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Titlebook: Biological Barriers to Protein Delivery; Kenneth L. Audus,Thomas J. Raub Book 1993 Springer Science+Business Media New York 1993 biochemis

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樓主: melancholy
31#
發(fā)表于 2025-3-26 21:47:10 | 只看該作者
Book 1993relating to the delivery of endogenous andrecombinant proteins to mammalian organs, tissues, and cells. It willpromote fruitful collaboration among academic and industrialscientists in the fields of pharmacology, cell biology, biochemistry,physiology, and immunology.
32#
發(fā)表于 2025-3-27 05:04:42 | 只看該作者
33#
發(fā)表于 2025-3-27 06:12:56 | 只看該作者
Biological Barriers to Protein Delivery978-1-4615-2898-2Series ISSN 1078-0467
34#
發(fā)表于 2025-3-27 13:09:48 | 只看該作者
https://doi.org/10.1007/978-3-322-92267-0 ways of delivering drugs into cells—for instance, with the purpose of irreversibly inhibiting the protein synthesis machinery of cancer cells—mechanisms by which various protein ligands are internalized by cells and subsequently translocated across the membrane of intracellular compartments are coming into focus.
35#
發(fā)表于 2025-3-27 16:36:10 | 只看該作者
Der frühe A. S. Neill in Gro?britannien play significant roles in fluid homeostasis, particularly in the alveolar region. Yet the knowledge of the mechanisms responsible for the maintenance of protein gradients across respiratory epithelia is primitive in relation to similar knowledge regarding ion gradients.
36#
發(fā)表于 2025-3-27 21:20:25 | 只看該作者
37#
發(fā)表于 2025-3-27 23:40:15 | 只看該作者
38#
發(fā)表于 2025-3-28 03:31:28 | 只看該作者
Karl Friedrich Bohler,Tobias Franzheld M.A. another species and has a different amino acid sequence, or it may be perceived as foreign due to a more subtle difference, such as being denatured or aggregated. Low-molecular-weight drugs generally do not initiate an immune reaction unless they become conjugated to protein, as occasionally occurs with penicillin.
39#
發(fā)表于 2025-3-28 06:50:07 | 只看該作者
40#
發(fā)表于 2025-3-28 11:41:00 | 只看該作者
Psychoanalytische Heilerziehungt especially for small- or medium-size peptide drugs. Potential advantages for intraoral delivery are the avoidance of gastrointestinal or liver first-pass effect, the feasibility of locally controlled absorption enhancement, the ease of administration and removal of an administered device, and the sustainment of drug action.
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