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| 1 | Development of an efficient, scalable, aldolase-catalyzed process for enantioselective synthesis of statin intermediates 显示文摘 | Greenberg W Varvak A Hanson S | 2004 | Proc Nat Acad Sci USA2004，101，16： | 1 |
| 2 | Engineering hyperthermostability into a GHI 1 xylanase is mediated by subtle changes to protein structure显示文摘 | Dumon C Varvak A Wall M A | 2008 | J Biol Chem2008，283，22： | 1 |
| 3 | Engineering hyperther- mostability into a GH11 xylanase is mediated by subtle changes to pro- tein structure显示文摘 | DUMON C VARVAK A WALL M A | 2008 | J Biol Chem2008，283，22： | 1 |
| 4 | Engineering hyperthermostability into a GHll xylanase is mediated by subtle changes to protein structure 显示文摘 | DUMON C VARVAK A WALL M A | 2008 | Journal of Biological Chemistry2008，283，22： | 1 |
| 5 | Development of an efficient,scalable,aldolase-catalyzed process for enantioselective synthesis of statin intermediates显示文摘 | Greenberg W A Varvak A Hanson S R | 2004 | Proc Natl Acad Sci USA2004，101，16： | 1 |
| 6 | Development of an efficient,scalable,aldolase-catalyzed process for enantioselective syhthesis of statin intermediates显示文摘 | GREENBERG WA VARVAK A HANSON SR | 2004 | PNAS2004，101，16： | 1 |
| 7 | Development of an efficient, scalable, aldolase-catalyzed process for enantioselective synthesis of statin intermediates 显示文摘 | Greenberg W A Varvak A Hanson S R | 2004 | PANS2004，101，16： | 1 |
| 8 | Development of an efficient, scalable, aldolasecatalyzed process for enantioselective synthesis of statin intermediates显示文摘 | GREENBERG W A VARVAK A HANSON S R | 2004 | Proc Natl Aead Sci U S A2004，101，16： | 1 |
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