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1 icing in C. merolae may occur without the U1 small nuclear ribonucleoprotein particle.
2 component that associates with the yeast U1 small nuclear ribonucleoprotein particle.
3 Prp18 forms a bridge between Slu7 and the U5 small nuclear ribonucleoprotein particles.
4 o alpha-helices and may interact with the U5 small nuclear ribonucleoprotein particles.
5 was detected in association with a subset of small nuclear ribonucleoprotein particle and Ser-Arg pro
6 strictive temperature (39.5 degrees C), both small nuclear ribonucleoprotein particles and a general
7 ceosome assembly within the mature U2 snRNP (small nuclear ribonucleoprotein particle), and its displ
8 esidues 885-2413) in complex with Aar2, a U5 small nuclear ribonucleoprotein particle assembly factor
9 nd in a manner independent of Prp16p, the U5 small nuclear ribonucleoprotein particle-associated prot
11 important for the biogenesis of spliceosomal small nuclear ribonucleoprotein particles, but downstrea
12 tion occurred after inactivation of U1 or U2 small nuclear ribonucleoprotein particles, compatible wi
15 and trans-splicing using the specialized SL2 small nuclear ribonucleoprotein particle for downstream
16 thereby promoting the dissociation of the U1 small nuclear ribonucleoprotein particle from the 5' spl
17 hat SmD1, a core component of the Drosophila small nuclear ribonucleoprotein particle implicated in s
20 ose) polymerase, the 70-kD protein of the U1 small nuclear ribonucleoprotein particle, lamin B, the n
21 the 5' splice site, cross-linking of the U5 small nuclear ribonucleoprotein particle protein, U5(200
23 ates that these complexes contain additional small nuclear ribonucleoprotein particle proteins and th
24 l nuclear ribonucleoprotein (snRNP) is a 25S small nuclear ribonucleoprotein particle similar in size
25 x, SF3B3 and SF3B5, that form part of the U2 small nuclear ribonucleoprotein particle (snRNP) are als
27 snRNP and the polypyrimidine tract by the U2 small nuclear ribonucleoprotein particle (snRNP) auxilia
30 k9-cyclin T modules from large, inactive 7SK small nuclear ribonucleoprotein particle (snRNP) complex
31 he 5' splice site, and a component of the U2 small nuclear ribonucleoprotein particle (snRNP) complex
32 In this investigation, we made use of anti-small nuclear ribonucleoprotein particle (snRNP) Ig tran
33 The current model for the function of the U5 small nuclear ribonucleoprotein particle (snRNP) in the
34 t dephosphorylated SRp38 interacts with a U1 small nuclear ribonucleoprotein particle (snRNP) protein
35 s shown to promote the recruitment of the U1 small nuclear ribonucleoprotein particle (snRNP) to the
39 odes a protein factor that contributes to U1 small nuclear ribonucleoprotein particle (snRNP)-pre-mRN
42 -B7.2 Abs expressed significantly lower anti-small nuclear ribonucleoprotein particles (snRNP) and an
44 of these introns requires a different set of small nuclear ribonucleoprotein particles (snRNPs) (U11,
45 When Prp24 is absent, unpaired U4 and U6 small nuclear ribonucleoprotein particles (snRNPs) accum
46 functions in the biogenesis of spliceosomal small nuclear ribonucleoprotein particles (snRNPs) and p
49 site for the Sm proteins, both hallmarks of small nuclear ribonucleoprotein particles (snRNPs) that
50 cipitation (ChIP) analysis of U1, U2, and U5 small nuclear ribonucleoprotein particles (snRNPs) to in
51 e interactions between the five spliceosomal small nuclear ribonucleoprotein particles (snRNPs) U1, U
52 r messenger RNA substrate bound to U1 and U2 small nuclear ribonucleoprotein particles (snRNPs), and
54 tion as an assembly machine for spliceosomal small nuclear ribonucleoprotein particles (snRNPs), the
62 ke proteins are stable components of several small nuclear ribonucleoprotein particles that function
63 IIF (TFIIF), TFIIS, splicing factors, the U7 small nuclear ribonucleoprotein particle, the stem-loop
66 d the spliceosome, which is composed of five small nuclear ribonucleoprotein particles, U1, U2, U4/U6
67 ) domain of spliceosomal A protein of the U1 small nuclear ribonucleoprotein particle (U1A) interacti
69 of Sm core structures of spliceosomal U-rich small nuclear ribonucleoprotein particles (UsnRNPs) requ
70 which facilitates the interaction of the U2 small nuclear ribonucleoprotein particle with the branch
71 autoreactive B cells that recognize self-Ag small nuclear ribonucleoprotein particles with activated
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