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

1 -bound (mIg) B cell receptors (BCRs) through alternative RNA splicing.

2 vary at their C termini as a consequence of alternative RNA splicing.

3 w viral E6 and E7 expression is regulated by alternative RNA splicing.

4 expression events through the regulation of alternative RNA splicing.

5 re B cells express together with IgM through alternative RNA splicing.

6 steroid receptor-mediated transcription and alternative RNA splicing.

7 h are generated by alternative promoters and alternative RNA splicing.

8 e-specific isoforms and is also regulated by alternative RNA splicing.

9 nsmembrane glycoprotein CD44 are produced by alternative RNA splicing.

10 f an RNA recognition motif (RRM) and affects alternative RNA splicing.

11 licing, no helicases have been implicated in alternative RNA splicing.

12 M-RAR molecules are expressed as a result of alternative RNA splicing.

13 r from a single promoter in association with alternative RNA splicing.

14 s numbers of EGF-like domains as a result of alternative RNA splicing.

15 biologically active isotypes resulting from alternative RNA splicing.

16 This isoform resulted from alternative RNA splicing.

17 P1L) and short (CD2BP1S) variants arising by alternative RNA splicing.

18 ence suggests that the deletion is caused by alternative RNA splicing.

19 espectively, and these appear to result from alternative RNA splicing.

20 oplasm and plays a role in the regulation of alternative RNA splicing.

21 specific mRNA isoforms would be generated by alternative RNA splicing.

22 and 206 amino acids/monomer) resulting from alternative RNA splicing.

23 is known to regulate homeotic genes through alternative RNA splicing.

24 gene yields various isoforms as a result of alternative RNA splicing.

25 DNA binding domain and the leucine zipper by alternative RNA splicing and differential polyadenylatio

26 tio-temporal patterns of GluR expression, by alternative RNA splicing and editing and by targeting an

27 pp52 and S37 mRNA isoforms are generated by alternative RNA splicing and establish that they are ind

28 eome has millions of protein variants due to alternative RNA splicing and post-translational modifica

29 is elegans gene mec-8 encodes a regulator of alternative RNA splicing and that mec-8 null mutants hav

30 rent genes (NFI-A, NFI-B, NFI-C, and NFI-X), alternative RNA splicing, and protein heterodimerization

31 Alternative RNA splicing (AS) regulates proteome diversi

32 Oct2 alpha and beta isoforms are derived by alternative RNA splicing; as determined by Southern anal

33 mmunoprecipitation-chip studies, analysis of alternative RNA splicing, characterization of the methyl

34 tional activity also directly participate in alternative RNA splicing decisions.

35 known as A2BP1), as a prominent regulator of alternative RNA splicing during heart failure.

36 The latter mutation has the same alternative RNA splicing effect as a reported synonymous

37 Here we describe a unique alternative RNA splicing event that occurs during the de

38 of higher organisms, for example, detecting alternative RNA splicing events and oncogenic chromosoma

39 e transmembrane domain and are the result of alternative RNA splicing events between exons IV and VII

40 roteomic diversity is frequently achieved by alternative RNA-splicing events that can be fine-tuned i

41 L4-33K is a virus-encoded alternative RNA splicing factor which activates splicing

42 includes a variety of molecules generated by alternative RNA splicing from 10 variant exons (v1-v10).

43 forms (alpha and beta) that are generated by alternative RNA splicing from a single SpOtx gene.

44 The structure-function relationship of the alternative RNA splicing-generated NH2-terminal variable

45 We have now determined that alternative RNA splicing gives rise to at least five dif

46 Alternative RNA splicing greatly expands the repertoire

47 Alternative RNA splicing greatly increases proteome dive

48 Alternative RNA splicing has been reported at three site

49 Since its discovery in 1977, the study of alternative RNA splicing has revealed a plethora of mech

50 d trans-acting factors contributing to HPV18 alternative RNA splicing have been discovered in this st

51 generation sequencing and analysis of global alternative RNA splicing identified that the mRNA splici

52 Dysregulation in patterns of alternative RNA splicing in cancer cells is emerging as

53 We report on the involvement of alternative RNA splicing in generating multiple function

54 Alternative RNA splicing is an essential process to yiel

55 Taking these data together, we propose that alternative RNA splicing is involved in hypothalamic dev

56 The molecular cloning of Rgh3 suggests that alternative RNA splicing is needed for cell differentiat

57 Alternative RNA splicing is now known to be pervasive th

58 n was performed to identify tumor-associated alternative RNA splicing isoforms.

59 ggest that posttranscriptional regulation by alternative RNA splicing may play an important role in M

60 Alternative RNA splicing may provide unique opportunitie

61 ssing results primarily from a novel form of alternative RNA splicing mediated by multiple exonic spl

62 hanges in the two isozymes, originating from alternative RNA splicing, occur at a stretch of 55 amino

63 group of polypeptide factors that arise from alternative RNA splicing of a single gene.

64 e of CAPER coactivators in the regulation of alternative RNA splicing of an endogenous cellular gene

65 Therefore, we investigated whether the alternative RNA splicing of Bcl-x pre-mRNA was modulated

66 D-containing NMDA receptors are modulated by alternative RNA splicing of GluN1.

67 stinguish these cells is IgD, which, through alternative RNA splicing of H chain transcripts, begins

68 study provides important observations on how alternative RNA splicing of HPV18 pre-mRNAs is subject t

69 ese data provide the first evidence that the alternative RNA splicing of HPV18 pre-mRNAs is subject t

70 Jmjd6 is shown to change alternative RNA splicing of some, but not all, of the en

71 Exclusion of the alpha-exon by alternative RNA splicing of the fibroblast growth factor

72 There is no evidence for alternative RNA splicing of this gene product.

73 Expression of HPV18 genes is regulated by alternative RNA splicing of viral polycistronic pre-mRNA

74 s troponin T (TnT) isoforms are generated by alternative RNA splicing primarily in its N-terminal hyp

75 Developmentally regulated alternative RNA splicing produces TnT isoforms differing

76 tudy was to investigate chicken TERT (cTERT) alternative RNA splicing profiles of samples varying for

77 d trans-acting factors contributing to HPV18 alternative RNA splicing remain unknown.

78 F) A is generated as two isoform families by alternative RNA splicing, represented by VEGF-A165a and

79 olycistronic pre-mRNAs that are regulated by alternative RNA splicing to produce a repertoire of vira

80 RGMc is a 4-exon gene that undergoes alternative RNA splicing to yield 3 mRNAs with 5' differ

81 POT1 gene encodes four other variants due to alternative RNA splicing (variants v2, v3, v4, and v5),

82 identify cis-acting elements regulating this alternative RNA splicing, we sequenced the 3' end of Mhc

83 SC35, SRp40, SRp55, and SF2/ASF involved in alternative RNA splicing were predicted in exon 12.

84 These results correlate alternative RNA splicing with the expression of two GPHe

85 and deletion of one or more coding exons by alternative RNA splicing would not shift the downstream