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

1 ls in the tumour core and edge differ due to alternative RNA splicing.

2 f DDX39B, plays a similar role in regulating alternative RNA splicing.

3 a function of O-glycosylation in regulating alternative RNA splicing.

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

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

6 expression events through the regulation of alternative RNA splicing.

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

8 steroid receptor-mediated transcription and alternative RNA splicing.

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

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

11 nsmembrane glycoprotein CD44 are produced by alternative RNA splicing.

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

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

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

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

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

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

18 biologically active isotypes resulting from alternative RNA splicing.

19 This isoform resulted from alternative RNA splicing.

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

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

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

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

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

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

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

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

28 and investigates the potential link between alternative RNA splicing and autism-related behaviors in

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

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

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

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

33 tion factors and RNA-binding proteins affect alternative RNA splicing and synaptic development, poten

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

35 Entropy calculated from alternative RNA splicing and transcription start/end pre

36 to base pair with its pre-mRNA and regulate alternative RNA splicing and/or A-to-I RNA editing.

37 s, usage of non-canonical initiation codons, alternative RNA splicing, and defective ribosomal RNA pr

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

39 Functionally, AGGF1 regulates alternative RNA splicing as it decreases the exon skippi

40 evere midline facial clefting and widespread alternative RNA splicing (AS) changes.

41 Misregulated alternative RNA splicing (AS) contributes to the tumorig

42 Alternative RNA splicing (AS) regulates proteome diversi

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

44 Alternative RNA splicing can generate distinct protein i

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

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

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

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

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

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

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

52 ons of these RNA-binding proteins influenced alternative RNA splicing events within key autism-relate

53 TRX, and TP53 mutations cooperatively impact alternative RNA splicing events, particularly suppressio

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

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

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

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

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

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

60 Alternative RNA splicing greatly expands the repertoire

61 Alternative RNA splicing greatly increases proteome dive

62 Alternative RNA splicing has been reported at three site

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

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

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

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

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

68 NA isoform sequencing (scISO-Seq) can reveal alternative RNA splicing in individual cells, it suffers

69 the RUNX1/RUNX1T1 oncogene is a regulator of alternative RNA splicing in leukemic cells.

70 nisms by which prenatal BPA exposure affects alternative RNA splicing in the prefrontal cortex and in

71 Alternative RNA splicing is an essential and dynamic pro

72 Alternative RNA splicing is an essential process to yiel

73 Collectively, our findings reveal that alternative RNA splicing is an important mechanism of ge

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

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

76 Alternative RNA splicing is now known to be pervasive th

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

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

79 Alternative RNA splicing may provide unique opportunitie

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

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

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

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

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

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

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

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

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

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

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

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

92 Finally, we show that Srsf3 regulates the alternative RNA splicing of transcripts encoding protein

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

94 ch correlated with the observed sex-specific alternative RNA splicing patterns.

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

96 Developmentally regulated alternative RNA splicing produces TnT isoforms differing

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

98 Alternative RNA splicing provides an important means to

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

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

101 We review recent findings pertaining to alternative RNA splicing, the formation of multiple dist

102 ral variability of NRG isoforms generated by alternative RNA splicing, the use of multiple promoters

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

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

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

106 AKT-phosphorylated IWS1 regulates alternative RNA splicing via a pathway that is active in

107 thin the positively selecting CD69+DP cells, alternative RNA splicing was dysregulated in the double

108 s in Htr2c RNA editing profiles, while Htr2c alternative RNA splicing was unchanged.

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

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

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

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