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Artykuły w czasopismach na temat "Molecular probes"

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Bubien, James K., i Dale J. Benos. "Molecular pH Probes". Circulation Research 99, nr 5 (wrzesień 2006): 453–54. http://dx.doi.org/10.1161/01.res.0000241052.33145.54.

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Zhang, Yujin, i Wei Hu. "Sensing Performance and Efficiency of Two Energy Transfer-Based Two-Photon Fluorescent Probes for pH". Sensors 18, nr 12 (13.12.2018): 4407. http://dx.doi.org/10.3390/s18124407.

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The design and synthesis of fluorescent probes for monitoring pH values inside living cells have attracted great attention, due to the important role pH plays in many biological processes. In this study, the optical properties of two different two-photon fluorescent probes for pH are studied. The ratiometric sensing of the probes are theoretically illustrated. Meanwhile, the recognitional mechanisms of the probes are investigated, which shows the energy transfer process when react with H+. Specially, the calculated results demonstrate that Probe1 possesses a higher energy transfer efficiency and a larger two-photon absorption cross-section than Probe2, indicating it to be a preferable pH fluorescent probe. Therefore, the influence of connection between the donor and the acceptor on the sensing performances of the probe is demonstrated. Our results help to understand the experimental observations and provide a theoretical basis to synthesize efficient two-photon fluorescent probes for monitoring pH changes.
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Mahmood, U., i L. Josephson. "Molecular MR Imaging Probes". Proceedings of the IEEE 93, nr 4 (kwiecień 2005): 800–808. http://dx.doi.org/10.1109/jproc.2005.844264.

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Strack, Rita. "Probes for molecular crowding". Nature Methods 15, nr 8 (31.07.2018): 570. http://dx.doi.org/10.1038/s41592-018-0098-8.

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Diwu, Zhenjun, Cailan Zhang, Dieter H. Klaubert i Richard P. Haugland. "Fluorescent molecular probes VI". Journal of Photochemistry and Photobiology A: Chemistry 131, nr 1-3 (luty 2000): 95–100. http://dx.doi.org/10.1016/s1010-6030(99)00240-3.

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Butler, John E. "Molecular probes and immunodiagnostics". Veterinary Immunology and Immunopathology 35 (luty 1993): 205–12. http://dx.doi.org/10.1016/0165-2427(93)90150-3.

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Wood, EJ. "Molecular probes: Handbook of fluorescent probes and research chemicals". Biochemical Education 22, nr 2 (kwiecień 1994): 83. http://dx.doi.org/10.1016/0307-4412(94)90083-3.

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Kele, Péter. "Advanced molecular (bio)probes—probes that are good, better, smarter". Methods and Applications in Fluorescence 3, nr 4 (8.09.2015): 040201. http://dx.doi.org/10.1088/2050-6120/3/4/040201.

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Barakat, Sarah, Melike Berksöz, Pegah Zahedimaram, Sofia Piepoli i Batu Erman. "Nanobodies as molecular imaging probes". Free Radical Biology and Medicine 182 (marzec 2022): 260–75. http://dx.doi.org/10.1016/j.freeradbiomed.2022.02.031.

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Nagano, T. "Molecular design of bioimaging probes". Seibutsu Butsuri 43, supplement (2003): S15. http://dx.doi.org/10.2142/biophys.43.s15_2.

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Rozprawy doktorskie na temat "Molecular probes"

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Nathubhai, Amit. "Molecular probes for mammalian chitinases". Thesis, University of Bath, 2010. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.518107.

