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23篇 您的检索式:作者名="Bankston D"
    题名 作者 年代 出处 被引量
1Ascaleable synthesis of BAY 43-9006 : a potent Raf ki-nase inhibitor for the treatment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002OrgProc Res Dev2002,6,6:1
2A scaleable synthesis of Bay 43-9006:a potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Dev2002,6,6:1
3A scalable synthesis of BAY 43-9006:A potent Rafkinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
4Central solar heating plants with seasonal tank 显示文摘BERGER D S BANKSTON C A 1992ASHRAE1992,,5:1
5A scaleable synthesis of BAY 43-9006: a potent Raf kinase inhibitor for the treatment of cancer 显示文摘Bankston D Dumas J Natero R 2002Org Proc Res Dev2002,6,:1
6A scaleable synthesis of BAY 43-9006: a potent Raf kinase inhibitor for the treatment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002Org Process Res Dev2002,6,6:1
7Lactational transfer of volatile chemicals in breast milk 显示文摘 Mahle D Bankston L 1997Am Ind Hygiene Assoc J1997,58,6:1
8A scalable synthesis of BAY 43-9006:A potent Raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
9Lactational transfer of volatile chemicals in breast milk显示文摘 Mahle D Bankston L 1997Am Ind Hygiene Assoc J1997,58,6:1
10查看详情显示文摘Bankston D Dumas J Natero R Riedl B. Monahan M. Sibley R 0,,:1
11Central solar heating plants with seasonal tank显示文摘Breger D S Bankston C A 1992ASHRAE J1992,34,5:1
12Structural basis for vinculin activation at sites of cell adhesion 显示文摘Bakolitsa C Cohen D M Bankston L A 2004Nature2004,430,6999:1
13Omega-Carboxypyridyl Substituted Ureas as Raf Kinase Inhibitors; SAR of the Amide Substituent显示文摘 Bankston D Barbosa J 2004Bioorg Mcd Chem Lett2004,14,3:1
14A scaleable synthesis of BAY 43-9006: A potent raf kinase inhibitor for the treatment of cancer显示文摘BANKSTON D DUMAS J NATERO R 2002Org Proc Res Dev2002,6,6:1
15Central solar heating plants with seasonal tank 显示文摘BREGER D S BANKSTON C A SUNDERLAND J E 1991ASHRAE1991,,5:1
16A scaleable synthesis of BAY 43-9006:a potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Dev2002,6,6:1
17A scaleable synthesis of BAY43-9006:A potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
18Structural and functional bases for broad-spectrum neutralization of avian and human influenza A viruses 显示文摘Sui J Hwang WC Perez S Wei G Aird D Chen LM Santelli E Stec B Cadwell G Ali M Wan H Murakami A Yammanuru A Han T Cox NJ Bankston LA Donis RO Liddington RC Marasco WA 2009Nat Struct Mol Biol2009,16,3:1
19A scaleable syn- thesis of BAY 43-9006: a potent raf kinase Inhibitor for the treat- ment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002Org Process Res Dev2002,6,6:1
20A scaleable synthesis of BAY 43-9006: A potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Deve2002,6,6:1
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