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Correction to cooperative binding of ferrocenylnaphthalene diimide carrying β-cyclodextrin converts double-stranded DNA to a rod-like structure.

Bioconjugate chemistry

Sato S, Umeda Y, Fujii S, Takenaka S.
PMID: 25815900
Bioconjug Chem. 2015 Apr 15;26(4):790. doi: 10.1021/acs.bioconjchem.5b00149. Epub 2015 Mar 27.

No abstract available.

Cite
Sato S, Umeda Y, Fujii S, et al. Correction to cooperative binding of ferrocenylnaphthalene diimide carrying β-cyclodextrin converts double-stranded DNA to a rod-like structure. Bioconjug Chem. 2015;26(4):790doi: 10.1021/acs.bioconjchem.5b00149.
Sato, S., Umeda, Y., Fujii, S., & Takenaka, S. (2015). Correction to cooperative binding of ferrocenylnaphthalene diimide carrying β-cyclodextrin converts double-stranded DNA to a rod-like structure. Bioconjugate chemistry, 26(4), 790. https://doi.org/10.1021/acs.bioconjchem.5b00149
Sato, Shinobu, et al. "Correction to cooperative binding of ferrocenylnaphthalene diimide carrying β-cyclodextrin converts double-stranded DNA to a rod-like structure." Bioconjugate chemistry vol. 26,4 (2015): 790. doi: https://doi.org/10.1021/acs.bioconjchem.5b00149
Sato S, Umeda Y, Fujii S, Takenaka S. Correction to cooperative binding of ferrocenylnaphthalene diimide carrying β-cyclodextrin converts double-stranded DNA to a rod-like structure. Bioconjug Chem. 2015 Apr 15;26(4):790. doi: 10.1021/acs.bioconjchem.5b00149. Epub 2015 Mar 27. PMID: 25815900.
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Correction to Glycans of Antibodies as a Specific Site for Drug Conjugation Using Glycosyltransferases.

Bioconjugate chemistry

Qasba PK.
PMID: 26653670
Bioconjug Chem. 2016 Jan 20;27(1):264. doi: 10.1021/acs.bioconjchem.5b00658. Epub 2015 Dec 14.

No abstract available.

Cite
Qasba PK. Correction to Glycans of Antibodies as a Specific Site for Drug Conjugation Using Glycosyltransferases. Bioconjug Chem. 2015;27(1):264doi: 10.1021/acs.bioconjchem.5b00658.
Qasba, P. K. (2016). Correction to Glycans of Antibodies as a Specific Site for Drug Conjugation Using Glycosyltransferases. Bioconjugate chemistry, 27(1), 264. https://doi.org/10.1021/acs.bioconjchem.5b00658
Qasba, Pradman K. "Correction to Glycans of Antibodies as a Specific Site for Drug Conjugation Using Glycosyltransferases." Bioconjugate chemistry vol. 27,1 (2016): 264. doi: https://doi.org/10.1021/acs.bioconjchem.5b00658
Qasba PK. Correction to Glycans of Antibodies as a Specific Site for Drug Conjugation Using Glycosyltransferases. Bioconjug Chem. 2016 Jan 20;27(1):264. doi: 10.1021/acs.bioconjchem.5b00658. Epub 2015 Dec 14. PMID: 26653670.
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Antimicrobial Silver Nanoclusters Bearing Biocompatible Phosphorylcholine-Based Zwitterionic Protection.

Bioconjugate chemistry

Sangsuwan A, Kawasaki H, Matsumura Y, Iwasaki Y.
PMID: 27689806
Bioconjug Chem. 2016 Oct 19;27(10):2527-2533. doi: 10.1021/acs.bioconjchem.6b00455. Epub 2016 Oct 07.

Infection is one of the most serious issues in medical treatments leading to the development of several antimicrobial agents. In particular, silver ions released from silver substrates is well-known as a reliable antimicrobial agent that either kills the microorganisms...

