|1.||Li, Zongbin: 4 articles (10/2014 - 03/2008)|
|2.||Liu, Yuqi: 4 articles (10/2014 - 03/2008)|
|3.||Taylor, Robert W: 4 articles (07/2013 - 10/2002)|
|4.||Guan, Min-Xin: 4 articles (06/2013 - 03/2008)|
|5.||Yang, Li: 3 articles (04/2011 - 03/2008)|
|6.||Guan, Minxin: 2 articles (10/2014 - 01/2014)|
|7.||Gao, Jinliao: 2 articles (10/2014 - 01/2014)|
|8.||Zhu, Chao: 2 articles (10/2014 - 01/2014)|
|9.||Nuoffer, J-M: 2 articles (10/2014 - 05/2011)|
|10.||Lan, Yunfeng: 2 articles (10/2014 - 01/2014)|
|1.||Chronic Progressive External Ophthalmoplegia (Progressive External Ophthalmoplegia)
10/01/2014 - "Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype."
05/01/2011 - "Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia."
01/15/2011 - "A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia."
03/01/2010 - "A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)."
11/01/2007 - "Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle."
|2.||Cytochrome-c Oxidase Deficiency
|3.||Mitochondrial Encephalomyopathies (Mitochondrial Encephalomyopathy)
08/01/1995 - "Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural study."
08/01/1995 - "This is the first report with histochemical and immunohistochemical techniques of an autopsy case with mitochondrial encephalomyopathy caused by the mitochondrial tRNA(Ile) (nt4269) A to G mutation showing focal cytochrome c oxidase (COX) deficiency of neuronal cells. "
02/04/1998 - "We report a new mutation, a G to A transition at nucleotide position 4298 within the mitochondrial tRNA(Ile) gene in a patient with chronic progressive external ophthalmoplegia and multiple sclerosis. "
02/04/1998 - "A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis."
03/01/2004 - "The A4269G mutation in the human mitochondrial (mt) tRNA(Ile) gene is associated with fatal cardiomyopathy. "
03/01/1998 - "Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene."
07/15/1992 - "Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy."
07/01/2013 - "We describe the morphologic, biochemical, and molecular features of hearts from 3 transplanted patients with isolated mitochondrial cardiomyopathy caused by homoplasmic mutations in the MTTI gene, coding for mitochondrial isoleucine tRNA (mt-tRNA(Ile)). "
06/01/2009 - "We have studied a homoplasmic mtDNA mutation in the tRNA(Ile) gene that segregates exclusively with cardiomyopathy in two unrelated families. "
|1.||Mitochondrial DNA (mtDNA)
|2.||Transfer RNA (tRNA)
|3.||Val Transfer RNA
|4.||Tyr Transfer RNA
|5.||Gln Transfer RNA
|6.||Leu Transfer RNA
|8.||12S ribosomal RNA
|10.||Small Interfering RNA (siRNA)