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Showing 1 to 12 of 25 entries
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Cross-linked Polymer-Blend Gate Dielectrics through Thermal Click Chemistry.

Chemistry (Weinheim an der Bergstrasse, Germany)

Li S, Tang W, Zhang W, Guo X, Zhang Q.
PMID: 26477514
Chemistry. 2015 Dec 01;21(49):17762-8. doi: 10.1002/chem.201502825. Epub 2015 Oct 19.

New cross-linking reagents were synthesized and mixed with polystyrene (PS) in solution to form a blend. Thin-films were spin-coated from the blend and then cross-linked by thermal activation at relatively low temperature (100 °C) to form cross-linked gate dielectrics....

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Li S, Tang W, Zhang W, et al. Cross-linked Polymer-Blend Gate Dielectrics through Thermal Click Chemistry. Chemistry. 2015;21(49):17762-8doi: 10.1002/chem.201502825.
Li, S., Tang, W., Zhang, W., Guo, X., & Zhang, Q. (2015). Cross-linked Polymer-Blend Gate Dielectrics through Thermal Click Chemistry. Chemistry (Weinheim an der Bergstrasse, Germany), 21(49), 17762-8. https://doi.org/10.1002/chem.201502825
Li, Shengxia, et al. "Cross-linked Polymer-Blend Gate Dielectrics through Thermal Click Chemistry." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,49 (2015): 17762-8. doi: https://doi.org/10.1002/chem.201502825
Li S, Tang W, Zhang W, Guo X, Zhang Q. Cross-linked Polymer-Blend Gate Dielectrics through Thermal Click Chemistry. Chemistry. 2015 Dec 01;21(49):17762-8. doi: 10.1002/chem.201502825. Epub 2015 Oct 19. PMID: 26477514.
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Quaternary structure and reconstitution of acetylcholine receptor from Torpedo Californica.

Neurochemistry international

Schiebler W, Bandini G, Hucho F.
PMID: 20487794
Neurochem Int. 1980;2:281-90. doi: 10.1016/0197-0186(80)90035-2.

The nicotinic acetylcholine receptor (AChR) from Torpedo californica electric tissue is a protein complex of MW 270 000 consisting of a binding moiety (receptor) and an ion channel (effector). Reconstitution experiments present evidence that receptor and effector may be...

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Schiebler W, Bandini G, Hucho F. Quaternary structure and reconstitution of acetylcholine receptor from Torpedo Californica. Neurochem Int. 1980;2:281-90doi: 10.1016/0197-0186(80)90035-2.
Schiebler, W., Bandini, G., & Hucho, F. (1980). Quaternary structure and reconstitution of acetylcholine receptor from Torpedo Californica. Neurochemistry international, 2281-90. https://doi.org/10.1016/0197-0186(80)90035-2
Schiebler, W, et al. "Quaternary structure and reconstitution of acetylcholine receptor from Torpedo Californica." Neurochemistry international vol. 2 (1980): 281-90. doi: https://doi.org/10.1016/0197-0186(80)90035-2
Schiebler W, Bandini G, Hucho F. Quaternary structure and reconstitution of acetylcholine receptor from Torpedo Californica. Neurochem Int. 1980;2:281-90. doi: 10.1016/0197-0186(80)90035-2. PMID: 20487794.
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Stabilization of restriction endonuclease Bam HI by cross-linking reagents.

Biotechnology and bioengineering

Dubey AK, Bisaria VS, Mukhopadhyay SN, Ghose TK.
PMID: 18587865
Biotechnol Bioeng. 1989 Apr 20;33(10):1311-6. doi: 10.1002/bit.260331013.

Bacillus amyloliquefaciens H produces a restriction endonuclease enzyme BamHl which is heat labile even at low temperatures. Studies were conducted to enhance thermal stability of BamHl using cross-linking reagents, namely, glutaraldehyde, dimethyl adipimidate (DMA), dimethyl suberimidate (DMS), and dimethyl...