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Sangsuwan A, Kawasaki H, Matsumura Y, et al. Antimicrobial Silver Nanoclusters Bearing Biocompatible Phosphorylcholine-Based Zwitterionic Protection. Bioconjug Chem. 2016;27(10):2527-2533doi: 10.1021/acs.bioconjchem.6b00455.
Sangsuwan, A., Kawasaki, H., Matsumura, Y., & Iwasaki, Y. (2016). Antimicrobial Silver Nanoclusters Bearing Biocompatible Phosphorylcholine-Based Zwitterionic Protection. Bioconjugate chemistry, 27(10), 2527-2533. https://doi.org/10.1021/acs.bioconjchem.6b00455
Sangsuwan, Arunee, et al. "Antimicrobial Silver Nanoclusters Bearing Biocompatible Phosphorylcholine-Based Zwitterionic Protection." Bioconjugate chemistry vol. 27,10 (2016): 2527-2533. doi: https://doi.org/10.1021/acs.bioconjchem.6b00455
Sangsuwan A, Kawasaki H, Matsumura Y, Iwasaki Y. Antimicrobial Silver Nanoclusters Bearing Biocompatible Phosphorylcholine-Based Zwitterionic Protection. Bioconjug Chem. 2016 Oct 19;27(10):2527-2533. doi: 10.1021/acs.bioconjchem.6b00455. Epub 2016 Oct 07. PMID: 27689806.
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Bioorthogonal Strategy for Bioprocessing of Specific-Site-Functionalized Enveloped Influenza-Virus-Like Particles.

Bioconjugate chemistry

Carvalho SB, Freire JM, Moleirinho MG, Monteiro F, Gaspar D, Castanho MARB, Carrondo MJT, Alves PM, Bernardes GJL, Peixoto C.
PMID: 27652605
Bioconjug Chem. 2016 Oct 19;27(10):2386-2399. doi: 10.1021/acs.bioconjchem.6b00372. Epub 2016 Oct 07.

Virus-like particles (VLPs) constitute a promising platform in vaccine development and targeted drug delivery. To date, most applications use simple nonenveloped VLPs as human papillomavirus or hepatitis B vaccines, even though the envelope is known to be critical to...

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Carvalho SB, Freire JM, Moleirinho MG, et al. Bioorthogonal Strategy for Bioprocessing of Specific-Site-Functionalized Enveloped Influenza-Virus-Like Particles. Bioconjug Chem. 2016;27(10):2386-2399doi: 10.1021/acs.bioconjchem.6b00372.
Carvalho, S. B., Freire, J. M., Moleirinho, M. G., Monteiro, F., Gaspar, D., Castanho, M. A. R. B., Carrondo, M. J. T., Alves, P. M., Bernardes, G. J. L., & Peixoto, C. (2016). Bioorthogonal Strategy for Bioprocessing of Specific-Site-Functionalized Enveloped Influenza-Virus-Like Particles. Bioconjugate chemistry, 27(10), 2386-2399. https://doi.org/10.1021/acs.bioconjchem.6b00372
Carvalho, Sofia B, et al. "Bioorthogonal Strategy for Bioprocessing of Specific-Site-Functionalized Enveloped Influenza-Virus-Like Particles." Bioconjugate chemistry vol. 27,10 (2016): 2386-2399. doi: https://doi.org/10.1021/acs.bioconjchem.6b00372
Carvalho SB, Freire JM, Moleirinho MG, Monteiro F, Gaspar D, Castanho MARB, Carrondo MJT, Alves PM, Bernardes GJL, Peixoto C. Bioorthogonal Strategy for Bioprocessing of Specific-Site-Functionalized Enveloped Influenza-Virus-Like Particles. Bioconjug Chem. 2016 Oct 19;27(10):2386-2399. doi: 10.1021/acs.bioconjchem.6b00372. Epub 2016 Oct 07. PMID: 27652605; PMCID: PMC5080633.
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Correction to Exploring the Effect of Conjugation Site and Chemistry on the Immunogenicity of an anti-Group B Streptococcus Glycoconjugate Vaccine Based on GBS67 Pilus Protein and Type V Polysaccharide.

