Готові списки джерел за темами / Quantum Dot - Cellular Imaging

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Автор: Grafiati
Опубліковано: 7 вересня 2023

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Статті в журналах з теми "Quantum Dot - Cellular Imaging"

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Smith, Andrew M., Xiaohu Gao, and Shuming Nie. "Quantum Dot Nanocrystals for In Vivo Molecular and Cellular Imaging¶." Photochemistry and Photobiology 80, no. 3 (2004): 377. http://dx.doi.org/10.1562/0031-8655(2004)080<0377:qdnfiv>2.0.co;2.

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Smith, Andrew M., Xiaohu Gao, and Shuming Nie. "Quantum Dot Nanocrystals for In Vivo Molecular and Cellular Imaging¶." Photochemistry and Photobiology 80, no. 3 (2004): 377. http://dx.doi.org/10.1562/2004-06-21-ir-209.1.

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Smith, Andrew M., Xiaohu Gao, and Shuming Nie. "Quantum Dot Nanocrystals for In Vivo Molecular and Cellular Imaging¶." Photochemistry and Photobiology 80, no. 3 (April 30, 2007): 377–85. http://dx.doi.org/10.1111/j.1751-1097.2004.tb00102.x.

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Jiang, Tongtong, Naiqiang Yin, Ling Liu, Jiangluqi Song, Qianpeng Huang, Lixin Zhu, and Xiaoliang Xu. "A Au nanoflower@SiO2@CdTe/CdS/ZnS quantum dot multi-functional nanoprobe for photothermal treatment and cellular imaging." RSC Adv. 4, no. 45 (2014): 23630–36. http://dx.doi.org/10.1039/c4ra02965h.

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Zhang, Yu-Hui, Ying-Ming Zhang, Yang Yang, Li-Xia Chen, and Yu Liu. "Controlled DNA condensation and targeted cellular imaging by ligand exchange in a polysaccharide–quantum dot conjugate." Chemical Communications 52, no. 36 (2016): 6087–90. http://dx.doi.org/10.1039/c6cc01571a.

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Zheng, Jianing, Arezou Ghazani, Qiang Song, Sawitri Mardyani, Warren Chan, and Chen Wang. "Cellular Imaging and Surface Marker Labeling of Hematopoietic Cells Using Quantum Dot Bioconjugates." Laboratory Hematology 12, no. 2 (June 1, 2006): 94–98. http://dx.doi.org/10.1532/lh96.04073.

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Lee, Jiyeon, Gyoyeon Hwang, Yeon Sun Hong, and Taebo Sim. "One step synthesis of quantum dot–magnetic nanoparticle heterodimers for dual modal imaging applications." Analyst 140, no. 8 (2015): 2864–68. http://dx.doi.org/10.1039/c4an02322f.

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8

Zhang, Mengying, Brittany P. Bishop, Nicole L. Thompson, Kate Hildahl, Binh Dang, Olesya Mironchuk, Nina Chen, Reyn Aoki, Vincent C. Holmberg, and Elizabeth Nance. "Quantum dot cellular uptake and toxicity in the developing brain: implications for use as imaging probes." Nanoscale Advances 1, no. 9 (2019): 3424–42. http://dx.doi.org/10.1039/c9na00334g.

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Park, Junwon, Sankarprasad Bhuniya, Hyunseung Lee, Young-Woock Noh, Yong Taik Lim, Jong Hwa Jung, Kwan Soo Hong, and Jong Seung Kim. "A DTTA-ligated uridine–quantum dot conjugate as a bimodal contrast agent for cellular imaging." Chemical Communications 48, no. 26 (2012): 3218. http://dx.doi.org/10.1039/c2cc17555j.

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Jooken, Stijn, Yovan de Coene, Olivier Deschaume, Dániel Zámbó, Tangi Aubert, Zeger Hens, Dirk Dorfs, et al. "Enhanced electric field sensitivity of quantum dot/rod two-photon fluorescence and its relevance for cell transmembrane voltage imaging." Nanophotonics 10, no. 9 (May 21, 2021): 2407–20. http://dx.doi.org/10.1515/nanoph-2021-0077.

