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Artykuły w czasopismach na temat "Masse spectrometry":
Zoppi, Ugo. "Radiocarbon AMS Data Analysis: From Measured Isotopic Ratios to 14C Concentrations". Radiocarbon 52, nr 1 (2010): 165–70. http://dx.doi.org/10.1017/s0033822200045112.
Helena Pereira, Maria, Luiz de Castro i Ricardo Michel. "Investigating Molecular Masses Formed during the Heat Treatment of Petroleum Pitches by Mass Spectrometry". Chemistry & Chemical Technology 7, nr 2 (10.06.2013): 131–39. http://dx.doi.org/10.23939/chcht07.02.131.
Antonation, Kym, Dobryan Tracz, Ashley Dreger i Cindi Corbett. "Identification des bactéries à cote de sécurité élevée, basée sur la spectrométrie de masse à temps de vol après désorption/ionisation laser assistée par matrice : considérations pour les utilisateurs canadiens de Bruker". Relevé des maladies transmissibles au Canada 46, nr 10 (1.10.2020): 376–82. http://dx.doi.org/10.14745/ccdr.v46i10a04f.
Bieleń, Wojciech, i Marek Janiga. "Spektrometria masowa i analiza izotopowa biomarkerów frakcji nasyconej". Nafta-Gaz 77, nr 8 (sierpień 2021): 512–28. http://dx.doi.org/10.18668/ng.2021.08.02.
Kim, Hyub, i Byung-Soo Ahn. "The Study on the Composition in Pharmacopunctures of Eight Principles by Gas Chromatography/Mass Spectrometry". Journal of Korean Institute of Herbal Acupuncture 11, nr 3 (30.09.2008): 79–91. http://dx.doi.org/10.3831/kpi.2008.11.3.079.
Gambier, Dominique, Hélène Valladas, Nadine Tisnérat-Laborde, Maurice Arnold i Frédérique Bresson. "Datation de vestiges humains présumés du Paléolithique supérieur par la méthode du Carbone 14 en spectrométrie de masse par accélérateur / Accelerator mass spectrometry radiocarbon dates of human remains from Upper Palaeolithic". Paléo 12, nr 1 (2000): 201–12. http://dx.doi.org/10.3406/pal.2000.1602.
Hoenicke, K., H. Fritz, R. Gatermann i S. Weidemann. "Analysis of furan in different foodstuffs using gas chromatography mass spectrometry". Czech Journal of Food Sciences 22, SI - Chem. Reactions in Foods V (1.01.2004): S357—S358. http://dx.doi.org/10.17221/10702-cjfs.
Kim, Jin Hyo, Cho-Long Jin, Geun-Hyoung Choi i Byung-Jun Park. "Sample Preparation Method for Perfluorochemicals with LC-Tandem Mass Spectrometry in Agricultural Water". Korean Journal of Pesticide Science 19, nr 1 (31.03.2015): 1–4. http://dx.doi.org/10.7585/kjps.2015.19.1.1.
Botek, P., J. Poustka i J. Hajšlová. "Determination of banned dyes in spices by liquid chromatography−mass spectrometry". Czech Journal of Food Sciences 25, No. 1 (7.01.2008): 17–24. http://dx.doi.org/10.17221/737-cjfs.
Decesari, S., J. Allan, C. Plass-Duelmer, B. J. Williams, M. Paglione, M. C. Facchini, C. O'Dowd i in. "Measurements of the aerosol chemical composition and mixing state in the Po Valley using multiple spectroscopic techniques". Atmospheric Chemistry and Physics 14, nr 22 (18.11.2014): 12109–32. http://dx.doi.org/10.5194/acp-14-12109-2014.
Rozprawy doktorskie na temat "Masse spectrometry":
Halim, Mohammad Abdul. "Coupling Laser with Mass Spectrometry for Biomolecules Characterization : From Peptides towards Protein Fibrils". Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE1088/document.
