209 related articles for article (PubMed ID: 28954229)
1. Microprocessor Recruitment to Elongating RNA Polymerase II Is Required for Differential Expression of MicroRNAs.
Church VA; Pressman S; Isaji M; Truscott M; Cizmecioglu NT; Buratowski S; Frolov MV; Carthew RW
Cell Rep; 2017 Sep; 20(13):3123-3134. PubMed ID: 28954229
[TBL] [Abstract][Full Text] [Related]
2. SRSF3 recruits DROSHA to the basal junction of primary microRNAs.
Kim K; Nguyen TD; Li S; Nguyen TA
RNA; 2018 Jul; 24(7):892-898. PubMed ID: 29615481
[TBL] [Abstract][Full Text] [Related]
3. Select amino acids in DGCR8 are essential for the UGU-pri-miRNA interaction and processing.
Dang TL; Le CT; Le MN; Nguyen TD; Nguyen TL; Bao S; Li S; Nguyen TA
Commun Biol; 2020 Jul; 3(1):344. PubMed ID: 32620823
[TBL] [Abstract][Full Text] [Related]
4. Microprocessor depends on hemin to recognize the apical loop of primary microRNA.
Nguyen TA; Park J; Dang TL; Choi YG; Kim VN
Nucleic Acids Res; 2018 Jun; 46(11):5726-5736. PubMed ID: 29750274
[TBL] [Abstract][Full Text] [Related]
5. The kinase ABL phosphorylates the microprocessor subunit DGCR8 to stimulate primary microRNA processing in response to DNA damage.
Tu CC; Zhong Y; Nguyen L; Tsai A; Sridevi P; Tarn WY; Wang JY
Sci Signal; 2015 Jun; 8(383):ra64. PubMed ID: 26126715
[TBL] [Abstract][Full Text] [Related]
6. Characterization of DGCR8/Pasha, the essential cofactor for Drosha in primary miRNA processing.
Yeom KH; Lee Y; Han J; Suh MR; Kim VN
Nucleic Acids Res; 2006; 34(16):4622-9. PubMed ID: 16963499
[TBL] [Abstract][Full Text] [Related]
7. Autoregulatory mechanisms controlling the microprocessor.
Triboulet R; Gregory RI
Adv Exp Med Biol; 2011; 700():56-66. PubMed ID: 21755473
[TBL] [Abstract][Full Text] [Related]
8. Functional Anatomy of the Human Microprocessor.
Nguyen TA; Jo MH; Choi YG; Park J; Kwon SC; Hohng S; Kim VN; Woo JS
Cell; 2015 Jun; 161(6):1374-87. PubMed ID: 26027739
[TBL] [Abstract][Full Text] [Related]
9. Primary microRNA processing is functionally coupled to RNAP II transcription in vitro.
Yin S; Yu Y; Reed R
Sci Rep; 2015 Jul; 5():11992. PubMed ID: 26149087
[TBL] [Abstract][Full Text] [Related]
10. HP1BP3, a Chromatin Retention Factor for Co-transcriptional MicroRNA Processing.
Liu H; Liang C; Kollipara RK; Matsui M; Ke X; Jeong BC; Wang Z; Yoo KS; Yadav GP; Kinch LN; Grishin NV; Nam Y; Corey DR; Kittler R; Liu Q
Mol Cell; 2016 Aug; 63(3):420-32. PubMed ID: 27425409
[TBL] [Abstract][Full Text] [Related]
11. N6-methyladenosine marks primary microRNAs for processing.
Alarcón CR; Lee H; Goodarzi H; Halberg N; Tavazoie SF
Nature; 2015 Mar; 519(7544):482-5. PubMed ID: 25799998
[TBL] [Abstract][Full Text] [Related]
12. SUMOylation at K707 of DGCR8 controls direct function of primary microRNA.
Zhu C; Chen C; Huang J; Zhang H; Zhao X; Deng R; Dou J; Jin H; Chen R; Xu M; Chen Q; Wang Y; Yu J
Nucleic Acids Res; 2015 Sep; 43(16):7945-60. PubMed ID: 26202964
[TBL] [Abstract][Full Text] [Related]
13. DGCR8-dependent efficient pri-miRNA processing of human pri-miR-9-2.
Nogami M; Miyamoto K; Hayakawa-Yano Y; Nakanishi A; Yano M; Okano H
J Biol Chem; 2021; 296():100409. PubMed ID: 33581109
[TBL] [Abstract][Full Text] [Related]
14. Human disease-associated single nucleotide polymorphism changes the orientation of DROSHA on pri-mir-146a.
Le CT; Nguyen TL; Nguyen TD; Nguyen TA
RNA; 2020 Dec; 26(12):1777-1786. PubMed ID: 32994184
[TBL] [Abstract][Full Text] [Related]
15. The DGCR8 RNA-binding heme domain recognizes primary microRNAs by clamping the hairpin.
Quick-Cleveland J; Jacob JP; Weitz SH; Shoffner G; Senturia R; Guo F
Cell Rep; 2014 Jun; 7(6):1994-2005. PubMed ID: 24910438
[TBL] [Abstract][Full Text] [Related]
16. MicroRNA biogenesis: isolation and characterization of the microprocessor complex.
Gregory RI; Chendrimada TP; Shiekhattar R
Methods Mol Biol; 2006; 342():33-47. PubMed ID: 16957365
[TBL] [Abstract][Full Text] [Related]
17. Dissection of the Caenorhabditis elegans Microprocessor.
Nguyen TL; Nguyen TD; Ngo MK; Nguyen TA
Nucleic Acids Res; 2023 Feb; 51(4):1512-1527. PubMed ID: 36598924
[TBL] [Abstract][Full Text] [Related]
18. Two MicroRNAs Are Sufficient for Embryonic Patterning in C. elegans.
Dexheimer PJ; Wang J; Cochella L
Curr Biol; 2020 Dec; 30(24):5058-5065.e5. PubMed ID: 33125867
[TBL] [Abstract][Full Text] [Related]
19. Pri-miRNA cleavage assays for the Microprocessor complex.
Le TN; Le CT; Nguyen TA
Methods Enzymol; 2023; 692():217-230. PubMed ID: 37925180
[TBL] [Abstract][Full Text] [Related]
20. The core microprocessor component DiGeorge syndrome critical region 8 (DGCR8) is a nonspecific RNA-binding protein.
Roth BM; Ishimaru D; Hennig M
J Biol Chem; 2013 Sep; 288(37):26785-99. PubMed ID: 23893406
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
