Literatura académica sobre el tema "MALDI"
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Artículos de revistas sobre el tema "MALDI"
Osa, Morichika, Maria Cecilia Belo, Zita Dela Merced, Annavi Marie G. Villanueva, Jaira Mauhay, Alyannah Celis, Melissa Catli et al. "Performance of MALDI–TOF Mass Spectrometry in the Philippines". Tropical Medicine and Infectious Disease 6, n.º 3 (26 de junio de 2021): 112. http://dx.doi.org/10.3390/tropicalmed6030112.
Texto completoKAWABATA, Shin-ichirou. "MALDI-TOFMS". Journal of the Japan Society of Colour Material 79, n.º 6 (2006): 257–62. http://dx.doi.org/10.4011/shikizai1937.79.257.
Texto completoKajiwara, Hideyuki. "MALDI biotyping". Nippon Shokuhin Kagaku Kogaku Kaishi 65, n.º 11 (15 de noviembre de 2018): 541. http://dx.doi.org/10.3136/nskkk.65.541.
Texto completoWisztorski, Maxence, Rémi Lemaire, Jonathan Stauber, Sonia Ait Menguellet, Olivia Jardin-Mathé, Robert Day, Michel Salzet y Isabelle Fournier. "Imagerie MALDI". médecine/sciences 23 (marzo de 2007): 31–38. http://dx.doi.org/10.1051/medsci/2007231s31.
Texto completoChakrabarti, A. "MALDI-TOF". International Journal of Infectious Diseases 45 (abril de 2016): 26. http://dx.doi.org/10.1016/j.ijid.2016.02.090.
Texto completoChin, Jefferson, Elizabeth Wood, Grace S. Peters y Dieter M. Drexler. "Acoustic Sample Deposition MALDI-MS (ASD-MALDI-MS)". Journal of Laboratory Automation 21, n.º 1 (febrero de 2016): 204–7. http://dx.doi.org/10.1177/2211068215594769.
Texto completoRim, John Hoon, Yangsoon Lee, Sung Kuk Hong, Yongjung Park, MyungSook Kim, Roshan D’Souza, Eun Suk Park, Dongeun Yong y Kyungwon Lee. "Insufficient Discriminatory Power of Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry Dendrograms to Determine the Clonality of Multi-Drug-ResistantAcinetobacter baumanniiIsolates from an Intensive Care Unit". BioMed Research International 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/535027.
Texto completoNIRASAWA, TAKASHI. "MALDI-TOF-MS." Kagaku To Seibutsu 34, n.º 4 (1996): 255–59. http://dx.doi.org/10.1271/kagakutoseibutsu1962.34.255.
Texto completoKriegsmann, J., R. Casadonte, F. Zweynert, M. Kriegsmann, M. Otto y S. Deininger. "MALDI-TOF-Bildgebung". Zeitschrift für Rheumatologie 72, n.º 7 (16 de agosto de 2013): 724–28. http://dx.doi.org/10.1007/s00393-013-1239-1.
Texto completoChen, Xin-Fei, Xin Hou, Meng Xiao, Li Zhang, Jing-Wei Cheng, Meng-Lan Zhou, Jing-Jing Huang, Jing-Jia Zhang, Ying-Chun Xu y Po-Ren Hsueh. "Matrix-Assisted Laser Desorption/Ionization Time of Flight Mass Spectrometry (MALDI-TOF MS) Analysis for the Identification of Pathogenic Microorganisms: A Review". Microorganisms 9, n.º 7 (19 de julio de 2021): 1536. http://dx.doi.org/10.3390/microorganisms9071536.
Texto completoTesis sobre el tema "MALDI"
Rodrigues, Lívia Riberti 1988. "Análise de impurezas de formas farmacêuticas sólidas por MALDI Mass Spectrometry Imaging (MALDI-MSI)". [s.n.], 2014. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312437.
