Littérature scientifique sur le sujet « SILICO ANALYSIS »
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Articles de revues sur le sujet "SILICO ANALYSIS"
Barik, Dr Bibhuti Prasad. « In Silico Observations and Analysis of Metabolic Pathways ». International Journal of Scientific Research 2, no 11 (1 juin 2012) : 44–48. http://dx.doi.org/10.15373/22778179/nov2013/14.
Texte intégralChaudhary, Hammad Tufail, et Shahida Hasnain. « IN-SILICO ANALYSIS ». Professional Medical Journal 23, no 02 (10 octobre 2016) : 217–22. http://dx.doi.org/10.29309/tpmj/2016.23.02.1074.
Texte intégralGunamalai, Lavanya, et C. Jaynthy C.Jaynthy. « In Silico Molecular Interaction Analysis Of Type I Collagen Telopeptides With Cyclodextrins ». International Journal of Scientific Research 3, no 8 (1 juin 2012) : 25–27. http://dx.doi.org/10.15373/22778179/august2014/8.
Texte intégralTADA, Yukio, et Mie TOGAWA. « Biomechanical Analysis of Hip Joint in Silico ». Proceedings of Conference of Kansai Branch 2002.77 (2002) : _4–45_—_4–46_. http://dx.doi.org/10.1299/jsmekansai.2002.77._4-45_.
Texte intégralJoy, Amitha. « MLH1 gene : An in silico analysis ». Journal of Computational Biology and Bioinformatics Research 5, no 1 (30 avril 2013) : 1–5. http://dx.doi.org/10.5897/jcbbr12.012.
Texte intégralBarbosa, Aulus Estevão, et Paulo Marinho. « In silico analysis of Eucalyptus thioredoxins ». Genetics and Molecular Biology 28, no 3 suppl (2005) : 539–47. http://dx.doi.org/10.1590/s1415-47572005000400008.
Texte intégralDenomme, Gregory. « In Silico Analysis in Transfusion Medicine ». Vox Sanguinis 83 (août 2002) : 111–13. http://dx.doi.org/10.1111/j.1423-0410.2002.tb05280.x.
Texte intégralGunn, S., J. R. Hotchkiss et P. Crooke. « In silico analysis of mechanical ventilation ». Journal of Critical Care 21, no 4 (décembre 2006) : 358–59. http://dx.doi.org/10.1016/j.jcrc.2006.10.027.
Texte intégralFlorczuk, Patrycja, et Joanna Gruszczyńska. « GENETIC BACKGROUND OF CHONDRODYSPLASIA IN DOMESTIC DOG (CANIS LUPUS FAMILIARIS) – IN SILICO ANALYSIS ». Acta Scientiarum Polonorum Zootechnica 15, no 4 (10 janvier 2017) : 5–14. http://dx.doi.org/10.21005/asp.2016.15.4.01.
Texte intégralKaplarević, Milica, Marija GaÄić, Georgia Karanasiou, Dimitris Fotiadis et Nenad Filipović. « COST-EFFECTIVENESS ANALYSIS OF IN SILICO CLINICAL TRIALS OF VASCULAR STENTS ». Journal of the Serbian Society for Computational Mechanics 16, no 2 (1 décembre 2022) : 105–16. http://dx.doi.org/10.24874/jsscm.2022.16.02.08.
Texte intégralThèses sur le sujet "SILICO ANALYSIS"
Chen, Ming. « In silico systems analysis of biopathways ». [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972067272.
Texte intégralValejev, Najl V. « In silico analysis of signal transduction proteins ». Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.432258.
Texte intégralFerreira, Susana Duarte Barros Lopes. « In silico analysis of regenerating spinal cord transcriptomes ». Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/19034.
