Pathology-related substitutions in human mitochondrial tRNA Ile reduce precursor 3′ end processing efficiency in vitro

By Levinger L.   Giegé R.   Florentz C.  

Nucleic Acids Research, Vol. 31, Iss. 7, 2003-04 ,pp. : 1904-1912

Oxford University Press

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Long 5" leaders inhibit removal of a 3" trailer from a precursor tRNA by mammalian tRNA 3" processing endoribonuclease

By Nashimoto Masayuki   Wesemann Duane R.   Geary Susanna   Tamura Masato   Kaspar Roger L.   Sprague K.U.   Westaway S.K.   Altman S.   Deutscher M.P.   Zasloff M.   Thomann H.-U.   Nashimoto M.   Nashimoto M.   Frendewey D.   Levinger L.   Solari A.   Engelke D.R.   Garber R.L.   Castano J.G.   O’Connor J.P.   Nashimoto M.   Nashimoto M.   Nashimoto M.   Nashimoto M.   Vnencak-Jones   Nashimoto M.   Guo Q.  

Nucleic Acids Research, Vol. 27, Iss. 13, 1999-07 ,pp. : 2770-2776

Oxford University Press

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In vitro 3′-end endonucleolytic processing defect in a human mitochondrial tRNA Ser(UCN) precursor with the U7445C substitution, which causes non-syndromic deafness

By Levinger L.   Jacobs O.   James M.  

Nucleic Acids Research, Vol. 29, Iss. 21, 2001-11 ,pp. : 4334-4340

Oxford University Press

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Characterization of Human Mitochondrial RNase P: Novel Aspects in tRNA Processing

By Rossmanith W.   Karwan R.M.  

Biochemical and Biophysical Research Communications, Vol. 247, Iss. 2, 1998-06 ,pp. : 234-241

Elsevier

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Mitochondrial tRNA 3′ end metabolism and human disease

By Levinger Louis  

Nucleic Acids Research, Vol. 32, Iss. 18, 2004-01 ,pp. : 5430-5441

Oxford University Press

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