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Titlebook: US Nuclear Strategy; A Reader Philip Bobbitt (Professor of Law, Fellow),Lawrence Book 1989 Palgrave Macmillan, a division of Macmillan Publ

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樓主: necrosis
51#
發(fā)表于 2025-3-30 09:28:51 | 只看該作者
Gregory F. Trevertonl, gender-conscious and interdisciplinary study, this collection offers a cutting edge account of how power has been exercised and demonstrated in various cultures of some bygone eras.978-1-349-93084-5978-1-137-58381-9
52#
發(fā)表于 2025-3-30 13:47:39 | 只看該作者
Bernard Brodiere we propose as a working hypothesis that it may be the actin-binding region of subfragment-1 around the SH-1 group which by, interacting with actin, is capable of “turning on” actin, so that calcium responsiveness increases.
53#
發(fā)表于 2025-3-30 19:44:28 | 只看該作者
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發(fā)表于 2025-3-30 22:01:08 | 只看該作者
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發(fā)表于 2025-3-31 03:44:42 | 只看該作者
Lawrence Freedmanatum [1]. The loss of striatal dopamine and the consequent dysfunction of the nigrostriatal pathway lead to the cardinal symptoms of PD: resting tremor, cogwheel rigidity, bradykinesia (or difficulty to initiate movement) and loss of postural reflex. Current pharmacological treatment strategies for
56#
發(fā)表于 2025-3-31 07:51:55 | 只看該作者
Giulio Douhet biotechnology companies. Designer peptide drugs overcome the unattractive pharmacological properties of native peptides and protein fragments and frequently feature nonnatural amino acid or backbone replacements, cyclic or multimeric structures, or peptidic or nonpeptidic delivery modules. With the
57#
發(fā)表于 2025-3-31 11:28:14 | 只看該作者
58#
發(fā)表于 2025-3-31 15:38:36 | 只看該作者
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發(fā)表于 2025-3-31 18:30:50 | 只看該作者
Lawrence Freedmanrey. The peptides within this venom have been the focus of many drug design efforts as they exhibit potent and selective targeting of therapeutically important receptors, transporters and channels, particularly in relation to the treatment of chronic pain. The most well studied class of . peptides a
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