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Chitin is a glycopolymer consisting of +-(1, 4)-linked N-acetyl-D-glucosamine residues that occurs widely in nature and is a constituent of many organisms that are pathogenic to humans, including insects, fungi, and parasitic nematodes. As these organisms depend on the ability to break down chitin at key points of their life-cycle, inhibitors of the enzymes termed chitinases that catalyse the hydrolysis of chitin, are of considerable interest as potential drugs and insecticides. Although chitin is absent from mammalian physiology, two human chitinases along with several chitin-binding proteins (chi-lectins) have been associated with the onset or transmission of several major human diseases such as asthma, Legionnaire’s disease and osteoarthritis. Therefore, selective inhibitors of chitinases are now of considerable interest as new drug leads and biochemical probes. Until recently, few broad spectrum chitinase inhibitors had been identified. The natural cyclopentapeptide, argifin, has been shown to be a potent inhibitor of several bacterial-type family 18 chitinases including Aspergillus fumigatus chitinase B1 (AfChiB1). With the aid of high resolution X-ray structures we have designed and prepared linear fragments of the natural product cyclopentapeptide argifin using a combination of SPPS and solution phase synthesis. This has allowed us to determine that the Nmethyl guanylurea motif serves as a starting point for the generation of novel, drug-like, peptidomimetic inhibitors family 18 chitinases. We have also demonstrated that the cis configuration about the Arg(MC)-N-MePhe peptide bond is essential to retain any significant biological activity. This dipeptide motif is also found in another naturally occurring cyclopentapeptide, banyasin A, extracted from the cyanobacteruim Nostoc sp. Banyasin A also contains a rare +-amino acid, 3-amino-2-methyl-5E-octenoic acid (Amoa), in which the stereochemistry at the C3 and C5 of Amoa has not been resolved. The diastereoselective synthesis of Amoa for the preparation of banyasin A has also been established using chiral oxazolidinone-based aldol chemistry, which has allowed us to successfully prepare a single diastereoisomer of the natural product cyclopentapeptide incorporating this +-amino acid. New methodology for the preparation of argifin has also been developed to reduce the propensity towards the formation of undesired side products and to prepare the natural product on a larger scale.
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Sapkal, S. "Spectroscopic investigation of molecular probes". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2021. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/6010.

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Wang, Lei. "Molecular Probes for Pancreatic Cancer Imaging". PDXScholar, 2016. http://pdxscholar.library.pdx.edu/open_access_etds/3108.

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Pancreatic ductal adenocarcinoma (PDAC) has the poorest five-year survival rate of any cancer. Currently, there are no effective diagnostics or chemotherapeutics. Surgical resection is the only curative therapy. However, most patients experience recurrence due largely to challenges in assessing tumor margin status in the operating room. Molecular probes that selectively highlight pancreatic cancer tissue, having the potential to improve PDAC margin assessment intraoperatively, are urgently needed. In this work, a series of red and near-infrared fluorescent probes is reported. Two were found to distribute to normal pancreas following systemic administration. One selectively accumulates in genetically modified mouse models of PDAC, providing cancer-specific fluorescence. In contrast to the small molecule probes reported previously, it possesses inherent affinity for PDAC cells and tissue, and thus does not require conjugation to targeting agents. Moreover, the probe exhibits intracellular accumulation and enables visualization of four levels of structure including the whole organ, tissue, individual cells and subcellular organelles. It can thus promote new strategies for precision image-guided surgery, pancreatic cancer detection, the monitoring of therapeutic outcomes and basic research.
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Willcocks, T. C. "Mapping of human genes with molecular probes". Thesis, University of Oxford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370272.

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James, David Thomas. "Developing structural probes for designed molecular architectures". Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/10732.

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This thesis is concerned with the development of techniques to probe and control molecular morphology in organic semiconductors and investigate structure-property relationships. An angle-dependent polarised Raman technique is developed to probe molecular order and orientation in 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS-pentacene) thin lms, and applied to understand the role of blending with polystyrene on morphology and charge transport properties in inkjet-printed organic field-effect transistors (OFETs). Compared to pristine devices, blending improves film uniformity in terms of device coverage and molecular orientation and increases saturation mobility from [Mathematical formula appears here. To view, please open pdf attachment]. A zone-casting apparatus is developed to systematically control the grain size and molecular orientation of TIPS-pentacene thin films. Processing parameters such as solvent, solution temperature, substrate temperature and casting speed are systematically controlled to study film coverage, grain size, alignment and orientation, and applied to investigate charge transport properties in TIPS-pentacene and 6,13-bis(triethylsilylethynyl) pentacene (TES-pentacene) OFETs. Casting speed and grain orientation strongly influence device performance. TIPS- pentacene shows higher mobilities and grain-boundary-limited transport while TES-pentacene charge transport is limited by crystal orientation. The anisotropic structural and optical properties of TIPS-pentacene and TES-pentacene films are characterised using polarised UV-visible absorption and Raman spectroscopy. Evidence for J- and H-aggregation is found from a packing-induced red-shifted and blue-shifted absorption transition, respectively. Angle-dependent polarised Raman spectroscopy is used to probe the molecular orientation and order in the films. The pentacene long-axis orientation is found to be ±(50-60)° relative to the zone-casting direction for both materials, while TIPS-pentacene shows a higher Raman anisotropy than TES-pentacene. Quantum-chemical studies are performed on a range of conjugated polymer systems. Using simulated structure-property relationships, the effect of side chain placement & positioning, blending with small molecules, thermal annealing and heavy-atom substitution on the opto- electronic and charge transport properties of the polymers are discussed.
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Caries, Christopher Cain. "Organometallics : a platform for molecular imaging probes /". May be available electronically:, 2009. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.

