Artigos de revistas sobre o tema "Fluorogenic dyes"
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Pham, Ha H., Christopher Szent-Gyorgyi, Wendy L. Brotherton, Brigitte F. Schmidt, Kimberly J. Zanotti, Alan S. Waggoner e Bruce A. Armitage. "Bichromophoric dyes for wavelength shifting of dye-protein fluoromodules". Organic & Biomolecular Chemistry 13, n.º 12 (2015): 3699–710. http://dx.doi.org/10.1039/c4ob02522a.
Texto completo da fonteMartin, Annabell, e Pablo Rivera Fuentes. "A Baldwin-favored Cyclization Inspires the Development of Fluorogenic Polymethine Dyes for Bioimaging". CHIMIA 78, n.º 4 (24 de abril de 2024): 196–99. http://dx.doi.org/10.2533/chimia.2024.196.
Texto completo da fonteMamaeva, Anastasiya A., Vladimir I. Martynov, Sergey M. Deyev e Alexey A. Pakhomov. "Comparison of Colorimetric and Fluorometric Chemosensors for Protein Concentration Determination and Approaches for Estimation of Their Limits of Detection". Chemosensors 10, n.º 12 (17 de dezembro de 2022): 542. http://dx.doi.org/10.3390/chemosensors10120542.
Texto completo da fonteKrell, Katja, e Hans-Achim Wagenknecht. "Fluorogenic and Bioorthogonal Modification of RNA Using Photoclick Chemistry". Biomolecules 10, n.º 3 (21 de março de 2020): 480. http://dx.doi.org/10.3390/biom10030480.
Texto completo da fonteMartin, Annabell, e Pablo Rivera-Fuentes. "Fluorogenic polymethine dyes by intramolecular cyclization". Current Opinion in Chemical Biology 80 (junho de 2024): 102444. http://dx.doi.org/10.1016/j.cbpa.2024.102444.
Texto completo da fonteLi, Chenge, Marie-Aude Plamont, Hanna L. Sladitschek, Vanessa Rodrigues, Isabelle Aujard, Pierre Neveu, Thomas Le Saux, Ludovic Jullien e Arnaud Gautier. "Dynamic multicolor protein labeling in living cells". Chemical Science 8, n.º 8 (2017): 5598–605. http://dx.doi.org/10.1039/c7sc01364g.
Texto completo da fonteBruchez, Marcel P. "Dark dyes–bright complexes: fluorogenic protein labeling". Current Opinion in Chemical Biology 27 (agosto de 2015): 18–23. http://dx.doi.org/10.1016/j.cbpa.2015.05.014.
Texto completo da fonteQi, Jianjun, e Ching-Hsuan Tung. "Development of benzothiazole ‘click-on’ fluorogenic dyes". Bioorganic & Medicinal Chemistry Letters 21, n.º 1 (janeiro de 2011): 320–23. http://dx.doi.org/10.1016/j.bmcl.2010.11.009.
Texto completo da fonteGu, Lingyue, Kévin Renault, Anthony Romieu, Jean-Alexandre Richard e Rajavel Srinivasan. "Synthesis and spectral properties of 6′-triazolyl-dihydroxanthene-hemicyanine fused near-infrared dyes". New Journal of Chemistry 44, n.º 28 (2020): 12208–15. http://dx.doi.org/10.1039/d0nj01724h.
Texto completo da fonteKarpenko, Iuliia A., Yosuke Niko, Viktor P. Yakubovskyi, Andriy O. Gerasov, Dominique Bonnet, Yuriy P. Kovtun e Andrey S. Klymchenko. "Push–pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand–receptor interactions". Journal of Materials Chemistry C 4, n.º 14 (2016): 3002–9. http://dx.doi.org/10.1039/c5tc03411f.
Texto completo da fonteWang, Xiaoqing, Qingsong Liu, Fen Qi, Lin Li, Hai-Dong Yu, Zhipeng Liu e Wei Huang. "Benzothiazole–pyrimidine-based BODIPY analogues: promising luminophores with fluorescence sensing and imaging ability and asymmetrization-induced solid-state emission". Dalton Transactions 45, n.º 43 (2016): 17274–80. http://dx.doi.org/10.1039/c6dt03469a.
