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Items: 10

1.

Losing the stem-loop structure from metazoan mitochondrial tRNAs and co-evolution of interacting factors.

Watanabe Y, Suematsu T, Ohtsuki T.

Front Genet. 2014 May 1;5:109. doi: 10.3389/fgene.2014.00109. eCollection 2014. Review.

2.

A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome.

Rivera H, Martín-Hernández E, Delmiro A, García-Silva MT, Quijada-Fraile P, Muley R, Arenas J, Martín MA, Martínez-Azorín F.

BMC Nephrol. 2013 Sep 13;14:195. doi: 10.1186/1471-2369-14-195.

3.

tRNA Modification and Genetic Code Variations in Animal Mitochondria.

Watanabe K, Yokobori S.

J Nucleic Acids. 2011;2011:623095. doi: 10.4061/2011/623095. Epub 2011 Oct 9.

4.

Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

Belostotsky R, Ben-Shalom E, Rinat C, Becker-Cohen R, Feinstein S, Zeligson S, Segel R, Elpeleg O, Nassar S, Frishberg Y.

Am J Hum Genet. 2011 Feb 11;88(2):193-200. doi: 10.1016/j.ajhg.2010.12.010. Epub 2011 Jan 20.

6.
7.

Post-transcriptional nucleotide modification and alternative folding of RNA.

Helm M.

Nucleic Acids Res. 2006 Feb 1;34(2):721-33. Print 2006. Review. Erratum in: Nucleic Acids Res. 2007;35(20):7041.

8.

Dual-mode recognition of noncanonical tRNAs(Ser) by seryl-tRNA synthetase in mammalian mitochondria.

Chimnaronk S, Gravers Jeppesen M, Suzuki T, Nyborg J, Watanabe K.

EMBO J. 2005 Oct 5;24(19):3369-79. Epub 2005 Sep 15.

9.

Mitochondrial tRNA 3' end metabolism and human disease.

Levinger L, Mörl M, Florentz C.

Nucleic Acids Res. 2004 Oct 11;32(18):5430-41. Print 2004. Review.

10.

Changing identities: tRNA duplication and remolding within animal mitochondrial genomes.

Rawlings TA, Collins TM, Bieler R.

Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15700-5. Epub 2003 Dec 12.

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