Bioconjugate chemistry

Nilo A, Passalacqua I, Fabbrini M, Allan M, Usera A, Carboni F, Brogioni B, Pezzicoli A, Cobb J, Romano MR, Margarit I, Hu QY, Berti F, Adamo R.
PMID: 26355285
Bioconjug Chem. 2015 Oct 21;26(10):2167. doi: 10.1021/acs.bioconjchem.5b00480. Epub 2015 Sep 10.

No abstract available.

Cite
Nilo A, Passalacqua I, Fabbrini M, et al. Correction to Exploring the Effect of Conjugation Site and Chemistry on the Immunogenicity of an anti-Group B Streptococcus Glycoconjugate Vaccine Based on GBS67 Pilus Protein and Type V Polysaccharide. Bioconjug Chem. 2015;26(10):2167doi: 10.1021/acs.bioconjchem.5b00480.
Nilo, A., Passalacqua, I., Fabbrini, M., Allan, M., Usera, A., Carboni, F., Brogioni, B., Pezzicoli, A., Cobb, J., Romano, M. R., Margarit, I., Hu, Q. Y., Berti, F., & Adamo, R. (2015). Correction to Exploring the Effect of Conjugation Site and Chemistry on the Immunogenicity of an anti-Group B Streptococcus Glycoconjugate Vaccine Based on GBS67 Pilus Protein and Type V Polysaccharide. Bioconjugate chemistry, 26(10), 2167. https://doi.org/10.1021/acs.bioconjchem.5b00480
Nilo, Alberto, et al. "Correction to Exploring the Effect of Conjugation Site and Chemistry on the Immunogenicity of an anti-Group B Streptococcus Glycoconjugate Vaccine Based on GBS67 Pilus Protein and Type V Polysaccharide." Bioconjugate chemistry vol. 26,10 (2015): 2167. doi: https://doi.org/10.1021/acs.bioconjchem.5b00480
Nilo A, Passalacqua I, Fabbrini M, Allan M, Usera A, Carboni F, Brogioni B, Pezzicoli A, Cobb J, Romano MR, Margarit I, Hu QY, Berti F, Adamo R. Correction to Exploring the Effect of Conjugation Site and Chemistry on the Immunogenicity of an anti-Group B Streptococcus Glycoconjugate Vaccine Based on GBS67 Pilus Protein and Type V Polysaccharide. Bioconjug Chem. 2015 Oct 21;26(10):2167. doi: 10.1021/acs.bioconjchem.5b00480. Epub 2015 Sep 10. PMID: 26355285.
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Correction to Novel Bispecific PSMA/GRPr Targeting Radioligands with Optimized Pharmacokinetics for Improved PET Imaging of Prostate Cancer.

Bioconjugate chemistry

Liolios C, Schäfer M, Haberkorn U, Eder M, Kopka K.
PMID: 27367305
Bioconjug Chem. 2016 Jul 20;27(7):1770. doi: 10.1021/acs.bioconjchem.6b00311. Epub 2016 Jul 01.

No abstract available.

