Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 1103 entries
Sorted by: Best Match Show Resources per page
MutS-mediated enrichment of mutated DNA produced by directed evolution in vitro.

World journal of microbiology & biotechnology

Zhong T, Zhou Y, Bi L, Zhang XE.
PMID: 25187136
World J Microbiol Biotechnol. 2011 Jun;27(6):1367-72. doi: 10.1007/s11274-010-0587-0. Epub 2010 Oct 10.

Directed evolution in vitro is a powerful tool in the study and design of protein function. However, screening the desired mutants is a difficult task. To facilitate the screening, a method is proposed to eliminate wild type sequences and...

Cite
Zhong T, Zhou Y, Bi L, et al. MutS-mediated enrichment of mutated DNA produced by directed evolution in vitro. World J Microbiol Biotechnol. 2010;27(6):1367-72doi: 10.1007/s11274-010-0587-0.
Zhong, T., Zhou, Y., Bi, L., & Zhang, X. E. (2011). MutS-mediated enrichment of mutated DNA produced by directed evolution in vitro. World journal of microbiology & biotechnology, 27(6), 1367-72. https://doi.org/10.1007/s11274-010-0587-0
Zhong, Tianying, et al. "MutS-mediated enrichment of mutated DNA produced by directed evolution in vitro." World journal of microbiology & biotechnology vol. 27,6 (2011): 1367-72. doi: https://doi.org/10.1007/s11274-010-0587-0
Zhong T, Zhou Y, Bi L, Zhang XE. MutS-mediated enrichment of mutated DNA produced by directed evolution in vitro. World J Microbiol Biotechnol. 2011 Jun;27(6):1367-72. doi: 10.1007/s11274-010-0587-0. Epub 2010 Oct 10. PMID: 25187136.
Copy Download .nbib Format: NLM
A Coarse Grained Model for Atomic-Detailed DNA Simulations with Explicit Electrostatics.

Journal of chemical theory and computation

Dans PD, Zeida A, Machado MR, Pantano S.
PMID: 26615701
J Chem Theory Comput. 2010 May 11;6(5):1711-25. doi: 10.1021/ct900653p. Epub 2010 Apr 14.

Coarse-grain (CG) techniques allow considerable extension of the accessible size and time scales in simulations of biological systems. Although many CG representations are available for the most common biomacromolecules, very few have been reported for nucleic acids. Here, we...

Cite
Dans PD, Zeida A, Machado MR, et al. A Coarse Grained Model for Atomic-Detailed DNA Simulations with Explicit Electrostatics. J Chem Theory Comput. 2010;6(5):1711-25doi: 10.1021/ct900653p.
Dans, P. D., Zeida, A., Machado, M. R., & Pantano, S. (2010). A Coarse Grained Model for Atomic-Detailed DNA Simulations with Explicit Electrostatics. Journal of chemical theory and computation, 6(5), 1711-25. https://doi.org/10.1021/ct900653p
Dans, Pablo D, et al. "A Coarse Grained Model for Atomic-Detailed DNA Simulations with Explicit Electrostatics." Journal of chemical theory and computation vol. 6,5 (2010): 1711-25. doi: https://doi.org/10.1021/ct900653p
Dans PD, Zeida A, Machado MR, Pantano S. A Coarse Grained Model for Atomic-Detailed DNA Simulations with Explicit Electrostatics. J Chem Theory Comput. 2010 May 11;6(5):1711-25. doi: 10.1021/ct900653p. Epub 2010 Apr 14. PMID: 26615701.
Copy Download .nbib Format: NLM
Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments.

Nature communications

Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J.
PMID: 27677239
Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761.

Small-molecule fragments binding to biomacromolecules can be starting points for the development of drugs, but are often difficult to detect due to low affinities. Here we present a strategy that identifies protein-binding fragments through their potential to induce the...