The structural characterization of proteins often required them to be fragmented into small units containing only few amino acids. In bottom-up approach, proteins are cleaved into small peptides by enzyme then these peptides are subjected to further fragmentation in a collision cell of a tandem mass spectrometer. However, in top-down approach, proteins can directly be dissociated (without enzyme) into small fragments by collision, electron and photon-driven dissociations. Photon-based activation methods including ultraviolet photodissociation (UVPD) and infrared multiphoton dissociation (IRMPD) have received great attention as an alternative to electron-driven and collision induced dissociation methods. Absorption of the high-energy UV photon is dispersed over the whole peptide or protein and stimulates extensive C?Ca backbone fragmentation while the low-energy IR photons gradually increases the internal energy and thus favorably dissociates the most labile amide (C?N) bonds. This thesis focuses on the method development and applications for characterizing biomolecules by photon-based activation methods. The interest of combining high-energy UV photons and low-energy IR photons in an Orbitrap mass spectrometer, for protein and post-translationally modified peptide characterization, has been evaluated. Moreover, infrared multiphoton dissociation has been implemented in a gated electrostatic ion trap to push forward the limit of fragmentation methods to large megadalton ions. One of the main breakthroughs in this thesis is the ability to adapt these method developments and applications to biomolecular objects ranging from small peptides (in kilodalton mass range) to entire protein fibrils (in megadalton mass range)
Fu, Tingting. "3D and High Sensitivity Micrometric Mass Spectrometry Imaging". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS218/document.
Mass spectrometry imaging has been shown of great interest in addressing biological questions by providing simultaneously chemical and spatial information. Particularly, TOF-SIMS is well recognized for its high spatial resolution (< 1 µm) which is essential in disclosing chemical information within a submicron area. The increasing use of TOF-SIMS in characterizing biological samples has greatly benefited from the introduction of new cluster ion sources. However, the ionization/desorption of the analytes under impacts of large clusters is still poorly understood. On the other hand, technically, current commercial TOF-SIMS instruments generally cannot provide sufficient mass resolution or mass accuracy for molecular identification, making analyses of complex biological systems especially challenging when no MS/MS fragmentation is available. Thus this thesis is aimed to get a better understanding of ion production under cluster impacts, to explore the MS/MS capability of the parallel imaging MS/MS Spectrometer (PHI nanoTOF II), as well as to apply TOF-SIMS to map important wood metabolites with high spatial resolution.In order to understand ion production under impacts of massive argon clusters, internal energy distributions of secondary ions were measured using survival yield method which involves the analyses of a series of benzylpyridinium ions. Investigation of various impacting conditions (energy, velocity, cluster size) suggested that velocity of the clusters play a major role in internal energy distribution and molecular fragmentation in the low energy per atom regime (E/n < 10 eV). The MS/MS fragmentation and parallel imaging capabilities of the newly designed PHI nanoTOF II spectrometer were evaluated by in situ MS/MS mapping of bioactive metabolites rubrynolide and rubrenolide in Amazonia wood species Sextonia rubra. Then this parallel imaging MS/MS technique was applied to perform in situ identification of related precursor metabolites in the same tree species. 2D and 3D TOF-SIMS imaging were carried out to target the plant cells that biosynthesize rubrynolide and rubrenolide. The results led to the proposal of a possible biosynthesis pathway of these two metabolites. In addition, to expand the application of TOF-SIMS imaging in wood chemistry analysis, radial distribution of wood extractives in the heartwood of European larch was also investigated
Vaca, Jacome Alvaro Sebastian. "Progress towards a better proteome characterization by quantitative mass spectrometry method development and proteogenomics". Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF020/document.
