Literatura académica sobre el tema "DNA nanoarrays"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "DNA nanoarrays".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "DNA nanoarrays"
Yang, Yang y Chenxiang Lin. "Directing reconfigurable DNA nanoarrays". Science 357, n.º 6349 (27 de julio de 2017): 352–53. http://dx.doi.org/10.1126/science.aao0599.
Texto completoHao, X., E. A. Josephs, Q. Gu y T. Ye. "Molecular conformations of DNA targets captured by model nanoarrays". Nanoscale 9, n.º 36 (2017): 13419–24. http://dx.doi.org/10.1039/c7nr04715k.
Texto completoNAKAO, Hidenobu, Futoshi IWATA, Hidenori KARASAWA, Hideki HAYASHI y Kazushi MIKI. "Fabrication of Metallic Nanoarrays using DNA Templates". Hyomen Kagaku 28, n.º 7 (2007): 372–77. http://dx.doi.org/10.1380/jsssj.28.372.
Texto completoHawkes, William, Da Huang, Paul Reynolds, Linda Hammond, Matthew Ward, Nikolaj Gadegaard, John F. Marshall, Thomas Iskratsch y Matteo Palma. "Probing the nanoscale organisation and multivalency of cell surface receptors: DNA origami nanoarrays for cellular studies with single-molecule control". Faraday Discussions 219 (2019): 203–19. http://dx.doi.org/10.1039/c9fd00023b.
Texto completoPiccone, Ashley. "DNA origami folds proteins into nanoarrays with precision". Scilight 2022, n.º 34 (19 de agosto de 2022): 341107. http://dx.doi.org/10.1063/10.0013751.
Texto completoLiu, Yan, Yonggang Ke y Hao Yan. "Self-Assembly of Symmetric Finite-Size DNA Nanoarrays". Journal of the American Chemical Society 127, n.º 49 (diciembre de 2005): 17140–41. http://dx.doi.org/10.1021/ja055614o.
Texto completoMei, Qian, Xixi Wei, Fengyu Su, Yan Liu, Cody Youngbull, Roger Johnson, Stuart Lindsay, Hao Yan y Deirdre Meldrum. "Stability of DNA Origami Nanoarrays in Cell Lysate". Nano Letters 11, n.º 4 (13 de abril de 2011): 1477–82. http://dx.doi.org/10.1021/nl1040836.
Texto completoGhosh, Sumana y Eric Defrancq. "Metal-Complex/DNA Conjugates: A Versatile Building Block for DNA Nanoarrays". Chemistry - A European Journal 16, n.º 43 (4 de octubre de 2010): 12780–87. http://dx.doi.org/10.1002/chem.201001590.
Texto completoCervantes-Salguero, K., M. Freeley, R. E. A. Gwyther, D. D. Jones, J. L. Chávez y M. Palma. "Single molecule DNA origami nanoarrays with controlled protein orientation". Biophysics Reviews 3, n.º 3 (septiembre de 2022): 031401. http://dx.doi.org/10.1063/5.0099294.
Texto completoSathish, Shivani, Sébastien G. Ricoult, Kazumi Toda-Peters y Amy Q. Shen. "Microcontact printing with aminosilanes: creating biomolecule micro- and nanoarrays for multiplexed microfluidic bioassays". Analyst 142, n.º 10 (2017): 1772–81. http://dx.doi.org/10.1039/c7an00273d.
Texto completoTesis sobre el tema "DNA nanoarrays"
White, Jenifer Christine. "Novel functionalised, nanoarrays of DNA binding supramolecular helicates". Thesis, University of Birmingham, 2016. http://etheses.bham.ac.uk//id/eprint/6625/.
Texto completoZhang, Fan. "DNA directed assembly of two dimensional fluorophore nanoarrays". Huntington, WV : [Marshall University Libraries], 2004. http://www.marshall.edu/etd/descript.asp?ref=396.
Texto completoTitle from document title page. Abstract included. Document formatted into pages; contains viii, 96 p. including illustrations. Includes abstract. Includes bibliographical references (p. 95-96).
Akbulut, Halatci Özge. "Extending the realm of SuNS to DNA nanoarrays and peptide features". Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/59218.
Texto completoIncludes bibliographical references.
