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Titlebook: EJB Reviews 1991; P. Christen,E. Hofmann Book 1992 Federation of European Biochemical Societies 1992 Biochemie.Biophysik.agriculture.bioch

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發(fā)表于 2025-3-23 12:58:27 | 只看該作者
Nuclear skeleton, DNA domains and control of replication and transcription, origin was found to possess enhancer activity lacking tissue specificity. Hence, the domain organization of DNA is related to the organization of replication process. Other sets of data indicate that the integrity of DNA domains is important for maintaining transcription within the domain. Accordin
12#
發(fā)表于 2025-3-23 15:16:44 | 只看該作者
13#
發(fā)表于 2025-3-23 18:57:21 | 只看該作者
Cell-free immunity in Cecropia,ins and in the isolation of immune RNA, used for the preparation of a cDNA library. After a short period of RNA synthesis, the insects respond to live bacteria by the production of a potent antibacterial activity which is due to the synthesis of 15–20 immune proteins.
14#
發(fā)表于 2025-3-24 01:26:59 | 只看該作者
15#
發(fā)表于 2025-3-24 05:09:39 | 只看該作者
,The molecular action of tumor necrosis factor-α,-binding regulatory proteins (G proteins), its amplification through activation of adenyl cyclase, phospholipases and protein kinases with the generation of second messenger pathways. The transduction of selected genes in different cell types determines the characteristics of the cell response to TN
16#
發(fā)表于 2025-3-24 09:19:20 | 只看該作者
17#
發(fā)表于 2025-3-24 10:57:31 | 只看該作者
18#
發(fā)表于 2025-3-24 16:06:25 | 只看該作者
Book 1992imulatebiochemical research are alsoincluded. The authors of thereviews are explicitly asked to be critical, selective,evaluative and interdisciplinarily oriented. The reviewsshould encourage young scientists toward independentandcreative thinking, and inform active investigators about thestateof the art in a given field.
19#
發(fā)表于 2025-3-24 20:52:30 | 只看該作者
20#
發(fā)表于 2025-3-25 01:35:59 | 只看該作者
The respiratory-chain NADH dehydrogenase (complex I) of mitochondria,tase (cytochrome oxidase or complex IV). The function of these enzyme complexes is to link electron transfer with proton translocation out of the mitochondrion. In doing so, they generate a transmembraneous proton motive force which subsequently drives ATP synthesis by the H.-ATPase (complex V, for a review see [1]).
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