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Items: 1 to 20 of 102

1.

A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.

Soldà G, Robusto M, Primignani P, Castorina P, Benzoni E, Cesarani A, Ambrosetti U, Asselta R, Duga S.

Hum Mol Genet. 2012 Feb 1;21(3):577-85. doi: 10.1093/hmg/ddr493. Epub 2011 Oct 28.

2.

A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.

Faletra F, Girotto G, D'Adamo AP, Vozzi D, Morgan A, Gasparini P.

Gene. 2014 Jan 25;534(2):236-9. doi: 10.1016/j.gene.2013.10.052. Epub 2013 Nov 6.

PMID:
24211385
3.

Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA.

Duan R, Pak C, Jin P.

Hum Mol Genet. 2007 May 1;16(9):1124-31. Epub 2007 Mar 30.

PMID:
17400653
4.

Genetic variation of miRNA sequence in pancreatic cancer.

Zhu Z, Gao W, Qian Z, Miao Y.

Acta Biochim Biophys Sin (Shanghai). 2009 May;41(5):407-13.

5.

miRNA mutations are not a common cause of deafness.

Hildebrand MS, Witmer PD, Xu S, Newton SS, Kahrizi K, Najmabadi H, Valle D, Smith RJ.

Am J Med Genet A. 2010 Mar;152A(3):646-52. doi: 10.1002/ajmg.a.33299.

6.

DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics.

Vona B, Hofrichter MA, Neuner C, Schröder J, Gehrig A, Hennermann JB, Kraus F, Shehata-Dieler W, Klopocki E, Nanda I, Haaf T.

Clin Genet. 2015;87(1):49-55. doi: 10.1111/cge.12332. Epub 2014 Jan 21.

7.

IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family.

Li-Yang MN, Shen XF, Wei QJ, Yao J, Lu YJ, Cao X, Xing GQ.

Chin Med J (Engl). 2015 Sep 20;128(18):2510-5. doi: 10.4103/0366-6999.164980.

8.

Intertwined pathways for Argonaute-mediated microRNA biogenesis in Drosophila.

Yang JS, Smibert P, Westholm JO, Jee D, Maurin T, Lai EC.

Nucleic Acids Res. 2014 Feb;42(3):1987-2002. doi: 10.1093/nar/gkt1038. Epub 2013 Nov 12.

9.

Novel TECTA mutations identified in stable sensorineural hearing loss and their clinical implications.

Kim AR, Chang MY, Koo JW, Oh SH, Choi BY.

Audiol Neurootol. 2015;20(1):17-25. doi: 10.1159/000366514. Epub 2014 Nov 19.

PMID:
25413827
10.

Discrimination of the expression of paralogous microRNA precursors that share the same major mature form.

Wang M, Wang W, Zhang P, Xiao J, Wang J, Huang C.

PLoS One. 2014 Mar 3;9(3):e90591. doi: 10.1371/journal.pone.0090591. eCollection 2014.

11.

Loop nucleotides control primary and mature miRNA function in target recognition and repression.

Yue SB, Trujillo RD, Tang Y, O'Gorman WE, Chen CZ.

RNA Biol. 2011 Nov-Dec;8(6):1115-23. doi: 10.4161/rna.8.6.17626.

12.

DDX6 post-transcriptionally down-regulates miR-143/145 expression through host gene NCR143/145 in cancer cells.

Iio A, Takagi T, Miki K, Naoe T, Nakayama A, Akao Y.

Biochim Biophys Acta. 2013 Oct;1829(10):1102-10. doi: 10.1016/j.bbagrm.2013.07.010. Epub 2013 Aug 9.

PMID:
23932921
13.

Conserved vertebrate mir-451 provides a platform for Dicer-independent, Ago2-mediated microRNA biogenesis.

Yang JS, Maurin T, Robine N, Rasmussen KD, Jeffrey KL, Chandwani R, Papapetrou EP, Sadelain M, O'Carroll D, Lai EC.

Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15163-8. doi: 10.1073/pnas.1006432107. Epub 2010 Aug 10.

14.

MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness.

Friedman LM, Avraham KB.

Mamm Genome. 2009 Sep-Oct;20(9-10):581-603. doi: 10.1007/s00335-009-9230-5. Epub 2009 Oct 30. Review.

PMID:
19876605
15.

The role of the precursor structure in the biogenesis of microRNA.

Starega-Roslan J, Koscianska E, Kozlowski P, Krzyzosiak WJ.

Cell Mol Life Sci. 2011 Sep;68(17):2859-71. doi: 10.1007/s00018-011-0726-2. Epub 2011 May 24. Review.

16.

Transcriptional, post-transcriptional and chromatin-associated regulation of pri-miRNAs, pre-miRNAs and moRNAs.

Nepal C, Coolen M, Hadzhiev Y, Cussigh D, Mydel P, Steen VM, Carninci P, Andersen JB, Bally-Cuif L, Müller F, Lenhard B.

Nucleic Acids Res. 2016 Apr 20;44(7):3070-81. doi: 10.1093/nar/gkv1354. Epub 2015 Dec 15.

17.

Developmentally regulated expression and complex processing of barley pri-microRNAs.

Kruszka K, Pacak A, Swida-Barteczka A, Stefaniak AK, Kaja E, Sierocka I, Karlowski W, Jarmolowski A, Szweykowska-Kulinska Z.

BMC Genomics. 2013 Jan 16;14:34. doi: 10.1186/1471-2164-14-34.

18.

The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation.

Zhou Y, Qing J, Dong Y, Nie J, Li J, Wang C, Liu Y, Peng T, Duan M, Liu X, Xie D.

Acta Otolaryngol. 2016;136(3):277-82. doi: 10.3109/00016489.2015.1109706. Epub 2015 Dec 4.

PMID:
26634621
19.

Small indels induced by CRISPR/Cas9 in the 5' region of microRNA lead to its depletion and Drosha processing retardance.

Jiang Q, Meng X, Meng L, Chang N, Xiong J, Cao H, Liang Z.

RNA Biol. 2014;11(10):1243-9. doi: 10.1080/15476286.2014.996067.

20.

A novel miRNA processing pathway independent of Dicer requires Argonaute2 catalytic activity.

Cifuentes D, Xue H, Taylor DW, Patnode H, Mishima Y, Cheloufi S, Ma E, Mane S, Hannon GJ, Lawson ND, Wolfe SA, Giraldez AJ.

Science. 2010 Jun 25;328(5986):1694-8. doi: 10.1126/science.1190809. Epub 2010 May 6.

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