Cite
Liolios C, Schäfer M, Haberkorn U, et al. Correction to Novel Bispecific PSMA/GRPr Targeting Radioligands with Optimized Pharmacokinetics for Improved PET Imaging of Prostate Cancer. Bioconjug Chem. 2016;27(7):1770doi: 10.1021/acs.bioconjchem.6b00311.
Liolios, C., Schäfer, M., Haberkorn, U., Eder, M., & Kopka, K. (2016). Correction to Novel Bispecific PSMA/GRPr Targeting Radioligands with Optimized Pharmacokinetics for Improved PET Imaging of Prostate Cancer. Bioconjugate chemistry, 27(7), 1770. https://doi.org/10.1021/acs.bioconjchem.6b00311
Liolios, Christos, et al. "Correction to Novel Bispecific PSMA/GRPr Targeting Radioligands with Optimized Pharmacokinetics for Improved PET Imaging of Prostate Cancer." Bioconjugate chemistry vol. 27,7 (2016): 1770. doi: https://doi.org/10.1021/acs.bioconjchem.6b00311
Liolios C, Schäfer M, Haberkorn U, Eder M, Kopka K. Correction to Novel Bispecific PSMA/GRPr Targeting Radioligands with Optimized Pharmacokinetics for Improved PET Imaging of Prostate Cancer. Bioconjug Chem. 2016 Jul 20;27(7):1770. doi: 10.1021/acs.bioconjchem.6b00311. Epub 2016 Jul 01. PMID: 27367305.
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Correction to Magnetically Guided Viral Transduction of Gene-Based Sensitization for Localized Photodynamic Therapy To Overcome Multidrug Resistance in Breast Cancer Cells.

Bioconjugate chemistry

Liao ZX, Kempson IM, Fa YC, Liu MC, Hsieh LC, Huang KY, Wang LF.
PMID: 29812919
Bioconjug Chem. 2018 Jun 20;29(6):2126. doi: 10.1021/acs.bioconjchem.8b00356. Epub 2018 May 29.

No abstract available.

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Liao ZX, Kempson IM, Fa YC, et al. Correction to Magnetically Guided Viral Transduction of Gene-Based Sensitization for Localized Photodynamic Therapy To Overcome Multidrug Resistance in Breast Cancer Cells. Bioconjug Chem. 2018;29(6):2126doi: 10.1021/acs.bioconjchem.8b00356.
Liao, Z. X., Kempson, I. M., Fa, Y. C., Liu, M. C., Hsieh, L. C., Huang, K. Y., & Wang, L. F. (2018). Correction to Magnetically Guided Viral Transduction of Gene-Based Sensitization for Localized Photodynamic Therapy To Overcome Multidrug Resistance in Breast Cancer Cells. Bioconjugate chemistry, 29(6), 2126. https://doi.org/10.1021/acs.bioconjchem.8b00356
Liao, Zi-Xian, et al. "Correction to Magnetically Guided Viral Transduction of Gene-Based Sensitization for Localized Photodynamic Therapy To Overcome Multidrug Resistance in Breast Cancer Cells." Bioconjugate chemistry vol. 29,6 (2018): 2126. doi: https://doi.org/10.1021/acs.bioconjchem.8b00356
Liao ZX, Kempson IM, Fa YC, Liu MC, Hsieh LC, Huang KY, Wang LF. Correction to Magnetically Guided Viral Transduction of Gene-Based Sensitization for Localized Photodynamic Therapy To Overcome Multidrug Resistance in Breast Cancer Cells. Bioconjug Chem. 2018 Jun 20;29(6):2126. doi: 10.1021/acs.bioconjchem.8b00356. Epub 2018 May 29. PMID: 29812919.
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Perspectives on the Future of Nanomedicine to Impact Patients: An Analysis of US Federal Funding and Interventional Clinical Trials.

Bioconjugate chemistry

McGoron AJ.
PMID: 31922742
Bioconjug Chem. 2020 Mar 18;31(3):436-447. doi: 10.1021/acs.bioconjchem.9b00818. Epub 2020 Jan 23.

The US and governments around the world, and companies, have made a considerable investment in nanomedicine, and there have been important discoveries. Nevertheless, there has been considerable debate as to whether the investment, both in money and in time,...