Texte intégralAs lesões na medula espinal são uma desordem neurológica comum com um impacto significativo na sociedade moderna do ponto de visto físico, psicosocial e socioeconómico. Apesar de vários vertebrados serem capazes de regenerar lesões do sistema nervoso central, nomeadamente da medula espinal (ex. Rã, Peixe-zebra, Salamandra), está bem estabelecido que os seres humanos, e outros mamíferos adultos, não o conseguem fazer. Como tal, em consequência de lesões traumáticas no cérebro ou medula espinal, há incapacidade dos axónios crescerem extensivamente no tecido lesado. No entanto, um estudo importante realizado no virar do século por Ramón y Cajal, comprovou que a incapacidade das fibras nervosas regenerarem “deriva de condições externas, da presença ou ausência de fatores auxiliares que são indispensáveis para o processo regenerativo”, trazendo assim esperança que a neuroregeneração possa ser alcançada por modulação de condições celulares e moleculares. Esta dissertação tem como objetivo adquirir uma melhor e mais extensa compreensão dos genes e processos fisiológicos que são cruciais durante a regeneração da medula espinal, usando estudos de expressão genómica de modelos regenerativos, tais como Xenopus laevis, Xenopus tropicalis e Danio rerio, estabelecendo-se simultaneamente um paralelismo com os respetivos ortólogos humanos com o objetivo de encontrar genes candidatos no genoma humano passíveis de serem modulados com vista a alterar o estatuto não-regenerativo dos mamíferos adultos.
Spinal cord injuries are a common neurologic disorder that have devastating impacts on modern society, be it from physical, psychosocial, or socioeconomic point of view. Although many small vertebrates are capable of regenerating lesions to the central nervous system, namely the spinal cord, (e.g. frog, zebrafish, salamander) it is well established that humans and other adult mammals cannot. As so, failure of axons to grow extensively through damaged central nervous system (CNS) tissues is a common consequence of injury to the brain and spinal cord on adult mammals. However, an important study made at the turn of the century by Ramón y Cajal, proved that the failure of central fibers to regrow “derives from external conditions, the presence or absence of auxiliary factors that are indispensable to the regenerative process”, thus bringing hope that neuroregeneration can be achieved by modulating cellular and molecular conditions. Through this dissertation, we aim to get a better understanding of the involvement of the genes and physiological processes that are crucial during regeneration of the spinal cord, using genome wide expression studies of regenerative models such as Xenopus laevis, Xenopus tropicalis, and Danio rerio, while drawing parallel to its human orthologues. Being our goal to find perfect gene candidates in the human genome that are predictably capable of being modulated so we can alter the non-regenerative status of the adult mammals.
Bassot, Claudio. « In silico analysis of membrane transport/permeability mechanisms ». Doctoral thesis, Università degli studi di Padova, 2017. http://hdl.handle.net/11577/3425730.
Texte intégralLe membrane lipidiche sono una componente fondamentale delle cellule viventi, separano fisicamente le componenti intracellulari dall’ambiente esterno e i diversi organelli del citoplasma. Le proteine di trasporto conferiscono permeabilità alle membrane lipidiche, proprietà essenziale per la traslocazione di nutrienti e la conservazione dell’energia. La cristallografia di proteine transmembrana è problematica a causa della loro localizzazione e proprietà chimiche, e solo un numero piuttosto ridotto di strutture è disponibile. L’analisi in silico può essere applicata con successo per investigare le strutture e il funzionamento proporre modelli testabili di trasportatori e delle loro funzioni. Il lavoro del mio dottorato sì è focalizzato su due modelli: la pendrina (SLC26A4) e il poro di transizione di permeabilità (PTP). Questi due sistemi proteici mi hanno permesso di studiare due differenti tipi di membrana e meccanismi di permeabilità: la membrana plasmatica con scambio specifico di anioni (SLC26A4) e la membrana interna mitocondriale con la permeabilità non selettiva mitocondriale (PTP). Le mutazioni della pendrina sono stimate essere la seconda causa genetica più comune della sordità umana, ma la struttura della proteina non è stata ancora determinata. Scopo del mio lavoro è stato quello di sopperire all’assenza di informazioni strutturali per il dominio transmembrana della