Texto completo da fonteKormos, Attila, Alexandra Egyed, Jasmine M. Olvany, Ágnes Szatmári, Adrienn Biró, Zsóka Csorba, Péter Kele e Krisztina Németh. "A Bioorthogonal Double Fluorogenic Probe to Visualize Protein–DNA Interaction". Chemosensors 10, n.º 1 (17 de janeiro de 2022): 37. http://dx.doi.org/10.3390/chemosensors10010037.
Texto completo da fonteLow, Michelle, Khin Yin Win, Enyi Ye, Shuhua Liu, Soon Huat Ng, Xiaoqun Zhou e Ming-Yong Han. "Fluorogenic Quantification of Albumin". Australian Journal of Chemistry 67, n.º 10 (2014): 1382. http://dx.doi.org/10.1071/ch14083.
Texto completo da fonteStensrud, Kenneth F., Kimberly J. Zanotti, Alan S. Waggoner e Bruce A. Armitage. "Spectral Properties of Fluorogenic Thiophene-derived Triarylmethane Dyes". Photochemistry and Photobiology 95, n.º 1 (23 de novembro de 2018): 406–10. http://dx.doi.org/10.1111/php.13037.
Texto completo da fonteLiu, Pei, Vincent Grenier, Wootack Hong, Vikram R. Muller e Evan W. Miller. "Fluorogenic Targeting of Voltage-Sensitive Dyes to Neurons". Journal of the American Chemical Society 139, n.º 48 (20 de novembro de 2017): 17334–40. http://dx.doi.org/10.1021/jacs.7b07047.
Texto completo da fonteSokolov, A. I., A. A. Gorshkova, N. S. Baleeva e M. S. Baranov. "Keto-Analogs of Arylidene-Imidazolones as Fluorogenic Dyes". Russian Journal of Bioorganic Chemistry 48, n.º 6 (dezembro de 2022): 1367–71. http://dx.doi.org/10.1134/s1068162022060243.
Texto completo da fonteBhasikuttan, Achikanath C., e Jyotirmayee Mohanty. "Targeting G-quadruplex structures with extrinsic fluorogenic dyes: promising fluorescence sensors". Chemical Communications 51, n.º 36 (2015): 7581–97. http://dx.doi.org/10.1039/c4cc10030a.
Texto completo da fonteVasilev, Aleksey A., Meglena I. Kandinska, Stanimir S. Stoyanov, Stanislava B. Yordanova, David Sucunza, Juan J. Vaquero, Obis D. Castaño, Stanislav Baluschev e Silvia E. Angelova. "Halogen-containing thiazole orange analogues – new fluorogenic DNA stains". Beilstein Journal of Organic Chemistry 13 (28 de dezembro de 2017): 2902–14. http://dx.doi.org/10.3762/bjoc.13.283.
Texto completo da fonteDou, Wei-Tao, Ying Lv, Chunyan Tan, Guo-Rong Chen e Xiao-Peng He. "Irreversible destruction of amyloid fibril plaques by conjugated polymer based fluorogenic nanogrenades". Journal of Materials Chemistry B 4, n.º 26 (2016): 4502–6. http://dx.doi.org/10.1039/c6tb01351a.
Texto completo da fonteAlfindee, Madher N., Yagya P. Subedi, Michelle M. Grilley, Jon Y. Takemoto e Cheng-Wei T. Chang. "Antifungal Activities of 4″,6″-Disubstituted Amphiphilic Kanamycins". Molecules 24, n.º 10 (16 de maio de 2019): 1882. http://dx.doi.org/10.3390/molecules24101882.