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McGoron AJ. Perspectives on the Future of Nanomedicine to Impact Patients: An Analysis of US Federal Funding and Interventional Clinical Trials. Bioconjug Chem. 2020;31(3):436-447doi: 10.1021/acs.bioconjchem.9b00818.
McGoron, A. J. (2020). Perspectives on the Future of Nanomedicine to Impact Patients: An Analysis of US Federal Funding and Interventional Clinical Trials. Bioconjugate chemistry, 31(3), 436-447. https://doi.org/10.1021/acs.bioconjchem.9b00818
McGoron, Anthony J. "Perspectives on the Future of Nanomedicine to Impact Patients: An Analysis of US Federal Funding and Interventional Clinical Trials." Bioconjugate chemistry vol. 31,3 (2020): 436-447. doi: https://doi.org/10.1021/acs.bioconjchem.9b00818
McGoron AJ. Perspectives on the Future of Nanomedicine to Impact Patients: An Analysis of US Federal Funding and Interventional Clinical Trials. Bioconjug Chem. 2020 Mar 18;31(3):436-447. doi: 10.1021/acs.bioconjchem.9b00818. Epub 2020 Jan 23. PMID: 31922742.
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Correction to Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles.

Bioconjugate chemistry

Galmarini S, Hanusch U, Giraud M, Cayla N, Chiappe D, von Moos N, Hofmann H, Maurizi L.
PMID: 31090399
Bioconjug Chem. 2019 Jun 19;30(6):1832. doi: 10.1021/acs.bioconjchem.9b00329. Epub 2019 May 15.

No abstract available.

Cite
Galmarini S, Hanusch U, Giraud M, et al. Correction to Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles. Bioconjug Chem. 2019;30(6):1832doi: 10.1021/acs.bioconjchem.9b00329.
Galmarini, S., Hanusch, U., Giraud, M., Cayla, N., Chiappe, D., von Moos, N., Hofmann, H., & Maurizi, L. (2019). Correction to Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles. Bioconjugate chemistry, 30(6), 1832. https://doi.org/10.1021/acs.bioconjchem.9b00329
Galmarini, Sandra, et al. "Correction to Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles." Bioconjugate chemistry vol. 30,6 (2019): 1832. doi: https://doi.org/10.1021/acs.bioconjchem.9b00329
Galmarini S, Hanusch U, Giraud M, Cayla N, Chiappe D, von Moos N, Hofmann H, Maurizi L. Correction to Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles. Bioconjug Chem. 2019 Jun 19;30(6):1832. doi: 10.1021/acs.bioconjchem.9b00329. Epub 2019 May 15. PMID: 31090399.
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Correction to Drug Delivery Systems Based on Hydroxyethyl Starch.

Bioconjugate chemistry

Paleos CM, Sideratou Z, Tsiourvas D.
PMID: 28753265
Bioconjug Chem. 2017 Aug 16;28(8):2208-2209. doi: 10.1021/acs.bioconjchem.7b00400. Epub 2017 Jul 28.

No abstract available.

Cite
Paleos CM, Sideratou Z, Tsiourvas D. Correction to Drug Delivery Systems Based on Hydroxyethyl Starch. Bioconjug Chem. 2017;28(8):2208-2209doi: 10.1021/acs.bioconjchem.7b00400.
Paleos, C. M., Sideratou, Z., & Tsiourvas, D. (2017). Correction to Drug Delivery Systems Based on Hydroxyethyl Starch. Bioconjugate chemistry, 28(8), 2208-2209. https://doi.org/10.1021/acs.bioconjchem.7b00400
Paleos, Constantinos M, et al. "Correction to Drug Delivery Systems Based on Hydroxyethyl Starch." Bioconjugate chemistry vol. 28,8 (2017): 2208-2209. doi: https://doi.org/10.1021/acs.bioconjchem.7b00400
Paleos CM, Sideratou Z, Tsiourvas D. Correction to Drug Delivery Systems Based on Hydroxyethyl Starch. Bioconjug Chem. 2017 Aug 16;28(8):2208-2209. doi: 10.1021/acs.bioconjchem.7b00400. Epub 2017 Jul 28. PMID: 28753265.
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Enhanced Cell Killing by Paclitaxel-Loaded Recombinant Protein Micelles Bearing Integrin-Binding and Cell-Penetrating Peptides.