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Chang, Yuan-Pin. "Novel probes of angular momentum polarization". Thesis, University of Oxford, 2010. http://ora.ox.ac.uk/objects/uuid:d3880edf-436a-415e-8a74-6b1c0fd26e65.

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New dynamical applications of quantum beat spectroscopy (QBS) to molecular dynamics are employed to probe the angular momentum polarization effects in photodissociation and molecular collisions. The magnitude and the dynamical behaviour of angular momentum alignment and orientation, two types of polarization, can be measured via QBS technique on a shot-by-shot basis. The first part of this thesis describes the experimental studies of collisional angular momentum depolarization for the electronically excited state radicals in the presence of the collider partners. Depolarization accompanies both inelastic collisions, giving rise to rotational energy transfer (RET), and elastic collisions. Experimental results also have a fairly good agreement with the results of quasi-classical trajectory scattering calculations. Chapter 1 provides the brief theories about the application of the QBS technique and collisional depolarization. Chapter 2 describes the method and instrumentation employed in the experiments of this work. In Chapter 3, the QBS technique is used to measure the total elastic plus elastic depolarization rate constants under thermal conditions for NO(A,v=0) in the presence of He, Ar, N2, and O2. In the case of NO(A) with Ar, and particularly with He, collisional depolarization is significantly smaller than RET, reflecting the weak long-range forces in these systems. In the case of NO(A)+N2/O2, collisional depolarization and RET are comparable, reflecting the relatively strong long-range forces in these systems. In Chapter 4, the QBS technique is used to measure the elastic and inelastic depolarization and total RET rate constants for OH(A,v=0) under thermal conditions in the presence of He and Ar, as well as the total depolarization rate constants under superthermal conditions. In the case of OH(A)+He, elastic depolarization is sensitive to the N rotational state, and inelastic depolarization is strongly dependent on the collision energy. In the case of OH(A)+Ar, elastic depolarization is insensitive to N, and inelastic depolarization is less sensitive to the collision energy, reflecting that the relatively strong long-range force in OH(A)+Ar system. The second part of this thesis describes the experimental studies of photodissociation under thermal conditions. Chapter 5 provides a brief introduction about several polarization parameter formalisms used for photodissociation, and the incorporation of the QBS technique to measure these polarization parameters. In this thesis, most polarization parameters of the molecular photofragments are measured using the LIF method, and the QBS technique is used as a complementary tool to probe these polarization parameters. In Chapter 6, rotational orientation in the OH(X,v=0) photofragments from H2O2 photodissociation using circularly polarized light at 193 nm is observed. Although H2O2 can be excited to both the A and B electronic states by 193 nm, the observed orientation is only related to the A state dynamics. A proposed mechanism about the coupling between a polarized photon and the H2O2 parent rotation is simulated, and the good agreement between the experimental and simulation results further confirms the validity of this mechanism. In Chapter 7, rotational orientation in the NO(X,v) photofragments from NO2 photodissociation using circularly polarized light at 306 nm (v=0,1,2) and at 355 nm (v=0,1) is observed. Two possible mechanisms, the parent molecular rotation and the coherent effect between multiple electronic states, are discussed. NOCl is photodissociated using circularly polarized light at 306 nm, and NO(X,v) rotational distributions (v=0,1) and rotational orientation (v=0) are measured. For the case of NOCl, the generation of orientation is attributed to the coherent effect.
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Kujala, Naresh Gandhi Yu Ping. "Frequency domain fluorescent molecular tomography and molecular probes for small animal imaging". Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/7021.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 26, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dissertation advisor: Dr. Ping Yu. Vita. Includes bibliographical references.
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Mastrodonato, Cristiano Matteo. "Elaboration of fluorescent molecular probes and molecular-based nanoparticles for bioimaging purposes". Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0652/document.