Texto completo da fonteDiana, Rosita, Barbara Panunzi, Simona Concilio, Francesco Marrafino, Rafi Shikler, Tonino Caruso e Ugo Caruso. "The Effect of Bulky Substituents on Two π-Conjugated Mesogenic Fluorophores. Their Organic Polymers and Zinc-Bridged Luminescent Networks". Polymers 11, n.º 9 (22 de agosto de 2019): 1379. http://dx.doi.org/10.3390/polym11091379.
Texto completo da fonteSmith, H. V., A. M. Grimason, C. Benton e J. F. W. Parker. "The Occurrence of Cryptosporidium Spp. Oocysts in Scottish Waters, and the Development of a Fluorogenic Viability Assay for Individual Cryptosporidium spp. Oocysts". Water Science and Technology 24, n.º 2 (1 de julho de 1991): 169–72. http://dx.doi.org/10.2166/wst.1991.0051.
Texto completo da fonteSilva, Gloria L., Volkan Ediz, David Yaron e Bruce A. Armitage. "Experimental and Computational Investigation of Unsymmetrical Cyanine Dyes: Understanding Torsionally Responsive Fluorogenic Dyes". Journal of the American Chemical Society 129, n.º 17 (maio de 2007): 5710–18. http://dx.doi.org/10.1021/ja070025z.
Texto completo da fonteQi, Jianjun, Myung-Shin Han, Yu-Cheng Chang e Ching-Hsuan Tung. "Developing Visible Fluorogenic ‘Click-On’ Dyes for Cellular Imaging". Bioconjugate Chemistry 22, n.º 9 (21 de setembro de 2011): 1758–62. http://dx.doi.org/10.1021/bc200282t.
Texto completo da fonteKisin-Finfer, Einat, e Doron Shabat. "New repertoire of ‘donor-two-acceptor’ NIR fluorogenic dyes". Bioorganic & Medicinal Chemistry 21, n.º 12 (junho de 2013): 3602–8. http://dx.doi.org/10.1016/j.bmc.2013.02.049.
Texto completo da fonteQi, Jianjun, e Ching-Hsuan Tung. "ChemInform Abstract: Development of Benzothiazole “Click-On” Fluorogenic Dyes." ChemInform 42, n.º 20 (21 de abril de 2011): no. http://dx.doi.org/10.1002/chin.201120179.
Texto completo da fonteVincent, Steve, Suman Mallick, Guillaume Barnoin, Hoang-Ngoan Le, Benoît Y. Michel e Alain Burger. "An Expeditious Approach towards the Synthesis and Application of Water-Soluble and Photostable Fluorogenic Chromones for DNA Detection". Molecules 27, n.º 7 (31 de março de 2022): 2267. http://dx.doi.org/10.3390/molecules27072267.
Texto completo da fonteYan, Qi, Brigitte F. Schmidt, Lydia A. Perkins, Matharishwan Naganbabu, Saumya Saurabh, Susan K. Andreko e Marcel P. Bruchez. "Near-instant surface-selective fluorogenic protein quantification using sulfonated triarylmethane dyes and fluorogen activating proteins". Organic & Biomolecular Chemistry 13, n.º 7 (2015): 2078–86. http://dx.doi.org/10.1039/c4ob02309a.
Texto completo da fonteDebieu, Sylvain, e Anthony Romieu. "In situ formation of pyronin dyes for fluorescence protease sensing". Organic & Biomolecular Chemistry 15, n.º 12 (2017): 2575–84. http://dx.doi.org/10.1039/c7ob00370f.
Texto completo da fonteChi, Weijie, Lu Huang, Chao Wang, Davin Tan, Zhaochao Xu e Xiaogang Liu. "A unified fluorescence quenching mechanism of tetrazine-based fluorogenic dyes: energy transfer to a dark state". Materials Chemistry Frontiers 5, n.º 18 (2021): 7012–21. http://dx.doi.org/10.1039/d1qm00852h.