Texto completoTexto em português e inglês
Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas
Made available in DSpace on 2018-08-25T05:33:49Z (GMT). No. of bitstreams: 1 Rodrigues_LiviaRiberti_M.pdf: 1203619 bytes, checksum: a17baf81fa013532bd6c9d451b2336f2 (MD5) Previous issue date: 2014
Resumo: Atualmente, as doenças cardiovasculares constituem uma das primeiras causas de mortes no Brasil e no mundo. Neste cenário, as estatinas constituem uma notável classe de medicamentos redutores de colesterol e têm sido associadas com uma expressiva diminuição da morbidade e mortalidade cardiovascular para pacientes em prevenção primária ou secundária da doença coronariana. Elas agem inibindo competitivamente a enzima HMG-CoA redutase, através da afinidade destes fármacos pelo sítio ativo da enzima. Esta enzima é responsável por catalisar a conversão do substrato HMG-CoA em mevalonato, um dos precursores do colesterol. A crescente necessidade e busca por medicamentos cada vez mais efetivos traz a preocupação na segurança destes produtos para seus usuários. Neste sentido, o conhecimento das impurezas e produtos de degradação torna-se necessário para garantir sua qualidade. Uma técnica muito utilizada para análises de impurezas e degradantes é a espectrometria de massas, pois é uma técnica sensível e seletiva e permite elucidar as estruturas químicas presentes na formulação do medicamento. Sendo assim, amostras de Atorvastatina cálcica foram analisadas pela técnica de espectrometria de massas por imagem (MALDI-MSI), permitindo a quantificação de impurezas do medicamento através da imagem da distribuição dessa impureza no comprimido. Dessa forma, é possível minimizar o preparo de amostra e obter um melhor conhecimento da formulação
Abstract: Currently, cardiovascular diseases constitute one of the first causes of deaths in Brazil and in the world. In this scenario, the statins are a notable class of medicines and cholesterol reducers have been associated with a significant reduction in cardiovascular morbidity and mortality for patients in primary or secondary prevention of coronary heart disease. They act by inhibiting competitively the enzyme HMG-CoA reductase, through the affinity of these drugs by the active site of the enzyme. This enzyme is responsible for catalyzing the conversion of HMG-CoA to mevalonate substrate, one of the precursors of cholesterol. The growing need and search for increasingly effective drugs brings the concern on the safety of these drugs for their users. In this sense, the knowledge of the impurities and degradation products becomes necessary to ensure their quality. A widely used technique for analysis of impurities and degrading is mass spectrometry, because it is a sensitive and selective technique and allows elucidating the chemical structures of the present formulation of the medicinal product. Thus, samples of Atorvastatin calcium were analyzed by the technique of mass spectrometry imaging (MALDI-MSI), which allows the quantification of impurities from the medicine through the image of the distribution of impurity in the tablet. That way, it is possible minimize sample preparation and get a better understanding of the formulation
Mestrado
Ciencias Biomedicas
Mestra em Ciências Médicas
Lai-Rowcroft, Lindsay Ling Gi. "Novel surfaces for MALDI-MS". Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/novel-surfaces-for-maldims(331dd97a-881e-4ed0-908f-d5947f3ebeba).html.
Texto completoTandina, Fatalmoudou. "Mise au point et application de technologies innovantes pour l'étude des moustiques, de leur préférence trophique et de leur microbiote". Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0277/document.
Texto completoMosquitoes are the main vectors involved in the transmission of pathogens to humans. Accurate identification of mosquito species is crucial to distinguish between vector and non-vector species. The mosquito blood meal determination is fundamental in understanding the behavior of vector species. Thus, we have listed 106 mosquito species currently recorded in Mali, including 28 Anophelinae and 78 Culicinae. Then, we evaluated the effectiveness of MALDI-TOF MS for identified mosquitoes collected in Mali and to determine their blood meal source. The results obtained show the ability of MALDI-TOF MS to identify mosquitoes collected in Mali and their source of blood meal. Subsequently, we were able to confirm the robustness of MALDI-TOF MS to identify other animal blood samples. We artificially engorged Anopheles gambiae and Anopheles coluzzii on eight animal bloods samples. We obtained 100% correct identification of the blood source for samples taken 1 to 24 hours after feeding. Then, we experimentally engorged An. gambiae, An. coluzzii and Ae. albopictus on successive and mixed blood meals using MALDI-TOF MS. The results revealed that MALDI-TOF MS is able to identify mixed blood meals. In addition we used MALDI-TOF and culturomics for the microbiota study of the mosquito collected in the field, notably in Marseille and Mali. The culturomics approach revealed a great diversity of the digestive microbiota of the An. gambiae, Ae. albopictus and Cx. quinquefasciatus mosquitoes
Krüger, Ralf. "Untersuchungen zum Einbau von Analytionen in MALDI-Matrizes sowie zur Ionisation und Adduktbildung in der MALDI-Massenspektrometrie". [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969681682.