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Abstract The optoelectronic properties of semiconductor nanoparticles make them valuable candidates for the long-term monitoring of transmembrane electric fields in excitable cells. In this work, we show that the electric field sensitivity of the fluorescence intensity of type-I and quasi-type-II quantum dots and quantum rods is enhanced under two-photon excitation compared to single-photon excitation. Based on the superior electric field sensitivity of the two-photon excited fluorescence, we demonstrate the ability of quantum dots and rods to track fast switching E-fields. These findings indicate the potential of semiconductor nanoparticles as cellular voltage probes in multiphoton imaging.
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Дисертації з теми "Quantum Dot - Cellular Imaging"

1

East, Daniel. "Characterisation and functional analysis of fission yeast tropomyosin mutants and development of quantum dot-antibody conjugates for cellular imaging." Thesis, University of Kent, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.527598.

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Wang, Weili. "Bright, compact and biocompatible quantum dot/rod-bioconjugates for Förster resonance energy transfer based ratiometric biosensing and cellular imaging." Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/16881/.

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Cancer, a generic group of diseases, can affect distant sites of the human body to cause sever health consequences. According to the World Health Organization, 9.8 million people died from cancer in 2015 worldwide, about 1600 people per day. More seriously, the number of new cases is expected to increase 70% by 2030 to cause 12 million deaths globally. Early detection, accurate diagnosis and effective treatment are crucial in increasing cancer survival rates and reducing patients’ suffering. In particular, precise cancer positioning that can guide surgery, chemotherapy and radiotherapy has important clinical significance in successful treatment. The nanotechnology-based diagnosis (e.g. QD/QR-bioconjugate probes) and/or treatment of different cancers have received great attention, which is growing to be a promising field in medical research. Over the past 20 years, not only have QD based probes been widely used in developing immunoassays, cellular labeling, cellular imaging, tissue imaging and in vivo imaging, but also being extended to researches such as the drug target and drug delivery system. And this thesis is composed of two parts: Part I An ultra-efficient ligand-exchange protocol (UCEP) to render commercial hydrophobic QDs completely water-soluble using >50-fold less of the air-stable lipoic acid (LA) based functional ligands with a rapid in situ reduction by tris(2-carboxylethyl phosphine, TECP) has been developed. The resulting water-soluble QDs are compact (Dh <10 nm), bright (retaining >90% of original fluorescence), resisting nonspecific adsorption and displaying good stabilities in biological buffers even with high salt contents (e.g. 2 M NaCl), making them well-suited for cell imaging and ratiometric biosensing. A DHLA-zwitterion capped QD prepared by the UCEP is readily biofunctionalized with hexa-histidine (His8)-tagged small antibody mimetic proteins (also known as Affimers), allowing for rapid, ratiometric detection of its target protein down to 5 pM via the QD-sensitized Förster resonance energy transfer (FRET) readout signal. Moreover, compact biotin functionalized QDs are prepared by a facile, one-step cap-exchange process for ratiometric quantitation detection of 5 pM protein such as NeutrAvidin as well as for fluorescence imaging of target model cancer cells. Part II A stable, water-soluble rod-shaped fluorescence semiconductor nanocrystal (CdSe/CdS core/shell quantum rod, QR) was made by an efficient cap exchange protocol as described in Part I. However, in most cases the fluorescence of the cap-exchanged QR was almost quenched, hindering their biomedical applications. Herein I have solved this problem by discovering a simple method that allows for efficient recovery of the QR quantum yield, making them suitable for biological applications. The resulting water-soluble QRs are compact (Dh < 20 nm), bright (recovering to > 67% of original fluorescence), resisting nonspecific adsorption and displaying good stabilities in biological buffers, making them well-suited for ratiometric biosensing. After tris(2-carboxylethyl phosphine, (TECP) reduction, a dihydrolipoic acid-zwitterion ligand (DHLA-ZW) capped QR was self-assembled with (His8)-tagged anti-yeast SUMO non-antibody binding proteins (nABPs), allowing for ratiometric detection of its target protein down to 5 pM by the QR-sensitized Förster resonance energy transfer (FRET) signal. Furthermore, compact biotin functionalized QRs are prepared by a facile, one-step cap-exchange process for ratiometric quantitation of labelled neutravidin down to 5 pM. Such sensitivity is among the very best for QR-FRET based biosensors.
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Hafian, Hilal. "IMAGERIE CELLULAIRE ET TISSULAIRE DE BIO-MARQUEURS TUMORAUX : EXCITATION MULTI-PHOTONIQUE DE QUANTUM DOTS CONJUGUES AVEC DES ANTICORPS DE DOMAINE SIMPLE." Thesis, Reims, 2016. http://www.theses.fr/2016REIMP201.

