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1 tions of missense alleles of unc-15 (encodes paramyosin).
2 library revealed that UNC-89 interacts with paramyosin.
3 eviously described component of M-lines, and paramyosin.
4 ization of a major thick filament component, paramyosin.
5 oform-specific interaction between MHC A and paramyosin.
6 erhaps through phosphorylation of myosin and paramyosin.
7 he binding of CaGC to native and recombinant paramyosin, 125I-CaGC was used as a binding tracer in SD
9 analysis of normal embryos demonstrated that paramyosin accumulates as a cytoplasmic protein in early
10 UNC-98 and anti-paramyosin colocalize in the paramyosin accumulations of missense alleles of unc-15 (
13 (calreticulin, tropomyosin 1, tropomyosin 2, paramyosin, and triose phosphate isomerase) did not.
14 nstrated that Th2-biased immune responses to paramyosin are associated with resistance to reinfection
15 tokine responses, these data further support paramyosin as a leading vaccine candidate for human schi
17 a periodicity matching the 72-nm repeats of paramyosin, as revealed by immunoelectron microscopy.
20 ngent needles, which contain both UNC-98 and paramyosin, can be suppressed by starvation or by exposu
25 tudied the core proteins that, together with paramyosin, form the core structure of the thick filamen
26 d colocalized with abnormal accumulations of paramyosin found in unc-98, -96, and -15 (encodes paramy
27 e responses is confirmed by experiments with paramyosin from the tropical parasites Onchocerca volvul
28 onally disrupted the Drosophila melanogaster paramyosin gene by mobilizing a P element located in its
29 in the pilot-scale production of schistosome paramyosin have hampered further studies of this promisi
30 s mediating close contacts between MHC A and paramyosin in an antiparallel arrangement at the filamen
32 one isoform of myosin heavy chain (MHC) and paramyosin in Caenorhabditis elegans to probe the molecu
34 diates an avid interaction between MHC A and paramyosin in parallel arrangement in formation of the f
37 ilagenin assembled with the myosin homologue paramyosin into the tubular cores of wild-type nematodes
43 hat N-terminal phosphorylation of Drosophila paramyosin is essential for optimal force and oscillator
47 red strains had decreases in the most acidic paramyosin isoforms, with a corresponding increase in mo
50 ramyosin-specific by rescuing the homozygous paramyosin mutant to adulthood with a paramyosin transge
52 ed by an embryonic version; the other group (paramyosin mutants) had one or more putative phosphoryla
55 horylation sites in Drosophila suggests that paramyosin phosphorylation is important for maintaining
56 mechanical defects observed upon disrupting paramyosin phosphorylation sites in Drosophila suggests
59 ing purified proteins, UNC-98 interacts with paramyosin residues 31-693, whereas UNC-96 interacts wit
63 ess in IFM myofibrils, probably by affecting paramyosin's interaction with other sarcomeric proteins.
67 e-rich consensus sequence, but the region of paramyosin that interacts with UNC-89's SH3 is alpha-hel
73 -scale production of recombinant full-length paramyosin will facilitate preclinical evaluation of par
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