Articoli di riviste sul 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. 12 (2015): 3699–710. http://dx.doi.org/10.1039/c4ob02522a.
Martin, Annabell, e Pablo Rivera Fuentes. "A Baldwin-favored Cyclization Inspires the Development of Fluorogenic Polymethine Dyes for Bioimaging". CHIMIA 78, n. 4 (24 aprile 2024): 196–99. http://dx.doi.org/10.2533/chimia.2024.196.
Mamaeva, 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. 12 (17 dicembre 2022): 542. http://dx.doi.org/10.3390/chemosensors10120542.
Krell, Katja, e Hans-Achim Wagenknecht. "Fluorogenic and Bioorthogonal Modification of RNA Using Photoclick Chemistry". Biomolecules 10, n. 3 (21 marzo 2020): 480. http://dx.doi.org/10.3390/biom10030480.
Martin, Annabell, e Pablo Rivera-Fuentes. "Fluorogenic polymethine dyes by intramolecular cyclization". Current Opinion in Chemical Biology 80 (giugno 2024): 102444. http://dx.doi.org/10.1016/j.cbpa.2024.102444.
Li, 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. 8 (2017): 5598–605. http://dx.doi.org/10.1039/c7sc01364g.
Bruchez, Marcel P. "Dark dyes–bright complexes: fluorogenic protein labeling". Current Opinion in Chemical Biology 27 (agosto 2015): 18–23. http://dx.doi.org/10.1016/j.cbpa.2015.05.014.
Qi, Jianjun, e Ching-Hsuan Tung. "Development of benzothiazole ‘click-on’ fluorogenic dyes". Bioorganic & Medicinal Chemistry Letters 21, n. 1 (gennaio 2011): 320–23. http://dx.doi.org/10.1016/j.bmcl.2010.11.009.
Gu, 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. 28 (2020): 12208–15. http://dx.doi.org/10.1039/d0nj01724h.
Karpenko, 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. 14 (2016): 3002–9. http://dx.doi.org/10.1039/c5tc03411f.
Wang, 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. 43 (2016): 17274–80. http://dx.doi.org/10.1039/c6dt03469a.
Kormos, 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. 1 (17 gennaio 2022): 37. http://dx.doi.org/10.3390/chemosensors10010037.
Low, 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. 10 (2014): 1382. http://dx.doi.org/10.1071/ch14083.
Stensrud, 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. 1 (23 novembre 2018): 406–10. http://dx.doi.org/10.1111/php.13037.
Liu, 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. 48 (20 novembre 2017): 17334–40. http://dx.doi.org/10.1021/jacs.7b07047.
Sokolov, 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. 6 (dicembre 2022): 1367–71. http://dx.doi.org/10.1134/s1068162022060243.
Bhasikuttan, Achikanath C., e Jyotirmayee Mohanty. "Targeting G-quadruplex structures with extrinsic fluorogenic dyes: promising fluorescence sensors". Chemical Communications 51, n. 36 (2015): 7581–97. http://dx.doi.org/10.1039/c4cc10030a.
Vasilev, 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 dicembre 2017): 2902–14. http://dx.doi.org/10.3762/bjoc.13.283.
Dou, 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. 26 (2016): 4502–6. http://dx.doi.org/10.1039/c6tb01351a.
Alfindee, 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. 10 (16 maggio 2019): 1882. http://dx.doi.org/10.3390/molecules24101882.
Diana, 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. 9 (22 agosto 2019): 1379. http://dx.doi.org/10.3390/polym11091379.
Smith, 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. 2 (1 luglio 1991): 169–72. http://dx.doi.org/10.2166/wst.1991.0051.
Silva, 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. 17 (maggio 2007): 5710–18. http://dx.doi.org/10.1021/ja070025z.
Qi, Jianjun, Myung-Shin Han, Yu-Cheng Chang e Ching-Hsuan Tung. "Developing Visible Fluorogenic ‘Click-On’ Dyes for Cellular Imaging". Bioconjugate Chemistry 22, n. 9 (21 settembre 2011): 1758–62. http://dx.doi.org/10.1021/bc200282t.
Kisin-Finfer, Einat, e Doron Shabat. "New repertoire of ‘donor-two-acceptor’ NIR fluorogenic dyes". Bioorganic & Medicinal Chemistry 21, n. 12 (giugno 2013): 3602–8. http://dx.doi.org/10.1016/j.bmc.2013.02.049.
Qi, Jianjun, e Ching-Hsuan Tung. "ChemInform Abstract: Development of Benzothiazole “Click-On” Fluorogenic Dyes." ChemInform 42, n. 20 (21 aprile 2011): no. http://dx.doi.org/10.1002/chin.201120179.
