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1 crotubule formation with purified tubulin or microtubule protein.
2 associated with the accumulation of rings of microtubule protein.
3 nship of midwall LV fractional shortening to microtubule protein.
4 termediate filament protein vimentin and the microtubule protein alpha-tubulin as components of these
5 enting the C-2, C-4, C-13 side chains to the microtubule protein and (2) service as a hydrogen-bond a
6 e antimitotic agent estramustine with bovine microtubule proteins and purified tubulin was investigat
7 ween NF-E2, platelet formation, and selected microtubule proteins, and they also provide novel molecu
8 clitaxel (Taxol(R)) in cultured cells and on microtubule protein, but differ from paclitaxel in retai
9 six had decreased LV function and increased microtubule protein concentration, and three had borderl
10 on, and three had borderline LV function and microtubule protein concentration, such that there was a
11 Four AS patients had normal LV function and microtubule protein concentration; six had decreased LV
12 on of Hsp90 copurifies with taxol-stabilized microtubule proteins in Drosophila embryo extracts, but
13 the polymerization of purified bovine brain microtubule protein into microtubules, and it depolymeri
14 : it assembled GTP-tubulin, GDP-tubulin, and microtubule protein into normal microtubules and stabili
17 the role of an angiosperm-specific TPX2-like microtubule protein MAP20 in pit formation using Brachyp
19 ffects on intact cells, cryptophycin-treated microtubule protein remained polymerization-defective ev
20 ease pathogenesis.SIGNIFICANCE STATEMENT The microtubule protein tau aggregates and forms insoluble i
21 id-beta (Abeta) peptide into plaques and the microtubule protein tau into neurofibrillary tangles (NF
22 domain of Stu1(CLASP), a conserved plus-end microtubule protein that is important for chromosome cap
25 lpha1 tubulin (alpha1T) is a neuron-specific microtubule protein whose expression is induced in the d
27 nt study we investigate TUBA4A, a structural microtubule protein with mutations causal to familial AL