01107nam0-2200361---450-99000859615040332120080107140743.0689934000859615FED01000859615(Aleph)000859615FED0100085961520071217d1968----km-y0itay50------baitaITy-------001yySui fatti di Cecoslovacchia[l'atteggiamento dei comunisti italiani di fronte all'intervento militare sovietico in Cecoslovacchia]Luigi LongoRomaEditori riunitic1968201 p.19 cm<<Il >>punto13In appendice interventi di Palmiro TogliattiCecoslovacchia - 1968FI943.716943.717Longo,Luigi<1900-1980>322373Togliatti,Palmiro<1893-1964>ITUNINARICAUNIMARCBK990008596150403321XXXI B 1567687NAP02NAP02Sui fatti di Cecoslovacchia712796UNINA03200nam 22004935 450 991030075790332120200705032740.09781484239391148423939310.1007/978-1-4842-3939-1(CKB)4100000007127597(MiAaPQ)EBC5598584(DE-He213)978-1-4842-3939-1(CaSebORM)9781484239391(PPN)232474591(OCoLC)1082522728(OCoLC)on1082522728(EXLCZ)99410000000712759720181112d2018 u| 0engurcnu||||||||txtrdacontentcrdamediacrrdacarrierPractical React Native Build Two Full Projects and One Full Game using React Native /by Frank Zammetti1st ed. 2018.Berkeley, CA :Apress :Imprint: Apress,2018.1 online resource (342 pages)9781484239384 1484239385 1. React Native: A Gentle Introduction -- 2. Getting to Know React Native -- 3. Restaurant Chooser, Part 1 -- 4. Restaurant Chooser, Part 2 -- 5. React Native Trivia, Part 1 -- 6. React Native Trivia, Part 2 -- 7. Time for Some Fun: A React Native Game, Part 1 -- 8. Time for Some Fun: A React Native Game, Part 2.Discover how to use React Native in the real world, from scratch. This book shows you what React Native has to offer, where it came from, and where it’s going. You'll begin with a solid foundation of practical knowledge, and then build on it immediately by constructing three different apps. You'll learn how to use each feature of React Native by working on two full projects and one full game. These aren’t just simple React Native Hello World examples (although you’ll naturally start there!) but are apps that you can, if you so choose, install on your mobile devices and use for real. Throughout this book, you'll gain real-world familiarity with React Native as well as supporting components from Expo, NativeBase, React Navigation and the Redux and Lodash libraries. You'll also build server-side code for a mobile React Native app to talk to using the popular Node.js and Socket.io library, providing you a holistic view of things even beyond React Native. And, you'll see many helpful tips, tricks and gotchas to watch out for along the way! Practical React Native offers practical exercises that will give you a solid grasp of building apps with React Native, allowing you to springboard into creating more advanced apps on your own.Creating a game with React Native will allow you to see a whole other perspective on what React Native can do.Computer programmingWeb Developmenthttps://scigraph.springernature.com/ontologies/product-market-codes/I29050Computer programming.Web Development.650.0285535Zammetti Frankauthttp://id.loc.gov/vocabulary/relators/aut872331UMIUMIBOOK9910300757903321Practical React Native2528355UNINA05299nam 2200697Ia 450 991102022910332120200520144314.09786612292057978128229205512822920569783527626687352762668997835276266943527626697(CKB)1000000000767195(EBL)481485(OCoLC)437416793(SSID)ssj0000137586(PQKBManifestationID)11159659(PQKBTitleCode)TC0000137586(PQKBWorkID)10088690(PQKB)11399282(MiAaPQ)EBC481485(PPN)194575683(Perlego)2757605(EXLCZ)99100000000076719520080107d2009 uy 0engur|n|---|||||txtccrDetection of highly dangerous pathogens microarray methods for BSL 3 and BSL 4 agents /edited by Tanja Kostic, Patrick Butaye, and Jacques SchrenzelWeinheim Wiley-VCH20091 online resource (193 p.)Description