The high intrinsic complexity of biological samples, the technical variability and the dependency of Bottom-up Proteomics to consensus protein sequence databases handicap the comprehensive analysis of an entire Proteome. My doctoral work was focused on method development in quantitative Proteomics and Proteogenomics in order to achieve a better proteome characterization. First, I focused on the development of global and targeted quantitative methods. The introduction and development of standard samples to assess the performances at any level of the analytical workflow is also described. These methods were applied to answer different biological questions. My PhD also focused on Proteogenomic method development. A high throughput N-terminomic analysis approach was developed and applied to the analysis of the human mitochondria. Finally, this manuscript presents a personalized multi-omics profiling strategy to improve the proteome analysis with the use of personalized databases
Dupont-Gervais, Annick. "Etude de supermolecules par spectrometrie de masse en mode d'ionisation electrospray. Suivi de la formation d'edifices supramoleculaires en solution". Université Louis Pasteur (Strasbourg) (1971-2008), 1996. http://www.theses.fr/1996STR13062.
Ayciriex, Sophie. "Caractérisation de lysolipide acyltransférases chez S. cerevisiae - Apport de la Spectrométrie de Masse". Thesis, Bordeaux 2, 2010. http://www.theses.fr/2010BOR21737/document.
In addition to their structural properties as main constituents of biological membranes, lipids play a multitude of roles such as in cell signalling, energy storage, and protein transport. Their biological importance has led to an increasing focus on analytical methods for the characterisation of their individual molecular species. Improvements in mass spectrometric technology has provided a great advantage for the characterisation and quantification of molecular lipid species in total lipid extracts (Han and Gross, 2005; Murphy et al., 2001). For instance, phospholipid molecular species can be identified on the basis of a characteristic fragment of the lipid class, the nature of the acyl chains and their positions on the glycerol backbone.A method allowing the quantitative profiling of the yeast lipidome was developed in a recent study using automated shotgun infusion strategy (Ejsing et al., 2009). We applied this method to characterise several lysophospholipid acyltransferase yeast mutants produced using reverse-genetics. These enzymes are involved in essential biological processes like de novo synthesis or remodelling of the phospholipid membrane component (Testet et al., 2005; Le Guedard et al., 2009). The comparative analysis of phospholipid molecular species from the wild-type strain and the corresponding deletion mutants has allowed us to identify lipid compositional changes, and has given us significant indications about the in vivo function of the encoded lysophospholipid acyltransferases
Fouquet, Thierry. "Mass spectrometry of synthetic polysiloxanes : from linear models to plasma-polymer networks". Thesis, Aix-Marseille, 2012. http://www.theses.fr/2012AIXM4756/document.
This thesis work aimed at describing the molecular and structural composition of silicon-based plasma-polymers (ppHMDSO) by mass spectrometry. Deposited under a micro-discharge regime at atmospheric pressure, these plasma-polymers exhibit a very low solubility in common solvents, assigned to their highly cross-linked structures, and are hence not easily amenable to ionization. Moreover, structural information cannot be readily deduced from fragmentation data obtained from species extractable from the studied thin films due to the lack of appropriate rules to understand dissociation of the observed gas-phase ions. This research work has thus consisted of developing an analytical strategy to address both of these challenging issues.Owing to the very limited number of articles dealing with tandem mass spectrometry of silicon-containing oligomers, mechanistic investigations were performed on the collision-induced decomposition of selected polymer standards holding different end-groups, expected to be relevant to characterize oligomers suspected to be present in the soluble part of the ppHMDSO samples. Focusing on ammonium adducts, fragmentation routes have first been established for symmetric poly(dimethylsiloxane) (PDMS) polymers holding trimethylsilyl, hydride, or methoxy terminations. POSS molecules were also investigated to understand the influence of cross-linked structures on PDMS adduct dissociation. Some discrepancies between MS/MS spectra of the standards and of the analytes were evidenced, assigned to random branching which could not be modeled by any commercially available compounds
Piccolo, Stefano. "Biophysical characterization of aptamer-ligand interactions by native mass spectrometry". Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0276.
