|1.||Holme, E: 2 articles (12/2003 - 04/2003)|
|2.||Tulinius, M: 2 articles (12/2003 - 04/2003)|
|3.||Moslemi, A-R: 2 articles (12/2003 - 04/2003)|
|4.||Oldfors, A: 2 articles (12/2003 - 04/2003)|
|5.||Darin, N: 2 articles (12/2003 - 04/2003)|
|6.||Le, Han-Bo: 1 article (01/2015)|
|7.||Chen, Zhi-Jun: 1 article (01/2015)|
|8.||Wang, Lie: 1 article (01/2015)|
|9.||Zhang, Yong-Kui: 1 article (01/2015)|
|10.||Mayr, Johannes A: 1 article (08/2013)|
03/01/2008 - "In this study, we examined the roles of AT synthesis and tRNA(Trp) charging in mediating physiological responses to tryptophan starvation. "
06/01/1984 - "Consistent with this conclusion is the observation that when tryptophan starvation was sufficient to relieve repression 50 to 60%, 65% of the tRNATrp of the bacterium was charged. "
|2.||Mitochondrial Myopathies (Mitochondrial Myopathy)
08/01/2013 - "Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene."
06/01/1998 - "We detected a novel pathogenic mutation, a G-->A transition at position 5521 of mitochondrial tRNA(Trp) gene, in association with familial late-onset mitochondrial myopathy. "
02/01/2005 - "The mutation in patient 1 (T5543C) was associated with isolated mitochondrial myopathy, and occurred in the anticodon loop of tRNA(Trp). "
06/01/1998 - "A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene."
|3.||Leigh Disease (Leigh's Disease)
07/01/2009 - "Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndrome."
12/01/2003 - "SURF1-mutations were identified in three out of four cases with Leigh syndrome while a mutation in the mitochondrial tRNA (trp) gene was identified in the fourth. "
04/01/2003 - "Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene."
04/01/2003 - "We report a nine-year-old boy with the features of Leigh syndrome (LS) and a severe cytochrome-c oxidase (COX) deficiency with a single thymidine insertion at nucleotide position 5537 (T 5537i) in the tRNA Trp gene of mitochondrial DNA. "
07/01/2009 - "We sequenced the encoded complex I units: ND2, ND3, ND4, ND5 and ND6 genes and the mitochondrial ATPase 6, tRNA(Val), tRNA(Leu(UUR)), tRNA(Trp) and tRNA(Lys) genes in 10 unrelated patients with Leigh syndrome. "
|4.||Cytochrome-c Oxidase Deficiency
|5.||Spinocerebellar Ataxias (Spinocerebellar Ataxia)
|2.||Transfer RNA (tRNA)
|4.||Mitochondrial DNA (mtDNA)
|6.||Val Transfer RNA
|7.||Tyr Transfer RNA
|8.||Ser Transfer RNA
|9.||Lys Transfer RNA
|10.||Leu Transfer RNA