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1 ith myosin rod and, to a lesser extent, with light meromyosin.
2 consistent with cross-linking two RLC to one light meromyosin.
3  cross-linked between the RLC of one head to light meromyosin between leucine 1554 and glutamate 1583
4                            The subfragment 2/light meromyosin "hinge" region has been proposed to sig
5                            The subfragment 2/light meromyosin "hinge" region of the MHC rod, located
6                                              Light meromyosin (LMM 77), the C-terminal proteolytic pe
7          The dimerization specificity of the light meromyosin (LMM) domain of chicken neonatal and ad
8 eromyosin (HMM), the S1 subfragment, and two light meromyosin (LMM) peptides containing amino acid se
9 MyBP-C (cMyBP-C(C10mut)), which binds to the light meromyosin (LMM) region of the myosin heavy chain,
10 ble mutations have not been described in the light meromyosin (LMM) region of the myosin rod, nor wou
11 ction between the heavy meromyosin (HMM) and light meromyosin (LMM) regions is expected to disrupt th
12 ndividuals reacted with distinctly different light meromyosin peptides.
13 in is in the rod region, particularly to the light meromyosin portion of the rod.
14 d regions spanning residues 1428-1571 in the light meromyosin portion of the tail, consistent with cr
15 s of a single molecule can cross-link to the light meromyosin portion of the tail.
16                         Different regions of light meromyosin produced valvulitis (residues 1685 to 1
17 n Abs recognized synthetic peptides from the light meromyosin region of the human cardiac myosin mole
18 und to react with specific peptides from the light meromyosin region of the human cardiac myosin mole
19 t 2 (S2) region of the adult isoform and the light meromyosin region of the neonatal isoform.
20 ponin binding sites in the subfragment 2 and light meromyosin regions of myosin, and that the region
21 in, epitopes were demonstrated in the S2 and light meromyosin regions.
22  via interactions at its C-terminus with the light meromyosin section of the myosin rod and with titi
23 phosphorylated heavy meromyosin (lacking the light meromyosin), suggesting a structural rearrangement

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