Cite
Becker D, Kaczmarska Z, Arkona C, et al. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016;7:12761doi: 10.1038/ncomms12761.
Becker, D., Kaczmarska, Z., Arkona, C., Schulz, R., Tauber, C., Wolber, G., Hilgenfeld, R., Coll, M., & Rademann, J. (2016). Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nature communications, 712761. https://doi.org/10.1038/ncomms12761
Becker, Daniel, et al. "Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments." Nature communications vol. 7 (2016): 12761. doi: https://doi.org/10.1038/ncomms12761
Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761. PMID: 27677239; PMCID: PMC5052702.
Copy Download .nbib Format: NLM
An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells.

Biophysics reports

Chen Y, Xia Z, Wang L, Yu Y, Liu P, Song E, Xu T.
PMID: 26942217
Biophys Rep. 2015;1:34-40. doi: 10.1007/s41048-015-0008-x. Epub 2015 Aug 07.

Insulin is one of the key regulators for blood glucose homeostasis. More than 99% of insulin is secreted from the pancreatic β-cells. Within each β-cell, insulin is packaged and processed in insulin secretary granules (ISGs) before its exocytosis. Insulin...

Cite
Chen Y, Xia Z, Wang L, et al. An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells. Biophys Rep. 2015;1:34-40doi: 10.1007/s41048-015-0008-x.
Chen, Y., Xia, Z., Wang, L., Yu, Y., Liu, P., Song, E., & Xu, T. (2015). An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells. Biophysics reports, 134-40. https://doi.org/10.1007/s41048-015-0008-x
Chen, Yan, et al. "An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells." Biophysics reports vol. 1 (2015): 34-40. doi: https://doi.org/10.1007/s41048-015-0008-x
Chen Y, Xia Z, Wang L, Yu Y, Liu P, Song E, Xu T. An efficient two-step subcellular fractionation method for the enrichment of insulin granules from INS-1 cells. Biophys Rep. 2015;1:34-40. doi: 10.1007/s41048-015-0008-x. Epub 2015 Aug 07. PMID: 26942217; PMCID: PMC4762126.
Copy Download .nbib Format: NLM
Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis.

Proceedings. Mathematical, physical, and engineering sciences

Fehl C, Davis BG.
PMID: 27279776
Proc Math Phys Eng Sci. 2016 May;472(2189):20160078. doi: 10.1098/rspa.2016.0078.

Despite nature's prevalent use of metals as prosthetics to adapt or enhance the behaviour of proteins, our ability to programme such architectural organization remains underdeveloped. Multi-metal clusters buried in proteins underpin the most remarkable chemical transformations in nature, but...

Cite
Fehl C, Davis BG. Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis. Proc Math Phys Eng Sci. 2016;472(2189):20160078doi: 10.1098/rspa.2016.0078.
Fehl, C., & Davis, B. G. (2016). Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis. Proceedings. Mathematical, physical, and engineering sciences, 472(2189), 20160078. https://doi.org/10.1098/rspa.2016.0078
Fehl, Charlie, and Davis, Benjamin G. "Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis." Proceedings. Mathematical, physical, and engineering sciences vol. 472,2189 (2016): 20160078. doi: https://doi.org/10.1098/rspa.2016.0078
Fehl C, Davis BG. Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis. Proc Math Phys Eng Sci. 2016 May;472(2189):20160078. doi: 10.1098/rspa.2016.0078. PMID: 27279776; PMCID: PMC4893187.
Copy Download .nbib Format: NLM
Multi-Level Interactions Between Heat Shock Factors, Heat Shock Proteins, and the Redox System Regulate Acclimation to Heat.

Frontiers in plant science

Driedonks N, Xu J, Peters JL, Park S, Rieu I.
PMID: 26635827
Front Plant Sci. 2015 Nov 17;6:999. doi: 10.3389/fpls.2015.00999. eCollection 2015.

High temperature has become a global concern because it seriously affects the growth and reproduction of plants. Exposure of plant cells to high temperatures result in cellular damage and can even lead to cell death. Part of the damage...

