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Items: 1 to 20 of 50

1.

Primary microRNA precursor transcripts are localized at post-synaptic densities in adult mouse forebrain.

Lugli G, Larson J, Demars MP, Smalheiser NR.

J Neurochem. 2012 Nov;123(4):459-66. doi: 10.1111/j.1471-4159.2012.07921.x. Epub 2012 Sep 28.

2.

Expression of microRNAs and their precursors in synaptic fractions of adult mouse forebrain.

Lugli G, Torvik VI, Larson J, Smalheiser NR.

J Neurochem. 2008 Jul;106(2):650-61. doi: 10.1111/j.1471-4159.2008.05413.x. Epub 2008 Apr 12.

3.

Post-transcriptional control of DGCR8 expression by the Microprocessor.

Triboulet R, Chang HM, Lapierre RJ, Gregory RI.

RNA. 2009 Jun;15(6):1005-11. doi: 10.1261/rna.1591709. Epub 2009 Apr 21.

4.

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. Epub 2006 Sep 8.

5.

Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex.

Han J, Lee Y, Yeom KH, Nam JW, Heo I, Rhee JK, Sohn SY, Cho Y, Zhang BT, Kim VN.

Cell. 2006 Jun 2;125(5):887-901.

6.

Microprocessor dynamics and interactions at endogenous imprinted C19MC microRNA genes.

Bellemer C, Bortolin-Cavaillé ML, Schmidt U, Jensen SM, Kjems J, Bertrand E, Cavaillé J.

J Cell Sci. 2012 Jun 1;125(Pt 11):2709-20. doi: 10.1242/jcs.100354. Epub 2012 Mar 5.

7.

Primary microRNA processing assay reconstituted using recombinant Drosha and DGCR8.

Barr I, Guo F.

Methods Mol Biol. 2014;1095:73-86. doi: 10.1007/978-1-62703-703-7_5.

8.

Processing of microRNA primary transcripts requires heme in mammalian cells.

Weitz SH, Gong M, Barr I, Weiss S, Guo F.

Proc Natl Acad Sci U S A. 2014 Feb 4;111(5):1861-6. doi: 10.1073/pnas.1309915111. Epub 2014 Jan 21.

9.

MicroRNA-206 is overexpressed in the diaphragm but not the hindlimb muscle of mdx mouse.

McCarthy JJ, Esser KA, Andrade FH.

Am J Physiol Cell Physiol. 2007 Jul;293(1):C451-7. Epub 2007 Apr 25.

10.

Rare Drosha splice variants are deficient in microRNA processing but do not affect general microRNA expression in cancer cells.

Grund SE, Polycarpou-Schwarz M, Luo C, Eichmüller SB, Diederichs S.

Neoplasia. 2012 Mar;14(3):238-48.

11.

The nuclear RNase III Drosha initiates microRNA processing.

Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Rådmark O, Kim S, Kim VN.

Nature. 2003 Sep 25;425(6956):415-9.

12.

Drosha in primary microRNA processing.

Lee Y, Han J, Yeom KH, Jin H, Kim VN.

Cold Spring Harb Symp Quant Biol. 2006;71:51-7. Review.

PMID:
17381280
13.

Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences.

Zeng Y, Cullen BR.

J Biol Chem. 2005 Jul 29;280(30):27595-603. Epub 2005 Jun 1.

14.
15.

Smad proteins bind a conserved RNA sequence to promote microRNA maturation by Drosha.

Davis BN, Hilyard AC, Nguyen PH, Lagna G, Hata A.

Mol Cell. 2010 Aug 13;39(3):373-84. doi: 10.1016/j.molcel.2010.07.011.

16.

In vitro and in vivo assays for the activity of Drosha complex.

Lee Y, Kim VN.

Methods Enzymol. 2007;427:89-106.

PMID:
17720480
17.

The NF90-NF45 complex functions as a negative regulator in the microRNA processing pathway.

Sakamoto S, Aoki K, Higuchi T, Todaka H, Morisawa K, Tamaki N, Hatano E, Fukushima A, Taniguchi T, Agata Y.

Mol Cell Biol. 2009 Jul;29(13):3754-69. doi: 10.1128/MCB.01836-08. Epub 2009 Apr 27.

18.

Alternative splicing affects the subcellular localization of Drosha.

Link S, Grund SE, Diederichs S.

Nucleic Acids Res. 2016 Jun 20;44(11):5330-43. doi: 10.1093/nar/gkw400. Epub 2016 May 16.

19.

MicroRNA biogenesis: isolation and characterization of the microprocessor complex.

Gregory RI, Chendrimada TP, Shiekhattar R.

Methods Mol Biol. 2006;342:33-47. Review.

PMID:
16957365
20.

Drosha versus ADAR: wrangling over pri-miRNA.

O'Connell MA, Keegan LP.

Nat Struct Mol Biol. 2006 Jan;13(1):3-4.

PMID:
16395313

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