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Mutational analysis of mitochondrial tRNA genes in patients with lung cancer

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van der Aalst CM, Ten Haaf K, de Koning HJ. Lung cancer screening: Latest development and unanswered questions. Lancet Respir Med. 2016; 4(9): 749-761.van der AalstCM,Ten HaafK,de KoningHJ.Lung cancer screening: Latest development and unanswered questionsLancet Respir Med20164974976110.1016/S2213-2600(16)30200-4Search in Google Scholar

Mao Y, Yang D, He J, Krasna MJ. Epidemiology of lung cancer. Surg Oncol Clin N Am. 2016; 25(3): 439-445.MaoY,YangD,HeJ,KrasnaMJ.Epidemiology of lung cancerSurg Oncol Clin N Am201625343944510.1016/j.soc.2016.02.001Search in Google Scholar

Green DR, Galluzzi L, Kroemer G. Mitochondria and the autophagy-inflammation-cell death axis in organismal aging. Science. 2011; 333(6046): 1109-1112.GreenDR,GalluzziL,KroemerG.Mitochondria and the autophagy-inflammation-cell death axis in organismal agingScience201133360461109111210.1126/science.1201940Search in Google Scholar

Soysal D, Krzildağ S, Saatli B, Posaci C, Soysal S, Koyuncuoglu M, et al. A novel angiogenesis inhibitor bevacizumab induces apoptosis in the rat endometriosis model. Balkan J Med Genet. 2015; 17(2): 73-80.SoysalD,KrzildağS,SaatliB,PosaciC,SoysalS,KoyuncuogluM,et alA novel angiogenesis inhibitor bevacizumab induces apoptosis in the rat endometriosis modelBalkan J Med Genet2015172738010.2478/bjmg-2014-0077Search in Google Scholar

Lu J, Sharma LK, Bai Y. Implications of mitochondrial DNA mutations and mitochondrial dysfunction in tumorigenesis. Cell Res. 2009; 19(7): 802-815.LuJ,SharmaLK,BaiY.Implications of mitochondrial DNA mutations and mitochondrial dysfunction in tumorigenesisCell Res200919780281510.1038/cr.2009.69Search in Google Scholar

Wallace DC. Mitochondrial DNA variation in human radiation and disease. Cell. 2015; 163(1): 33-38.WallaceDC.Mitochondrial DNA variation in human radiation and diseaseCell20151631333810.1016/j.cell.2015.08.067Search in Google Scholar

Kara M, Tatar A, Borekci B, Dagli F, Oztas S. Mitochondrial DNA4977 bp deletion in chronic cervicitis and cervix cancers. Balkan J Med Genet. 2012; 15(1): 25-29.KaraM,TatarA,BorekciB,DagliF,OztasS.Mitochondrial DNA4977 bp deletion in chronic cervicitis and cervix cancersBalkan J Med Genet2012151252910.2478/v10034-012-0004-0Search in Google Scholar

Abbott JA, Francklyn CS, Robey-Bond SM. Transfer RNA and human disease. Front Genet. 2014; 5:158. doi: 10.3389/fgene.2014.00158.AbbottJA,FrancklynCS,Robey-BondSM.Transfer RNA and human diseaseFront Genet20145158doi: 10.3389/fgene.2014.00158Open DOISearch in Google Scholar

Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet. 1999; 23(2):147.AndrewsRM,KubackaI,ChinneryPF,LightowlersRN,TurnbullDM,HowellN.Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNANat Genet199923214710.1038/13779Search in Google Scholar

McFarland R, Elson JL, Taylor RW, Howell N, Turnbull DM. Assigning pathogenicity to mitochondrial tRNA mutations: When “definitely maybe” is not good enough. Trends Genet. 2004; 20(12): 591-596.McFarlandR,ElsonJL,TaylorRW,HowellN,TurnbullDM.Assigning pathogenicity to mitochondrial tRNA mutations: When “definitely maybe” is not good enoughTrends Genet2004201259159610.1016/j.tig.2004.09.014Search in Google Scholar

Yarham JW, Al-Dosary M, Blakely EL, Alston CL, Taylor RW, Elson JL, et al. A comparative analysis approach to determining the pathogenicity of mitochondrial tRNAmutations. Hum Mutat. 2011; 32(11): 1319-1325.YarhamJW,Al-DosaryM,BlakelyEL,AlstonCL,TaylorRW,ElsonJL,et alA comparative analysis approach to determining the pathogenicity of mitochondrial tRNAmutationsHum Mutat201132111319132510.1002/humu.21575Search in Google Scholar

Didkowska J, Wojciechowska U, Manczuk M, Lobaszewski J. Lung cancer epidemiology: Contemporary and future challenges worldwide. Ann Transl Med. 2016; 4(8): 150. doi: 10.21037/atm.2016.03.11.DidkowskaJ,WojciechowskaU,ManczukM,LobaszewskiJ.Lung cancer epidemiology: Contemporary and future challenges worldwideAnn Transl Med201648150doi: 10.21037/atm.2016.03.11Open DOISearch in Google Scholar

