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1 production of valvulitis were located in the rod region.
2 ues 1874 to 1902) near the C terminus of the rod region.
3 e nanocrystals organized into rods and inter-rod regions.
4                 The requirement for both the rod region and She3p can be bypassed by directly couplin
5  the hydrophobic character of the N-terminal rod region and, alternatively, activating the C-terminal
6 partial shortening (melting) in the proximal rod region and/or stiffening of the regulatory domain of
7 and the mechanisms by which mutations in the rod region disrupt nonmuscle myosin-IIA function, we exa
8 p- and downstream positions in both head and rod regions, indicating that residues 17 and 137 were th
9 ro binding studies suggest that the internal rod region is important for heterotypic associations of
10 aped GCs(10)) but that a relatively thick GC rod region is needed to enhance pore opening.
11 Tax binds to the domain corresponding to the rod region of alpha-internexin, which is essential for n
12 amino-terminal head region, an alpha-helical rod region of approximately310 amino acids, and a carbox
13  first insight into how mutations affect the rod region of muscle myosins, and provide a framework fo
14 chanism of pathogenesis for mutations in the rod region of muscle myosins.
15 ngly, the adaptor protein She3p binds to the rod region of Myo4p and forms a homogeneous single-heade
16                                          The rod region of Myo4p, but not the globular tail, is essen
17 hat the interaction between the head and the rod region of smooth muscle myosin at S2 is important fo
18                                          The rod region of talin1 consists of 62 alpha-helices bundle
19 Proline substitutions within the coiled-coil rod region of the beta-myosin gene (MYH7) are the predom
20  filament assembly, SM1 and SM2 myosins, the rod region of these myosin isoforms, and a rod with no t
21 The binding site of Mts1 on myosin is in the rod region, particularly to the light meromyosin portion
22                                              Rod regions show unusually high oxidation levels.
23 llow for significant portions of the protein rod regions to be occupied by conformations other than a
24 lecule's two-chain alpha-helical coiled-coil rod region--towards the carboxy terminus of the heavy ch
25 nt of keratin 8 corresponding to the central rod region was detected in the soluble fraction of chlam