Physiologic and pharmacologic roles for the cardiac Na+, K+Atpase transport system.
作者信息
Allen J C, Schwartz A
出版信息
Recent Adv Stud Cardiac Struct Metab. 1972;1:30-3.
PMID:4283442
Abstract
摘要
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1
Physiologic and pharmacologic roles for the cardiac Na+, K+Atpase transport system.心脏钠钾ATP酶转运系统的生理和药理作用。
Recent Adv Stud Cardiac Struct Metab. 1972;1:30-3.
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[Na, K-ATPase (author's transl)].[钠钾ATP酶（作者译）]
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Na+, K+-ATPase, the transport enzyme: evidence for its proposed role as pharmacologic receptor for cardiac glycosides.钠钾ATP酶，转运酶：关于其作为强心苷药理学受体的推测作用的证据。
Ann N Y Acad Sci. 1974;242(0):646-57. doi: 10.1111/j.1749-6632.1974.tb19123.x.
7
Cardiac glycoside receptor in potassium depletion.低钾血症时的强心苷受体
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Ouabain: temporal relationship between the inotropic effect and the in vitro binding to, and dissociation from, (Na + + K + )- activated ATPase.哇巴因：变力作用与体外与（钠+ +钾+）激活的ATP酶结合及解离之间的时间关系。
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The function of (Na+, K+)-ATPase in the thick ascending limb of Henles loop.
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