Aptamers are single-stranded nucleic acids capable to bind selectively to a ligand or to a family of molecules. Aptamers are the sensing part of riboswitches, which are regulatory segments of messenger RNA involved in gene expression. Aptamers are also promising artificial probes, sensors and stimuli-responsive elements. In the development of aptamer-based technology, it is crucial to understand how binding is occurring, to quantify affinities, and ligand-induced conformational changes. The objective of this thesis is to explore the applicability of native IM-MS to DNA and RNA aptamers to quantify binding and to detect conformational change upon binding.In the first part, we evaluated the quantitative determination of equilibrium dissociation constants (KD) by mass spectrometry (MS), and the necessity of including a correction for relative response factors of free and bound aptamers. We compared isothermal titration calorimetry and MS titrations to validate the quantifications. Two RNA aptamers were taken as models: the malachite green aptamer, extensively studied by ITC, and the riboflavin mononucleotide aptamer, a case of Mg2+-dependent ligand binding. We observed that typical volatile electrolytes ammonium acetate and trimethyl ammonium acetate are suitable to study RNA aptamer binding, and that comparable KD values are obtained from ITC and native MS. The neomycin and tobramycin RNA aptamers were chosen to test the limit of detection of native MS. We found that native MS is appropriate to determine KD values in the range from 50 nM to 30 µM. The relative response factor correction was relatively modest in all cases, suggesting that the ligand binding is not associated to a significant conformational difference upon ionization. For these aptamers, we conclude that assuming equal response factors is acceptable.In the second part, we evaluated whether the aptamers’ “adaptive binding” mechanism can be revealed by ion mobility spectrometry (IMS). To this aim, in addition to the systems listed above we studied the tetracycline RNA aptamer and a series of cocaine-binding DNA aptamers, for which the conformational change upon binding is reported in literature. For all aptamers except the tetracycline aptamer, we did not observe a significant difference in the shape of the gas-phase structure upon ligand or Mg2+ binding. However, a significant change was observed in tetracycline RNA aptamer’s ion mobilities, at biologically relevant concentration of Mg2+ (100 µM), and we found that Mg2+ is essential for ligand binding, in agreement with previous solution studies. For the cocaine-binding DNA aptamer series, although we observed similar compactness for the free and bound aptamers in soft pre-IMS conditions, a conformational extension occurs at high pre-IMS activation, best revealed by charge state 7-, suggesting gas-phase rearrangements. To better investigate whether the energetics of these rearrangements depend on pre-folding or on ligand binding, we modified the sequences with dA overhangs, to compare systems with similar numbers of degrees of freedom without altering the core structure. We also propose new ways of presenting the data, adapted to the cases where ligand dissociation, declustering and unfolding occur at similar voltages. The gradual increase of the pre-IMS collisional activation revealed that the unfolding energetics is correlated with the base pairs content, suggesting that base pairs are conserved in the gas-phase structures. We also found that ligand is lost at lower energies than unfolding.In summary, gas-phase compaction occur for both the free aptamers and bound aptamers, and memories of the solution-phase structures can only be revealed in some particular cases. However, the compaction towards similar shapes might constitute an advantage for the quantification, because molecular systems of similar shapes have similar electrospray responses. Consequently, native MS provides reliable estimations of KD values
Guigues, Elodie. "Mesure en ligne des produits de fission gazeux par spectrométrie de masse". Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4706.