pendrina e di dare una spiegazione funzionale per le mutazioni raccolte nel MORL Deafness Variation Database. Il modello 3D della pendrina è basato sull’omologia con SLC26Dg (3) ed è stato validato analizzando la distribuzione sulla superfice dei residui idrofobici. L’alta qualità risultante dal modello è stata usata per mappare 147 mutazioni patologiche umane. Tre cluster di mutazioni sono stati trovati e la loro localizzazione suggerisce per pendrina un innovativa struttura a 14 domini transmembrana. Anche la natura del PTP è rimasta a lungo misteriosa. Nel 2013 Giorgio et al. hanno suggerito che i dimeri di F1FO (F)-ATP sintasi formino il poro, tuttavia l’esatta composizione e il modo in cui il poro di transizione si possa formare è ancora materia di dibattito. L’apertura del PTP è innescata da un aumento della concentrazione di Ca2+ nella matrice mitocondriale ed è favorita dallo stress ossidativo. Per fare luce sul funzionamento del PTP ho studiato l’effetto del legame del Ca2+ al sito per i cationi divalenti (Me2+) nel dominio F1 attraverso la dinamica molecolare (MD). Un approccio simile è stato anche applicato alla mutazione T163S, che fa variare l’affinità relativa per Mg2+ e Ca2+. I dati sperimentali mostrano come la mutazione induca resistenza all’apertura del PTP. La MD ha dimostrato come il legame del Ca2+ irrigidisca la struttura del complesso. Il riarrangiamento del sito catalitico indotto dai differenti ioni che lo occupano, così come la mutazione T163S, causa rilevanti variazioni delle interazioni tra il dominio F1 e la subunità OSCP. Suggerisco che un loop non strutturato tra i residui 82-131 della subunità β trasmetta il riarrangiamento strutturale originato nel sito catalitico a OSCP e quindi alla membrana interna attraverso il rigido stalk laterale. Il ruolo critico che emerge per OSCP nella regolazione del PTP apre due domande collegate: (i) come il segnale di apertura mediato da OSCP venga trasmesso alla regione trans-membrana e (ii) quali siano i componenti transmembrana del PTP. Le variazioni di conduttanza del poro osservate in specie diverse suggeriscono che le subunità che formano il canale debbano avere delle differenze significative. E’ stato prodotto un allineamento di sequenze per tutte le subunità della F-ATP sintasi. I risultati preliminari ci hanno spinto a focalizzarci sulle subunità e, g e b a causa della loro localizzazione e conservazione di sequenza. Basandomi sugli allineamenti multipli ho suggerito mutazioni puntiformi per testare l’importanza di specifici residui ai fini dell’apertura del poro. In parallelo la presenza delle subunità e e g tra gli eucarioti è stata indagata attraverso un analisi filogenetica. Proteine omologhe di queste specifiche subunità sono presenti in tutti gli eucarioti: dai lieviti alle piante, tuttavia gli Oomiceti sono risultati mancanti delle subunità e e g e le alghe verdi della subunità e. Questi risultati suggeriscono un’origine antica per le subunità di dimerizzazione della F-ATP sintasi e probabilmente anche del PTP. Per chiarire questo aspetto saranno necessarie ulteriori analisi e verifiche sperimentali.
Bellora, Pereyra Nicolás. « In silico analysis of regulatory motifs in gene promoters ». Doctoral thesis, Universitat Pompeu Fabra, 2010. http://hdl.handle.net/10803/7202.
Texte intégralLa regulació de la transcripció dels gens és un procés complex que implica moltes proteïnes diferents, algunes de les quals s'unexien a motius específics d'ADN localitzats a la regió promotora dels gens. S'espera que la necessitat de mantenir les interaccions específiques entre els factors de transcripció i les proteïnes implicades en el complex de la ARN polimerasa II imposi limitacions en la posició relativa i l'espaiat dels motius d'interacció amb l'ADN. La feina presentada en aquesta tesi inclou el desenvolupament d'un nou metode per l'identificació de motius que mostren una localització preferencial en seqüències d'ADN i l'implementació d'una aplicació web pública anomenada PEAKS. Hem investigat si la col·locació i la naturalesa de la majoria dels motius comuns depen del rang d'expresió del gen. Hem trobat diferències que serveixen per il·lustrar el fet que moltes senyals clau de regulació gènica poden estar presents en la regió proximal del promotor dels gens de mamífers. També hem aplicat altres mètodes per a l'identificació de factors de transcripció (TFs) específics involucrats en la co-regulació d'un grup de gens. Dades de llocs d'unio dels TFs (TFBSs) verificats experimentalment recolzen la rellevància biològica dels nostres resultats.
