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In vivo kinetics and biodistribution analysis of neoglycoproteins: Effects of chemically introduced glycans on proteinsBiodistribution and in vivo kinetics analysis of chemically prepared neoglycoproteins are reviewed
Chemical glycan conjugation controls the biodistribution and kinetics of proteins in live animals© 2014 Bentham Science Publishers. The biodistributions and in vivo kinetics of chemically prepared
In vivo kinetics and biodistribution analysis of neoglycoproteins: Effects of chemically introduced glycans on proteinsBiodistribution and in vivo kinetics analysis of chemically prepared neoglycoproteins are reviewed
Chemical glycan conjugation controls the biodistribution and kinetics of proteins in live animals© 2014 Bentham Science Publishers. The biodistributions and in vivo kinetics of chemically prepared
Gene transfer to mice organs using non-viral systems for targeted delivery with different hydrophobicity and with lactose addressing group. It is shown that biodistribution doesn't depend on lipoplex lipid composition under i.p. administration
Gene transfer to mice organs using non-viral systems for targeted delivery with different hydrophobicity and with lactose addressing group. It is shown that biodistribution doesn't depend on lipoplex lipid composition under i.p. administration
Use of submicron vaterite particles serves as an effective delivery vehicle to the respiratory portion of the lung administration particles of all three sizes were visible in the lung, with the deepest penetrance observed with 0
Visualizing Trimming Dependence of Biodistribution and Kinetics with Homo-and Heterogeneous N-Glycoclusters on Fluorescent Albumin, for the first time, a glycan-dependent shift from urinary to gall bladder excretion mediated by sequential
Submicron-Sized Nanocomposite Magnetic-Sensitive Carriers: Controllable Organ Distribution and Biological Effects are the lack of information about acute toxicity, the influence of the submicron size of the carrier
Visualizing Trimming Dependence of Biodistribution and Kinetics with Homo-and Heterogeneous N-Glycoclusters on Fluorescent Albumin, for the first time, a glycan-dependent shift from urinary to gall bladder excretion mediated by sequential
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