Papers associated with adar

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	The cytoplasm of Xenopus oocytes contains a factor that protects double-stranded RNA from adenosine-to-inosine modification., Saccomanno L, Bass BL., Mol Cell Biol. August 1, 1994; 14 (8): 5425-32.
	Deamination of mammalian glutamate receptor RNA by Xenopus dsRNA adenosine deaminase: similarities to in vivo RNA editing., Hurst SR, Hough RF, Aruscavage PJ, Bass BL., RNA. December 1, 1995; 1 (10): 1051-60.
	RNA editing of hepatitis delta virus antigenome by dsRNA-adenosine deaminase., Polson AG, Bass BL, Casey JL., Nature. April 4, 1996; 380 (6573): 454-6.
	Analysis of Xenopus dsRNA adenosine deaminase cDNAs reveals similarities to DNA methyltransferases., Hough RF, Bass BL., RNA. April 1, 1997; 3 (4): 356-70.
	The double-stranded RNA-binding domains of Xenopus laevis ADAR1 exhibit different RNA-binding behaviors., Brooks R, Eckmann CR, Jantsch MF., FEBS Lett. August 28, 1998; 434 (1-2): 121-6.
	A minor fraction of basic fibroblast growth factor mRNA is deaminated in Xenopus stage VI and matured oocytes., Saccomanno L, Bass BL., RNA. January 1, 1999; 5 (1): 39-48.
	The RNA-editing enzyme ADAR1 is localized to the nascent ribonucleoprotein matrix on Xenopus lampbrush chromosomes but specifically associates with an atypical loop., Eckmann CR, Jantsch MF., J Cell Biol. February 22, 1999; 144 (4): 603-15.
	The importance of internal loops within RNA substrates of ADAR1., Lehmann KA, Bass BL., J Mol Biol. August 6, 1999; 291 (1): 1-13.
	Double-stranded RNA adenosine deaminases ADAR1 and ADAR2 have overlapping specificities., Lehmann KA, Bass BL., Biochemistry. October 24, 2000; 39 (42): 12875-84.
	The human but not the Xenopus RNA-editing enzyme ADAR1 has an atypical nuclear localization signal and displays the characteristics of a shuttling protein., Eckmann CR, Neunteufl A, Pfaffstetter L, Jantsch MF., Mol Biol Cell. July 1, 2001; 12 (7): 1911-24.
	Nucleocytoplasmic distribution of human RNA-editing enzyme ADAR1 is modulated by double-stranded RNA-binding domains, a leucine-rich export signal, and a putative dimerization domain., Strehblow A, Hallegger M, Jantsch MF., Mol Biol Cell. November 1, 2002; 13 (11): 3822-35.
	Distinct in vivo roles for double-stranded RNA-binding domains of the Xenopus RNA-editing enzyme ADAR1 in chromosomal targeting., Doyle M, Jantsch MF., J Cell Biol. April 28, 2003; 161 (2): 309-19.
	The RISC subunit Tudor-SN binds to hyper-edited double-stranded RNA and promotes its cleavage., Scadden AD., Nat Struct Mol Biol. June 1, 2005; 12 (6): 489-96.
	Chromosomal storage of the RNA-editing enzyme ADAR1 in Xenopus oocytes., Sallacz NB, Jantsch MF., Mol Biol Cell. July 1, 2005; 16 (7): 3377-86.
	Cleavage of dsRNAs hyper-edited by ADARs occurs at preferred editing sites., Scadden AD, O'Connell MA., Nucleic Acids Res. October 27, 2005; 33 (18): 5954-64.
	RNA aptamers binding the double-stranded RNA-binding domain., Hallegger M, Taschner A, Jantsch MF., RNA. November 1, 2006; 12 (11): 1993-2004.
	SINE RNA induces severe developmental defects in Arabidopsis thaliana and interacts with HYL1 (DRB1), a key member of the DCL1 complex., Pouch-Pélissier MN, Pélissier T, Elmayan T, Vaucheret H, Boko D, Jantsch MF, Deragon JM., PLoS Genet. June 13, 2008; 4 (6): e1000096.
	A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing., Zaranek AW, Levanon EY, Zecharia T, Clegg T, Church GM., PLoS Genet. May 20, 2010; 6 (5): e1000954.
	Conserved microRNA editing in mammalian evolution, development and disease., Warnefors M, Liechti A, Halbert J, Valloton D, Kaessmann H., Genome Biol. June 25, 2014; 15 (6): R83.
	Evidence for multiple, distinct ADAR-containing complexes in Xenopus laevis., Schweidenback CT, Emerman AB, Jambhekar A, Blower MD., RNA. February 1, 2015; 21 (2): 279-95.
	Identification of Plasmodium falciparum Translation Initiation eIF2β Subunit: Direct Interaction with Protein Phosphatase Type 1., Tellier G, Lenne A, Cailliau-Maggio K, Cabezas-Cruz A, Valdés JJ, Martoriati A, Aliouat el M, Gosset P, Delaire B, Fréville A, Pierrot C, Khalife J., Front Microbiol. May 26, 2016; 7 777.
	Massive A-to-I RNA editing is common across the Metazoa and correlates with dsRNA abundance., Porath HT, Knisbacher BA, Eisenberg E, Levanon EY., Genome Biol. October 2, 2017; 18 (1): 185.
	Direct identification of A-to-I editing sites with nanopore native RNA sequencing., Nguyen TA, Heng JWJ, Kaewsapsak P, Kok EPL, Stanojević D, Liu H, Cardilla A, Praditya A, Yi Z, Lin M, Aw JGA, Ho YY, Peh KLE, Wang Y, Zhong Q, Heraud-Farlow J, Xue S, Reversade B, Walkley C, Ho YS, Šikić M, Wan Y, Tan MH., Nat Methods. July 1, 2022; 19 (7): 833-844.
	Deep transcriptome profiling reveals limited conservation of A-to-I RNA editing in Xenopus., Nguyen TA, Heng JWJ, Ng YT, Sun R, Fisher S, Oguz G, Kaewsapsak P, Xue S, Reversade B, Ramasamy A, Eisenberg E, Tan MH., BMC Biol. November 9, 2023; 21 (1): 251.

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