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Les conjugués QD-sdAbs sont des nano-sondes qui associent un quantum dot (QD) et des anticorps de domaine simple (sdAbs). Ces nano-sondes fluorescentes permettent des immunomarquages sur coupes tissulaires et sur cellules. L’objectif de ce travail est de montrer l’intérêt de l’excitation multi-photonique pour la détection et la localisation très spécifiques de biomarqueurs tumoraux.L’excitation multi-photonique des nano-sondes QD570-sdAb anti-CEA a été étudiée, sur coupes d’appendice et de carcinome du côlon humains pour optimiser le rapport signal/auto-fluorescence. L’utilisation du QD comme capteur d’énergie d’excitation dans un modéle de FRET QD-fluorophore organique a été démontré. Un modéle innovant pour une détéction ultra spécifique du CEA sur cellules MC38 CEA par double immunomarquage spécifique pour un transfert d’énergie résonnant entre QD et Alexa Fluor à été mis en oeuvre.Les résutats montrent l’intérêt de l’excitation multi-photonique par rapport à l’excitation à 458,9 nm pour la discrimination et l’optimisation du rapport signal/auto-fluorescence. Il est 40 fois supérieur en excitation à 800 nm qu’à 458,9 nm sur les coupes étudiées.L’utilisation des conjugués QD556-sdAb anti-CEA et d’un anticorps monoclonal permet un double immunomarquage du CEA membranaire sur cellules MC38 CEA. L’utilisation du QD comme nano-capteur d’énergie d’excitation multi-photonique permet une séléctivité d’excitation et un FRET entre QD et Alexa Fluor. Ce schéma permet une détéction spectrale aisée du FRET et une localisation très spécifique et sensible du CEA membranaire. Ceci est conforté par la diminution du temps de déclin du QD556 donneur d’énergie non radiative
The QD-sdAbs conjugates are nano-sensors that combine a quantum dot (QD) and single domain antibodies (sdAbs). These fluorescent nanoprobes allow immunostaining on tissue sections and cells. The objective of this work is to show the interest of the multi-photon excitation for the detection and highly specific location of tumor biomarkers.Multi-photon excitation of anti CEA QD570-sdAb nanoprobes was investigated on human appendix and colon carcinoma slides for specifical detection and an optimization of the signal/auto-fluorescence emission ratio. The use of QD as excitation energy sensor for a QD-organic fluorophore FRET model has been shown. An innovative model for ultra-specific detection of CEA on MC38 CEA membrane cells by double immunostaining for a resonant energy transfer between QD and Alexa Fluor has been implemented.Our results shows the great interest of the multi-photon excitation compared to 458.9 nm excitation for discrimination and optimization of the signal / autofluorescence. It is 40 times higher at 800 nm two photon excitation has 458.9 nm one photon excitation on the studied sections.The use of conjugated QD556-sdAb anti-CEA and a conventional monoclonal antibody allows a double immunostaining on CEA on MC38 CEA membrane cells. The QD is use as multi-photon excitation energy nano-sensor enables an excitation selectivity and FRET between QD and Alexa Fluor. This configuration enables easy spectral detection of FRET and a very specific and sensitive location of membrane CEA. This is reinforced by the decrease in decay time of QD556 as donor of non radiative energy
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4

Srivastava, Saket. "Probabilistic modeling of quantum-dot cellular automata." [Tampa, Fla.] : University of South Florida, 2007. http://purl.fcla.edu/usf/dc/et/SFE0002399.

