Half‐Life Extension through HESylation®
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[1] C. Won,et al. PEG-modified biopharmaceuticals , 2009 .
[2] J. Kressler,et al. Enzymatically catalyzed HES conjugation using microbial transglutaminase: Proof of feasibility. , 2009, Journal of pharmaceutical sciences.
[3] D. Spahn,et al. Repetitive Large-Dose Infusion of the Novel Hydroxyethyl Starch 130/0.4 in Patients with Severe Head Injury , 2003, Anesthesia and analgesia.
[4] H. Taegtmeyer,et al. Synthesis of polymer-bound hemoglobin samples , 1981 .
[5] W. Jurecka,et al. Human monocytes and keratinocytes in culture ingest hydroxyethylstarch , 2005, Archives of Dermatological Research.
[6] R. Whaley,et al. Pegademase Bovine: Replacement Therapy for Severe Combined Immunodeficiency Disease , 1991, DICP : the annals of pharmacotherapy.
[7] D. Cook,et al. Resuscitation fluid use in critically ill adults: an international cross-sectional study in 391 intensive care units , 2010, Critical care.
[8] Herbert J Meiselman,et al. Antibody against poly(ethylene glycol) adversely affects PEG‐asparaginase therapy in acute lymphoblastic leukemia patients , 2007, Cancer.
[9] M. Westphal,et al. Hydroxyethyl Starches: Different Products – Different Effects , 2009, Anesthesiology.
[10] I. Macdougall. Recent advances in erythropoietic agents in renal anemia. , 2006, Seminars in nephrology.
[11] T. Luger,et al. Differential storage of hydroxyethyl starch (HES) in the skin: an immunoelectron-microscopical long-term study , 2001, Cell and Tissue Research.
[12] P. Taupin,et al. PEG and PEG conjugates toxicity: towards an understanding of the toxicity of PEG and its relevance to PEGylated biologicals , 2009 .
[13] Zhi-xin Xu,et al. Rational design of a potent, long-lasting form of interferon: a 40 kDa branched polyethylene glycol-conjugated interferon alpha-2a for the treatment of hepatitis C. , 2001, Bioconjugate chemistry.
[14] A. N. de Belder,et al. Antibodies against hydroxyethylstarch produced in rabbits by immunization with a protein-hydroxyetylstarch conjugate. , 1976, International archives of allergy and applied immunology.
[15] M. Eichner,et al. Endothelial Accumulation of Hydroxyethyl Starch and Functional Consequences on Leukocyte-Endothelial Interactions , 2002, European Surgical Research.
[16] F. Davis,et al. Alteration of immunological properties of bovine serum albumin by covalent attachment of polyethylene glycol. , 1977, The Journal of biological chemistry.
[17] W. Schimetta,et al. Hydroxyethyl Starch Antibodies in Humans: Incidence and Clinical Relevance , 1998, Anesthesia and analgesia.
[18] M. Laxenaire,et al. Réactions anaphylactoïdes aux substituts colloïdaux du plasma : incidence, facteurs de risque, mécanismes. Enquête prospective multicentrique française , 1994 .
[19] Francesco M Veronese,et al. PEGylation, successful approach to drug delivery. , 2005, Drug discovery today.
[20] Robert M. Stroud,et al. Efficiency of signalling through cytokine receptors depends critically on receptor orientation , 1998, Nature.
[21] Kapp,et al. Decreased activity of acid α‐glucosidase in a patient with persistent periocular swelling after infusions of hydroxyethyl starch , 1998, The British journal of dermatology.
[22] M. Jarsch,et al. Comparative Erythropoietin Receptor Binding Kinetics of C.E.R.A. and Epoetin-β Determined by Surface Plasmon Resonance and Competition Binding Assay , 2007, Pharmacology.
[23] J. Egrie,et al. Development and characterization of novel erythropoiesis stimulating protein (NESP) , 2001, British Journal of Cancer.