Texto completoKirmess, Kristopher Michael. "Investigation of Primary Ion Formation Mechanisms in UV-MALDI-MS Using Excited State Dynamics of Common MALDI Matrices". OpenSIUC, 2015. https://opensiuc.lib.siu.edu/dissertations/1110.
Texto completoCollazo, Verena. "Reverse Sanger-Sequenzierung mittels MALDI-TOF-Massenspektrometrie". [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=964226871.
Texto completoEnebro, Jonas. "Characterization of carboxymethyl cellulose by MALDI-TOFMS /". Stockholm : [Fiber och polymerteknologi, Kungliga Tekniska högskolan], 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4376.
Texto completoLeander, Ellinor. "Artidentifiering av mögelsvamp med MALDI-TOF MS". Thesis, Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB), 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-80166.
Texto completoRapid and accurate species identification is crucial for successful treatment of fungal infections, especially among immunosuppressed patients. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) is used routinely at clinical laboratories to identify characteristic protein patterns of bacteria and yeast by the interpretation of protein spectra in a database for accurate species identification. The hard cell wall of the mold and the heterogeneous growth with varying protein expression due to maturation, complicates identification with MALDI-TOF MS. The potential benefits of this method compared to microscopy as traditional method are shortened turn-around times, safer species identification of more species that is independent on subjective morphological assessment. The purpose of the study was to investigate whether MALDI-TOF MS could be adapted and used for the identification of molds in clinical routine diagnostics. Four reference strains (Aspergillus niger, A.fumigatus, A.terreus, A.flavus) and a clinical isolate (A.terreus) were examined. The preparation methods (I) complete formic acid extraction, (II) direct application and (III) suspension in distilled water were used for analysis of spores and frontmycelium from younger and older mold cultures. Two different masspektradatabases for species identification were compared; routine database BDAL and the specialized mold database, Filamentous Fungi Library. Also the collecting technique of mold prior to analysis with MALDI-TOF MS was evaluated. Sometimes, the species identification improved after extraction of mold cultures, while in other cases direct application was sufficient. Cultures with a lot of spores tended to give slightly more species identifications in BDAL regardless of the age of cultures. Filamentous Fungi Library, in some cases, tended to improve the performance compared to BDAL for younger cultures. More studies are required to evaluate and optimize MALDI-TOF MS as a method of mold identification.
Stauber, Jonathan. "Imagerie MALDI : nouveaux développements et applications cliniques". Lille 1, 2007. https://pepite-depot.univ-lille.fr/LIBRE/Th_Num/2007/50376-2007-379.pdf.
Texto completoThe recent innovations in molecular biology were realized with the evolution of the imaging techniques in the field of Genomics, Transcriptomics, and recently in Proteomics with an essential tool, the mass spectrometry. This imaging technique create characteristic protein profiles of the cellular states, and appears today as an undissociable tool for research in biology and medicine. The last developments look to emerge the mass spectrometry to a molecular imaging to identify pathologies, to observe the drugs distributions in tissues, or the diseases diagnosis or prognosis. This unique and recent technology should be developed, improved, and standardized. It's in this point of view the my PhD training named MALDI imaging new developments and clinical applications was defined. The different results obtained during my PhD were permits to create a concept of Specific Imaging Mass Spectrometry, to develop Molecular MALDI imaging of frozen and FFPE tissues with many applications in the research of specific biomarkers in Parkinson disease and ovarian cancer. The evolution of this unique molecular imaging technique should be in the next years a complementary method of others in vivo imaging technique
Jacksén, Johan. "Improved techniques for CE-MALDI-MS off-line coupling and MALDI-MS analysis of primarily hydrophobic proteins and peptides". Licentiate thesis, KTH, Chemistry, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4599.
Texto completoDue to the hydrophobic nature of integral membrane proteins (IMP) they give rise to several difficulties concerning handling and analysis, which is not the case for the most water soluble proteins. New analysis methods are needed, where the insolubility problems of the hydrophobic proteins due to aggregation and adhesion are tackled. Those problems also affect digestion performance and equipment compatibility for the analysis.