In order to increase fuel rod performances, the basic mechanisms that promote gas (i.e. He, H2, Kr and Xe) release from irradiated nuclear fuels must be studied. In this context, the CEA fuel study department at Cadarache decided to improve its experimental facility devoted to fuel behaviour under thermal transient by modifying the existing annealing device, called MERARG-II.The first part of this dissertation adresses the fuel gas release monitoring from irradiated fuel during thermal transient. The device choice leads to a quadrupole mass filter as mass analyser according to the specification requirement, i.e. isotopic identification of Xe, Kr and masses at 4 and 2 u. It is commercialized Residual Gas Analyser, mounted in a small-volume vacuum chamber requiring adaptations to be connected to the MERARG II line. The resolution and sensitivity of the mass spectrometer have been evaluated. The calibrated device is being installed in MERARG II replica.The second part of this dissertation relates adaptation to low-mass analysis of an RF 3D ion trap operated a Fourier Transform mode. Theoretically, using this operating mode, the lower the mass, the higher the resolution. More particularly, an ion injection device and its operating mode are studied in order to gain position and velocity distributions of confinable ions. The knowledge of these initial conditions is of a great concern as they fix the signal dynamic (peak height) and the signal fluctuation, respectively. This feasibility study, using simulation, allows us to obtain the optimal values of trap operating condition for 1-6 u mass injection and confinement with high resolution
Ndiaye, Massamba. "Miniaturisation de la préparation d'échantillon en protéomique bottom-up pour la quantification de l'oxydation des cystéines". Thesis, Paris Sciences et Lettres (ComUE), 2019. https://pastel.archives-ouvertes.fr/tel-03003473.
Bottom-up proteomics is the most commonly used approach for protein analysis by mass spectrometry. In this approach, enzymatic digestion is one step of a long and tedious sample preparation protocol. Specific care is needed to study post-translational changes, such as cysteine oxidation, with additional steps which makes the protocol even more complex. The OcSILAC protocol, developed in our laboratory for quantifying cysteine oxidation, is a perfect illustration of this. The miniaturization of the experimental setup is an opportunity for the OcSILAC protocol to be less time and sample consuming. It is the objective of my thesis project.A microfluidic device, inspired by the Filter Aided Sample Preparation (FASP) method, was developed during this project. It is a PDMS device, incorporating a regenerated cellulose molecular filtration membrane and manufactured by gentle photolithography. In the literature, the majority of microfluidic devices dedicated to proteomics stops at proof of concept on standard reference proteins. The microchip developed during this thesis allowed the analysis of biological complex protein samples: with ten times less sample and an eight-times shorter protocol than conventional procedures. Our ChipFilter Proteolysis protocol can identify more proteins and more peptides than the previously reported FASP method. For the miniaturization of the OcSILAC protocol, the development of a biotinylated peptide enrichment unit was started using avidin magnetic beads
Eskenazi, Nicolas. "Caractérisation structurale de la glycosylation des protéines : de la glycomique à la glycoprotéomique, une stratégie utile pour l’étude des gonadotrophines". Thesis, Paris Sciences et Lettres (ComUE), 2019. http://www.theses.fr/2019PSLET032.
Polysaccharides from glycoproteins play an important part in numerous biological processes and pathologies. Their structural elucidation requires performant and sensitive tools capable of assessing the heterogeneity of such glycans. Different approaches were developed: N-glycan analysis by MALDI-TOF and LC-ESI-FTMS proteomics.Glycomics is the analysis of glycans independently of their linked-protein and can be using to obtain a glycosylation fingerprint of a protein, fluid etc. Developments of innovative sample and matrix preparation conditions, including glycan chemical modification, improved their mass spectrometry detection and fragmentation.Glycopeptide and glycoprotein analysis permits selective assessment of the glycan population across the protein hence allowing the characterization of molecular microheterogeneity of the different glycoforms. The development and integration of non-specific protease digestion and stepped-energy fragmentation produced more diverse and reliable identifications.Because of their critical role in gestation and embryo development, glycosylated gonadotropins are of major medical and veterinary interest. Combining analytical methodologies granted access to the characterization of population-specific glycosylation motifs
Książki na temat "Masse spectrometry":
G, Harrison Alex. Chemical ionization mass spectrometry. Wyd. 2. Boca Raton, Fla: CRC Press, 1992.
Watson, J. Throck. Introduction to mass spectrometry. New York: Raven Press, 1985.
Watson, J. Throck. Introduction to mass spectrometry. Wyd. 3. Philadelphia: Lippincott-Raven, 1997.
White, Frederick Andrew. Mass spectrometry: Applications in science and engineering. New York: Wiley, 1986.
Niessen, W. M. A. Liquid chromatography-mass spectrometry. Wyd. 2. New York: M. Dekker, 1999.