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Les techniques de fluorescence sont des outils de choix pour l’étude et la compréhension fine des processus biologiques. Ceci requiert toutefois l’utilisation de sondes fluorescentes parfaitement adaptées au but visé et répondant aux différentes exigences requises pour l’application visée. Dans ce cadre, nous nous sommes plus particulièrement intéressés à l’élaboration de sondes biphotoniques de pH adaptées à une mesure très sensible de faibles variations de pH autour du pH neutre. Les variations et gradients de pH sont en effet impliqués dans un certain nombre de processus biologiques importants et peuvent être associées à des dysfonctionnements liés à certaines maladies. Dans ce cadre, nous avons développé de nouvelles sondes fluorescentes de pH fluorescentes présentant à la fois un comportement ratiométrique, une forte sensibilité autour du pH neutre et facilement excitables dans le proche IR par absorption à deux photons. Ces sondes de structure quadrupolaire et bolamamphiphile permettent ainsi la détection ratiométrique du pH dans des environnements biologiques au moyen d'une excitation biphotonique dans le proche IR. En parallèle, nous nous sommes intéressés à l’élaboration de nanoparticules hyperbrillantes dédiées à l’imagerie biologique par microscopie de fluorescence induite par excitation à deux photons. Nous nous sommes plus particulièrement attachées au design de nanoparticules organiques fluorescentes constituées de molécules organiques de bas poids moléculaire (FONs). Cette approche offre en effet une grande flexibilité et la possibilité d’accéder à des nanosondes ayant des brillances comparables aux très populaires quantum dots mais moins toxiques et plus facilement dégradables. L’ingénierie moléculaire des fluorophores utilisés pour la préparation des FON est cruciale puisqu’elle influence fortement à la fois les propriétés photophysiques (brillance, couleur…) et leur propriétés physico-chimiques (stabilité chimique et structurale, stabilité colloïdale). Dans ce contexte, une librairie de nouveaux chromophores dipolaires a été synthétisée et utilisées pour la préparation de FON par la méthode de nano-précipitation. Leurs propriétés ont été étudiées afin de déterminer la relation entre la structure du chromophore et les propriétés globales des nanoparticules constituées de ces colorants. Ce travail a permis d’identifier les paramètres structuraux permettant d’accéder à des nanoparticules présentant à la fois une brillance exceptionnelle, une émission modulable du vert au rouge et proche IR et une remarquable stabilité colloïdale. Ces nanoparticules présentent des potentialités majeures pour l’imagerie in vivo par excitation et détection dans le proche IR
Fluorescence-based techniques are popular tools for the study and understanding of biological processes. This has prompted continuous research aimed at the development of a wide range of fluorescent probes specifically designed for specific applications. Among them, fluorescent pH probes are of much interest as pH variations or gradients are involved in many biological events and anomalous alterations are often related to the onset of dysfunctions and diseases. In this framework we have developed a series of promising two-photon pH fluorescent molecular probes. These quadrupolar bolaamphiphilic probes are of great interest, as they combine a steep pH dependence of their optical properties close to neutral pH, ratiometric behavior and large response to two-photon (2P) excitation in the NIR region. As such they offer much promise for ratiometric detection of the pH in biological environments and in situ monitoring of acidification. In parallel, we have been interest in the design of ultrabright nanoparticles for bioimaging purpose (in particular highly sensitive optical imaging). We chose to focus on Fluorescent Organic Nanoparticles made of organic molecules with low molecular weight (FONs) as they offer a flexible route and promising alternatives to toxic quantum dots. In this case the design of the dye used as building blocks of the FONs is of crucial importance and strongly influence the chemical and physical properties of the nanoparticles generated, such as their one and two-photon brightness and both their structural and colloidal stability. In that context a library of novel dipolar chromophores have been synthesized and used to prepare FONs using the nanoprecipitation method. Their properties were thoroughly investigated in order to determine the relationship between the molecular design of the isolated dye and the overall properties of the nanoparticles made of these dyes. As a result, Hyperbright FONs emitting in the green to NIR region and combining giant brightness and remarkable stability have been achieved. They offer major promise for bioimaging based on both excitation and detection in the NIR region
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Lenaerts, Jeremy. "Molecular beacons as hybridisation probes in microbial ecology". Thesis, University of Exeter, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493638.

