ライフサイエンスコーパス: alternative splicing factor

1 site recognition and is a frequent target of alternative splicing factors.

2 otein isoform expression and is regulated by alternative splicing factors.

3 that serve as binding sites for trans-acting alternative splicing factors.

4 Nova proteins are a neuron-specific alternative splicing factors.

5 n-protein interactions with constitutive and alternative splicing factors.

6 lice donors and, likely, novel exon-specific alternative splicing factors.

7 whereas cytokine-inducible nuclear protein, alternative splicing factor 2, and beta-hydroxyisobutyry

8 The alternative splicing factor 45 (SPF45) is overexpressed

9 ine rich) protein ASF/SF2 (also called human alternative splicing factor), an essential splicing fact

10 licing factor 1) (SF2/ASF, splicing factor 2/alternative splicing factor), an essential splicing regu

11 e functional homologues of the human ASF/SF2 alternative splicing factor and they indicate a diversit

12 The human alternative splicing factor ASF/SF2, an SR (serine-argin

13 5 and the splicing factor SF2 (also known as alternative splicing factor (ASF)).

14 The UHM-containing alternative splicing factor CAPERalpha regulates splicin

15 The prototypical SR protein ASF/SF2 (human alternative splicing factor) contains two N-terminal RNA

16 A-binding protein motifs and found that some alternative splicing factors could affect tumor-specific

17 hnRNP H and F are alternative splicing factors for numerous U2- and U12-de

18 Splicing factor 45 kDa (SPF45) is an alternative splicing factor implicated in breast and lun

19 The predominant alternative splicing factor in neutrophils is SRp30c, wh

20 hey indicate a diversity of the ASF/SF2-like alternative splicing factors in monocot plant cells.

21 imidine tract-binding protein (PTB) is a key alternative splicing factor involved in exon repression.

22 The alternative splicing factor MBNL1 is sequestered to the

23 fbn-1 mRNA processing requires the conserved alternative splicing factor MEC-8/RBPMS.

24 The RNA binding protein and alternative splicing factor Muscleblind-like 1 (MBNL1) h

25 nt study, we have identified the predominant alternative splicing factor present in human neutrophils

26 In PH, miR-124, through the alternative splicing factor PTBP1, regulates the PKM2/PK

27 We hypothesized that alternative splicing factors RBFOX2 and RBFOX1 might med

28 s), and its application to the developmental alternative splicing factors RBFOX2, CELF1/CUGBP1, and M

29 Thus, this well characterized alternative splicing factor regulates at least one targe

30 R1 is a plant homologue of the human general/alternative splicing factor SF2/ASF.

31 he serine arginine protein splicing factor 2/alternative splicing factor (SF2/ASF) enhances the expre

32 lts suggest that increased splicing factor 2/alternative splicing factor (SF2/ASF) expression in diff

33 plicing factor (SRSF) 1 or splicing factor 2/alternative splicing factor (SF2/ASF) to be important in

34 amily of proteins, such as splicing factor 2/alternative splicing factor (SF2/ASF), which recruit bas

35 We have investigated the role of the alternative-splicing factor Sfrs1, an arginine/serine-ri

36 Alternative splicing factor/splicing factor 2 (ASF/SF2)

37 Tnpo3 in its free as well as GTPase Ran- and alternative splicing factor/splicing factor 2 (ASF/SF2)-

38 otide, which identified the splicing protein alternative splicing factor/splicing factor 2 (ASF/SF2).

39 mall nuclear ribonucleoproteins (snRNPs) and alternative splicing factor/splicing factor 2 (ASF/SF2).

40 cing enhancers, each containing two ASF/SF2 (alternative splicing factor/splicing factor 2) binding s

41 (SR) proteins, and the AG-rich 3' end binds alternative splicing factor/splicing factor 2.

42 MBNL1 (muscleblind-like protein 1) is an alternative splicing factor that becomes highly concentr

43 s nuclear ribonucleoprotein (hnRNP) A1 is an alternative splicing factor that is mainly nuclear, alth

44 The muscleblind-like (MBNL) genes encode alternative splicing factors that are essential for the

45 ctedly, we found that the ability of a given alternative splicing factor to behave as an enhancer or

46 identified a large group of constitutive and alternative splicing factors, two nucleoporins involved

47 f-white-apricot (SWAP) and Transformer (Tra) alternative splicing factors, we found that the RS domai