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Titlebook: Wasser, Energie und Umwelt; Aktuelle Beitr?ge au Markus Porth,Holger Schüttrumpf Book 2022 Der/die Herausgeber bzw. der/die Autor(en), exkl

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樓主: 警察在苦笑
61#
發(fā)表于 2025-4-1 05:54:53 | 只看該作者
62#
發(fā)表于 2025-4-1 07:45:51 | 只看該作者
Christian Hagelükenass. Finally, this system is applied to the experiment and the weld region shows good quality so the gap can be filled without defect. Therefore, the system developed in this study can support to optimize and correct the welding condition depending on the disturbance.
63#
發(fā)表于 2025-4-1 10:17:35 | 只看該作者
J?rg Woidasky,Sebastian Jeanvréide some insight into the variety of formats available for screening, together with some of their inherent advantages and limitations. Particular emphasis is placed on the mechanistic basis of drug-target interaction and those aspects of structure/function that are of prime importance in potassium channel drug discovery.
64#
發(fā)表于 2025-4-1 15:56:37 | 只看該作者
65#
發(fā)表于 2025-4-1 19:28:34 | 只看該作者
pdoor. Both the constructions are instantiated in prime-order bilinear groups and are proven anonymous CPA-secure under SXDH assumption by extending Jutla-Roy technique. Our proposed solutions improve upon the only other adaptively secure schemes that can be obtained using the generic technique of Ambrona et al.
66#
發(fā)表于 2025-4-1 23:38:20 | 只看該作者
67#
發(fā)表于 2025-4-2 03:56:53 | 只看該作者
68#
發(fā)表于 2025-4-2 09:42:17 | 只看該作者
J?rg Demmicher. This is presumably due to a horizontal gene transfer. The mechanism of this inter-species gene transfer can be mimicked in therapeutic gene delivery. Mimicking specifics or principles of chemical evolution including experimental and test-tube evolution also provides leads for new drug discovery.
69#
發(fā)表于 2025-4-2 12:16:28 | 只看該作者
r tool, the area are much better than the circuits converted by DC synthesizers from the lookup tables (LUT). At last, we use our tool to find implementations of 5-bit S-boxes, such as those used in KECCAK and ASCON.
70#
發(fā)表于 2025-4-2 15:55:10 | 只看該作者
Christian Hagelükenhe development of inactivators which are selective for the isoforms of polyamine oxidase. Isozyme-selective inhibitors will give more profound insights into and reveal a diversity of specific functions of polyamine oxidase.
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