Behera, Jyoti, et Aruna Kilaru. « Comparative in Silico Analysis of WRINKLED1 Paralogs in Angiosperms ». Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etsu-works/7723.
Texte intégralBehera, Jyoti, Shina Bhatia et Aruna Kilaru. « Comparative in Silico Analysis of WRINKLED1 Paralogs in Angiosperms ». Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etsu-works/7724.
Texte intégralAzevedo, Ana do Carmo Ramalho Moreira. « Familial amyloid polyneuropathy : TTR sequencing and "in silico" analysis ». Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/15608.
Texte intégralFamilial amyloid polyneuropathy (FAP) or paramiloidosis is an autosomal dominant neurodegenerative disease with onset on adult age that is characterized by mutated protein deposition in the form of amyloid substance. FAP is due to a point alteration in the transthyretin (TTR) gene and until now more than 100 amyloidogenic mutations have been described in TTR gene. FAP shows a wide variation in age-at-onset (AO) (19-82 years, in Portuguese cases) and the V30M mutation often runs through several generation of asymptomatic carriers, before expressing in a proband, but the protective effect disappear in a single generation, with offspring of late-onset cases having early onset. V30M mutation does not explain alone the symptoms and AO variability of the disease observed in the same family. Our aim in this study was to identify genetic factors associated with AO variability and reduced penetrance which can have important clinical implications. To accomplish this we genotyped 230 individuals, using a directautomated sequencing approach in order to identify possible genetic modifiers within the TTR locus. After genotyping, we assessed a putative association of the SNPs found with AO and an intensive in silico analysis was performed in order to understand a possible regulation of gene expression. Although we did not find any significant association between SNPs and AO, we found very interesting and unreported results in the in silico analysis since we observed some alterations in the mechanism of splicing, transcription factors binding and miRNAs binding. All of these mechanisms when altered can lead to dysregulation of gene expression, which can have an impact in AO and phenotypic variability. These putative mechanisms of regulation of gene expression within the TTR gene could be used in the future as potential therapeutical targets, and could improve genetic counselling and follow-up of mutation carriers.
A Polineuropatia amiloidótica familiar (FAP) ou paramiloidose é uma doença neurodegenerativa autossómica dominante com início na vida adulta sendo caracterizada pela deposição da proteína mutada na forma de substância amilóide. A FAP é devida a uma mutação pontual no gene transtirretina (TTR) e até agora mais de 100 mutações amiloidogénicas foram descritas neste gene. A FAP apresenta uma grande variação na idade de início (AO) (19-82 anos, nos casos portugueses) e a mutação V30M pode segregar através de várias gerações de portadores assintomáticos, antes de se expressar num probando. No entanto, este efeito protetor pode desaparecer numa única geração, com os filhos de casos tardios a apresentarem um início precoce. A mutação V30M não explica por si só os sintomas e a variabilidade da AO observada dentro de uma mesma família. O nosso objetivo neste trabalho foi identificar fatores genéticos associados com a variabilidade da AO e a penetrância reduzida. De modo a cumprir este objetivo genotipámos 230 doentes, por sequenciação automática, para identificar possíveis modificadores genéticos dentro do locus da TTR. Após a genotipagem, investigamos uma possível associação dos SNPs encontrados com a AO e realizamos uma intensiva análise in silico de modo a perceber uma possível regulação da expressão génica. Apesar de não termos encontrado nenhuma associação entre os SNPs e a AO, encontrámos resultados não descritos e muito interessantes na análise in silico dado termos observado algumas alterações a nível do mecanismo de splicing, ligação de fatores de transcrição e ligação de miRNAs. Todos estes mecanismos quando alterados podem levar à desregulação da expressão do gene, o que pode ter um impacto na AO e variabilidade fenotípica. Estes mecanismos hipotéticos da regulação da expressão génica no gene da TTR podem ser úteis para no futuro serem aplicados como potenciais alvos terapêuticos, beneficiando o aconselhamento genético e o follow-up dos portadores da mutação.
