| 493 - 502 |
Bioreactor cultivation enhances the efficiency of human embryoid body (hEB) formation and differentiation
Gerecht-Nir S, Cohen S, Itskovitz-Eldor J |
| 503 - 511 |
Inhibition of the Trichoderma reesei cellulases by cellobiose is strongly dependent on the nature of the substrate
Gruno M, Valjamae P, Pettersson G, Johansson G |
| 512 - 519 |
Partitioning of model toxins to hydrophobically terminated DAB dendrimers
King M, Duan X, Sheardown H |
| 520 - 530 |
Physiological significance of the cytometric distribution of fluorescent yeasts after viability staining
Bouchez JC, Cornu M, Danzart M, Leveau JY, Duchiron F, Bouix M |
| 531 - 542 |
Modeling and simulation of oxygen-limited partial nitritation in a membrane-assisted bioreactor (MBR)
Wyffels S, Van Hulle SWH, Boeckx P, Volcke EIP, Van Cleemput O, Vanrolleghem PA, Verstraete W |
| 543 - 549 |
Influence of beta-subunit on thermal and high-pressure process stability of tomato polygalacturonase
Peeters L, Fachin D, Smout C, van Loey A, Hendrickx ME |
| 550 - 557 |
Role of oxidative enzymatic treatments on enzymatic hydrolysis of softwood
Palonen H, Viikari L |
| 558 - 562 |
Encapsulation of crosslinked penicillin G acylase aggregates in lentikats: Evaluation of a novel biocatalyst in organic media
Wilson L, Illanes A, Pessela BCC, Abian O, Fernandez-Lafuente R, Guisan JM |
| 563 - 572 |
Production and characterization of liquid-core capsules made from cross-linked acrylamide copolymers for biotechnological applications
Wyss A, von Stockar U, Marison IW |
| 573 - 586 |
A mixed mechanistic-electrostatic model to explain pH dependence of glycosyl hydrolase enzyme activity
Olivera-Nappa A, Andrews BA, Asenjo JA |
| 587 - 594 |
Fermentation of biomass-generated producer gas to ethanol
Datar RP, Shenkman RM, Cateni BG, Huhnke RL, Lewis RS |
| 595 - 599 |
Novel synthetic jasmonates as highly efficient elicitors for taxoid production by suspension cultures of Taxus chinensis
Qian ZG, Zhao ZJ, Tian WH, Xu YF, Zhong JJ, Qian XH |
| 600 - 600 |
New-generation multicistronic expression platform: pTRIDENT vectors containing size-optimized IRES elements enable homing endonuclease-based cistron swapping into lenitviral expression vectors (vol 86, pg 174, 2004)
Fux C, Langer D, Kelm JM, Weber W, Fussenegger M |