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Dubey AK, Bisaria VS, Mukhopadhyay SN, et al. Stabilization of restriction endonuclease Bam HI by cross-linking reagents. Biotechnol Bioeng. 1989;33(10):1311-6doi: 10.1002/bit.260331013.
Dubey, A. K., Bisaria, V. S., Mukhopadhyay, S. N., & Ghose, T. K. (1989). Stabilization of restriction endonuclease Bam HI by cross-linking reagents. Biotechnology and bioengineering, 33(10), 1311-6. https://doi.org/10.1002/bit.260331013
Dubey, A K, et al. "Stabilization of restriction endonuclease Bam HI by cross-linking reagents." Biotechnology and bioengineering vol. 33,10 (1989): 1311-6. doi: https://doi.org/10.1002/bit.260331013
Dubey AK, Bisaria VS, Mukhopadhyay SN, Ghose TK. Stabilization of restriction endonuclease Bam HI by cross-linking reagents. Biotechnol Bioeng. 1989 Apr 20;33(10):1311-6. doi: 10.1002/bit.260331013. PMID: 18587865.
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Outcome of Corneal Collagen Cross-Linking in Keratoconus: Introducing the Predictive Factors.

Journal of current ophthalmology

Peyman A, Feizi A, Ganjalikhani-Hakemi M, Hosseini-Nasab F, Pourazizi M.
PMID: 32510009
J Curr Ophthalmol. 2020 Mar 23;32(1):19-25. doi: 10.4103/JOCO.JOCO_48_20. eCollection 2020.

PURPOSE: To evaluate the multiple pretreatment characteristics and topographic factors of keratoconus (KC) patients and their relationship to clinical outcomes of corneal collagen cross-linking (CXL).METHODS: In this prospective study, 61 patients (106 eyes) with KC as candidates for CXL...

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Peyman A, Feizi A, Ganjalikhani-Hakemi M, et al. Outcome of Corneal Collagen Cross-Linking in Keratoconus: Introducing the Predictive Factors. J Curr Ophthalmol. 2020;32(1):19-25doi: 10.4103/JOCO.JOCO_48_20.
Peyman, A., Feizi, A., Ganjalikhani-Hakemi, M., Hosseini-Nasab, F., & Pourazizi, M. (2020). Outcome of Corneal Collagen Cross-Linking in Keratoconus: Introducing the Predictive Factors. Journal of current ophthalmology, 32(1), 19-25. https://doi.org/10.4103/JOCO.JOCO_48_20
Peyman, Alireza, et al. "Outcome of Corneal Collagen Cross-Linking in Keratoconus: Introducing the Predictive Factors." Journal of current ophthalmology vol. 32,1 (2020): 19-25. doi: https://doi.org/10.4103/JOCO.JOCO_48_20
Peyman A, Feizi A, Ganjalikhani-Hakemi M, Hosseini-Nasab F, Pourazizi M. Outcome of Corneal Collagen Cross-Linking in Keratoconus: Introducing the Predictive Factors. J Curr Ophthalmol. 2020 Mar 23;32(1):19-25. doi: 10.4103/JOCO.JOCO_48_20. eCollection 2020. PMID: 32510009; PMCID: PMC7265260.
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Integrating gold nanoclusters, folic acid and reduced graphene oxide for nanosensing of glutathione based on "turn-off" fluorescence.

Scientific reports

Wong XY, Quesada-González D, Manickam S, New SY, Muthoosamy K, Merkoçi A.
PMID: 33504892
Sci Rep. 2021 Jan 27;11(1):2375. doi: 10.1038/s41598-021-81677-8.

Glutathione (GSH) is a useful biomarker in the development, diagnosis and treatment of cancer. However, most of the reported GSH biosensors are expensive, time-consuming and often require complex sample treatment, which limit its biological applications. Herein, a nanobiosensor for...

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Wong XY, Quesada-González D, Manickam S, et al. Integrating gold nanoclusters, folic acid and reduced graphene oxide for nanosensing of glutathione based on "turn-off" fluorescence. Sci Rep. 2021;11(1):2375doi: 10.1038/s41598-021-81677-8.
Wong, X. Y., Quesada-González, D., Manickam, S., New, S. Y., Muthoosamy, K., & Merkoçi, A. (2021). Integrating gold nanoclusters, folic acid and reduced graphene oxide for nanosensing of glutathione based on "turn-off" fluorescence. Scientific reports, 11(1), 2375. https://doi.org/10.1038/s41598-021-81677-8
Wong, Xin Yi, et al. "Integrating gold nanoclusters, folic acid and reduced graphene oxide for nanosensing of glutathione based on "turn-off" fluorescence." Scientific reports vol. 11,1 (2021): 2375. doi: https://doi.org/10.1038/s41598-021-81677-8
Wong XY, Quesada-González D, Manickam S, New SY, Muthoosamy K, Merkoçi A. Integrating gold nanoclusters, folic acid and reduced graphene oxide for nanosensing of glutathione based on "turn-off" fluorescence. Sci Rep. 2021 Jan 27;11(1):2375. doi: 10.1038/s41598-021-81677-8. PMID: 33504892; PMCID: PMC7841173.
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Natural Extracellular Matrix for Cellular and Tissue Biomanufacturing.