Huang, Yi. « In silico analysis of a novel human coronavirus, coronavirus HKU1 ». Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/hkuto/record/B39793825.
Texte intégralSaeed, Hanaa. « «In planta» and «in silico» analysis of soybean lectin promoters ». Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=18806.
Texte intégralChez le soja (Glycine max), le promoteur du gene lectine Le1 dirige l'expression spécifique dans les graines. Des homologues de Le1 existent dans le genome du soja et sont exprimées ailleurs dans la plante. Nous avons isolé deux promoteurs de ces homologues de lectine, et décrivons le patron d'expression qu'ils dirigent. Un total de 1.3 kilobase des regions 5' des promoteurs, en amont du gène, a été isolé pour chacune des copies Le2 et Le3, et fusionné avec le gène rapporteur GUS. Le promoteur de Le1 étant déjà connu, il sert de controle. L'Arabidopsis transformée avec ces constructions, montre que le promoteur de Le3 dirige l'expression dans les tissues végétatifs, tandis que le promoteur de Le2 procure un niveau minimal d'expression dans tous les tissus examinés. De plus, des analyses bioinformatiques identifient des motifs spécifiques dans les sequences de promoteurs qui confirment les patrons d'expression que nous avons démontrés.
Livres sur le sujet "SILICO ANALYSIS"
Center, Lewis Research, dir. Stability and rheology of dispersions of silicon nitride and silicon carbide. [Cleveland, Ohio] : National Aeronautics and Space Administration, 1987.
Trouver le texte intégralAmpian, Sarkis G. Crystalline silica overview : Occurrence and analysis. Washington, D.C : U.S. Dept. of the Interior, Bureau of Mines, 1992.
Trouver le texte intégralTrust, Western Australian Silicon, et Maunsell & Partners., dir. Western Australian Silicon Project. [W.A.] : Maunsell & Partners, 1986.
Trouver le texte intégralInternational, ASTM, dir. Silica and associated respirable mineral particles. West Conshohocken, PA : ASTM International, 2014.
Trouver le texte intégralUnited States. National Aeronautics and Space Administration., dir. Stress and efficiency studies in EFG. Waltham, Mass : Mobil Solar Energy Corp., 1987.
Trouver le texte intégralJet Propulsion Laboratory (U.S.), dir. Stress and efficiency studies in EFG : Quarterly progress report, subcontract no. 956312, covering period October 1, 1984 - December 31, 1984. Waltham, Mass : Mobil Solar Energy Corp., 1985.
Trouver le texte intégralUnited States. National Aeronautics and Space Administration, dir. Stress and efficiency studies in EFG : Quarterly progress report ... covering period January 1, 1985 to March 31, 1985. Waltham, Mass : Mobil Solar Energy Corp., 1985.
Trouver le texte intégralAdachi, Sadao. Properties of semiconductor alloys : Group-IV, III-V and II-VI semiconductors. Chichester, West Sussex, U.K : Wiley, 2009.
Trouver le texte intégralProperties of semiconductor alloys : Group-IV, III-V and II-VI semiconductors. Chichester, West Sussex, U.K : Wiley, 2009.
Trouver le texte intégralNed, Tenekedjiev, Thomas Susan P et American Foundrymen's Society, dir. Microstructures and thermal analysis of strontium-treated aluminum-silicon alloys. Des Plains, Ill : American Foundrymen's Society, 1995.
Trouver le texte intégralChapitres de livres sur le sujet "SILICO ANALYSIS"
Yu, Bing, et Changbin Zhang. « In Silico PCR Analysis ». Dans Methods in Molecular Biology, 91–107. Totowa, NJ : Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-176-5_6.
Texte intégralBolívar, Julio, Reinhard Hehl et Lorenz Bülow. « In Silico Expression Analysis ». Dans Methods in Molecular Biology, 247–57. New York, NY : Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6396-6_16.