Vincent, 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. 7 (31 marzo 2022): 2267. http://dx.doi.org/10.3390/molecules27072267.
Yan, 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. 7 (2015): 2078–86. http://dx.doi.org/10.1039/c4ob02309a.
Debieu, Sylvain, e Anthony Romieu. "In situ formation of pyronin dyes for fluorescence protease sensing". Organic & Biomolecular Chemistry 15, n. 12 (2017): 2575–84. http://dx.doi.org/10.1039/c7ob00370f.
Chi, 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. 18 (2021): 7012–21. http://dx.doi.org/10.1039/d1qm00852h.
Ilieva, 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. 1 (23 dicembre 2023): 114. http://dx.doi.org/10.3390/molecules29010114.
Constantin, 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. 8 (aprile 2008): 1561–64. http://dx.doi.org/10.1021/ol702920e.
Chauhan, Dinesh Pratapsinh, Tanmoy Saha, Mayurika Lahiri e Pinaki Talukdar. "BODIPY based ‘click on’ fluorogenic dyes: application in live cell imaging". Tetrahedron Letters 55, n. 1 (gennaio 2014): 244–47. http://dx.doi.org/10.1016/j.tetlet.2013.11.003.
O’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. 1 (19 dicembre 2016): 20–30. http://dx.doi.org/10.1021/acscentsci.6b00276.
Zhang, 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. 17 (30 agosto 2013): 8710–17. http://dx.doi.org/10.1021/am402361w.
Ho, Nan-hui, Ralph Weissleder e Ching-Hsuan Tung. "Development of water-soluble far-red fluorogenic dyes for enzyme sensing". Tetrahedron 62, n. 4 (gennaio 2006): 578–85. http://dx.doi.org/10.1016/j.tet.2005.10.020.
NISHIZAWA, 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. 3 (5 marzo 2024): 79–86. http://dx.doi.org/10.2116/bunsekikagaku.73.79.
Choi, Sang-Kee, Jonghoon Kim e Eunha Kim. "Overview of Syntheses and Molecular-Design Strategies for Tetrazine-Based Fluorogenic Probes". Molecules 26, n. 7 (26 marzo 2021): 1868. http://dx.doi.org/10.3390/molecules26071868.
Zanotti, 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. 4 (2011): 1012–20. http://dx.doi.org/10.1039/c0ob00444h.
Demeter, 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. 5 (28 aprile 2017): 1552–59. http://dx.doi.org/10.1021/acs.bioconjchem.7b00178.
Bozhanova, 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. 12 (28 novembre 2018): 3778. http://dx.doi.org/10.3390/ijms19123778.
Patalag, Lukas J., e Daniel B. Werz. "Benzothiadiazole oligoene fatty acids: fluorescent dyes with large Stokes shifts". Beilstein Journal of Organic Chemistry 12 (14 dicembre 2016): 2739–47. http://dx.doi.org/10.3762/bjoc.12.270.
Hannig, Christian, Marie Follo, Elmar Hellwig e Ali Al-Ahmad. "Visualization of adherent micro-organisms using different techniques". Journal of Medical Microbiology 59, n. 1 (1 gennaio 2010): 1–7. http://dx.doi.org/10.1099/jmm.0.015420-0.
Ediz, 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. 40 (9 ottobre 2008): 9692–701. http://dx.doi.org/10.1021/jp805546s.
Klymchenko, Andrey S. "Solvatochromic and Fluorogenic Dyes as Environment-Sensitive Probes: Design and Biological Applications". Accounts of Chemical Research 50, n. 2 (9 gennaio 2017): 366–75. http://dx.doi.org/10.1021/acs.accounts.6b00517.
Chen, 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 (giugno 2020): 108313. http://dx.doi.org/10.1016/j.dyepig.2020.108313.
Collot, 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. 96 (2015): 17136–39. http://dx.doi.org/10.1039/c5cc06094j.
Ta, Daniel D., e Sergei V. Dzyuba. "Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions". Chemosensors 9, n. 11 (25 ottobre 2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.
Ryazantsev, 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. 11 (2014): 2867–72. http://dx.doi.org/10.1039/c4an00081a.
Muñoz Resta, Ignacio, e Francisco Galindo. "Phenol-based styrylpyrylium dyes for trace water detection via chromogenic and fluorogenic responses". Dyes and Pigments 197 (gennaio 2022): 109908. http://dx.doi.org/10.1016/j.dyepig.2021.109908.