Protocols for analysis and separation specified for IMP are presented in Paper I and III.
The instrumentation used in this work was capillary electrophoresis (CE) and matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). Both instruments are suitable for peptide/proteins analysis.
In Paper I, protocols for a CE separation of bacteriorhodopsin (BR) peptides as model IMP peptides are established. Also, a partially automated manufacturing procedure of a concentration MALDI-target is presented, suitable for fractions from CE. The MS analysis detected 9 out of 10 cyanogen bromide (CNBr) digested BR peptides. A novel technique for the off-line integration of CE to MALDI-MS using a closed-open-closed system is presented in Paper II, where the open part is a microcanal functioning as a MALDI target window. Investigation of the microcanal electro-osmotic flow (EOF) properties and band broadening characteristics was performed. A protein separation was obtained and detected with MALDI-MS analysis in the microcanal. Different protein digestion methods were evaluated using BR in Paper III through MALDI-MS. Several digestion methods as well as MS media were investigated alongside different MALDI matrices. For example, matrices as the hydrophobic 2,6-dihydroxyacetophenone (DHAP) and 2-Hydroxy-3-methoxybenzoic acid (2H3MBA) or 2-Hydroxy-5-methoxybenzoic acid (2H5MBA) mixed with DHB, appeared to be promising matrices for analysis of BR.
Med anledning av integrala membranproteiners (IMP) hydrofoba egenskaper uppstår flera svårigheter vid hantering och analys av IMP, vilket inte är fallet för vattenlösliga proteiner. Nya analysmetoder krävs, som löser löslighetsproblemen för de hydrofoba proteinerna som tex flockning och adsorbtion. Dessa problem påverkar även klyvningsgrad och kompatibilitet med analysutrustningen.
I Artikel I och Artikel III presenteras protokoll för analys och separation specifikt för IMP. Instrumenteringen som har använts i detta arbete är kapillärelektrofores (CE) och matris-assisterad laserdesorptions-joniserings-masspektrometri (MALDI-MS). Båda instrumenten är lämpade för peptid/protein analyser.
I Artikel I, presenteras protokoll för en CE separation av peptider från bacteriorhodopsin (BR), som användes som modellpeptider för IMP. En delvis automatiserat tillverkningsprocedur för en koncentrerande MALDI-platta, som är anpassad för CE fraktionerna beskrivs också. MS-analysen detekterade 9 av 10 BR-peptider från cyanobromid-klyvning (CNBr). En ny teknik för off line-integrering av CE till MALDI-MS genom ett slutet-öppet-slutet system presenteras i Artikel II, där den öppna delen är en mikrokanal som fungerar som detektionsfönster i MALDI. Undersökning av mikrokanalens egenskaper som tex det elektroosmotiska flödet (EOF) och bandbreddningen utvärderades. En proteinseparation genomfördes och detekterades med MALDI–MS i mikrokanalen. Olika proteinklyvningsmetoder för BR undersöktes i Artikel III med MALDI-MS. Flera proteinklyvningsmetoder samt MS-medier utvärderades tillsammans med olika MALDI-matriser. Den hydrofoba matrisen 2,6-dihydroxyacetophenone (DHAP) och 2-Hydroxy-3-methoxybenzoic acid (2H3MBA) eller 2-Hydroxy-5-methoxybenzoic acid (2H5MBA) blandade med DHB, visade sig exempelvis vara lovande matriser för BR-analyser.
Libros sobre el tema "MALDI"
Hillenkamp, Franz y Jasna Peter-Katalinic, eds. MALDI MS. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.
Texto completoPorta Siegel, Tiffany, ed. MALDI Mass Spectrometry Imaging. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839165191.
Texto completoCole, Richard B., ed. Electrospray and MALDI Mass Spectrometry. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470588901.
Texto completoCai, Zongwei y Shuying Liu, eds. Applications of MALDI-TOF Spectroscopy. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35665-0.
Texto completoHosseini, Samira y Sergio O. Martinez-Chapa. Fundamentals of MALDI-ToF-MS Analysis. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-2356-9.
Texto completoLi, Liang, ed. Maldi Mass Spectrometry for Synthetic Polymer Analysis. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470567234.