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5

Zimmer, John P. (John Philip). "Quantum dot-based nanomaterials for biological imaging." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/37888.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2006.
Vita.
Includes bibliographical references.
Quantum dot-based fluorescent probes were synthesized and applied to biological imaging in two distinct size regimes: (1) 100-1000 nm and (2) < 10 nm in diameter. The larger diameter range was accessed by doping CdSe/ZnS or CdS/ZnS quantum dots (QDs) into shells grown on the surfaces of pre-formed sub-micron SiO2 microspheres. The smaller diameter range was accessed with two different materials: very small InAs/ZnSe QDs and CdSe/ZnS QDs, each water solubilized with small molecule ligands chosen for their ability not only to stabilize QDs in water but also to minimize the total hydrodynamic size of the QD-ligand conjugates. Indium arsenide QDs were synthesized because nanocrystals of this material can be tuned to fluoresce in the near infrared (NIR) portion of the electromagnetic spectrum, especially in the 700-900 nm window where many tissues in the body absorb and scatter minimally, while maintaining core sizes of 2 nm or less. The QD-containing microspheres were used to image tumor vasculature in living animals, and to generate maps of size-dependent extravasation. With subcutaneously delivered nAs/ZnSe QDs, multiple lymph node mapping was demonstrated in vivo for the first time with nanocrystals. When administered intravenously, < 10 nm QDs escaped from the vasculature, or were efficiently cleared from circulation by the kidney. Both of these behaviors, previously unreported, mark key milestones in the realization of an ideal fluorescent QD probe for imaging specific compartments in vivo. Also presented in this thesis is the growth of single-crystalline cobalt nanorods through the oriented attachment of spherical cobalt nanocrystal monomers.
(cont.) When administered intravenously, < 10 nm QDs escaped from the vasculature, or were efficiently cleared from circulation by the kidney. Both of these behaviors, previously unreported, mark key milestones in the realization of an ideal fluorescent QD probe for imaging specific compartments in vivo. Also presented in this thesis is the growth of single-crystalline cobalt nanorods through the oriented attachment of spherical cobalt nanocrystal monomers.
by John P. Zimmer.
Ph.D.
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6

Pelling, Stephen. "Terahertz imaging using a quantum dot detector." Thesis, Royal Holloway, University of London, 2011. http://repository.royalholloway.ac.uk/items/2311f672-f705-ab41-a5b9-78f87a192faf/8/.

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Mandell, Eric S. "Theoretical studies of inter-dot potential barrier modulation in quantum-dot cellular automata." Virtual Press, 2001. http://liblink.bsu.edu/uhtbin/catkey/1221305.