Texte intégralDovrolis, Nikolas. « In Silico Metagenomics Analysis ». Dans Gut Microbiome-Related Diseases and Therapies, 29–39. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-59642-2_2.
Texte intégralHone, Andrew, et Hugo van den Berg. « Mathematical Analysis of Artificial Immune System Dynamics and Performance ». Dans In Silico Immunology, 351–74. Boston, MA : Springer US, 2007. http://dx.doi.org/10.1007/978-0-387-39241-7_17.
Texte intégralWoodrow, Ian E. « Flux Control Analysis of the Rate of Photosynthetic CO2 Assimilation ». Dans Photosynthesis in silico, 349–60. Dordrecht : Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-1-4020-9237-4_15.
Texte intégralParis, Margot, et Laurence Després. « In Silico Fingerprinting (ISIF) : A User-Friendly In Silico AFLP Program ». Dans Data Production and Analysis in Population Genomics, 55–64. Totowa, NJ : Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-870-2_4.
Texte intégralZhu, Xin-Guang, et Stephen P. Long. « Can Increase in Rubisco Specificity Increase Carbon Gain by Whole Canopy ? A Modeling Analysis ». Dans Photosynthesis in silico, 401–16. Dordrecht : Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-1-4020-9237-4_17.
Texte intégralLiu, Hanqing, Tim N. Beck, Erica A. Golemis et Ilya G. Serebriiskii. « Integrating In Silico Resources to Map a Signaling Network ». Dans Gene Function Analysis, 197–245. Totowa, NJ : Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-721-1_11.
Texte intégralPruess, Manuela, Paul Kersey, Tamara Kulikova et Rolf Apweiler. « Databases and Resources for in silico Proteome Analysis ». Dans Methods of Biochemical Analysis, 395–414. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471973165.ch21.
Texte intégralSquazzoni, Flaminio, et Federico Bianchi. « Exploring Interventions on Social Outcomes with In Silico, Agent-Based Experiments ». Dans Texts in Quantitative Political Analysis, 217–34. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-12982-7_9.
Texte intégralActes de conférences sur le sujet "SILICO ANALYSIS"
Rossinelli, Diego, Yu-Hang Tang, Kirill Lykov, Dmitry Alexeev, Massimo Bernaschi, Panagiotis Hadjidoukas, Mauro Bisson et al. « The in-silico lab-on-a-chip ». Dans SC15 : The International Conference for High Performance Computing, Networking, Storage and Analysis. New York, NY, USA : ACM, 2015. http://dx.doi.org/10.1145/2807591.2807677.
Texte intégralL., Yeo S., Shazilah K., Suhaila S., Abu Bakar F. D. et Murad A. M. A. « In-silico analysis of Aspergillus niger beta-glucosidases ». Dans THE 2014 UKM FST POSTGRADUATE COLLOQUIUM : Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895257.
Texte intégralSpanu, Michele, et Matteo Bruno Lodi. « In silico analysis of farmlands disinfection using microwave ». Dans 2017 International Applied Computational Electromagnetics Society Symposium - Italy (ACES). IEEE, 2017. http://dx.doi.org/10.23919/ropaces.2017.7916419.
Texte intégralArshad, Abida, Rashda Abbasi, Christian MK Sieber, Muhammad Arshad et Nafees Ahmad. « In silico analysis of mutations in PITX3 gene ». Dans 2014 8th International Conference on Systems Biology (ISB). IEEE, 2014. http://dx.doi.org/10.1109/isb.2014.6990430.
Texte intégralMundayoor, Sathish. « Session details : In silico analysis in biomedical research ». Dans ISB '10 : International Symposium on BioComputing. New York, NY, USA : ACM, 2010. http://dx.doi.org/10.1145/3250321.
Texte intégralAbreu, Carlos, Francisco Miranda et Paula Felgueiras. « Towards patient-specific carbohydrate counting accuracy : An in silico study ». Dans INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2020. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0081330.