Niessen, W. M. A. Liquid chromatography--mass spectrometry. Wyd. 3. Boca Raton: CRC/Taylor & Francis, 2006.
Davis, R. Mass spectrometry: Analytical chemistry by open learning. Redaktorzy Frearson Martin, Prichard F. Elizabeth 1937- i ACOL. Chichester: Published on behalf of ACOL by Wiley, 1987.
Kinter, Michael. Protein sequencing and identification using tandem mass spectrometry. New York: John Wiley, 2000.
Niessen, W. M. A. Liquid chromatography--mass spectrometry: Principles and applications. New York: M. Dekker, 1992.
Watson, J. Throck. Introduction to mass spectrometry: Instrumentation, applications, and strategies for data interpretation. Wyd. 4. Hoboken, N.J: John Wiley, 2007.
Części książek na temat "Masse spectrometry":
Rozanova, Svitlana, Katalin Barkovits, Miroslav Nikolov, Carla Schmidt, Henning Urlaub i Katrin Marcus. "Quantitative Mass Spectrometry-Based Proteomics: An Overview". W Methods in Molecular Biology, 85–116. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1024-4_8.
Dass, Chhabil. "Mass Spectrometry". W Mass Spectrometry, 1–52. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1748-5_1.
Westman-Brinkmalm, Ann, i Gunnar Brinkmalm. "Definitions and Explanations". W Mass Spectrometry, 3–13. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch1.
Sheldon, Robert. "Space Sciences". W Mass Spectrometry, 253–66. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch11.
Delvecchio, Vito G., i Cesar V. Mujer. "Bioterrorism". W Mass Spectrometry, 267–73. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch12.
Szynkowska, Małgorzata Iwona. "Imaging of Small Molecules". W Mass Spectrometry, 275–85. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch13.
Chace, Donald H. "Utilization of Mass Spectrometry in Clinical Chemistry". W Mass Spectrometry, 287–97. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch14.
Montaudo, Maurizio S. "Polymers". W Mass Spectrometry, 299–307. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch15.
Kala, Maria. "Forensic Sciences". W Mass Spectrometry, 309–19. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch16.
Bergquist, Jonas, Jerzy Silberring i Rolf Ekman. "New Approaches to Neurochemistry". W Mass Spectrometry, 321–35. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470395813.ch17.
Streszczenia konferencji na temat "Masse spectrometry":
Veličković, Suzana, i Xianglei Kong. "„Superalkali” clusters, production, potential application like energy storage materials". W 8th International Conference on Renewable Electrical Power Sources. SMEITS, 2020. http://dx.doi.org/10.24094/mkoiee.020.8.1.15.
Sarycheva, Anastasia, Anton Grigoryev, Evgeny N. Nikolaev i Yury Kostyukevich. "Robust Simulation Of Imaging Mass Spectrometry Data". W 35th ECMS International Conference on Modelling and Simulation. ECMS, 2021. http://dx.doi.org/10.7148/2021-0192.
Kitagawa, Kuniyuki, Shigeaki Morita, Kenji Kodama i Kozo Matsumoto. "Spectroscopic Monitoring of Energy Systems (Calvin W. Rice Lecture)". W ASME 2009 Power Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/power2009-81047.
Kawai, Yosuke, Kentaro Terada, Toshinobu Hondo, Jun Aoki, Morio Ishihara, Michisato Toyoda i Ryosuke Nakamura. "Development of a Secondary Neutral Mass Spectrometer for Submicron Imaging Mass Spectrometry". W Proceedings of the 15th International Symposium on Origin of Matter and Evolution of Galaxies (OMEG15). Journal of the Physical Society of Japan, 2020. http://dx.doi.org/10.7566/jpscp.31.011065.
Brennwald, Matthias, Y. Tomonaga i R. Kipfer. "Compensation of Mass Spectrometric Interferences with the miniRUEDI Portable Mass Spectrometer". W Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.260.
