These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 25274738)

  • 41. TREND-DB-a transcriptome-wide atlas of the dynamic landscape of alternative polyadenylation.
    Marini F; Scherzinger D; Danckwardt S
    Nucleic Acids Res; 2021 Jan; 49(D1):D243-D253. PubMed ID: 32976578
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 3'UTR shortening and EGF signaling: implications for breast cancer.
    Akman HB; Oyken M; Tuncer T; Can T; Erson-Bensan AE
    Hum Mol Genet; 2015 Dec; 24(24):6910-20. PubMed ID: 26395459
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The early noncoding region of human papillomavirus type 16 is regulated by cytoplasmic polyadenylation factors.
    Glahder JA; Kristiansen K; Durand M; Vinther J; Norrild B
    Virus Res; 2010 May; 149(2):217-23. PubMed ID: 20144904
    [TBL] [Abstract][Full Text] [Related]  

  • 44. THOC5 couples M-CSF receptor signaling to transcription factor expression.
    Carney L; Pierce A; Rijnen M; Gonzalez Sanchez MB; Hamzah HG; Zhang L; Tamura T; Whetton AD
    Cell Signal; 2009 Feb; 21(2):309-16. PubMed ID: 19015024
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Direct interactions between subunits of CPSF and the U2 snRNP contribute to the coupling of pre-mRNA 3' end processing and splicing.
    Kyburz A; Friedlein A; Langen H; Keller W
    Mol Cell; 2006 Jul; 23(2):195-205. PubMed ID: 16857586
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Cellular stress alters 3'UTR landscape through alternative polyadenylation and isoform-specific degradation.
    Zheng D; Wang R; Ding Q; Wang T; Xie B; Wei L; Zhong Z; Tian B
    Nat Commun; 2018 Jun; 9(1):2268. PubMed ID: 29891946
    [TBL] [Abstract][Full Text] [Related]  

  • 47. RNAP II CTD phosphorylated on threonine-4 is required for histone mRNA 3' end processing.
    Hsin JP; Sheth A; Manley JL
    Science; 2011 Nov; 334(6056):683-6. PubMed ID: 22053051
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genome-wide profiling reveals alternative polyadenylation of mRNA in human non-small cell lung cancer.
    Zhang S; Zhang X; Lei W; Liang J; Xu Y; Liu H; Ma S
    J Transl Med; 2019 Aug; 17(1):257. PubMed ID: 31391087
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genes involved in pre-mRNA 3'-end formation and transcription termination revealed by a lin-15 operon Muv suppressor screen.
    Cui M; Allen MA; Larsen A; Macmorris M; Han M; Blumenthal T
    Proc Natl Acad Sci U S A; 2008 Oct; 105(43):16665-70. PubMed ID: 18946043
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Cleavage and polyadenylation: Ending the message expands gene regulation.
    Neve J; Patel R; Wang Z; Louey A; Furger AM
    RNA Biol; 2017 Jul; 14(7):865-890. PubMed ID: 28453393
    [TBL] [Abstract][Full Text] [Related]  

  • 51. αCP Poly(C) binding proteins act as global regulators of alternative polyadenylation.
    Ji X; Wan J; Vishnu M; Xing Y; Liebhaber SA
    Mol Cell Biol; 2013 Jul; 33(13):2560-73. PubMed ID: 23629627
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Distinct Functions of the Cap-Binding Complex in Stimulation of Nuclear mRNA Export.
    Sen R; Barman P; Kaja A; Ferdoush J; Lahudkar S; Roy A; Bhaumik SR
    Mol Cell Biol; 2019 Apr; 39(8):. PubMed ID: 30745412
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A snoRNA modulates mRNA 3' end processing and regulates the expression of a subset of mRNAs.
    Huang C; Shi J; Guo Y; Huang W; Huang S; Ming S; Wu X; Zhang R; Ding J; Zhao W; Jia J; Huang X; Xiang AP; Shi Y; Yao C
    Nucleic Acids Res; 2017 Sep; 45(15):8647-8660. PubMed ID: 28911119
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Nuclear eIF4E Stimulates 3'-End Cleavage of Target RNAs.
    Davis MR; Delaleau M; Borden KLB
    Cell Rep; 2019 Apr; 27(5):1397-1408.e4. PubMed ID: 31042468
    [TBL] [Abstract][Full Text] [Related]  

  • 55. CSTF2-Induced Shortening of the
    Chen X; Zhang JX; Luo JH; Wu S; Yuan GJ; Ma NF; Feng Y; Cai MY; Chen RX; Lu J; Jiang LJ; Chen JW; Jin XH; Liu HL; Chen W; Guan XY; Kang TB; Zhou FJ; Xie D
    Cancer Res; 2018 Oct; 78(20):5848-5862. PubMed ID: 30143523
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Activation and repression of cellular immediate early genes by serum response factor cofactors.
    Lee SM; Vasishtha M; Prywes R
    J Biol Chem; 2010 Jul; 285(29):22036-49. PubMed ID: 20466732
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Different expression of immediate-early genes in the rat paraventricular nucleus induced by stress: relation to corticotropin-releasing factor gene transcription.
    Imaki T; Shibasaki T; Chikada N; Harada S; Naruse M; Demura H
    Endocr J; 1996 Dec; 43(6):629-38. PubMed ID: 9075602
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Alternative polyadenylation produces multiple 3' untranslated regions of odorant receptor mRNAs in mouse olfactory sensory neurons.
    Doulazmi M; Cros C; Dusart I; Trembleau A; Dubacq C
    BMC Genomics; 2019 Jul; 20(1):577. PubMed ID: 31299892
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Systematic profiling of poly(A)+ transcripts modulated by core 3' end processing and splicing factors reveals regulatory rules of alternative cleavage and polyadenylation.
    Li W; You B; Hoque M; Zheng D; Luo W; Ji Z; Park JY; Gunderson SI; Kalsotra A; Manley JL; Tian B
    PLoS Genet; 2015 Apr; 11(4):e1005166. PubMed ID: 25906188
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A pathway from leukemogenic oncogenes and stem cell chemokines to RNA processing via THOC5.
    Griaud F; Pierce A; Gonzalez Sanchez MB; Scott M; Abraham SA; Holyoake TL; Tran DD; Tamura T; Whetton AD
    Leukemia; 2013 Apr; 27(4):932-40. PubMed ID: 23032722
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.