ACS biomaterials science & engineering

Xing Q, Qian Z, Jia W, Ghosh A, Tahtinen M, Zhao F.
PMID: 33429633
ACS Biomater Sci Eng. 2017 Aug 14;3(8):1462-1476. doi: 10.1021/acsbiomaterials.6b00235. Epub 2016 Dec 20.

Natural extracellular matrices (ECM) derived from native tissues or cultured cells are extensively employed to fabricate biocompatible scaffolds or living tissue constructs for the application in cellular and tissue engineering. The composition and structure of ECM are not only...

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Xing Q, Qian Z, Jia W, et al. Natural Extracellular Matrix for Cellular and Tissue Biomanufacturing. ACS Biomater Sci Eng. 2016;3(8):1462-1476doi: 10.1021/acsbiomaterials.6b00235.
Xing, Q., Qian, Z., Jia, W., Ghosh, A., Tahtinen, M., & Zhao, F. (2017). Natural Extracellular Matrix for Cellular and Tissue Biomanufacturing. ACS biomaterials science & engineering, 3(8), 1462-1476. https://doi.org/10.1021/acsbiomaterials.6b00235
Xing, Qi, et al. "Natural Extracellular Matrix for Cellular and Tissue Biomanufacturing." ACS biomaterials science & engineering vol. 3,8 (2017): 1462-1476. doi: https://doi.org/10.1021/acsbiomaterials.6b00235
Xing Q, Qian Z, Jia W, Ghosh A, Tahtinen M, Zhao F. Natural Extracellular Matrix for Cellular and Tissue Biomanufacturing. ACS Biomater Sci Eng. 2017 Aug 14;3(8):1462-1476. doi: 10.1021/acsbiomaterials.6b00235. Epub 2016 Dec 20. PMID: 33429633.
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Highly cross-linked self-assembled monolayer stationary phases: an approach to greatly enhancing the low pH stability of silica-based stationary phases.

Analytical chemistry

Trammell BC, Ma L, Luo H, Jin D, Hillmyer MA, Carr PW.
PMID: 12349964
Anal Chem. 2002 Sep 15;74(18):4634-9. doi: 10.1021/ac020206d.

A new type of silica-based stationary phase with dramatically improved acid stability compared to any currently available silica-based stationary phase has been developed. Superior low pH stability is achieved by first self-assembling a densely bonded monolayer of (chloromethyl)-phenylethyltrichlorosilane (CMPES)....

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Trammell BC, Ma L, Luo H, et al. Highly cross-linked self-assembled monolayer stationary phases: an approach to greatly enhancing the low pH stability of silica-based stationary phases. Anal Chem. 2002;74(18):4634-9doi: 10.1021/ac020206d.
Trammell, B. C., Ma, L., Luo, H., Jin, D., Hillmyer, M. A., & Carr, P. W. (2002). Highly cross-linked self-assembled monolayer stationary phases: an approach to greatly enhancing the low pH stability of silica-based stationary phases. Analytical chemistry, 74(18), 4634-9. https://doi.org/10.1021/ac020206d
Trammell, Brian C, et al. "Highly cross-linked self-assembled monolayer stationary phases: an approach to greatly enhancing the low pH stability of silica-based stationary phases." Analytical chemistry vol. 74,18 (2002): 4634-9. doi: https://doi.org/10.1021/ac020206d
Trammell BC, Ma L, Luo H, Jin D, Hillmyer MA, Carr PW. Highly cross-linked self-assembled monolayer stationary phases: an approach to greatly enhancing the low pH stability of silica-based stationary phases. Anal Chem. 2002 Sep 15;74(18):4634-9. doi: 10.1021/ac020206d. PMID: 12349964.
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Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ.

ACS medicinal chemistry letters

Nepomuceno GM, Chan KM, Huynh V, Martin KS, Moore JT, O'Brien TE, Pollo LA, Sarabia FJ, Tadeus C, Yao Z, Anderson DE, Ames JB, Shaw JT.
PMID: 25815151
ACS Med Chem Lett. 2015 Jan 07;6(3):308-12. doi: 10.1021/ml500497s. eCollection 2015 Mar 12.