Cite
Driedonks N, Xu J, Peters JL, et al. Multi-Level Interactions Between Heat Shock Factors, Heat Shock Proteins, and the Redox System Regulate Acclimation to Heat. Front Plant Sci. 2015;6:999doi: 10.3389/fpls.2015.00999.
Driedonks, N., Xu, J., Peters, J. L., Park, S., & Rieu, I. (2015). Multi-Level Interactions Between Heat Shock Factors, Heat Shock Proteins, and the Redox System Regulate Acclimation to Heat. Frontiers in plant science, 6999. https://doi.org/10.3389/fpls.2015.00999
Driedonks, Nicky, et al. "Multi-Level Interactions Between Heat Shock Factors, Heat Shock Proteins, and the Redox System Regulate Acclimation to Heat." Frontiers in plant science vol. 6 (2015): 999. doi: https://doi.org/10.3389/fpls.2015.00999
Driedonks N, Xu J, Peters JL, Park S, Rieu I. Multi-Level Interactions Between Heat Shock Factors, Heat Shock Proteins, and the Redox System Regulate Acclimation to Heat. Front Plant Sci. 2015 Nov 17;6:999. doi: 10.3389/fpls.2015.00999. eCollection 2015. PMID: 26635827; PMCID: PMC4647109.
Copy Download .nbib Format: NLM
Encapsulation of Inorganic Nanomaterials inside Virus-Based Nanoparticles for Bioimaging.

Nanotheranostics

Zhang W, Xu C, Yin GQ, Zhang XE, Wang Q, Li F.
PMID: 29071199
Nanotheranostics. 2017 Aug 18;1(4):358-368. doi: 10.7150/ntno.21384. eCollection 2017.

Virus-based nanoparticles (VNPs) can serve as containers for inorganic nanomaterials with excellent physical and chemical properties. Incorporation of nanomaterials inside the inner cavity of VNPs has opened up lots of possibilities for imaging applications in the field of biology...

Cite
Zhang W, Xu C, Yin GQ, et al. Encapsulation of Inorganic Nanomaterials inside Virus-Based Nanoparticles for Bioimaging. Nanotheranostics. 2017;1(4):358-368doi: 10.7150/ntno.21384.
Zhang, W., Xu, C., Yin, G. Q., Zhang, X. E., Wang, Q., & Li, F. (2017). Encapsulation of Inorganic Nanomaterials inside Virus-Based Nanoparticles for Bioimaging. Nanotheranostics, 1(4), 358-368. https://doi.org/10.7150/ntno.21384
Zhang, Wenjing, et al. "Encapsulation of Inorganic Nanomaterials inside Virus-Based Nanoparticles for Bioimaging." Nanotheranostics vol. 1,4 (2017): 358-368. doi: https://doi.org/10.7150/ntno.21384
Zhang W, Xu C, Yin GQ, Zhang XE, Wang Q, Li F. Encapsulation of Inorganic Nanomaterials inside Virus-Based Nanoparticles for Bioimaging. Nanotheranostics. 2017 Aug 18;1(4):358-368. doi: 10.7150/ntno.21384. eCollection 2017. PMID: 29071199; PMCID: PMC5646737.
Copy Download .nbib Format: NLM
Dipeptide concave nanospheres based on interfacially controlled self-assembly: from crescent to solid.

Physical chemistry chemical physics : PCCP

Wang J, Shen G, Ma K, Jiao T, Liu K, Yan X.
PMID: 27722335
Phys Chem Chem Phys. 2016 Nov 16;18(45):30926-30930. doi: 10.1039/c6cp06150h.

Concave nanospheres based on the self-assembly of simple dipeptides not only provide alternatives for modeling the interactions between biomacromolecules, but also present a range of applications for purification and separation, and delivery of active species. The kinetic control of...

