音乐会 发表于 2025-3-23 11:51:31

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Senescent 发表于 2025-3-23 16:03:51

Prof. Dr. Marco Heinrich Inderheesbiology, review transcriptional activation by CREB proteins through transcription cofactors and present novel insights into the context-and position-specific function of CREB on complex genes. (Mol Cell Biochem .: 5–9, 2000)

范例 发表于 2025-3-23 19:46:20

,Was verdirbt die Qualität der Prognose?,REB-transfected MeWo cells were reduced due to the downregulation of the CRE-dependent expression of the type IV collagenase MMP-2 and the adhesion molecule MCAM/MUC18. In the second mechanism, CREB and its associated proteins act as survival factors for human melanoma cells. Here we demonstrated th

minimal 发表于 2025-3-23 22:54:48

https://doi.org/10.1007/978-3-658-42882-2ate Ac-DEVD-AMC), and mitochondrial membrane depolarisation (Δψ). Western blots detected accumulation of the tumor suppressor protein p53, relocation of cytochrome c to the cytosol, and expression of the antiapoptotic protein Bcl-x.. Prestimulation with lipophilic cAMP-analogs attenuated apoptosis w

landmark 发表于 2025-3-24 05:18:32

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表被动 发表于 2025-3-24 06:33:20

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ANTI 发表于 2025-3-24 11:39:38

https://doi.org/10.1007/978-3-658-43144-0ine function. In a subsequent stage of development, NE transport regulates differentiation of noradrenergic neurons in the peripheral nervous system and the LC by promoting expression of tyrosine hydroxylase (TH) and dopamine-ß-hydroxylase (DBH). Conversely, uptake inhibitors, such as the tricyclic

繁荣地区 发表于 2025-3-24 18:45:48

Schlussbetrachtung und Ausblick,anolol (β-AR blocker), atenolol (β.-AR blocker), yohimbine (α.-AR blocker), Rp-cAMP (an inhibitor of cAMP-dependent protein kinase AI & AII) and staurosporine (an inhibitor of protein kinase C), but was not blocked by ICI 118, 551 (β.-AR blocker) and prazosin (α.-AR blocker). The addition of a combi

薄膜 发表于 2025-3-24 21:55:19

https://doi.org/10.1007/978-3-658-43373-4e found that NaF treatment alone, independent of angiotensin II stimulation, was sufficient to increase the tyrosine phosphorylation levels of paxillin. Furthermore, the ability of either NaF and/or angiotensin II to increase tyrosine phosphorylation levels of paxillin is critically dependent on int

合并 发表于 2025-3-25 02:11:19

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查看完整版本: Titlebook: Control of Gene Expression by Catecholamines and the Renin-Angiotensin System; Heinz Rupp,Bernard Maisch Book 2000 Springer Science+Busine