The bacterial cell division protein FtsZ is one of many potential targets for the development of novel antibiotics. Recently, zantrin Z3 was shown to be a cross-species inhibitor of FtsZ; however, its specific interactions with the protein are still...

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Nepomuceno GM, Chan KM, Huynh V, et al. Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ. ACS Med Chem Lett. 2015;6(3):308-12doi: 10.1021/ml500497s.
Nepomuceno, G. M., Chan, K. M., Huynh, V., Martin, K. S., Moore, J. T., O'Brien, T. E., Pollo, L. A., Sarabia, F. J., Tadeus, C., Yao, Z., Anderson, D. E., Ames, J. B., & Shaw, J. T. (2015). Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ. ACS medicinal chemistry letters, 6(3), 308-12. https://doi.org/10.1021/ml500497s
Nepomuceno, Gabriella M, et al. "Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ." ACS medicinal chemistry letters vol. 6,3 (2015): 308-12. doi: https://doi.org/10.1021/ml500497s
Nepomuceno GM, Chan KM, Huynh V, Martin KS, Moore JT, O'Brien TE, Pollo LA, Sarabia FJ, Tadeus C, Yao Z, Anderson DE, Ames JB, Shaw JT. Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ. ACS Med Chem Lett. 2015 Jan 07;6(3):308-12. doi: 10.1021/ml500497s. eCollection 2015 Mar 12. PMID: 25815151; PMCID: PMC4360151.
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Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds.

Journal of the American Chemical Society

Kim C, Wang Z, Choi HJ, Ha YG, Facchetti A, Marks TJ.
PMID: 18454529
J Am Chem Soc. 2008 May 28;130(21):6867-78. doi: 10.1021/ja801047g. Epub 2008 May 03.

We report here the synthesis and dielectric properties of optimized, cross-linked polymer blend (CPB) dielectrics for application in organic field-effect transistors (OFETs). Novel silane cross-linking reagents enable the synthesis of CPB films having excellent quality and tunable thickness (from...

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Kim C, Wang Z, Choi HJ, et al. Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds. J Am Chem Soc. 2008;130(21):6867-78doi: 10.1021/ja801047g.
Kim, C., Wang, Z., Choi, H. J., Ha, Y. G., Facchetti, A., & Marks, T. J. (2008). Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds. Journal of the American Chemical Society, 130(21), 6867-78. https://doi.org/10.1021/ja801047g
Kim, Choongik, et al. "Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds." Journal of the American Chemical Society vol. 130,21 (2008): 6867-78. doi: https://doi.org/10.1021/ja801047g
Kim C, Wang Z, Choi HJ, Ha YG, Facchetti A, Marks TJ. Printable cross-linked polymer blend dielectrics. Design strategies, synthesis, microstructures, and electrical properties, with organic field-effect transistors as testbeds. J Am Chem Soc. 2008 May 28;130(21):6867-78. doi: 10.1021/ja801047g. Epub 2008 May 03. PMID: 18454529.
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Rapid Fabrication of Cell-Laden Alginate Hydrogel 3D Structures by Micro Dip-Coating.

Frontiers in bioengineering and biotechnology

Ghanizadeh Tabriz A, Mills CG, Mullins JJ, Davies JA, Shu W.
PMID: 28286747
Front Bioeng Biotechnol. 2017 Feb 24;5:13. doi: 10.3389/fbioe.2017.00013. eCollection 2017.

Development of a simple, straightforward 3D fabrication method to culture cells in 3D, without relying on any complex fabrication methods, remains a challenge. In this paper, we describe a new technique that allows fabrication of scalable 3D cell-laden hydrogel...

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Ghanizadeh Tabriz A, Mills CG, Mullins JJ, et al. Rapid Fabrication of Cell-Laden Alginate Hydrogel 3D Structures by Micro Dip-Coating. Front Bioeng Biotechnol. 2017;5:13doi: 10.3389/fbioe.2017.00013.
Ghanizadeh Tabriz, A., Mills, C. G., Mullins, J. J., Davies, J. A., & Shu, W. (2017). Rapid Fabrication of Cell-Laden Alginate Hydrogel 3D Structures by Micro Dip-Coating. Frontiers in bioengineering and biotechnology, 513. https://doi.org/10.3389/fbioe.2017.00013
Ghanizadeh Tabriz, Atabak, et al. "Rapid Fabrication of Cell-Laden Alginate Hydrogel 3D Structures by Micro Dip-Coating." Frontiers in bioengineering and biotechnology vol. 5 (2017): 13. doi: https://doi.org/10.3389/fbioe.2017.00013
Ghanizadeh Tabriz A, Mills CG, Mullins JJ, Davies JA, Shu W. Rapid Fabrication of Cell-Laden Alginate Hydrogel 3D Structures by Micro Dip-Coating. Front Bioeng Biotechnol. 2017 Feb 24;5:13. doi: 10.3389/fbioe.2017.00013. eCollection 2017. PMID: 28286747; PMCID: PMC5323421.
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A disposable biosensor based on immobilization of laccase with silica spheres on the MWCNTs-doped screen-printed electrode.