Texto completo da fonteIlieva, Sonia, Nadezhda Bozova, Miroslav Rangelov, Nadezhda Todorova, Aleksey Vasilev e Diana Cheshmedzhieva. "Asymmetric Monomethine Cyanine Dyes with Hydrophobic Functionalities for Fluorescent Intercalator Displacement Assay". Molecules 29, n.º 1 (23 de dezembro de 2023): 114. http://dx.doi.org/10.3390/molecules29010114.
Texto completo da fonteConstantin, Tudor P., Gloria L. Silva, Kelly L. Robertson, Tamara P. Hamilton, Kaitlin Fague, Alan S. Waggoner e Bruce A. Armitage. "Synthesis of New Fluorogenic Cyanine Dyes and Incorporation into RNA Fluoromodules". Organic Letters 10, n.º 8 (abril de 2008): 1561–64. http://dx.doi.org/10.1021/ol702920e.
Texto completo da fonteChauhan, Dinesh Pratapsinh, Tanmoy Saha, Mayurika Lahiri e Pinaki Talukdar. "BODIPY based ‘click on’ fluorogenic dyes: application in live cell imaging". Tetrahedron Letters 55, n.º 1 (janeiro de 2014): 244–47. http://dx.doi.org/10.1016/j.tetlet.2013.11.003.
Texto completo da fonteO’Connor, Liam J., Ishna N. Mistry, Sarah L. Collins, Lisa K. Folkes, Graham Brown, Stuart J. Conway e Ester M. Hammond. "CYP450 Enzymes Effect Oxygen-Dependent Reduction of Azide-Based Fluorogenic Dyes". ACS Central Science 3, n.º 1 (19 de dezembro de 2016): 20–30. http://dx.doi.org/10.1021/acscentsci.6b00276.
Texto completo da fonteZhang, Yuanwei, Xiling Yue, Bosung Kim, Sheng Yao, Mykhailo V. Bondar e Kevin D. Belfield. "Bovine Serum Albumin Nanoparticles with Fluorogenic Near-IR-Emitting Squaraine Dyes". ACS Applied Materials & Interfaces 5, n.º 17 (30 de agosto de 2013): 8710–17. http://dx.doi.org/10.1021/am402361w.
Texto completo da fonteHo, Nan-hui, Ralph Weissleder e Ching-Hsuan Tung. "Development of water-soluble far-red fluorogenic dyes for enzyme sensing". Tetrahedron 62, n.º 4 (janeiro de 2006): 578–85. http://dx.doi.org/10.1016/j.tet.2005.10.020.
Texto completo da fonteNISHIZAWA, Seiichi, Yukina YOSHINO, Mengmeng HE, Kei HIGUCHI, Nao TOGASHI, Michiyuki SUZUKI, Yugo IGARASHI e Yusuke SATO. "Fluorogenic Monomethine Cyanine Dyes for Nucleolar RNA Imaging in Living Cells". BUNSEKI KAGAKU 73, n.º 3 (5 de março de 2024): 79–86. http://dx.doi.org/10.2116/bunsekikagaku.73.79.
Texto completo da fonteChoi, Sang-Kee, Jonghoon Kim e Eunha Kim. "Overview of Syntheses and Molecular-Design Strategies for Tetrazine-Based Fluorogenic Probes". Molecules 26, n.º 7 (26 de março de 2021): 1868. http://dx.doi.org/10.3390/molecules26071868.
Texto completo da fonteZanotti, Kimberly J., Gloria L. Silva, Yehuda Creeger, Kelly L. Robertson, Alan S. Waggoner, Peter B. Berget e Bruce A. Armitage. "Blue fluorescent dye-protein complexes based on fluorogenic cyanine dyes and single chain antibody fragments". Org. Biomol. Chem. 9, n.º 4 (2011): 1012–20. http://dx.doi.org/10.1039/c0ob00444h.
Texto completo da fonteDemeter, Orsolya, Attila Kormos, Christine Koehler, Gábor Mező, Krisztina Németh, Eszter Kozma, Levente B. Takács, Edward A. Lemke e Péter Kele. "Bisazide Cyanine Dyes as Fluorogenic Probes for Bis-Cyclooctynylated Peptide Tags and as Fluorogenic Cross-Linkers of Cyclooctynylated Proteins". Bioconjugate Chemistry 28, n.º 5 (28 de abril de 2017): 1552–59. http://dx.doi.org/10.1021/acs.bioconjchem.7b00178.