based upon print version of record.9783527322756 3527322752 Includes bibliographical references and index.Detection of Highly Dangerous Pathogens: Microarray Methods for the Detection of BSL 3 and BSL 4 Agents; Contents; This Publication is Supported by COST; Preface; List of Contributors; 1 Introduction to Microarray-Based Detection Methods; 1.1 Introduction to Microarray Technology; 1.2 Technical Aspects of Microarray Technology; 1.2.1 Probes; 1.2.1.1 Genome Fragments; 1.2.1.2 PCR Products; 1.2.1.3 Oligonucleotide Probes; 1.2.2 Substrates for Printing; 1.2.2.1 Slides with Poly-L-lysine Coating; 1.2.2.2 Slides with Amino Silane Coating; 1.2.2.3 Slides with Aldehyde Coating1.2.2.4 Slides with Epoxy Coating1.2.2.5 Proprietary Surface Chemistries; 1.2.2.6 Probe Spacers; 1.2.3 Targets for Microarray Analysis; 1.2.3.1 Target Amplifications and Sensitivity Issues; 1.2.3.2 Labeling of the Targets; 1.2.3.3 Hybridization and Wash Conditions; 1.2.4 Classical Commercially Available Microarray Formats; 1.2.4.1 Spotting Approaches; 1.2.4.2 In Situ Synthesis; 1.2.5 Alternative Methods for Improving Microarray-Based Detection Sensitivity; 1.2.5.1 Resonance-Light Scattering (RLS); 1.2.5.2 Planar-Waveguide Technology (PWT); 1.2.5.3 Liquid Arrays1.2.5.4 Three-Dimensional Microarray Formats1.2.6 Marker Genes Used on MDMs; 1.3 Analysis and Quality Control Aspects; 1.4 Applications of Microarray Technology in Microbial Diagnostics; 1.4.1 Gene Expression Studies; 1.4.2 Comparative Genomic Hybridization (CGH); 1.4.3 Generic or Universal Microarrays; 1.4.4 Microarrays for Sequence Analysis; 1.4.5 Microbial Diagnostic Microarrays (MDMs); 1.5 Further Developments and New Perspectives Regarding Array Sensitivity and Specificity; 1.6 Conclusions; References; Part I: Methods; 2 Long Oligonucleotide Microarray-Based Microbial Detection2.1 Introduction2.2 Method; 2.2.1 DNA Extraction; 2.2.2 Ф29 Amplification; 2.2.3 Klenow Amplification/Labeling; 2.2.4 Probe and Slide Preparation; 2.2.5 Slide Processing Protocol (for Amino Surfaces); 2.2.6 Hybridization and Slide Washing; 2.2.7 Comments; 2.3 Our Test System and Results; 2.4 Conclusions; References; 3 Sequence-Specific End-Labeling of Oligonucleotides; 3.1 Introduction; 3.2 Probe Design; 3.3 Slide Preparation (Spotting); 3.4 Slide Processing Protocol ( for Aldehyde Surfaces); 3.5 DNA Extraction and PCR Amplification of the Targeted Gene3.6 Shrimp Alkaline Phosphatase Treatment3.7 Labeling; 3.8 Hybridization and Slide Washing; 3.9 Data Analysis; 3.10 Costs; 3.11 Microarray for Detection of Pathogenic Bacteria; References; 4 Non-Cognate Approaches for Pathogen Detection on Microarrays; 4.1 Introduction; 4.2 Non-Cognate Hybridization System; 4.2.1 Concept; 4.2.2 Definition of the Optimal Probe Length; 4.2.3 Virtual Assessment of Array Performances (in Silico Experiments); 4.2.4 Array Manufacturing and Hybridization (Wet-Lab Experiments); 4.2.5 Analysis; 4.3 Perspectives; References; 5 Patterning Techniques for Array Platforms5.1 IntroductionWritten by leading experts in the field as part of an interdisciplinary pan-European research program funded by the EU, the results provided in this booklet provide a unique and comprehensive overview of how microarray technology can be used in safely tracking the most highly dangerous pathogens. A must-have for public health agencies focused on bioterrorism as well as all laboratories working with BSL3 and/or BSL 4 agents.Pathogenic microorganismsDetectionDNA microarraysPathogenic microorganismsDetection.DNA microarrays.579.165Kostic Tanja1838925Butaye Patrick1838926Schrenzel Jacques1838927MiAaPQMiAaPQMiAaPQBOOK9911020229103321Detection of highly dangerous pathogens4418021UNINA