Suzuki T - Search Results

1

Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome.

Limongelli A, Schaefer J, Jackson S, Invernizzi F, Kirino Y, Suzuki T, Reichmann H, Zeviani M. Limongelli A, et al. Among authors: suzuki t. J Med Genet. 2004 May;41(5):342-9. doi: 10.1136/jmg.2003.016048. J Med Genet. 2004. PMID: 15121771 Free PMC article.

2

Regulation of X11L-dependent amyloid precursor protein metabolism by XB51, a novel X11L-binding protein.

Lee DS, Tomita S, Kirino Y, Suzuki T. Lee DS, et al. Among authors: suzuki t. J Biol Chem. 2000 Jul 28;275(30):23134-8. doi: 10.1074/jbc.C000302200. J Biol Chem. 2000. PMID: 10833507 Free article.

3

Decoding property of C5 uridine modification at the wobble position of tRNA anticodon.

Kurata S, Ohtsuki T, Wada T, Kirino Y, Takai K, Saigo K, Watanabe K, Suzuki T. Kurata S, et al. Among authors: suzuki t. Nucleic Acids Res Suppl. 2003;(3):245-6. doi: 10.1093/nass/3.1.245. Nucleic Acids Res Suppl. 2003. PMID: 14510472

4

Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease.

Kirino Y, Yasukawa T, Ohta S, Akira S, Ishihara K, Watanabe K, Suzuki T. Kirino Y, et al. Among authors: suzuki t. Proc Natl Acad Sci U S A. 2004 Oct 19;101(42):15070-5. doi: 10.1073/pnas.0405173101. Epub 2004 Oct 11. Proc Natl Acad Sci U S A. 2004. PMID: 15477592 Free PMC article.

5

Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.

Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T. Kirino Y, et al. Among authors: suzuki t. Proc Natl Acad Sci U S A. 2005 May 17;102(20):7127-32. doi: 10.1073/pnas.0500563102. Epub 2005 May 3. Proc Natl Acad Sci U S A. 2005. PMID: 15870203 Free PMC article.

6

Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases.

Yasukawa T, Kirino Y, Ishii N, Holt IJ, Jacobs HT, Makifuchi T, Fukuhara N, Ohta S, Suzuki T, Watanabe K. Yasukawa T, et al. Among authors: suzuki t. FEBS Lett. 2005 May 23;579(13):2948-52. doi: 10.1016/j.febslet.2005.04.038. FEBS Lett. 2005. PMID: 15893315 Free article.

7

Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.

Kirino Y, Yasukawa T, Marjavaara SK, Jacobs HT, Holt IJ, Watanabe K, Suzuki T. Kirino Y, et al. Among authors: suzuki t. Hum Mol Genet. 2006 Mar 15;15(6):897-904. doi: 10.1093/hmg/ddl007. Epub 2006 Jan 30. Hum Mol Genet. 2006. PMID: 16446307

8

Biosynthesis of wybutosine, a hyper-modified nucleoside in eukaryotic phenylalanine tRNA.

Noma A, Kirino Y, Ikeuchi Y, Suzuki T. Noma A, et al. Among authors: suzuki t. EMBO J. 2006 May 17;25(10):2142-54. doi: 10.1038/sj.emboj.7601105. Epub 2006 Apr 27. EMBO J. 2006. PMID: 16642040 Free PMC article.

9

Human mitochondrial diseases associated with tRNA wobble modification deficiency.

Kirino Y, Suzuki T. Kirino Y, et al. Among authors: suzuki t. RNA Biol. 2005 Apr;2(2):41-4. doi: 10.4161/rna.2.2.1610. Epub 2005 Apr 14. RNA Biol. 2005. PMID: 17132941 Free article. Review.

10

Reversible infantile respiratory chain deficiency: a clinical and molecular study.

Mimaki M, Hatakeyama H, Komaki H, Yokoyama M, Arai H, Kirino Y, Suzuki T, Nishino I, Nonaka I, Goto Y. Mimaki M, et al. Among authors: suzuki t. Ann Neurol. 2010 Dec;68(6):845-54. doi: 10.1002/ana.22111. Ann Neurol. 2010. PMID: 21194154

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