Texte intégralTimkin, Pavel, E. Timofeev, A. Chupalov et Evgeniy Borodin. « ANALYSIS AND SELECTION OF LIGANDS FOR TRPM8 USING HARD DOCKING AND MACHINE LEARNING ». Dans XIV International Scientific Conference "System Analysis in Medicine". Far Eastern Scientific Center of Physiology and Pathology of Respiration, 2020. http://dx.doi.org/10.12737/conferencearticle_5fe01d9b233509.17835494.
Texte intégralSchoenrock, Andrew, Daniel Burnside, Houman Moteshareie, Alex Wong, Ashkan Golshani, Frank Dehne et James R. Green. « Engineering inhibitory proteins with InSiPS : the in-silico protein synthesizer ». Dans SC15 : The International Conference for High Performance Computing, Networking, Storage and Analysis. New York, NY, USA : ACM, 2015. http://dx.doi.org/10.1145/2807591.2807630.
Texte intégralMustafha, Siti Mardhiah, Abdul Munir Abdul Murad, Nor Muhammad Mahadi, Shazilah Kamaruddin et Farah Diba Abu Bakar. « In silico analysis of subtilisin from Glaciozyma antarctica PI12 ». Dans THE 2015 UKM FST POSTGRADUATE COLLOQUIUM : Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2015 Postgraduate Colloquium. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4931246.
Texte intégralHANAI, TOSHIHIKO, et TSUTOMU TACHIKAWA. « QUANTITATIVE ANALYSIS OF CHEMILUMINESCENCE INTENSITY AND TOXICITY IN SILICO ». Dans Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0094.
Texte intégralRapports d'organisations sur le sujet "SILICO ANALYSIS"
Lazzaro, John, et John Wawrzynek. Silicon Models for Auditory Scene Analysis. Fort Belvoir, VA : Defense Technical Information Center, janvier 1995. http://dx.doi.org/10.21236/ada327239.
Texte intégralPawlak, John. D0 Silicon Upgrade : Ladder Removal Stress Analysis. Office of Scientific and Technical Information (OSTI), octobre 1994. http://dx.doi.org/10.2172/1033317.
Texte intégralvan der Werf, I., F. Palmisano, Raffaele De Leo et Stefano Marrone. Chemical Analyses of Silicon Aerogel Samples. Office of Scientific and Technical Information (OSTI), avril 2008. http://dx.doi.org/10.2172/955880.
Texte intégralHaney, R. E., A. Neugroschel, K. Misiakos et F. A. Lindholm. Frequency-domain transient analysis of silicon solar cells. Office of Scientific and Technical Information (OSTI), mars 1989. http://dx.doi.org/10.2172/6346849.
Texte intégralRucinski, Russ. D0 Silicon Upgrade : D-Zero Assembly Hall ODH Analysis. Office of Scientific and Technical Information (OSTI), mars 1997. http://dx.doi.org/10.2172/1033268.
Texte intégralRucinski, Russ. D0 Silicon Upgrade : Lower Cleanroom Roof Quick Load Analysis. Office of Scientific and Technical Information (OSTI), novembre 1995. http://dx.doi.org/10.2172/1033291.
Texte intégralWilmarth, W. R. Silicon Analysis of Tank 8F and Tank 40H Turbidity Samples. Office of Scientific and Technical Information (OSTI), avril 2001. http://dx.doi.org/10.2172/779685.
Texte intégralAnderson, Brent. D0 Silicon Upgrade : A Layer Drawbridge Access : Platforms Calculations and Analysis. Office of Scientific and Technical Information (OSTI), mai 2000. http://dx.doi.org/10.2172/1481382.
Texte intégralUnderwood, J. H., P. J. Cote et G. N. Vigilante. Thermomechanical and Fracture Analysis of Silicon Carbide in Cannon Bore Applications. Fort Belvoir, VA : Defense Technical Information Center, juin 2003. http://dx.doi.org/10.21236/ada416282.
Texte intégralRatzmann, Paul M. D0 Silicon Upgrade : Thermal Analysis of the D0 Double Sided Ladders. Office of Scientific and Technical Information (OSTI), juillet 1996. http://dx.doi.org/10.2172/1033276.
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