ライフサイエンスコーパス: alternative splice site

1 titution, a G-->A, at the -1 position of the alternative splice site.

2 on simultaneously define amino acids and the alternative splice site.

3 exon sequences immediately downstream of an alternative splice site.

4 g complexes regulate utilization of pre-mRNA alternative splice sites.

5 plice site of intron 5 and is flanked by two alternative splice sites.

6 the temporal and cell-specific selection of alternative splice sites.

7 sium (BK) channel gene, which contains three alternative splice sites (A, B, and C) and encodes at le

8 t involved in any alternative splicing; (iv) alternative splice sites, a set of 209 splice sites wher

9 Alternative transcription start sites and alternative splice sites are used to generate a remarkab

10 Most human genes contain multiple alternative splice sites believed to extend the complexi

11 tive splicing at the normal and the upstream alternative splice site, but splicing at the downstream

12 has been shown to affect the choice between alternative splice sites by favoring the proximal as opp

13 Alternative splice site choice in the 5' UTR and relativ

14 Two alternative splice sites corresponding to known mRNA tra

15 f RNA degradation signals, identification of alternative splicing sites, etc.

16 The alternative splice sites for the smallest adducin isofor

17 ic isoforms termed VEGFAxxxb that utilise an alternative splice site in the final exon have been wide

18 r R-4 (CXCR-4) revealed a potential in-frame alternative splice site in the region encoding the N-ter

19 is alternatively spliced through the use of alternative splice sites in exons 3 and 4, although the

20 The activation of sex-specific alternative splice sites in the Drosophila melanogaster

21 ding domain is downstream of each of the two alternative splice sites in the intermediate chains.

22 ucture similar to that of neuregulins and an alternative splicing site in the epidermal growth factor

23 f bona fide novel elements of RNA processing-alternative splice sites, introns, and cleavage sites-wh

24 hese data suggest that 1) the ligand binding alternative splice site is functionally inert in terms o

25 The selection of alternative splice sites is governed by the dynamic form

26 s a homozygous base-pair substitution in the alternative splice site of the mu heavy-chain gene.

27 is far higher than previous estimates, with alternative splice sites on average activated at approxi

28 e both abundant and highly conserved between alternative splice site pairs and that mutation of ESSs

29 hat mutation of ESSs located between natural alternative splice site pairs consistently shifted splic

30 ted level of alternative splicing, including alternative splice site selection for over half of all a

31 titutive pre-mRNA splicing and also regulate alternative splice site selection in a concentration-dep

32 initiating methionines) and both 5'- and 3'-alternative splice site selection of the first intron.

33 at seemingly disparate roles for hnRNP A1 in alternative splice site selection, RNA processing, RNA t

34 fficiency of pre-mRNA splicing and regulates alternative splice site selection.

35 gulated by other splicing factors to control alternative splice site selection.

36 pressing constitutive splicing and switching alternative splice site selection.

37 effect of C6 pyridinium ceramide (PyrCer) on alternative splice site selection.

38 This processed snoRNA functions in alternative splice-site selection.

39 tion-dependent effects of this SR protein on alternative splice-site selection.

40 R family proteins modulates certain types of alternative splice-site selection.

41 PEG linker between an enhancer sequence and alternative splice sites, the interaction of these two e

42 specific differences in intron retention and alternative splice site usage are primarily attributable

43 ntial roles in general splicing and regulate alternative splice site utilization in a concentration-d

44 This contig is also an Ensembl annotated alternative splice-site variant of the UDG2 gene (Udg2v2

45 Alternative splice site variants of the 1226-amino acid

46 Three alternative splice-site variants of ADAR1 (ADAR1-a, -b,

47 splice site, but splicing at the downstream alternative splice site was consistently rare.

48 he majority of APLP2 mRNA generated from two alternative splicing sites was found to contain the exon

49 K4 transcription initiation site and several alternative splice sites with a 5'-RACE approach.

50 9R chimeric splicing, using either intact or alternative splice sites within the IL-9R gene.

51 Sequencing confirms that an alternative splicing site within exon 3 results in the t