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Items: 8

1.

Coding of Class I and II Aminoacyl-tRNA Synthetases.

Carter CW Jr.

Adv Exp Med Biol. 2017;966:103-148. doi: 10.1007/5584_2017_93.

2.

The phenotypic expression of mitochondrial tRNA-mutations can be modulated by either mitochondrial leucyl-tRNA synthetase or the C-terminal domain thereof.

Giordano C, Morea V, Perli E, d'Amati G.

Front Genet. 2015 Mar 23;6:113. doi: 10.3389/fgene.2015.00113. eCollection 2015.

3.

The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells.

Perli E, Giordano C, Pisano A, Montanari A, Campese AF, Reyes A, Ghezzi D, Nasca A, Tuppen HA, Orlandi M, Di Micco P, Poser E, Taylor RW, Colotti G, Francisci S, Morea V, Frontali L, Zeviani M, d'Amati G.

EMBO Mol Med. 2014 Feb;6(2):169-82. doi: 10.1002/emmm.201303198. Epub 2014 Jan 10.

4.

Emergence of the universal genetic code imprinted in an RNA record.

Hohn MJ, Park HS, O'Donoghue P, Schnitzbauer M, Söll D.

Proc Natl Acad Sci U S A. 2006 Nov 28;103(48):18095-100. Epub 2006 Nov 16.

5.

Mammalian polypeptide chain release factor and tryptophanyl-tRNA synthetase are distinct proteins.

Frolova LYu, Dalphin ME, Justesen J, Powell RJ, Drugeon G, McCaughan KK, Kisselev LL, Tate WP, Haenni AL.

EMBO J. 1993 Oct;12(10):4013-9.

6.
7.

Evolution and relatedness in two aminoacyl-tRNA synthetase families.

Nagel GM, Doolittle RF.

Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):8121-5.

8.

Editing of errors in selection of amino acids for protein synthesis.

Jakubowski H, Goldman E.

Microbiol Rev. 1992 Sep;56(3):412-29. Review.

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