Cite
Wang J, Shen G, Ma K, et al. Dipeptide concave nanospheres based on interfacially controlled self-assembly: from crescent to solid. Phys Chem Chem Phys. 2016;18(45):30926-30930doi: 10.1039/c6cp06150h.
Wang, J., Shen, G., Ma, K., Jiao, T., Liu, K., & Yan, X. (2016). Dipeptide concave nanospheres based on interfacially controlled self-assembly: from crescent to solid. Physical chemistry chemical physics : PCCP, 18(45), 30926-30930. https://doi.org/10.1039/c6cp06150h
Wang, Juan, et al. "Dipeptide concave nanospheres based on interfacially controlled self-assembly: from crescent to solid." Physical chemistry chemical physics : PCCP vol. 18,45 (2016): 30926-30930. doi: https://doi.org/10.1039/c6cp06150h
Wang J, Shen G, Ma K, Jiao T, Liu K, Yan X. Dipeptide concave nanospheres based on interfacially controlled self-assembly: from crescent to solid. Phys Chem Chem Phys. 2016 Nov 16;18(45):30926-30930. doi: 10.1039/c6cp06150h. PMID: 27722335.
Copy Download .nbib Format: NLM
Identification of natural products as novel ligands for the human 5-HT.

Biophysics reports

Peng Y, Zhao S, Wu Y, Cao H, Xu Y, Liu X, Shui W, Cheng J, Zhao S, Shen L, Ma J, Quinn RJ, Stevens RC, Zhong G, Liu ZJ.
PMID: 29577069
Biophys Rep. 2018;4(1):50-61. doi: 10.1007/s41048-018-0047-1. Epub 2018 Mar 09.

G protein-coupled receptors (GPCRs) constitute the largest human protein family with over 800 members, which are implicated in many important medical conditions. Serotonin receptors belong to the aminergic GPCR subfamily and play important roles in physiological and psychological activities....

Cite
Peng Y, Zhao S, Wu Y, et al. Identification of natural products as novel ligands for the human 5-HT. Biophys Rep. 2018;4(1):50-61doi: 10.1007/s41048-018-0047-1.
Peng, Y., Zhao, S., Wu, Y., Cao, H., Xu, Y., Liu, X., Shui, W., Cheng, J., Zhao, S., Shen, L., Ma, J., Quinn, R. J., Stevens, R. C., Zhong, G., & Liu, Z. J. (2018). Identification of natural products as novel ligands for the human 5-HT. Biophysics reports, 4(1), 50-61. https://doi.org/10.1007/s41048-018-0047-1
Peng, Yao, et al. "Identification of natural products as novel ligands for the human 5-HT." Biophysics reports vol. 4,1 (2018): 50-61. doi: https://doi.org/10.1007/s41048-018-0047-1
Peng Y, Zhao S, Wu Y, Cao H, Xu Y, Liu X, Shui W, Cheng J, Zhao S, Shen L, Ma J, Quinn RJ, Stevens RC, Zhong G, Liu ZJ. Identification of natural products as novel ligands for the human 5-HT. Biophys Rep. 2018;4(1):50-61. doi: 10.1007/s41048-018-0047-1. Epub 2018 Mar 09. PMID: 29577069; PMCID: PMC5860131.
Copy Download .nbib Format: NLM
Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization.

Polymer chemistry

Backlund CM, Sgolastra F, Otter R, Minter L, Takeuchi T, Futaki S, Tew GN.
PMID: 29093759
Polym Chem. 2016 Dec 28;7(48):7514-7521. doi: 10.1039/C6PY01615D. Epub 2016 Nov 14.

The plasma membrane is a major obstacle in the development and use of biomacromolecules for intracellular therapeutic applications. Protein transduction domains (PTDs) have been used to overcome this barrier, but often require covalent conjugation to their cargo and can...