Texto completo da fonteBozhanova, Nina, Mikhail Baranov, Nadezhda Baleeva, Alexey Gavrikov e Alexander Mishin. "Red-Shifted Aminated Derivatives of GFP Chromophore for Live-Cell Protein Labeling with Lipocalins". International Journal of Molecular Sciences 19, n.º 12 (28 de novembro de 2018): 3778. http://dx.doi.org/10.3390/ijms19123778.
Texto completo da fontePatalag, Lukas J., e Daniel B. Werz. "Benzothiadiazole oligoene fatty acids: fluorescent dyes with large Stokes shifts". Beilstein Journal of Organic Chemistry 12 (14 de dezembro de 2016): 2739–47. http://dx.doi.org/10.3762/bjoc.12.270.
Texto completo da fonteHannig, Christian, Marie Follo, Elmar Hellwig e Ali Al-Ahmad. "Visualization of adherent micro-organisms using different techniques". Journal of Medical Microbiology 59, n.º 1 (1 de janeiro de 2010): 1–7. http://dx.doi.org/10.1099/jmm.0.015420-0.
Texto completo da fonteEdiz, Volkan, Jihoon L. Lee, Bruce A. Armitage e David Yaron. "Molecular Engineering of Torsional Potentials in Fluorogenic Dyes via Electronic Substituent Effects". Journal of Physical Chemistry A 112, n.º 40 (9 de outubro de 2008): 9692–701. http://dx.doi.org/10.1021/jp805546s.
Texto completo da fonteKlymchenko, Andrey S. "Solvatochromic and Fluorogenic Dyes as Environment-Sensitive Probes: Design and Biological Applications". Accounts of Chemical Research 50, n.º 2 (9 de janeiro de 2017): 366–75. http://dx.doi.org/10.1021/acs.accounts.6b00517.
Texto completo da fonteChen, Lei, Fei Li, Mitoshi Nandi, Lu Huang, Zhizhong Chen, Junfa Wei, Weijie Chi, Xiaogang Liu e Jun Yang. "Towards tetrazine-based near-infrared fluorogenic dyes: Is there a wavelength limit?" Dyes and Pigments 177 (junho de 2020): 108313. http://dx.doi.org/10.1016/j.dyepig.2020.108313.
Texto completo da fonteCollot, Mayeul, Rémy Kreder, Anatoliy L. Tatarets, Leonid D. Patsenker, Yves Mely e Andrey S. Klymchenko. "Bright fluorogenic squaraines with tuned cell entry for selective imaging of plasma membrane vs. endoplasmic reticulum". Chemical Communications 51, n.º 96 (2015): 17136–39. http://dx.doi.org/10.1039/c5cc06094j.
Texto completo da fonteTa, Daniel D., e Sergei V. Dzyuba. "Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions". Chemosensors 9, n.º 11 (25 de outubro de 2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.
Texto completo da fonteRyazantsev, Dmitry Y., Maksim V. Kvach, Dmitry A. Tsybulsky, Igor A. Prokhorenko, Irina A. Stepanova, Yury V. Martynenko, Sergey V. Gontarev, Vadim V. Shmanai, Sergey K. Zavriev e Vladimir A. Korshun. "Design of molecular beacons: 3′ couple quenchers improve fluorogenic properties of a probe in real-time PCR assay". Analyst 139, n.º 11 (2014): 2867–72. http://dx.doi.org/10.1039/c4an00081a.
Texto completo da fonteMuñoz Resta, Ignacio, e Francisco Galindo. "Phenol-based styrylpyrylium dyes for trace water detection via chromogenic and fluorogenic responses". Dyes and Pigments 197 (janeiro de 2022): 109908. http://dx.doi.org/10.1016/j.dyepig.2021.109908.
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