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Items: 14

1.

Disruption in A-to-I Editing Levels Affects C. elegans Development More Than a Complete Lack of Editing.

Ganem NS, Ben-Asher N, Manning AC, Deffit SN, Washburn MC, Wheeler EC, Yeo GW, Zgayer OB, Mantsur E, Hundley HA, Lamm AT.

Cell Rep. 2019 Apr 23;27(4):1244-1253.e4. doi: 10.1016/j.celrep.2019.03.095.

2.

A-to-I RNA Editing Affects lncRNAs Expression after Heat Shock.

Haas R, Ganem NS, Keshet A, Orlov A, Fishman A, Lamm AT.

Genes (Basel). 2018 Dec 13;9(12). pii: E627. doi: 10.3390/genes9120627.

3.

Escherichia coli mediated resistance of Entamoeba histolytica to oxidative stress is triggered by oxaloacetate.

Shaulov Y, Shimokawa C, Trebicz-Geffen M, Nagaraja S, Methling K, Lalk M, Weiss-Cerem L, Lamm AT, Hisaeda H, Ankri S.

PLoS Pathog. 2018 Oct 11;14(10):e1007295. doi: 10.1371/journal.ppat.1007295. eCollection 2018 Oct.

4.

QsRNA-seq: a method for high-throughput profiling and quantifying small RNAs.

Fishman A, Light D, Lamm AT.

Genome Biol. 2018 Aug 14;19(1):113. doi: 10.1186/s13059-018-1495-0.

5.

In cancer, A-to-I RNA editing can be the driver, the passenger, or the mechanic.

Ganem NS, Ben-Asher N, Lamm AT.

Drug Resist Updat. 2017 May;32:16-22. doi: 10.1016/j.drup.2017.09.001. Epub 2017 Oct 4. Review.

PMID:
29145975
6.

A-to-I RNA editing - thinking beyond the single nucleotide.

Ganem NS, Lamm AT.

RNA Biol. 2017 Dec 2;14(12):1690-1694. doi: 10.1080/15476286.2017.1364830. Epub 2017 Oct 11. Review.

7.

A-to-I RNA editing promotes developmental stage-specific gene and lncRNA expression.

Goldstein B, Agranat-Tamir L, Light D, Ben-Naim Zgayer O, Fishman A, Lamm AT.

Genome Res. 2017 Mar;27(3):462-470. doi: 10.1101/gr.211169.116. Epub 2016 Dec 28.

8.

Function of cancer associated genes revealed by modern univariate and multivariate association tests.

Gorfine M, Goldstein B, Fishman A, Heller R, Heller Y, Lamm AT.

PLoS One. 2015 May 12;10(5):e0126544. doi: 10.1371/journal.pone.0126544. eCollection 2015.

9.

Co-option of the piRNA pathway for germline-specific alternative splicing of C. elegans TOR.

Barberán-Soler S, Fontrodona L, Ribó A, Lamm AT, Iannone C, Cerón J, Lehner B, Valcárcel J.

Cell Rep. 2014 Sep 25;8(6):1609-1616. doi: 10.1016/j.celrep.2014.08.016. Epub 2014 Sep 15.

10.

BAF-1 mobility is regulated by environmental stresses.

Bar DZ, Davidovich M, Lamm AT, Zer H, Wilson KL, Gruenbaum Y.

Mol Biol Cell. 2014 Apr;25(7):1127-36. doi: 10.1091/mbc.E13-08-0477. Epub 2014 Feb 5.

11.

Ce-emerin and LEM-2: essential roles in Caenorhabditis elegans development, muscle function, and mitosis.

Barkan R, Zahand AJ, Sharabi K, Lamm AT, Feinstein N, Haithcock E, Wilson KL, Liu J, Gruenbaum Y.

Mol Biol Cell. 2012 Feb;23(4):543-52. doi: 10.1091/mbc.E11-06-0505. Epub 2011 Dec 14.

12.

Competition between ADAR and RNAi pathways for an extensive class of RNA targets.

Wu D, Lamm AT, Fire AZ.

Nat Struct Mol Biol. 2011 Sep 11;18(10):1094-101. doi: 10.1038/nsmb.2129.

13.

Multimodal RNA-seq using single-strand, double-strand, and CircLigase-based capture yields a refined and extended description of the C. elegans transcriptome.

Lamm AT, Stadler MR, Zhang H, Gent JI, Fire AZ.

Genome Res. 2011 Feb;21(2):265-75. doi: 10.1101/gr.108845.110. Epub 2010 Dec 22.

14.

Distinct phases of siRNA synthesis in an endogenous RNAi pathway in C. elegans soma.

Gent JI, Lamm AT, Pavelec DM, Maniar JM, Parameswaran P, Tao L, Kennedy S, Fire AZ.

Mol Cell. 2010 Mar 12;37(5):679-89. doi: 10.1016/j.molcel.2010.01.012. Epub 2010 Jan 28.

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