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Microorganisms are of fundamental importance to global biogeochemical cycling, yet aspects of their ecology are poorly understood. Within the present methods used to study microbial ecology are limitations with regards to sensitivity, applicability and automation. This study aimed to investigate the potential application of novel nucleic acid probes (molecular beacons and locked nucleic acid probes) in microbial ecology.
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Książki na temat "Molecular probes"

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Susan, Hockfield, red. Molecular probes of the nervous system. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1993.

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Alberto, Albertini, Paoletti Rodolfo, Reisfeld Ralph A i International Symposium BIOTECH RIA '88, "Molecular Probes: Technology and Medical Applications" (1988 : Florence, Italy), red. Molecular probes: Technology and medical applications. New York: Raven Press, 1989.

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R, Walker Matthew, i Rapley Ralph, red. Molecular and antibody probes in diagnosis. Chichester: Wiley, 1993.

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Johnson, Iain D., i Michelle T. Z. Spence. The molecular probes handbook: A guide to fluorescent probes and labeling technologies. [Carlsbad, CA]: Live Technologies Corporation, 2010.

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Tycko, Robert, red. Nuclear Magnetic Resonance Probes of Molecular Dynamics. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1410-3.

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Jan, Slavík. Fluorescent probes in cellular and molecular biology. Boca Raton: CRC Press, 1994.

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Robert, Tycko, red. Nuclear magnetic resonance probes of molecular dynamics. Dordrecht: Kluwer Academic Publishers, 1994.

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Papkovsky, Dmitri B. Phosphorescent Oxygen-Sensitive Probes. Basel: Springer Basel, 2012.

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Prof, Miller Lawrence W., red. Probes and tags to study biomolecular function: For proteins, RNA, and membranes. Weinheim: Wiley-VCH Verlag, 2008.

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1946-, Swaminathan Bala, i Prakash Gyan 1956-, red. Nucleic acid and monoclonal antibody probes: Applications in diagnostic microbiology. New York: M. Dekker, 1989.

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Części książek na temat "Molecular probes"

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Khalil, Gamal, Christian Brückner i Masoud Ghandehari. "Molecular Probes". W Optical Phenomenology and Applications, 35–48. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-70715-0_4.

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Yang, Min, Yuping Xu, Xinyu Wang, Yu Liu, Yanting Wang, Huimin Zhao, Jie Sheng i Yaoqi Li. "Novel Molecular Probes". W Nuclear Medicine in Oncology, 315–46. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7458-6_20.

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van Pelt-Verkuil, E., i R. te Witt. "Primers and Probes". W Molecular Diagnostics, 51–95. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1604-3_3.

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Isaac, Peter G. "Nonradioactive Probes". W Molecular Tools for Screening Biodiversity, 96–97. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-009-0019-6_19.

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Bruford, Michael W. "VNTR Probes". W Molecular Tools for Screening Biodiversity, 286. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-009-0019-6_52.

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Silverman, Adam P., Hiroshi Abe i Eric T. Kool. "Quenched Autoligation Probes". W Methods in Molecular Biology, 161–70. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-040-3_11.

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Cunningham, Martin. "Preparation of radioactive probes". W Molecular Microbial Ecology Manual, 161–94. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0351-0_13.

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Gainer, Harold, Todd A. Ponzio, Chunmei Yue i Makoto Kawasaki. "Intron-Specific Neuropeptide Probes". W Methods in Molecular Biology, 89–110. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-310-3_5.

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Wong, Chi-Huey. "Molecular Probes for Glycosylation: Overview". W Glycoscience: Biology and Medicine, 1–4. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54836-2_108-1.

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Wong, Chi-Huey. "Molecular Probes for Glycosylation: Overview". W Glycoscience: Biology and Medicine, 455–57. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54841-6_108.

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Streszczenia konferencji na temat "Molecular probes"

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Contag, Chris. "Molecular Probes for Microendoscopy". W Frontiers in Optics. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/fio.2009.ftul1.

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Bogyo, Matthew. "Imaging cancer with protease activated optical probes". W Molecular-Guided Surgery: Molecules, Devices, and Applications VIII, redaktorzy Summer L. Gibbs, Brian W. Pogue i Sylvain Gioux. SPIE, 2022. http://dx.doi.org/10.1117/12.2617795.

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Min, Wei. "Seeing molecular vibrations: optical imaging of small molecules for biomedicine". W Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/omp.2015.jw2b.3.

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Gibbs, Summer L. "Near-infrared nerve-specific probes to guide surgery". W Molecular-Guided Surgery: Molecules, Devices, and Applications VII, redaktorzy Summer L. Gibbs, Brian W. Pogue i Sylvain Gioux. SPIE, 2021. http://dx.doi.org/10.1117/12.2596408.