Texto completoPasch, Harald y Wolfgang Schrepp. MALDI-TOF Mass Spectrometry of Synthetic Polymers. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05046-0.
Texto completoPasch, Harald. MALDI-TOF Mass Spectrometry of Synthetic Polymers. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003.
Buscar texto completoLiang, Li, ed. MALDI mass spectrometry for synthetic polymers analysis. Hoboken: Wiley, 2010.
Buscar texto completoShah, Haroun N. y Saheer E. Gharbia, eds. MALDI-TOF and Tandem MS for Clinical Microbiology. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781118960226.
Texto completoCapítulos de libros sobre el tema "MALDI"
Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, Ben J. Harrison, Christos Pantelis, Christof Baltes, Thomas Mueggler et al. "MALDI". En Encyclopedia of Psychopharmacology, 749. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4339.
Texto completoHillenkamp, Franz, Thorsten W. Jaskolla y Michael Karas. "The MALDI Process and Method". En MALDI MS, 1–40. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch1.
Texto completoPham, Thang V. y Connie R. Jimenez. "Computational Analysis of High-Throughput MALDI-TOF-MS-Based Peptide Profiling". En MALDI MS, 411–30. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch10.
Texto completoKostrzewa, Markus. "Biotyping of Microorganisms". En MALDI MS, 431–43. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch11.
Texto completoO'Connor, Peter B., Klaus Dreisewerd, Kerstin Strupat y Franz Hillenkamp. "MALDI Mass Spectrometry Instrumentation". En MALDI MS, 41–104. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch2.
Texto completoHjernø, Karin y Ole N. Jensen. "MALDI-MS in Protein Chemistry and Proteomics". En MALDI MS, 105–31. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch3.
Texto completoSpengler, Bernhard. "MALDI-Mass Spectrometry Imaging". En MALDI MS, 133–67. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch4.
Texto completoBerkenkamp, Stefan, Dirk van den Boom y Daniele Fabris. "Analysis of Nucleic Acids, and Practical Implementations in Genomics and Genetics". En MALDI MS, 169–238. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch5.
Texto completoPerreault, Hélène, Erika Lattová, Dijana Šagi y Jasna Peter-Katalinic. "MALDI-MS of Glycans and Glycoconjugates". En MALDI MS, 239–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch6.
Texto completoSchiller, Jürgen y Beate Fuchs. "Lipids". En MALDI MS, 273–311. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527335961.ch7.
Texto completoActas de conferencias sobre el tema "MALDI"
Murray, Kermit K., Michelle D. Beeson y David H. Russell. "Laser Ionization of Biomolecules in Solution". En Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/laca.1994.tha.5.
Texto completoKinsel, Gary R., Kent Gillig, Ricky Edmondson y David H. Russell. "Fundamental Investigations of the Mechanism of Laser Desorption and Ionization in Matrix Assisted Laser Desorption / Ionization". En Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/laca.1994.thb.1.
Texto completoPuapaiboon, Uraiwan, Jaran Jai-nhuknan y James A. Cowan. "Exonuclease reactivity using MALDI-TOF mass spectrometry". En BiOS 2000 The International Symposium on Biomedical Optics, editado por Darryl J. Bornhop y Kai Licha. SPIE, 2000. http://dx.doi.org/10.1117/12.384247.
Texto completoDing, Li, Eizoh Kawatoh, Koichi Tanaka, Alan J. Smith y Sumio Kumashiro. "High-efficiency MALDI-QIT-ToF mass spectrometer". En SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, editado por Eric Munro. SPIE, 1999. http://dx.doi.org/10.1117/12.370125.
Texto completoSILVA, J. A. DA, L. NAGY y L. G. AGUIAR. "CARACTERIZAÇÃO DE POLIÓIS INDUSTRIAIS POR MALDI-TOF". En Congresso Brasileiro de Engenharia Química em Iniciação Científica. São Paulo: Editora Blucher, 2017. http://dx.doi.org/10.5151/chemeng-cobeqic2017-312.
Texto completoNAOMI TAMI, MARIANA, RODRIGO RAMOS CATHARINO y DIOGO N. OLIVEIRA. "Avaliação de corantes alimentares por MALDI-Imaging". En XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil: Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-50969.