Cite
Backlund CM, Sgolastra F, Otter R, et al. Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization. Polym Chem. 2016;7(48):7514-7521doi: 10.1039/C6PY01615D.
Backlund, C. M., Sgolastra, F., Otter, R., Minter, L., Takeuchi, T., Futaki, S., & Tew, G. N. (2016). Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization. Polymer chemistry, 7(48), 7514-7521. https://doi.org/10.1039/C6PY01615D
Backlund, Coralie M, et al. "Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization." Polymer chemistry vol. 7,48 (2016): 7514-7521. doi: https://doi.org/10.1039/C6PY01615D
Backlund CM, Sgolastra F, Otter R, Minter L, Takeuchi T, Futaki S, Tew GN. Increased Hydrophobic Block Length of PTDMs Promotes Protein Internalization. Polym Chem. 2016 Dec 28;7(48):7514-7521. doi: 10.1039/C6PY01615D. Epub 2016 Nov 14. PMID: 29093759; PMCID: PMC5661863.
Copy Download .nbib Format: NLM
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation.

Chemical communications (Cambridge, England)

Shang E, Zhang J, Bai J, Wang Z, Li X, Zhu B, Lei X.
PMID: 27161847
Chem Commun (Camb). 2016 May 19;52(43):7028-31. doi: 10.1039/c6cc01976e.

A transition-metal-free oxidative N-N bond formation strategy was developed to generate various structurally interesting [1,2,4]triazolo[1,5-a]benzazoles efficiently. The mechanism of the key oxidative N-N bond formation was investigated by using an intramolecular competition reaction. Notably, the first single crystal structure...

Cite
Shang E, Zhang J, Bai J, et al. Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation. Chem Commun (Camb). 2016;52(43):7028-31doi: 10.1039/c6cc01976e.
Shang, E., Zhang, J., Bai, J., Wang, Z., Li, X., Zhu, B., & Lei, X. (2016). Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation. Chemical communications (Cambridge, England), 52(43), 7028-31. https://doi.org/10.1039/c6cc01976e
Shang, Erchang, et al. "Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation." Chemical communications (Cambridge, England) vol. 52,43 (2016): 7028-31. doi: https://doi.org/10.1039/c6cc01976e
Shang E, Zhang J, Bai J, Wang Z, Li X, Zhu B, Lei X. Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation. Chem Commun (Camb). 2016 May 19;52(43):7028-31. doi: 10.1039/c6cc01976e. PMID: 27161847.
Copy Download .nbib Format: NLM
Correction to Bacterial Cellulose As a Support for the Growth of Retinal Pigment Epithelium.

Biomacromolecules

Gonçalves S, Padrão J, Rodrigues IP, Silva JP, Sencadas V, Lanceros-Mendez S, Girão H, Dourado F, Rodrigues LR.
PMID: 26594905
Biomacromolecules. 2015 Dec 14;16(12):4032. doi: 10.1021/acs.biomac.5b01556. Epub 2015 Nov 23.

No abstract available.

Cite
Gonçalves S, Padrão J, Rodrigues IP, et al. Correction to Bacterial Cellulose As a Support for the Growth of Retinal Pigment Epithelium. Biomacromolecules. 2015;16(12):4032doi: 10.1021/acs.biomac.5b01556.
Gonçalves, S., Padrão, J., Rodrigues, I. P., Silva, J. P., Sencadas, V., Lanceros-Mendez, S., Girão, H., Dourado, F., & Rodrigues, L. R. (2015). Correction to Bacterial Cellulose As a Support for the Growth of Retinal Pigment Epithelium. Biomacromolecules, 16(12), 4032. https://doi.org/10.1021/acs.biomac.5b01556
Gonçalves, Sara, et al. "Correction to Bacterial Cellulose As a Support for the Growth of Retinal Pigment Epithelium." Biomacromolecules vol. 16,12 (2015): 4032. doi: https://doi.org/10.1021/acs.biomac.5b01556
Gonçalves S, Padrão J, Rodrigues IP, Silva JP, Sencadas V, Lanceros-Mendez S, Girão H, Dourado F, Rodrigues LR. Correction to Bacterial Cellulose As a Support for the Growth of Retinal Pigment Epithelium. Biomacromolecules. 2015 Dec 14;16(12):4032. doi: 10.1021/acs.biomac.5b01556. Epub 2015 Nov 23. PMID: 26594905.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 1103 entries