Titlebook: Cellular Fatty Acid-Binding Proteins II; Proceedings of the 2 Jan F. C. Glatz,Ger J. Vusse Conference proceedings 1993 Springer Science+Bus

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書目名稱Cellular Fatty Acid-Binding Proteins II影響因子(影響力)




書目名稱Cellular Fatty Acid-Binding Proteins II影響因子(影響力)學(xué)科排名




書目名稱Cellular Fatty Acid-Binding Proteins II網(wǎng)絡(luò)公開度




書目名稱Cellular Fatty Acid-Binding Proteins II網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Cellular Fatty Acid-Binding Proteins II被引頻次




書目名稱Cellular Fatty Acid-Binding Proteins II被引頻次學(xué)科排名




書目名稱Cellular Fatty Acid-Binding Proteins II年度引用




書目名稱Cellular Fatty Acid-Binding Proteins II年度引用學(xué)科排名




書目名稱Cellular Fatty Acid-Binding Proteins II讀者反饋




書目名稱Cellular Fatty Acid-Binding Proteins II讀者反饋學(xué)科排名

Anecdote

High resolution X-ray studies of mammalian intestinal and muscle fatty acid-binding proteins providith bound hexadecanoate (palmitate) and 9Z-octadecenoate (oleate), respectively. The structure of .-derived human muscle fatty acid-binding protein has also been solved to 2.1 ? with a C16 bacterial fatty acid. Both proteins contain 10 anti-parallel β-strands in a + 1, +1, +1… motif. The strands are

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男生戴手銬

充氣女

Titration calorimetry as a binding assay for lipid-binding proteins,pid-binding proteins. An important feature of this method was its ability to accurately determine binding constants in a non-perturbing manner. The equilibrium was not perturbed, since there was no requirement to separate bound and free ligand in order to obtain binding parameters. Also, the structu

圓柱

Identification of high affinity membrane-bound fatty acid-binding proteins using a photoreactive fang of these sites requires the use of low concentrations (nanomolar) of the photoreactive fatty acid 11-.-diazirinophenoxy-[11-.H]undecanoate. It was delivered as a bovine serum albumin (BSA) complex which serves as a reservoir for fatty acid and thus allows precise control of unbound fatty acid con

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Diversity of fatty acid-binding protein structure and function: studies with fluorescent ligands,ns and mechanisms of action . remain unknown. The present studies have sought to understand the relationships among these proteins, and to address the possible role of FABP in cellular fatty acid traffic. A series of anthroyloxy-labeled fluorescent fatty acids have been used to examine the physicoch

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Regulation of transcription factor mRNA accumulation during 3T3-L1 preadipocyte differentiation by transforming growth factor-β (TGF-β), attenuate this process. Inhibition of differentiation by these agents, thought to be at the level of transcription, has been investigated by examining the accumulation of mRNA for six transcription factors and the autocrine growth factor interleukin 6 (IL-6). Up

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