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1 ar protein called poly(A) binding protein 2 (PABP2).
2 in the context of the proposed functions for PABP2.
3                             We conclude that PABP2 analysis is a reliable non-invasive diagnostic tes
4 n in the gene for poly(A) binding protein 2 (PABP2) and is found in isolated cohorts throughout the w
5 ted one of the two poly(A)-binding proteins, PABP2, and one of the six cap-binding translation initia
6 e mammalian nuclear poly(A) binding protein, PABP2, controls the length of the newly synthesized poly
7 components of NMD-susceptible mRNP as CBP20, PABP2, eIF4G, and the NMD factors Upf2 and Upf3.
8                              Thus, the mouse Pabp2 gene is a retroposon, created by synthesizing a re
9 at the transcription start site of the mouse Pabp2 gene is located approximately 330 bases downstream
10                   First, the promoter of the Pabp2 gene is not derived from its intron-containing pro
11 of the human PABP1 mRNA, indicating that the Pabp2 gene lacks 5' flanking sequences of the parental P
12 e of genomic and cDNAs demonstrated that the Pabp2 gene lacks introns, whereas all other functional P
13 termined the transcription start site of the Pabp2 gene to clarify the source of its promoter, a prer
14 e family had a pathological expansion in the PABP2 gene, ranging from (GCG)(8) to (GCG)(13).
15 e triplet repeat expansion ([GCG](9)) in the PABP2 gene.
16 ic isoform of mouse poly(A) binding protein (Pabp2) has been isolated and sequenced.
17 o 10.0% of myocyte nuclei contained discreet PABP2 immunoreactive intranuclear inclusions, providing
18 xon 1 of the poly(A) binding protein 2 gene (PABP2), in which (GCG)(6) is the normal repeat length.
19 d early haploid spermatogenic cells, and the Pabp2 mRNA encodes a protein whose size and RNA-binding
20 that its promoter drives the accumulation of Pabp2 mRNA in meiotic and early haploid spermatogenic ce
21 as baits: poly(A)-binding proteins PABP1 and PABP2, mRNA export receptor MEX67, and the nucleoporin N
22                            The origin of the PABP2 mutation in New Mexican OPMD patients is unclear,
23   Maximum particle size is realized when the PABP2.poly(A) complex is formed with poly(A) molecules 2
24 l, we have investigated the structure of the PABP2.poly(A) complex.
25  gel mobility shift assays indicate that the PABP2.poly(A) particle formed on A(300) is not significa
26 psite of the PABP1 mRNA, indicating that the Pabp2 promoter is derived from the PABP1 5' UTR.
27                                    The mouse Pabp2 retroposon encodes an isoform of poly(A) binding p
28                      The 5' end of the mouse Pabp2 retroposon exhibits extensive similarity to the en
29                                          The Pabp2 retroposon is unusual because it is functional: pr
30 plicated in the retention of function of the Pabp2 retroposon.
31 canning force microscopy studies reveal that PABP2, when bound to poly(A), forms both linear filament