Texto completoJabbour, Rabih, Ashish Tripathi, Erik D. Emmons, Phillip G. Wilcox, Jason A. Guicheteau, Gregory Peterson y Jared Decoste. "Advancements in MOF characterization for enhanced MALDI sensing". En Chemical, Biological, Radiological, Nuclear, and Explosives (CBRNE) Sensing XIX, editado por Augustus W. Fountain, Jason A. Guicheteau y Chris R. Howle. SPIE, 2018. http://dx.doi.org/10.1117/12.2303501.
Texto completoKolibal, J. y D. Howard. "Novel Algorithm for MALDI-TOF Baseline Drift Removal". En 2005 IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology. IEEE, 2005. http://dx.doi.org/10.1109/cibcb.2005.1594946.
Texto completoGerhard, Marc, Soren-Oliver Deininger y Frank-Michael Schleif. "Statistical Classification and Visualization of MALDI-Imaging Data". En Twentieth IEEE International Symposium on Computer-Based Medical Systems. IEEE, 2007. http://dx.doi.org/10.1109/cbms.2007.99.
Texto completoVadlamudi, Ayyappa, Shao-Hui Chuang, Xiaoyan Sun, Lisa Cazares, Julius Nyalwidhe, Dean Troyer, O. John Semmes, Jiang Li y Frederic D. McKenzie. "Prostate cancer region prediction using MALDI mass spectra". En SPIE Medical Imaging, editado por Nico Karssemeijer y Ronald M. Summers. SPIE, 2010. http://dx.doi.org/10.1117/12.844494.
Texto completoInformes sobre el tema "MALDI"
Waite, J. H. Direct Analysis of Marine Interfaces: Mussels and MALDI. Fort Belvoir, VA: Defense Technical Information Center, enero de 2002. http://dx.doi.org/10.21236/ada397968.
Texto completoGillman, Amelie R. Correlating MALDI and MRI Biomarkers of Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, julio de 2010. http://dx.doi.org/10.21236/ada540714.
Texto completoWahl, Karen L., Kristin H. Jarman, Nancy B. Valentine, Mark T. Kingsley, Catherine E. Petersen, Sharon C. Wunschel y Adam J. Saenz. Analysis of Hazardous Biological Materials by MALDI Mass Spectrometry. Office of Scientific and Technical Information (OSTI), diciembre de 1999. http://dx.doi.org/10.2172/15002705.
Texto completoSamaraweera, Himali, Sun Hee Moon y Dong U. Ahn. Characterization of Phosvitin Phosphopeptides using MALDI-TOF Mass Spectrometry. Ames (Iowa): Iowa State University, enero de 2016. http://dx.doi.org/10.31274/ans_air-180814-1389.
Texto completoKL Wahl, KH Jarman, NB Valentine, MT Kingsley, CE Petersen, ST Cebula y AJ Saenz. Analysis of hazardous biological material by MALDI mass spectrometry. Office of Scientific and Technical Information (OSTI), marzo de 2000. http://dx.doi.org/10.2172/752459.
Texto completoPuretzky, A. A. y D. B. Geohegan. LIF-imaging and gas-phase diagnostics of laser desorbed MALDI-matrix plumes. Office of Scientific and Technical Information (OSTI), julio de 1997. http://dx.doi.org/10.2172/563317.
Texto completoFeenstra, Adam D. Technological Development of High-Performance MALDI Mass Spectrometry Imaging for the Study of Metabolic Biology. Office of Scientific and Technical Information (OSTI), diciembre de 2016. http://dx.doi.org/10.2172/1409181.
Texto completoKorte, Andrew R. Development of matrix-assisted laser desorption ionization-mass spectrometry imaging (MALDI-MSI) for plant metabolite analysis. Office of Scientific and Technical Information (OSTI), diciembre de 2014. http://dx.doi.org/10.2172/1226566.
Texto completoSriram, Subramaniam. MALDI/Mass Spectrometry of Normal Appearing and Dystrophic Axons in Spinal Cord of Multiple Sclerosis (MS). Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2012. http://dx.doi.org/10.21236/ada582356.
Texto completoSriram, Subramaniam. MALDI/Mass Spectrometry of Normal Appearing" and Dystrophic Axons in Spinal Cord of Multiple Sclerosis (MS)". Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2013. http://dx.doi.org/10.21236/ada592436.
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