Intense research on DNA arrays has been fostered by their applications in the field of biomedicine. DNA microarrays are composed of several different DNA sequences to be analyzed in parallel allowing high throughput information. Current methods to fabricate these arrays are serial in nature resulting in high prices that prevent their extensive utilization. Supramolecular Nanostamping is devised to solve this problem by harnessing the reversible bond formation between complementary DNA strands. This contact based technique is proven to replicate DNA arrays in a three step cycle: 1) Hybridization, 2) Contact and 3) Dehybridization. The overall goal of this thesis is to demonstrate the application of SuNS to DNA nanoarrays, i.e. increase the resolution of the current method, and broaden the printing capability to peptide arrays. The amount of analyte needed in an array scales with the feature size and spacing i.e. the total array size. The features of a DNA microarray are usually tens of micrometers in size with a spacing on the order of hundred micrometers. Therefore, miniaturization of such arrays is necessary for applications when analyte scarcity is an issue. DNA nanoarrays are promising lower analyte volumes due to their decreased feature size and spacing; namely high resolution. Unfortunately, DNA nanoarrays can only be fabricated by scanning probe microscopy based serial methods which generate each spot individually. To demonstrate SuNS is capable of dealing with the increasing demand to miniaturize DNA arrays, DNA features composed of a few DNA strands is replicated. The faithful printing of feature sizes as small as 14 nm with 70 nm spacing was shown. Apart from the capability to cope with features of various sizes, the strength of a printing method emerges from its ability to deal with different types of biomolecules. Coiled-coil peptides are treated analogously to complementary DNA strands due to the molecular recognition between two complementary peptide strands. Through Liquid Supramolecular Nanostamping (LiSuNS), the replication of coiled-coil motif peptides was demonstrated. To prove the multiplexing capability of the process, a master made of peptide and DNA features was successfully stamped via LiSuNS as well.
by Ozge Akbulut Halatci.
Ph.D.
Castronovo, Matteo. "Crowding effects on biochemical reactions of surface-bound DNA". Doctoral thesis, Università degli studi di Trieste, 2008. http://hdl.handle.net/10077/2616.
Texto completoNext-generation DNA detection arrays are expected to achieve unprecedented sensitivity, reducing the minimum amount of genetic material that can be directly (PCR-free and label-free) and quantitatively detected, up to the single cell limit. To realize these goals, we propose a new method for the miniaturization of DNA arrays to the nano-scale, which has the unique capability of controlling the packing quality of the deposited bio- molecules. We used NanoGrafting, a nano-lithography technique based on atomic force microscopy (AFM), to fabricate well ordered thiolated single stranded (ss)-DNA nano-patches within a self-assembled monolayer (SAM) of inert thiols on gold surfaces. By varying the “writing” parameters, in particular the number of scan lines, we were able to vary the density of the supported DNA molecules inside the nano-patches in a controlled manner. Our findings can be resumed in two parts: 1) Combining accurate height and compressibility measurements, before and after hybridization, we demonstrate that high-density ss-DNA nanografted patches hybridize with high efficiency, and that, contrary to current understanding, is not the density of probe molecules to be responsible for the lack of hybridization observed in high density ss-DNA SAMs, but the poor quality of their structure. 2) Dpn II enzymatic reactions were carried out over nanopatches with different molecular density and different geometries. Using nanopatch height measurements we are able to show that the capability of the Dpn II enzyme to reach and react at the recognition site significantly depends on the molecular density in the nanopatches. In particular the inhibition of the reaction follows a step-wise fashion at relatively low DNA densities. These findings suggest that, due to the enzyme size, it is possible to tune the efficiency of an enzymatic reaction within surface-bound DNA nanostructures by changing only the crowding of DNA on the surface and without introducing any further physical or chemical variable.
XIX Ciclo
1979
Actas de conferencias sobre el tema "DNA nanoarrays"
Cheng, Li-Jing, Akash Kannegulla, Ye Liu y Bo Wu. "Enhanced molecular beacon based DNA detection using plasmonic open-ring nanoarrays". En Biosensing and Nanomedicine XI, editado por Hooman Mohseni, Massoud H. Agahi y Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2321234.
Texto completoKannegulla, Akash, Ye Liu, Bo Wu y Li-Jing Cheng. "Broadband Fluorescence Enhancement and Ultrasensitive DNA Detection Using Plasmonic Open-Ring Nanoarrays". En CLEO: Applications and Technology. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/cleo_at.2018.atu3j.2.
Texto completoKim, Do-Kyun, Young-Soo Kwon, Yuzuru Takamura y Eiichi Tamiya. "Development of DNA chip nanoarray by Fluidic Self-assembly method for Detection of DNA Hybridization". En 2005 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2005. http://dx.doi.org/10.7567/ssdm.2005.p11-3.
Texto completo