维普中文期刊产品整合服务
17篇 您的检索式:作者名="Macchiarulo A"
    题名 作者 年代 出处 被引量
1Glueoeorticoid-induced leu- cine zipper inhibits the Raf-extracellular signal-regulated kinase path- way by binding to Raf-1 显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell BioI2002,22,22:1
2Novel potent and selective bile acid derivatives as TGR5 agonists: biological screening,structure-activity relationships,and molecular modeling studies显示文摘Sato H Macchiarulo A Thomas C 2008J Med Chem2008,51,6:1
3Glucocorticoid -induced leucine zipper inhibits the Rafextracellular signal - regulated kinase pathway by binding to Raf - 1 显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell Biol2002,22,22:1
4Discovery of 6α-ethyl-23 (S)-methylcholic acid (S-EMCA,INT-777) as a potent and selective agonist for the TGR5 receptor,a novel target for diabesity显示文摘Pellicciari R Gioiello A Macchiarulo A 2009J Med Chem2009,52,24:1
5Glucocorticoid-induced leucine zipper inhibits the Raf-extracellular signal-regulated kinase pathway by binding to Raf-1显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell Bio2002,22,22:1
6Glucocorticoid - induced leucine zipper inhibits the Raf - extracellular signal - regulated kinase pathway by binding to Raf - 1 显示文摘AYROLDI E ZOLLO O MACCHIARULO A 2002Mol Cell Biol2002,22,22:1
7Biochemical and molecular characterization of the novel BRAF (V599Ins) mutation detected in a classic papillary thyroid carcinoma显示文摘Moretti S Macchiarulo A De Falco V 2006Oncogene2006,25,30:1
8Novel potent and selective bile acid derivatives as TGR5 agonists:biological screening,structure-activity relationships,and molecular modeling studies显示文摘Sato H Macchiarulo A Thomas C 0,,:1
9Extending SAR of bile acids as FXR ligands: discovery of 23-N- (carbocinnamyloxy) -3ct,7a-dihydroxy-6a-ethyl- 24-nor-5显示文摘Gioiello A Macchiarulo A Pellicciari R 2011Bioorg Med Chem2011,19,8:1
10QSAR study of anticonvulsant negative allosteric modulators of the AMPA receptor显示文摘Macchiarulo A Luca L D Costantino G 2004Journal of Medicinal Chemistry2004,47,7:1
11Novel potent and se- lective bile acid derivatives as TGR5 agonists: biological screen-ing, structure-activity relationships, and molecular modeling studies显示文摘Sato H Macchiarulo A Thomas C 2008Med Chem2008,51,6:1
12Glucocorticoid-induced leucine zipper inhibits the Raf-extracellular signal-regulated kinase pathway by binding to Raf-1 显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell Biol2002,22,22:1
13Glucocorticoid-induced leucine zipper inhibits the Raf-extracellular signal-regulated kinase pathway by binding to Raf-1显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell Biol2002,22,22:1
14Highlights at the gate of tryptophan catabolism: a review on the mechanisms of activation and regulation of indoleamine 2, 3-dioxygenase (IDO), a novel target in cancer disease显示文摘Macchiarulo A Camaioni E Nuti R 2009Amino Acids2009,37,2:1
15Glucocorticoid-in- duced leucine zipper inhibits the Raf-extracellular signal-regula- ted kinase pathway by binding to Raf-1 显示文摘Ayroldi E Zollo O Macchiarulo A 2002Mol Cell Biol2002,22,22:1
16Discovery of 6alpha - ethyl - 23 (S) - methylcholic acid ( S - EMCA, INT - 777 ) as a potent and selective agonist for the TGR5 receptor, a novel target for diabesity显示文摘Pellicciari R Gioiello A Macchiarulo A 2009J Med Chem2009,52,24:1
17Extending SAR of bile acids as FXR ligands: discovery of 23-N- (carbocinnamyloxy)-3α,7α-dihydroxy-6β-ethyl-24-nor-5β-cholan-23-amine 显示文摘Gioiello A Macchiarulo A Carotti A 2011Bioorg Med Chem2011,19,:1
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费