Bioconjugate chemistry

Gao C, Lee V, Hammer DA.
PMID: 30777745
Bioconjug Chem. 2019 Feb 19; doi: 10.1021/acs.bioconjchem.8b00748. Epub 2019 Feb 19.

Peptide ligands are effective and specific vectors that can target cell surface receptors, and have shown great potential for targeting drug delivery vehicles. Often, materials used as drug delivery matrices are chemically synthesized and difficult to functionalize, which compromises...

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Gao C, Lee V, Hammer DA. Enhanced Cell Killing by Paclitaxel-Loaded Recombinant Protein Micelles Bearing Integrin-Binding and Cell-Penetrating Peptides. Bioconjug Chem. 2019;doi: 10.1021/acs.bioconjchem.8b00748.
Gao, C., Lee, V., & Hammer, D. A. (2019). Enhanced Cell Killing by Paclitaxel-Loaded Recombinant Protein Micelles Bearing Integrin-Binding and Cell-Penetrating Peptides. Bioconjugate chemistry, . https://doi.org/10.1021/acs.bioconjchem.8b00748
Gao, Chen, et al. "Enhanced Cell Killing by Paclitaxel-Loaded Recombinant Protein Micelles Bearing Integrin-Binding and Cell-Penetrating Peptides." Bioconjugate chemistry vol. (2019). doi: https://doi.org/10.1021/acs.bioconjchem.8b00748
Gao C, Lee V, Hammer DA. Enhanced Cell Killing by Paclitaxel-Loaded Recombinant Protein Micelles Bearing Integrin-Binding and Cell-Penetrating Peptides. Bioconjug Chem. 2019 Feb 19; doi: 10.1021/acs.bioconjchem.8b00748. Epub 2019 Feb 19. PMID: 30777745.
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GB Tags: Small Covalent Peptide Tags Based on Protein Fragment Reconstitution.

Bioconjugate chemistry

Wang R, Liu M, Wang H, Xia J, Li H.
PMID: 34329559
Bioconjug Chem. 2021 Aug 18;32(8):1926-1934. doi: 10.1021/acs.bioconjchem.1c00325. Epub 2021 Jul 30.

Developing peptide tags that can bind target proteins covalently under mild conditions is of great importance for a myriad of applications, ranging from chemical biology to biotechnology. Here we report the development of a small covalent peptide tag system,...

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Wang R, Liu M, Wang H, et al. GB Tags: Small Covalent Peptide Tags Based on Protein Fragment Reconstitution. Bioconjug Chem. 2021;32(8):1926-1934doi: 10.1021/acs.bioconjchem.1c00325.
Wang, R., Liu, M., Wang, H., Xia, J., & Li, H. (2021). GB Tags: Small Covalent Peptide Tags Based on Protein Fragment Reconstitution. Bioconjugate chemistry, 32(8), 1926-1934. https://doi.org/10.1021/acs.bioconjchem.1c00325
Wang, Ruidi, et al. "GB Tags: Small Covalent Peptide Tags Based on Protein Fragment Reconstitution." Bioconjugate chemistry vol. 32,8 (2021): 1926-1934. doi: https://doi.org/10.1021/acs.bioconjchem.1c00325
Wang R, Liu M, Wang H, Xia J, Li H. GB Tags: Small Covalent Peptide Tags Based on Protein Fragment Reconstitution. Bioconjug Chem. 2021 Aug 18;32(8):1926-1934. doi: 10.1021/acs.bioconjchem.1c00325. Epub 2021 Jul 30. PMID: 34329559.
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Showing 1 to 12 of 252 entries