Yarham JW, Elson JL, Blakely EL, McFarland R, Taylor RW. Mitochondrial tRNA mutations and disease. Wiley Interdiscip Rev RNA. 2010; 1(2): 304-324.YarhamJW,ElsonJL,BlakelyEL,McFarlandR,TaylorRW.Mitochondrial tRNA mutations and diseaseWiley Interdiscip Rev RNA20101230432410.1002/wrna.27Search in Google Scholar

Lv F, Qian G, You W, Lin H, Wang XF, Qiu GS, et al. Variants in mitochondrial tRNA gene may not be associated with thyroid carcinoma. Balkan J Med Genet. 2015; 18(2): 59-64.LvF,QianG,YouW,LinH,WangXF,QiuGS,et alVariants in mitochondrial tRNA gene may not be associated with thyroid carcinomaBalkan J Med Genet2015182596410.1515/bjmg-2015-0090Search in Google Scholar

Jiang P, Wang M, Xue L, Xiao Y, Yu J, Wang H, et al. A hypertension-associated tRNAAla mutation alters the tRNA metabolism and mitochondrial function. Mol Cell Biol. 2016; 36(14): 1920-1930.JiangP,WangM,XueL,XiaoY,YuJ,WangH,et alA hypertension-associated tRNAAla mutation alters the tRNA metabolism and mitochondrial functionMol Cell Biol201636141920193010.1128/MCB.00199-16Search in Google Scholar

Rose G, Passarino G, Carrieri G, Altomare K, Greco V, Bertolini S, et al. Paradoxes in longevity: Sequence analysis of mtDNA haplogroup J in centenarians. Eur J Hum Genet. 2001; 9(9): 701-707.RoseG,PassarinoG,CarrieriG,AltomareK,GrecoV,BertoliniS,et alParadoxes in longevity: Sequence analysis of mtDNA haplogroup J in centenariansEur J Hum Genet20019970170710.1038/sj.ejhg.5200703Search in Google Scholar

Young WY Zhao L, Qian Y, Li R, Chen J, Yuan H, et al. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNAA1555G mutation in three Han Chinese families with hearing loss. Am J Med Genet A. 2006; 140(20): 2188-2197.YoungWYZhaoL,QianY,LiR,ChenJ,YuanH,et alVariants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNAA1555G mutation in three Han Chinese families with hearing lossAm J Med Genet A2006140202188219710.1002/ajmg.a.31434Search in Google Scholar

Luo Z. Mitochondrial tRNAArg T10454C variant may not influence the clinical expression of deafness associated 12S rRNA A1555G mutation. Mitochondrial DNAADNA MappSeqAnal. 2016; 27(2): 1137-1140.LuoZ.Mitochondrial tRNAArg T10454C variant may not influence the clinical expression of deafness associated 12S rRNA A1555G mutationMitochondrial DNAADNA MappSeqAnal20162721137114010.3109/19401736.2014.933337Search in Google Scholar

Teng L, Zheng J, Leng J, Ding Y. Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension. Mitochondrial DNA. 2012; 23(6): 461-465.TengL,ZhengJ,LengJ,DingY.Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertensionMitochondrial DNA201223646146510.3109/19401736.2012.710205Search in Google Scholar

Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, et al Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family. Mol Genet Metab. 2010; 100(1): 57-64.TangX,LiR,ZhengJ,CaiQ,ZhangT,GongS,et alMaternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese familyMol Genet Metab20101001576410.1016/j.ymgme.2010.01.008Search in Google Scholar

Florentz C, Sohm B, Tryoen-Tyth P, Pütz J, Sissler M. Human mitochondrial tRNAs in health and disease. Cell Mol Life Sci. 2003; 60(7): 1356-1375.FlorentzC,SohmB,Tryoen-TythP,PützJ,SisslerM.Human mitochondrial tRNAs in health and diseaseCell Mol Life Sci20036071356137510.1007/s00018-003-2343-1Search in Google Scholar

Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, et al Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenet Genomics. 2008; 18(12): 1059-1070.WangX,LuJ,ZhuY,YangA,YangL,LiR,et alMitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese familiesPharmacogenet Genomics200818121059107010.1097/FPC.0b013e3283131661Search in Google Scholar

Jia Z, Wang X, Qin Y, Xue L, Jiang P, Meng Y, et al. Coronary heart disease is associated with a mutation in mitochondrial tRNA. Hum Mol Genet. 2013; 22(20): 4064-4073.JiaZ,WangX,QinY,XueL,JiangP,MengY,et alCoronary heart disease is associated with a mutation in mitochondrial tRNAHum Mol Genet201322204064407310.1093/hmg/ddt256Search in Google Scholar

Brulé H, Holmes WM, Keith G, Giegé R, Florentz C. Effect of a mutation in the anticodon of human mitochondrial tRNAPro on its post-transcriptional modification pattern. Nucleic Acids Res. 1998; 26(2): 537-543.BruléH,HolmesWM,KeithG,GiegéR,FlorentzC.Effect of a mutation in the anticodon of human mitochondrial tRNAPro on its post-transcriptional modification patternNucleic Acids Res199826253754310.1093/nar/26.2.537Search in Google Scholar

eISSN:
1311-0160
Lingua:
Inglese
Frequenza di pubblicazione:
2 volte all'anno
Argomenti della rivista:
Medicine, Basic Medical Science, other