Mri485 发表于 2025-3-25 03:33:39
Computational Design of Reaction-Diffusion Patterns Using DNA-Based Chemical Reaction Networks,ces, and that consensus in a spatial context results in the spontaneous formation of distinct spatial domains, in which one species is completely eliminated. Together, our results suggest that programmed spatial self-organisation of DNA, through a reaction diffusion mechanism, is achievable with current DNA strand displacement technology.Perigee 发表于 2025-3-25 08:39:10
0302-9743 lines (including mathematics, computer science, physics, chemistry, material science and biology) to address the analysis, design, and synthesis of information-based molecular systems.978-3-319-11294-7978-3-319-11295-4Series ISSN 0302-9743 Series E-ISSN 1611-3349Angioplasty 发表于 2025-3-25 13:55:14
http://reply.papertrans.cn/27/2602/260128/260128_23.png形容词 发表于 2025-3-25 17:01:31
Marianne Resch,Claudia Fenzl MBA offline model of computing by chemical reaction networks (CRNs)..Thus, the main results in this paper not only strengthen the previous result on Turing computability of RAs but also clarify the computing powers of inhibitors in RA computation.neutrophils 发表于 2025-3-25 21:10:24
Marianne Resch,Claudia Fenzl MBAocols (which is a central result for output stable CRDs). In particular, we observe that the computation-friendly class of totally stable CRDs has equal expressive power as the larger class of output stable CRDs.Anhydrous 发表于 2025-3-26 00:48:12
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The Computational Capability of Chemical Reaction Automata, offline model of computing by chemical reaction networks (CRNs)..Thus, the main results in this paper not only strengthen the previous result on Turing computability of RAs but also clarify the computing powers of inhibitors in RA computation.Gustatory 发表于 2025-3-26 10:53:01
http://reply.papertrans.cn/27/2602/260128/260128_28.png种子 发表于 2025-3-26 14:58:33
http://reply.papertrans.cn/27/2602/260128/260128_29.pngopportune 发表于 2025-3-26 17:28:59
Design Principles for Single-Stranded RNA Origami Structures, the RNA is being enzymatically produced, commonly referred to as cotranscriptional folding. To realize a general and scalable architecture we have developed a theoretical framework for determining RNA crossover geometries, long-distance interactions, and strand paths that are topologically compatib