Search Results - "Mannesse, Maurice L. M"

Recombinant C1 inhibitor in brain ischemic injury by Gesuete, Raffaella, Storini, Claudio, Fantin, Alessandro, Stravalaci, Matteo, Zanier, Elisa R., Orsini, Franca, Vietsch, Helene, Mannesse, M. L. Maurice, Ziere, Bertjan, Gobbi, Marco, De Simoni, Maria-Grazia

“…Objective C1 inhibitor (C1‐INH) is an endogenous inhibitor of complement and kinin systems. We have explored the efficacy and the therapeutic window of the…”
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N-glycans of recombinant human acid α-glucosidase expressed in the milk of transgenic rabbits by Jongen, Susanne P, Gerwig, Gerrit J, Leeflang, Bas R, Koles, Kate, Mannesse, Maurice LM, van Berkel, Patrick HC, Pieper, Frank R, Kroos, Marian A, Reuser, Arnold JJ, Zhou, Qun, Jin, Xiaoying, Zhang, Kate, Edmunds, Tim, Kamerling, Johannis P

“…Pompe disease is a lysosomal glycogen storage disorder characterized by acid α-glucosidase (GAA) deficiency. More than 110 different pathogenic mutations in…”
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Characterization of recombinant human C1 inhibitor secreted in milk of transgenic rabbits by van Veen, Harrie A., Koiter, Jaco, Vogelezang, Carla J.M., van Wessel, Noucha, van Dam, Tijtje, Velterop, Ingeborg, van Houdt, Kristina, Kupers, Luc, Horbach, Danielle, Salaheddine, Mourad, Nuijens, Jan H., Mannesse, Maurice L.M.

“…► Transgenic rabbits expressed high levels of recombinant human C1 inhibitor in milk. ► A highly purified rhC1INH product was obtained from transgenic rabbit…”
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Structural basis of the chiral selectivity of Pseudomonas cepacia lipase by Lang, Dietmar A., Mannesse, Maurice L. M., De Haas, Gerard H., Verheij, Hubertus M., Dijkstra, Bauke W.

“…To investigate the enantioselectivity of Pseudomonas cepacia lipase, inhibition studies were performed with SC‐ and RC‐(RP…”
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Cutinase from Fusarium solani pisi Hydrolyzing Triglyceride Analogs. Effect of Acyl Chain Length and Position in the Substrate Molecule on Activity and Enantioselectivity by Mannesse, Maurice L. M, Cox, Ruud C, Koops, Bart C, Verheij, Hubertus M, de Haas, Gerard H, Egmond, Maarten R, van der Hijden, Harry T. W. M, de Vlieg, Jacob

“…Triglyceride analogues were synthesized in which one of the primary acyl ester functions has been replaced by an alkyl group and the secondary acyl ester bond…”
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NMR Studies of Fusarium solani pisi Cutinase in Complex with Phosphonate Inhibitors by Prompers, Jeanine J, van Noorloos, Brigitte, Mannesse, Maurice L. M, Groenewegen, Anneke, Egmond, Maarten R, Verheij, Hubertus M, Hilbers, Cornelis W, Pepermans, Henri A. M

“…The backbone dynamics of Fusarium solani pisi cutinase in complex with a phosphonate inhibitor has been studied by a variety of nuclear magnetic resonance…”
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N- and O-glycans of recombinant human C1 inhibitor expressed in the milk of transgenic rabbits by Koles, Kate, van Berkel, Patrick H. C., Pieper, Frank R., Nuijens, Jan H., Mannesse, Maurice L.M., Vliegenthart, Johannes F.G., Kamerling, Johannis P.

“…Human C1 inhibitor (hC1INH) is a therapeutic N, O-glycoprotein with a growing number of clinical applications, but the current natural supplies are not likely…”
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Recombinant Cl Inhibitor in Brain Ischemic Injury by GESUETE, Raffaella, STORINI, Claudio, DE SIMONI, Maria-Grazia, FANTIN, Alessandro, STRAVALACI, Matteo, ZANIER, Elisa R, ORSINI, Franca, VIETSCH, Helene, MAURICE MANNESSE, M. L, ZIERE, Bertjan, GOBBI, Marco

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Influence of lactation parameters on the N-glycosylation of recombinant human C1 inhibitor isolated from the milk of transgenic rabbits by Koles, Kate, van Berkel, Patrick H.C., Mannesse, Maurice L.M., Zoetemelk, Raimon, Vliegenthart, Johannes F.G., Kamerling, Johannis P.

“…The large-scale production of recombinant biopharmaceutical glycoproteins in the milk of transgenic animals is becoming more widespread. However, in comparison…”
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N-glycans of recombinant human acid [alpha]-glucosidase expressed in the milk of transgenic rabbits by Jongen, Susanne P, Gerwig, Gerrit J, Leeflang, Bas R, Koles, Kate, Mannesse, Maurice LM, van Berkel, Patrick HC, Pieper, Frank R, Kroos, Marian A, Reuser, Arnold JJ, Zhou, Qun, Jin, Xiaoying, Zhang, Kate, Edmunds, Tim, Kamerling, Johannis P

“…Pompe disease is a lysosomal glycogen storage disorder characterized by acid α-glucosidase (GAA) deficiency. More than 110 different pathogenic mutations in…”
Get full text