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Titlebook: Activation and Desensitization of Transducing Pathways; T. M. Konijn,M. D. Houslay,P. J. M. Haastert Conference proceedings 1990 Springer-

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發(fā)表于 2025-3-25 03:47:48 | 只看該作者
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發(fā)表于 2025-3-25 07:57:35 | 只看該作者
Investment and Australian Economic Growth,phosphorylations by .-adrenergic receptor kinase (Benovic .. 1987); (3) a protein kinase C (PKC)-mediated heterologous desensitization which occurs in response to relatively high concentrations of the phorbol ester PMA with an EC. of about 100 nM (Johnson .. 1986); (4) a slow homologous down regulat
23#
發(fā)表于 2025-3-25 14:07:05 | 只看該作者
https://doi.org/10.1057/978-1-137-58130-3emonstrated an electronegative charge-shift following cAMP binding, indicating that the binding sites themselves were directly involved in the shift. The increase in surface electronegativity of the cyclic nucleotide binding sites may either be a reflection of an overall conformational change due to
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發(fā)表于 2025-3-25 17:05:09 | 只看該作者
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發(fā)表于 2025-3-26 02:57:30 | 只看該作者
Human Nature, Global War and Justice, adenosine, no good antagonists of P.-purinergic receptors are available, and cell surface hydrolases readily metabolize ATP and ADP to adenosine, which can then produce physiological effects through P.-purinergic receptors. However, the development of relatively non-hydrolyzable analogs of ATP help
27#
發(fā)表于 2025-3-26 05:34:35 | 只看該作者
Human Nature, Global War and Justice,racellular signalling hormonal factors, being in the range of one hundred, the number of G-proteins, known so far both from the protein and cDNA level, is rather small, in the range of ten to fifteen. Some of these G-proteins are apparently widely distributed in different cell types of the mammalian
28#
發(fā)表于 2025-3-26 09:31:25 | 只看該作者
29#
發(fā)表于 2025-3-26 14:41:01 | 只看該作者
Nato ASI Subseries H:http://image.papertrans.cn/a/image/144156.jpg
30#
發(fā)表于 2025-3-26 20:42:19 | 只看該作者
Elspeth Oppermann,Matt Brearleyrotein kinase that can phosphorylate two chemotaxis system components, the CheY and the CheB proteins. When CheY is phosphorylated it modulates bacterial flagellar rotation and thus effects the cells’ movement. When CheB is phosphorylated it increases its ability to modify the cell surface receptor
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