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Quantum-Dot Cellular Automata (QCA) is being investigated as a possible alternative for encoding and processing binary information in an attempt to realize dramatic improvements in device density and processing speed over conventional CMOS design. The binary information is encoded in the locations of two excess electrons in a system of four quantum dots. The dots are arranged with each on a corner of a square, and electrons are able to quantum-mechanically tunnel between dots. Each set of four dots and two excess electrons constitutes a QCA cell. Coulomb repulsion ensures that the electrons will tend to occupy antipodal sites, giving two possible polarizations, or lowest energy ground states for a QCA cell. The electrons would tend to align along one diagonal or the other. Arrangements of QCA cells can be used to pass along input binary information and perform necessary logic operations on the input signal.When electrons tunnel back and forth between dots, it is possible they will occupy excited states in the dots. Two undesirable effects result from this: 1) Energy will be dissipated to the environment and cause thermal heating, and 2) it is possible a cell could become locked in a metastable state, which may be a local energy minimum, but is not one of the ground state polarizations we desire. Through the modulation of the heights of the inter-dot potential barriers, it would be possible to allow electrons to more easily tunnel between dots. This would help prevent the system from reaching excited states. The time variance in the heights of the potential barriers must be greater than the time it takes for the electrons to tunnel between dots, thus, effectively clocking the QCA device.We present theoretical studies of controlling the inter-dot potential barriers in a QCA device using an electric field due to electrostatically charged rods. The amount of charge on the rods is varied in time to increase and decrease the electric field, which will raise and lower the inter-dot potential barriers as desired. Different arrangements of rods provide different time-dependent behavior in the electric field, which may be useful depending on the arrangements of QCA cells required to make a logic device.
Department of Physics and Astronomy
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Hendrichsen, Melissa K. "Thermal effect and fault tolerance in quantum dot cellular automata." Virtual Press, 2005. http://liblink.bsu.edu/uhtbin/catkey/1314329.

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To have a useful QCA device it is first necessary to study how to control data flow in a device, then study how temperature and manufacturing defects will affect the proper output of the device. Theoretically a "quantum wire" of perfectly aligned QCA cells at zero Kelvin temperature has been examined. However, QCA processors will not be operating at a temperature of zero Kelvin and inherently the manufacturing process will introduce defects into the system. Many different types of defects could occur at the device level and the individual cell level, both kinds of defects should be examined. Device defects include but are not limited to linear and/or rotational translation, and missing or extra cell(s). The internal cell defects would include an odd sized cell, and one or more miss-sized or dislocated quantum dot(s). These defects may have little effect on the operation of the QCA device, or could cause a complete failure. In addition, the thermal effect on the QCA devices may also cause a failure of the device or system. The defect and thermal operating limit of a QCA device must be determined.In the present investigation, the thermal and defect tolerance of clocked QCA devices will be studied. In order to study tolerance of QCA devices theoretical models will be developed. In particular, some existing computer simulation programs will be studied and expanded.
Department of Physics and Astronomy
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9

Kanuchok, Jonathan L. "The thermal effect and clocking in quantum-dot cellular automata." Virtual Press, 2004. http://liblink.bsu.edu/uhtbin/catkey/1286605.

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We present a theoretical study of quasi-adiabatic clocking and thermal effect in Quantum-dot Cellular Automata (QCA). Quasi-adiabatic clocking is the modulation of an inter-dot potential barrier in order to keep the QCA cells near the ground state throughout the switching process. A time-dependent electric field is calculated for arrays of charged rods. The electron tunneling between dots is controlled by raising and lowering a potential barrier in the cell.A quantum statistical model has been introduced to obtain the thermal average of polarization of a QCA cell. We have studied the thermal effect on QCA devices. The theoretical analysis has been approximated for a two-state model where the cells are in one of two possible eigenstates of the cell Hamiltonian. In general, the average polarization of each cell decreases with temperature and the distance from the driver cells. The results demonstrate the critical nature of temperature dependence for the operation of QCA.
Department of Physics and Astronomy
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10

Tung, Chia-Ching. "Implementation of multi-CLB designs using quantum-dot cellular automata /." Online version of thesis, 2010. http://hdl.handle.net/1850/11699.

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Книги з теми "Quantum Dot - Cellular Imaging"

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Sasamal, Trailokya, Hari Mohan Gaur, Ashutosh Kumar Singh, and Xiaoqing Wen. Quantum-Dot Cellular Automata Circuits for Nanocomputing Applications. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003361633.

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Kumar, Naresh. Memory Design Using Quantum Dot Cellular Automata (QCA) Technology. Saarbrücken: LAP LAMBERT Academic Publishing, 2017.

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Sridharan, K., and Vikramkumar Pudi. Design of Arithmetic Circuits in Quantum Dot Cellular Automata Nanotechnology. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-16688-9.