Hazama, Hisanao, Jun Aoki, Hirofumi Nagao, Hidetoshi Yoshimura, Yasuhide Naito, Michisato Toyoda, Katsuyoshi Masuda, Kenichi Fujii, Toshio Tashima i Kunio Awazu. "Stigmatic imaging mass spectrometry using a multi-turn time-of-flight mass spectrometer". W The Pacific Rim Conference on Lasers and Electro-Optics (CLEO/PACIFIC RIM). IEEE, 2009. http://dx.doi.org/10.1109/cleopr.2009.5292164.
Li, Xiang, Timothy Cornish, Scott Ecelberger, Stephanie A. Getty i William B. Brinckerhoff. "Tandem mass spectrometry on a miniaturized laser desorption time-of-flight mass spectrometer". W 2016 IEEE Aerospace Conference. IEEE, 2016. http://dx.doi.org/10.1109/aero.2016.7500615.
Kim, J. C. "Accelerator mass spectrometry". W HADRONS AND NUCLEI: First International Symposium. AIP, 2001. http://dx.doi.org/10.1063/1.1425525.
Blebea, Nicoleta Mirela, i Simona Negreș. "METHODS FOR QUANTIFICATION OF THE MAIN CANNABINOIDS IN CBD OIL". W GEOLINKS Conference Proceedings. Saima Consult Ltd, 2021. http://dx.doi.org/10.32008/geolinks2021/b1/v3/13.
Downey, Stephen W. "Comparison of secondary ion mass spectrometry and resonance ionization mass spectrometry". W OE/LASE '90, 14-19 Jan., Los Angeles, CA, redaktor Nicholas S. Nogar. SPIE, 1990. http://dx.doi.org/10.1117/12.17881.
Raporty organizacyjne na temat "Masse spectrometry":
Hastie, J. W., D. W. Bonnell i P. K. Schenck. Laser-assisted vaporization mass spectrometry:. Gaithersburg, MD: National Institute of Standards and Technology, 2001. http://dx.doi.org/10.6028/nist.ir.6793.
Benz, Frederick W. High Technology Mass Spectrometry Laboratory. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2010. http://dx.doi.org/10.21236/ada530590.
Hunka, Deborah E., i Daniel Austin. Ion Mobility Spectrometer / Mass Spectrometer (IMS-MS). Office of Scientific and Technical Information (OSTI), październik 2005. http://dx.doi.org/10.2172/1126945.
Hunka Deborah Elaine i Daniel E. Austin. Ion mobility spectrometer / mass spectrometer (IMS-MS). Office of Scientific and Technical Information (OSTI), lipiec 2005. http://dx.doi.org/10.2172/889413.
Gaffney, Amy. Guideline on Isotope Dilution Mass Spectrometry. Office of Scientific and Technical Information (OSTI), maj 2017. http://dx.doi.org/10.2172/1358328.
Hieftje, Gary M., i George H. Vickers. Developments in Plasma-Source Mass Spectrometry. Fort Belvoir, VA: Defense Technical Information Center, lipiec 1988. http://dx.doi.org/10.21236/ada197732.
Bach, Stephan B., i Walter Hubert. Radiation Biomarker Research Using Mass Spectrometry. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2007. http://dx.doi.org/10.21236/ada473187.
Perdian, David C. Direct analysis of samples by mass spectrometry: From elements to bio-molecules using laser ablation inductively couple plasma mass spectrometry and laser desorption/ionization mass spectrometry. Office of Scientific and Technical Information (OSTI), styczeń 2009. http://dx.doi.org/10.2172/972075.
Leckey, J. H., i M. D. Boeckmann. Rapid scanning mass spectrometer. Office of Scientific and Technical Information (OSTI), listopad 1996. http://dx.doi.org/10.2172/459358.
Vertes, Akos. New approaches for metabolomics by mass spectrometry. Office of Scientific and Technical Information (OSTI), lipiec 2017. http://dx.doi.org/10.2172/1368638.