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Hasan, Tayyaba. "Molecular probes in Photodynamic Therapy". W Biomedical Optics. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/biomed.2012.bm2a.1.

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Li, Lin, Chengwu Zhang i Wei Huang. "Two-photon Small Molecular Enzymatic Probes". W International Conference on Photonics and Imaging in Biology and Medicine. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/pibm.2017.w3a.126.

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Bogyo, Matthew. "Protease-activated probes for real-time ratiometric imaging of solid tumors". W Molecular-Guided Surgery: Molecules, Devices, and Applications X, redaktorzy Summer L. Gibbs, Brian W. Pogue i Sylvain Gioux. SPIE, 2024. http://dx.doi.org/10.1117/12.3009175.

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Pal, Rahul, i Anand T. Kumar. "Fluorescence lifetime-based tumor contrast enhancement using targeted near infrared probes (Conference Presentation)". W Molecular-Guided Surgery: Molecules, Devices, and Applications VI, redaktorzy Summer L. Gibbs, Brian W. Pogue i Sylvain Gioux. SPIE, 2020. http://dx.doi.org/10.1117/12.2545246.

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Bouvet, Michael. "Development of imaging probes for fluorescence guided surgery of GI and endocrine tumors". W Molecular-Guided Surgery: Molecules, Devices, and Applications X, redaktorzy Summer L. Gibbs, Brian W. Pogue i Sylvain Gioux. SPIE, 2024. http://dx.doi.org/10.1117/12.3009487.

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Blaskovich, Mark A., Wanida Phetsang, M. Rhia Stone, Urszula Lapinska, Stefano Pagliara, Rajiv Bhalla i Matthew A. Cooper. "Antibiotic-derived molecular probes for bacterial imaging". W Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases 2019, redaktorzy Tianhong Dai, Mei X. Wu i Jürgen Popp. SPIE, 2019. http://dx.doi.org/10.1117/12.2507329.

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Raporty organizacyjne na temat "Molecular probes"

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Wang, Lei. Molecular Probes for Pancreatic Cancer Imaging. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.3105.

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Johnson, P. M. Ionization probes of molecular structure and chemistry. Office of Scientific and Technical Information (OSTI), styczeń 1993. http://dx.doi.org/10.2172/7030747.

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Johnson, Philip M. Final Progress Report--Ionization probes of molecular structure and chemistry. Office of Scientific and Technical Information (OSTI), styczeń 2009. http://dx.doi.org/10.2172/948820.

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Lieber, Charles M. Development and Application of Molecular-Resolution Chemically-Sensitive Nanotube Probes. Fort Belvoir, VA: Defense Technical Information Center, listopad 2002. http://dx.doi.org/10.21236/ada419867.

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Zhang, W., I. Gaberman i M. Ciszkowska. Diffusion of Molecular Probes in Thermoresponsive Poly(N-isopropylacrylamide) Hydrogels: Electroanalytical Studies. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada390102.

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Thelen, M., A. Rowe, A. Siebers i Y. Jiao. 08-ERD-071 Final Report: New Molecular Probes and Catalysts for Bioenergy Research. Office of Scientific and Technical Information (OSTI), marzec 2011. http://dx.doi.org/10.2172/1021546.

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Asbury, John. Molecular and Structural Probes of Defect States in Quantum Dots for Solar Photoconversion. Office of Scientific and Technical Information (OSTI), lipiec 2019. http://dx.doi.org/10.2172/1542290.

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Greulich-Bode, Karin M., Mei Wang, Andreas P. Rhein, Jingly F. Weier i Heinz-Ulli G. Weier. Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA. Office of Scientific and Technical Information (OSTI), grudzień 2008. http://dx.doi.org/10.2172/982916.

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Hanson, Robert N. Training Grant in Radiochemistry and Radiotracer Development. Design and Synthesis of Molecular and Nanoparticulate Probes. Office of Scientific and Technical Information (OSTI), styczeń 2015. http://dx.doi.org/10.2172/1167275.

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Johnson, P. M. Ionization probes of molecular structure and chemistry. Progress report, January 15, 1992--January 14, 1993. Office of Scientific and Technical Information (OSTI), styczeń 1993. http://dx.doi.org/10.2172/10128812.

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