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Sasamal, Trailokya Nath, Ashutosh Kumar Singh, and Anand Mohan. Quantum-Dot Cellular Automata Based Digital Logic Circuits: A Design Perspective. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-1823-2.

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Sridharan, K., and Vikramkumar Pudi. Design of Arithmetic Circuits in Quantum Dot Cellular Automata Nanotechnology. Springer, 2016.

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Sridharan, K., and Vikramkumar Pudi. Design of Arithmetic Circuits in Quantum Dot Cellular Automata Nanotechnology. Springer, 2015.

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7

Sridharan, K., and Vikramkumar Pudi. Design of Arithmetic Circuits in Quantum Dot Cellular Automata Nanotechnology. Springer, 2015.

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8

Design and Test of Digital Circuits by Quantum-Dot Cellular Automata. Artech House Publishers, 2007.

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9

Mohan, Anand, Ashutosh Kumar Singh, and Trailokya Nath Sasamal. Quantum-Dot Cellular Automata Based Digital Logic Circuits: A Design Perspective. Springer, 2020.

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10

Mohan, Anand, Ashutosh Kumar Singh, and Trailokya Nath Sasamal. Quantum-Dot Cellular Automata Based Digital Logic Circuits: A Design Perspective. Springer Singapore Pte. Limited, 2021.

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Частини книг з теми "Quantum Dot - Cellular Imaging"

1

Rees, Kelly, Melissa Massey, Michael V. Tran, and W. Russ Algar. "Dextran-Functionalized Quantum Dot Immunoconjugates for Cellular Imaging." In Quantum Dots, 143–68. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0463-2_8.

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2

East, Daniel Alistair, Michael Todd, and Ian James Bruce. "Quantum Dot–Antibody Conjugates via Carbodiimide-Mediated Coupling for Cellular Imaging." In Quantum Dots: Applications in Biology, 67–83. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1280-3_5.

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Lent, C. S., G. L. Snider, G. Bernstein, W. Porod, A. Orlov, M. Lieberman, T. Fehlner, M. Niemier, and P. Kogge. "Quantum-Dot Cellular Automata." In Electron Transport in Quantum Dots, 397–431. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0437-5_10.

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4

Khanna, Vinod Kumar. "Quantum Dot Cellular Automata (QDCA)." In NanoScience and Technology, 323–39. New Delhi: Springer India, 2016. http://dx.doi.org/10.1007/978-81-322-3625-2_19.

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Silva, Gabriel A. "Quantum Dot Methods for Cellular Neuroimaging." In Nanotechnology for Biology and Medicine, 169–86. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-31296-5_8.

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Lent, Craig S., and Gregory L. Snider. "The Development of Quantum-Dot Cellular Automata." In Field-Coupled Nanocomputing, 3–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-43722-3_1.

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Lent, Craig S., and Gregory L. Snider. "The Development of Quantum-Dot Cellular Automata." In Field-Coupled Nanocomputing, 3–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-45908-9_1.

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Chang, Jerry C., and Sandra J. Rosenthal. "Single Quantum Dot Imaging in Living Cells." In Methods in Molecular Biology, 149–62. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-336-7_15.

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Sen, Bibhash, Manojit Dutta, Divyam Saran, and Biplab K. Sikdar. "An Efficient Multiplexer in Quantum-dot Cellular Automata." In Progress in VLSI Design and Test, 350–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-31494-0_40.

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Hänninen, Ismo, and Jarmo Takala. "Radix-4 Recoded Multiplier on Quantum-Dot Cellular Automata." In Lecture Notes in Computer Science, 118–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03138-0_13.

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Тези доповідей конференцій з теми "Quantum Dot - Cellular Imaging"

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Dahan, Maxime. "Probing Cellular Events with Single Quantum Dot Imaging." In Laser Science. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/ls.2009.lsthb4.

