Titlebook: Regulation of the Contractile Cycle in Smooth Muscle; Takeshi Nakano (Professor),David J. Hartshorne (Pr Conference proceedings 1995 Sprin

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Smooth Muscle Myosin Phosphatase,e was active with both isolated myosin light chain and intact myosin that had been phosphorylated by myosin light chain kinase as substrates, suggesting that phosphorylated myosin might be a substrate in situ. The 38-kDa subunit was identified as a catalytic subunit of a type lδ protein phosphatase

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Structure and Expression of Vascular Smooth Muscle Calponin,(SMCs). The NH.-terminal region of calponin shares homology with a putative negative regulatory domain of the GDP-GTP exchanger for Rho-like GTP-binding proteins. Expression of calponin is down-modulated in proliferating SMCs of atherosclerotic neointima and injured arterial media. Direct transfer o

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Smooth Muscle Cell Differentiation and Its Abnormality in Vascular Diseases,h muscles contain at least three MHC isoforms: SM1 (204 kDa), SM2 (200 kDa), and SMemb (200 kDa). SM1 and SM2 are specific to smooth muscles. SM1 is expressed from the early stage of fetal life into adulthood, but SM2 appears after birth. SMemb is a nonmuscle-type MHC abundantly expressed in the emb

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