Nanoscale size control of protein aggregates.
暂无分享,去创建一个
[1] Ying Y Hey,et al. Murine spleen contains a diversity of myeloid and dendritic cells distinct in antigen presenting function , 2012, Journal of cellular and molecular medicine.
[2] H. Kiyono,et al. Two Distinct Epitopes on the Ovalbumin 323-339 Peptide Differentiating CD4+T Cells into the Th2 or Th1 Phenotype , 2012, Bioscience, biotechnology, and biochemistry.
[3] M. Strømme,et al. Current status and future prospects of nanotechnology in cosmetics , 2012 .
[4] Esther Vázquez,et al. Bacterial inclusion bodies: making gold from waste. , 2012, Trends in biotechnology.
[5] Jian-Zhong Shao,et al. Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model , 2011, International journal of nanomedicine.
[6] T. Casale,et al. Immune modulation for treatment of allergic disease , 2011, Immunological reviews.
[7] R. Germain,et al. Protective T cell immunity in mice following protein-TLR7/8 agonist-conjugate immunization requires aggregation, type I IFN, and multiple DC subsets. , 2011, The Journal of clinical investigation.
[8] Fulin Wu,et al. Unfolding and refolding details of lysozyme in the presence of β-casein micelles. , 2011, Physical chemistry chemical physics : PCCP.
[9] A. Espino,et al. Effectiveness of intranasal vaccination against Angiostrongylus costaricensis using a serine/threonine phosphatase 2 A synthetic peptide and recombinant antigens. , 2010, Vaccine.
[10] T. Ficht,et al. Polymeric particles in vaccine delivery. , 2010, Current opinion in microbiology.
[11] M. Malmsten,et al. Nanomedicine: reshaping clinical practice , 2010, Journal of internal medicine.
[12] J. Veciana,et al. Surface Cell Growth Engineering Assisted by a Novel Bacterial Nanomaterial , 2009 .
[13] H. Benson,et al. Pharmaceutical aspects of intranasal delivery of vaccines using particulate systems. , 2009, Journal of pharmaceutical sciences.
[14] Rakesh K. Kumar,et al. The "classical" ovalbumin challenge model of asthma in mice. , 2008, Current drug targets.
[15] A. Renault,et al. Interfacial properties of heat-treated ovalbumin. , 2007, Journal of colloid and interface science.
[16] H. Wędrychowicz,et al. Vaccine potential of inclusion bodies containing cysteine proteinase of Fasciola hepatica in calves and lambs experimentally challenged with metacercariae of the fluke. , 2007, Veterinary parasitology.
[17] H. Wędrychowicz,et al. Enteral vaccination of rats against Fasciola hepatica using recombinant cysteine proteinase (cathepsin L1). , 2007, Vaccine.
[18] M. Løvik,et al. The allergy adjuvant effect of particles – genetic factors influence antibody and cytokine responses , 2005, BMC Immunology.
[19] T. Kündig,et al. Immunity in response to particulate antigen-delivery systems. , 2005, Advanced drug delivery reviews.
[20] F. Spertini,et al. Intranasal treatment with ovalbumin but not the major T cell epitope ovalbumin 323–339 generates interleukin‐10 secreting T cells and results in the induction of allergen systemic tolerance , 2004, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.
[21] B. Szewczyk,et al. Inclusion bodies from recombinant bacteria as a novel system for delivery of vaccine antigen by the oral route. , 2004, Immunology letters.
[22] A. Middelberg,et al. The influence of molecular variation on protein interactions. , 2003, Biotechnology and bioengineering.
[23] Hans P Kocher,et al. The likelihood of aggregation during protein renaturation can be assessed using the second virial coefficient , 2003, Protein science : a publication of the Protein Society.
[24] A. Villaverde,et al. Construction and deconstruction of bacterial inclusion bodies. , 2002, Journal of biotechnology.
[25] R. Kopito,et al. Aggresomes, inclusion bodies and protein aggregation. , 2000, Trends in cell biology.
[26] T. Root,et al. Protein retention in hydrophobic interaction chromatography: modeling variation with buffer ionic strength and column hydrophobicity , 1997 .
[27] J. Lowe,et al. The latent membrane protein‐1 in Epstein‐Barr virus‐transformed lymphoblastoid cells is found with ubiquitin‐protein conjugates and heat‐shock protein 70 in lysosomes oriented around the microtubule organizing centre , 1991, The Journal of pathology.
[28] D. Morrison,et al. Binding of polymyxin B to the lipid A portion of bacterial lipopolysaccharides. , 1976, Immunochemistry.
[29] P. Scott. Development and regulation of cell-mediated immunity in experimental Leishmaniasis , 2003, Immunologic research.