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Courty, Sébastien, Marcel Zevenbergen, Cédric Bouzigues, Marie-Virginie Ehrensperger, Camilla Luccardini, Assa Sittner, Stéphane Bonneau, and Maxime Dahan. "Single quantum dot imaging in live cells: toward a cellular GPS." In Biomedical Optics 2006, edited by Marek Osinski, Kenji Yamamoto, and Thomas M. Jovin. SPIE, 2006. http://dx.doi.org/10.1117/12.663348.

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3

Hoshino, K., G. Bhave, N. Triesault, P. Joshi, A. Zubieta, V. Wang, K. V. Sokolov, and X. J. Zhang. "Quantum dot based compact solid-state swept light source for hyperspectral cellular imaging." In 2013 Transducers & Eurosensors XXVII: The 17th International Conference on Solid-State Sensors, Actuators and Microsystems (TRANSDUCERS & EUROSENSORS XXVII). IEEE, 2013. http://dx.doi.org/10.1109/transducers.2013.6627336.

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Bernstein, Gary H. "Quantum-dot cellular automata." In the 40th conference. New York, New York, USA: ACM Press, 2003. http://dx.doi.org/10.1145/775832.775900.

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Lent, Craig S. "Molecular quantum-dot cellular automata." In 2006 IEEE Workshop on Signal Processing Systems Design and Implementation. IEEE, 2006. http://dx.doi.org/10.1109/sips.2006.352542.

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Snider, Gregory L., Alexei O. Orlov, Vishwanath Joshi, Robin A. Joyce, Hua Qi, Kameshwar K. Yadavalli, Gary H. Bernstein, Thomas P. Fehlner, and Craig S. Lent. "Electronic quantum-dot cellular automata." In 2008 9th International Conference on Solid-State and Integrated-Circuit Technology (ICSICT). IEEE, 2008. http://dx.doi.org/10.1109/icsict.2008.4734600.

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Krrabaj, Samedin, Ercan Canhasi, and Xhevahir Bajrami. "Quantum-Dot cellular automata divider." In 2017 6th Mediterranean Conference on Embedded Computing (MECO). IEEE, 2017. http://dx.doi.org/10.1109/meco.2017.7977215.

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Ghosh, Bahniman, Shoubhik Gupta, and Smriti Kumari. "Quantum dot cellular automata magnitude comparators." In 2012 IEEE International Conference of Electron Devices and Solid-State Circuits (EDSSC). IEEE, 2012. http://dx.doi.org/10.1109/edssc.2012.6482766.

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Lampreht, Blaz, Luka Stepancic, Igor Vizec, Bostjan Zankar, Miha Mraz, Iztok Lebar Bajec, and Primoz Pecar. "Quantum-Dot Cellular Automata Serial Comparator." In 2008 11th EUROMICRO Conference on Digital System Design Architectures, Methods and Tools. IEEE, 2008. http://dx.doi.org/10.1109/dsd.2008.49.

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Sen, Bibhash, Anshu S. Anand, Tanumoy Adak, and Biplab K. Sikdar. "Thresholding using Quantum-dot Cellular Automata." In 2011 International Conference on Innovations in Information Technology (IIT). IEEE, 2011. http://dx.doi.org/10.1109/innovations.2011.5893848.

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Звіти організацій з теми "Quantum Dot - Cellular Imaging"

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Ropp, Chad, Zachary Cummins, Sanghee Nah, John T. Fourkas, Benjamin Shapiro, and Edo Waks. Nanoscale Imaging with a Single Quantum Dot. Fort Belvoir, VA: Defense Technical Information Center, December 2011. http://dx.doi.org/10.21236/ada581052.

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Meier, Kristina. Quantum at LANL Quantum Ghost Imaging and Quantum Dot Single-Photon Sources. Office of Scientific and Technical Information (OSTI), January 2023. http://dx.doi.org/10.2172/1921988.

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Singhal, Rahul. Logic Realization Using Regular Structures in Quantum-Dot Cellular Automata (QCA). Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.196.

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