L. / Fedorov, O. / Gasser, C. / Filippakopoulos, P. / Bullock, A.N. / Fabbro, D. / Trappe, J. / Schwaller, J. / Knapp, S. et al. | 2012
- 403
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7,8-Dichloro-1-oxo-β-carbolines as a Versatile Scaffold for the Development of Potent and Selective Kinase Inhibitors with Unusual Binding ModesHuber, Kilian / Brault, Laurent / Fedorov, Oleg / Gasser, Christelle / Filippakopoulos, Panagis / Bullock, Alex N. / Fabbro, Doriano / Trappe, Jörg / Schwaller, Jürg / Knapp, Stefan et al. | 2012
- 414
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Optimization of 5-Pyridazin-3-one Phenoxypropylamines as Potent, Selective Histamine H3 Receptor Antagonists with Potent Cognition Enhancing ActivityTao, Ming / Aimone, Lisa D. / Huang, Zeqi / Mathiasen, Joanne / Raddatz, Rita / Lyons, Jacquelyn / Hudkins, Robert L. et al. | 2012
- 424
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Potent Galloyl-Based Selective Modulators Targeting Multidrug Resistance Associated Protein 1 and P-glycoproteinPellicani, Raffaella Zoe / Stefanachi, Angela / Niso, Mauro / Carotti, Angelo / Leonetti, Francesco / Nicolotti, Orazio / Perrone, Roberto / Berardi, Francesco / Cellamare, Saverio / Colabufo, Nicola Antonio et al. | 2012
- 437
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Boranophosphate Isoster Controls P2Y-Receptor Subtype Selectivity and Metabolic Stability of Dinucleoside Polyphosphate AnaloguesYelovitch, Shir / Camden, Jean / Weisman, Gary A. / Fischer, Bilha et al. | 2012
- 449
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Design, Synthesis, and Anaplastic Lymphoma Kinase (ALK) Inhibitory Activity for a Novel Series of 2,4,8,22-Tetraazatetracyclo[14.3.1.13,7.19,13]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene MacrocyclesBreslin, Henry J. / Lane, Brandon M. / Ott, Gregory R. / Ghose, Arup K. / Angeles, Thelma S. / Albom, Mark S. / Cheng, Mangeng / Wan, Weihua / Haltiwanger, R. Curtis / Wells-Knecht, Kevin J. et al. | 2012
- 465
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Nonquaternary Reactivators for Organophosphate-Inhibited CholinesterasesKalisiak, Jarosław / Ralph, Erik C. / Cashman, John R. et al. | 2012
- 475
-
Synthesis and Evaluation of 1,5-Disubstituted Tetrazoles as Rigid Analogues of Combretastatin A-4 with Potent Antiproliferative and Antitumor ActivityRomagnoli, Romeo / Baraldi, Pier Giovanni / Salvador, Maria Kimatrai / Preti, Delia / Aghazadeh Tabrizi, Mojgan / Brancale, Andrea / Fu, Xian-Hua / Li, Jun / Zhang, Su-Zhan / Hamel, Ernest et al. | 2012
- 489
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Cyclic Hydroxyamidines as Amide Isosteres: Discovery of Oxadiazolines and Oxadiazines as Potent and Highly Efficacious γ-Secretase Modulators in VivoSun, Zhong-Yue / Asberom, Theodros / Bara, Thomas / Bennett, Chad / Burnett, Duane / Chu, Inhou / Clader, John / Cohen-Williams, Mary / Cole, David / Czarniecki, Michael et al. | 2012
- 489
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Cyclic Hydroxyamidines as Amide Isosteres: Discovery of Oxadiazolines and Oxadiazines as Potent and Highly Efficacious gamma -Secretase Modulators in VivoSun, Z.-Y. / Asberom, T. / Bara, T. / Bennett, C. / Burnett, D. / Chu, I. / Clader, J. / Cohen-Williams, M. / Cole, D. / Czarniecki, M. et al. | 2012
- 503