Chemistry Central journal

Li Y, Zhang L, Li M, Pan Z, Li D.
PMID: 22986118
Chem Cent J. 2012 Sep 17;6(1):103. doi: 10.1186/1752-153X-6-103.

BACKGROUND: Biosensors have attracted increasing attention as reliable analytical instruments in in situ monitoring of public health and environmental pollution. For enzyme-based biosensors, the stabilization of enzymatic activity on the biological recognition element is of great importance. It is...

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Li Y, Zhang L, Li M, et al. A disposable biosensor based on immobilization of laccase with silica spheres on the MWCNTs-doped screen-printed electrode. Chem Cent J. 2012;6(1):103doi: 10.1186/1752-153X-6-103.
Li, Y., Zhang, L., Li, M., Pan, Z., & Li, D. (2012). A disposable biosensor based on immobilization of laccase with silica spheres on the MWCNTs-doped screen-printed electrode. Chemistry Central journal, 6(1), 103. https://doi.org/10.1186/1752-153X-6-103
Li, Yuanting, et al. "A disposable biosensor based on immobilization of laccase with silica spheres on the MWCNTs-doped screen-printed electrode." Chemistry Central journal vol. 6,1 (2012): 103. doi: https://doi.org/10.1186/1752-153X-6-103
Li Y, Zhang L, Li M, Pan Z, Li D. A disposable biosensor based on immobilization of laccase with silica spheres on the MWCNTs-doped screen-printed electrode. Chem Cent J. 2012 Sep 17;6(1):103. doi: 10.1186/1752-153X-6-103. PMID: 22986118; PMCID: PMC3505160.
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Nonglutaraldehyde Fixation for off the Shelf Decellularized Bovine Pericardium in Anticalcification Cardiac Valve Applications.

ACS biomaterials science & engineering

Liu J, Jing H, Qin Y, Li B, Sun Z, Kong D, Leng X, Wang Z.
PMID: 33405620
ACS Biomater Sci Eng. 2019 Mar 11;5(3):1452-1461. doi: 10.1021/acsbiomaterials.8b01311. Epub 2019 Feb 11.

In valvular replacement surgery, especially in the construction of bioprosthetic valves with decellularized pericardial xenograft, glutaraldehyde (GA) is routinely utilized as the golden standard reagent to fix bovine or porcine pericardial tissues. However, the apparent defects of GA, including...

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Liu J, Jing H, Qin Y, et al. Nonglutaraldehyde Fixation for off the Shelf Decellularized Bovine Pericardium in Anticalcification Cardiac Valve Applications. ACS Biomater Sci Eng. 2019;5(3):1452-1461doi: 10.1021/acsbiomaterials.8b01311.
Liu, J., Jing, H., Qin, Y., Li, B., Sun, Z., Kong, D., Leng, X., & Wang, Z. (2019). Nonglutaraldehyde Fixation for off the Shelf Decellularized Bovine Pericardium in Anticalcification Cardiac Valve Applications. ACS biomaterials science & engineering, 5(3), 1452-1461. https://doi.org/10.1021/acsbiomaterials.8b01311
Liu, Jing, et al. "Nonglutaraldehyde Fixation for off the Shelf Decellularized Bovine Pericardium in Anticalcification Cardiac Valve Applications." ACS biomaterials science & engineering vol. 5,3 (2019): 1452-1461. doi: https://doi.org/10.1021/acsbiomaterials.8b01311
Liu J, Jing H, Qin Y, Li B, Sun Z, Kong D, Leng X, Wang Z. Nonglutaraldehyde Fixation for off the Shelf Decellularized Bovine Pericardium in Anticalcification Cardiac Valve Applications. ACS Biomater Sci Eng. 2019 Mar 11;5(3):1452-1461. doi: 10.1021/acsbiomaterials.8b01311. Epub 2019 Feb 11. PMID: 33405620.
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Showing 1 to 12 of 25 entries