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c++ in a nutshell. c++ primer, 5th edition is for people who want to get up and running with c++ as quickly as possible. it is a complete c++ tutorial for beginners, with expert advice on every aspect of the language from the standard library to classes to templates to exceptions to memory management. the book s core is a complete c++ tutorial that provides a comprehensive view of the language with the right mix of theory, real world examples, and practical advice.
c++ primer, 5th edition is a complete c++ tutorial for beginners. the book s core is a complete c++ tutorial that provides a comprehensive view of the language with the right mix of theory, real world examples, and practical advice.
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in the following days, we will only have one rule: no, this is not a joke. we take the same three rules that we discussed earlier in this book, and we apply them to the c programming language. this is the first rule: the c programming language, first edition, by brian w. kernighan and dennis m. ritchie, is the first computer science book that i have ever read, and this is the reason why. it is a book that is both accessible and..
the c programming language, second edition, by brian w. kernighan and dennis m. ritchie, is the best computer science book i have ever read. you do not need to be a computer scientist to understand it. it is not a difficult book and is the best introduction to the c programming language, and the c programming language is the most important language in the world.
Total cellular RNA was purified from cell lines and frozen stored tissues of ESCC patients by the acid guanidine-phenol-chloroform method. Reverse transcription of total cellular RNA (5 g) was performed using a First-Strand cDNA Synthesis Kit (Amersham, Buckinghamshire, United Kingdom), and cDNA was subjected to PCR for 35 cycles of amplification using Advantage cDNA PCR kit (Becton Dickinson Biosciences, Palo Alto, CA). Amplification was performed for 30 s at 94C and 3 min at 68C. The final extension step was carried out for 3 min at 68C. The amplification products were separated on 1.5% agarose gels and visualized by ethidium bromide staining. PCR primers for TSLC1 were as follows: the forward primer was 5-CATCACAGTCCTGGTCCCACCACGTAATCT-3, and the reverse primer was 5-AATAGGGCCAGTTGGACACCTCATTGAAAC-3. For glyceraldehyde-3-phosphate dehydrogenase, the forward primer was 5-TGGTATCGTGGAAGGACTCATGAC-3, and the reverse primer was 5-ATGCCAGTGAGCTTCCCGTTCAGC-3. For the positive controls, normal human tissue cDNA of lung were purchased from Becton Dickinson Biosciences (Palo Alto, CA).
Making Website Work: The Complete Guide to Optimizing Mobile Performance is a tutorial, written by the website editors of each edition, that outlines how to use the knowledge of website design and development to create a website that is simple to use and understand, while also providing good speed and overall performance. It guides you through the basic steps needed to design a high performing website, including acquiring any requ…
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