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Niphatenones, Glycerol Ethers from the Sponge Niphates digitalis Block Androgen Receptor Transcriptional Activity in Prostate Cancer Cells: Structure Elucidation, Synthesis, and Biological ActivityMeimetis, Labros G. / Williams, David E. / Mawji, Nasrin R. / Banuelos, Carmen A. / Lal, Aaron A. / Park, Jacob J. / Tien, Amy H. / Fernandez, Javier Garcia / de Voogd, Nicole J. / Sadar, Marianne D. et al. | 2012
- 515
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ADME-Guided Design and Synthesis of Aryloxanyl Pyrazolone Derivatives To Block Mutant Superoxide Dismutase 1 (SOD1) Cytotoxicity and Protein Aggregation: Potential Application for the Treatment of Amyotrophic Lateral SclerosisChen, Tian / Benmohamed, Radhia / Kim, Jinho / Smith, Karen / Amante, Daniel / Morimoto, Richard I. / Kirsch, Donald R. / Ferrante, Robert J. / Silverman, Richard B. et al. | 2012
- 528
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Diarylpropionitrile (DPN) Enantiomers: Synthesis and Evaluation of Estrogen Receptor β-Selective LigandsCarroll, Vincent M. / Jeyakumar, M. / Carlson, Kathryn E. / Katzenellenbogen, John A. et al. | 2012
- 528
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Diarylpropionitrile (DPN) Enantiomers: Synthesis and Evaluation of Estrogen Receptor beta -Selective LigandsCarroll, V.M. / Jeyakumar, M. / Carlson, K.E. / Katzenellenbogen, J.A. et al. | 2012
- 538
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Evaluation of Molecular Modeling of Agonist Binding in Light of the Crystallographic Structure of an Agonist-Bound A2A Adenosine ReceptorDeflorian, Francesca / Kumar, T. Santhosh / Phan, Khai / Gao, Zhan-Guo / Xu, Fei / Wu, Huixian / Katritch, Vsevolod / Stevens, Raymond C. / Jacobson, Kenneth A. et al. | 2012
- 553
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Design, Synthesis, and Evaluation of Thiol-Activated Sources of Sulfur Dioxide (SO2) as Antimycobacterial AgentsMalwal, Satish R. / Sriram, Dharmarajan / Yogeeswari, Perumal / Konkimalla, V. Badireenath / Chakrapani, Harinath et al. | 2012
- 558
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Synthesis of Rocaglamide Hydroxamates and Related Compounds as Eukaryotic Translation Inhibitors: Synthetic and Biological StudiesRodrigo, Christina M. / Cencic, Regina / Roche, Stéphane P. / Pelletier, Jerry / Porco, John A. et al. | 2012
- 563
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Correction to Synthesis and SAR of 5-Amino- and 5-(Aminomethyl)benzofuran Histamine H3 Receptor Antagonists with Improved PotencySun, Minghua / Zhao, Chen / Gfesser, Gregory A. / Thiffault, Christine / Miller, Thomas R. / Marsh, Kennan / Wetter, Jill / Curtis, Michael / Faghih, Ramin / Esbenshade, Timothy A. et al. | 2012
- 564
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Correction to Tricyclic Series of Heat Shock Protein 90 (Hsp90) Inhibitors Part I: Discovery of Tricyclic Imidazo[4,5-c]pyridines as Potent Inhibitors of the Hsp90 Molecular ChaperoneVallée, François / Carrez, Chantal / Pilorge, Fabienne / Dupuy, Alain / Parent, Annick / Bertin, Luc / Thompson, Fabienne / Ferrari, Paul / Fassy, Florence / Lamberton, Annabelle et al. | 2012
- 565
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Correction to Targeting the Binding Function 3 (BF3) Site of the Human Androgen Receptor through Virtual ScreeningLack, Nathan A. / Axerio-Cilies, Peter / Tavassoli, Peyman / Han, Frank Q. / Chan, Ka Hong / Feau, Clementine / LeBlanc, Eric / Guns, Emma Tomlinson / Guy, R. Kiplin / Rennie, Paul S. et al. | 2012