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3 ions correlated with enhanced retention of a U5 snRNP subunit on transcription complexes downstream o
4 etically exacerbated by mutations in PRP8, a U5 snRNP protein that physically interacts with Snu114,
5 we propose that dephosphorylation of U2 and U5 snRNP components by PP1/PP2A family phosphatases faci
7 NAs, pre-mRNA splicing intermediates, U2 and U5 snRNP proteins, the Nineteen Complex (NTC), and secon
10 ntary to U12 or U5 demonstrates that U12 and U5 snRNPs perform essential roles in the AT-AC spliceoso
11 l electrophoresis reveals that U11, U12, and U5 snRNPs assemble onto the P120 pre-mRNA to form splici
12 e provide evidence that components of U2 and U5 snRNPs, specifically SAP155 and U5-116 kDa, are the k
16 The Sm core proteins of U1, U2, U4/U6 and U5 snRNPs include B(B1), B'(B2), N(B3), D1, D2, D3, E, F
17 al kinase that, in association with the both U5 snRNP and N-CoR deacetylase complexes, demonstrates a
19 vel mutation in the evolutionarily conserved U5 snRNP protein Prp8 suppresses the U4-cs1 growth defec
21 specific function to any part of the 280-kD U5 snRNP protein has been difficult, in part because Prp
22 A, the 3'-->5' helicase acts to disrupt mRNA/U5 snRNP contacts, thereby liberating the mRNA from the
25 tem promotes the assembly of a key module of U5 snRNP while assuring the quality control of PRPF8.
27 depleted splicing extracts with reassembled U5 snRNP particles, molecular neighbors were assessed as
28 Together, these observations suggest that U5 snRNP is positioned on the 3' splice site by an inter
30 d not detect Fl(2)d complexes containing the U5 snRNP protein U5-40K or with a protein that associate
31 chains increase the affinity of Prp3 for the U5 snRNP component Prp8, thereby allowing for the stabil
33 with RNA splicing regulators, including the U5 snRNP components of the spliceosome, such as EFTUD2.
35 g factor PRPF8 is a crucial component of the U5 snRNP, and together with EFTUD2 and SNRNP200, it form
40 igmentosa assemble less efficiently with the U5 snRNP and bind more strongly to R2TP, with one mutant
41 of PRP31 regulates its interaction with the U5 snRNP component PRP8, which is required for the effic
46 The purification of the low abundance U4/U6.U5 snRNP from yeast and the powerful sequencing methodol
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