This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Šeruga M, Makuc J, Završnik M, Cilenšek I, Ekart R, Petrovič D. Polymorphism of angiotensin-converting enzyme (rs4340) and diabetic nephropathy in Caucasians with type 2 diabetes mellitus. Balkan J Med Genet. 2017; 19(2): 29-34.ŠerugaMMakucJZavršnikMCilenšekIEkartRPetrovičDPolymorphism of angiotensin-converting enzyme (rs4340) and diabetic nephropathy in Caucasians with type 2 diabetes mellitusBalkan J Med Genet201719229–3410.1515/bjmg-2016-0033Search in Google Scholar
Popović D, Nikolajević Starčević J, Šantl Letonja M, Makuc J, Cokan Vujkovac A, Reschner H, et al. PECAM-1 gene polymorphism (rs668) and subclinical markers of carotid atherosclerosis in patients with type 2 diabetes mellitus. Balkan J Med Genet. 2016; 19(1): 63-70.PopovićDNikolajevićStarčević JŠantl LetonjaMMakucJCokan VujkovacAReschnerHPECAM-1 gene polymorphism (rs668) and subclinical markers of carotid atherosclerosis in patients with type 2 diabetes mellitusBalkan J Med Genet201619163–7010.1515/bjmg-2016-0008Search in Google Scholar
Lu J, Wang D, Li R, Li W, Ji J, Zhao J, et al. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family. Biochem Biophys Res Commun. 2006; 348(1): 115-119.LuJWangDLiRLiWJiJZhaoJMaternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese familyBiochem Biophys Res Commun20063481115–11910.1016/j.bbrc.2006.07.010Search in Google Scholar
Naing A, Kenchaiah M, Krishnan B, Mir F, Charnley A, Egan C, et al. Maternally inherited diabetes and deafness (MIDD): Diagnosis and management. J Diabetes Complications. 2014; 28(4): 542-546.NaingAKenchaiahMKrishnanBMirFCharnleyAEganCMaternally inherited diabetes and deafness (MIDD): Diagnosis and managementJ Diabetes Complications2014284542–54610.1016/j.jdiacomp.2014.03.006Search in Google Scholar
Tsukuda K, Suzuki Y, Kameoka K, Osawa N, Goto Y, Katagiri H, et al. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region. Diabet Med. 1997; 14(12): 1032-1037.TsukudaKSuzukiYKameokaKOsawaNGotoYKatagiriHScreening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] regionDiabet Med199714121032–103710.1002/(SICI)1096-9136(199712)14:12<1032::AID-DIA504>3.0.CO;2-YSearch in Google Scholar
Suzuki Y, Suzuki S, Hinokio Y, Chiba M, Atsumi Y, Hosokawa K, et al. Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation. Diabetes Care. 1997; 20(7): 1138-1140.SuzukiYSuzukiSHinokioYChibaMAtsumiYHosokawaKDiabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutationDiabetes Care19972071138–114010.2337/diacare.20.7.1138Search in Google Scholar
Leonard JV, Schapira AH. Mitochondrial respiratory chain disorders I: Mitochondrial DNA defects. Lancet. 2000; 355(9200): 299-304.LeonardJVSchapiraAHMitochondrial respiratory chain disorders I: Mitochondrial DNA defectsLancet20003559200299–30410.1016/S0140-6736(99)05225-3Search in Google Scholar
DiMauro S, Schon EA. Mitochondrial DNA mutations in human disease. Am J Med Genet. 2001; 106(1): 18-26.DiMauroSSchonEAMitochondrial DNA mutations in human diseaseAm J Med Genet2001106118–2610.1002/ajmg.1392Search in Google Scholar
Zhu Q, Zhou Y, Jin X, Lin X. The role of mitochondrial tRNAPhe C628T variant in deafness expression. Mitochondrial DNA. 2015; 26(1): 2-6.ZhuQZhouYJinXLinXThe role of mitochondrial tRNAPhe C628T variant in deafness expressionMitochondrial DNA20152612–610.3109/19401736.2013.823192Search in Google Scholar
Helm M, Brulé H, Friede D, Giegé R, Pütz D, Florentz C. Search for characteristic structural features of mammalian mitochondrial tRNAs. RNA. 2000; 6(10): 1356-1379.HelmMBruléHFriedeDGiegéRPützDFlorentzCSearch for characteristic structural features of mammalian mitochondrial tRNAsRNA20006101356–137910.1017/S1355838200001047Search in Google Scholar
van Oven M, Kayser M. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Hum Mutat. 2009; 30(2): E386-394.vanOven MKayserMUpdated comprehensive phylogenetic tree of global human mitochondrial DNA variationHum Mutat2009302E386–39410.1002/humu.20921Search in Google Scholar
Gruber AR, Lorenz R, Bernhart SH, Neuböck R, Hofacker IL. The Vienna RNA Website. Nucleic Acids Res. 2008; 36(Web Server issue): W70-W74.GruberARLorenzRBernhartSHNeuböckRHofackerILThe Vienna RNA WebsiteNucleic Acids Res200836Web Server issueW70–W7410.1093/nar/gkn188Search in Google Scholar
American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2011; 34(Suppl 1): S62-S71.American Diabetes AssociationDiagnosis and classification of diabetes mellitusDiabetes Care201134Suppl 1S62–S7110.2337/dc11-S062Search in Google Scholar
Andrews RM, Kubacka I, Chinnery PF, Light-owlers RN, Turnbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet. 1999; 23(2):147.AndrewsRMKubackaIChinneryPFLight-owlersRNTurnbullDMHowellNReanalysis and revision of the Cambridge reference sequence for human mitochondrial DNANat Genet199923214710.1038/13779Search in Google Scholar
Li W, Wen C, Li W, Wang H, Guan X, Zhang W, et al. The tRNA(Gly) T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNA(Gly), increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potential. Mol Cell Biochem. 2015; 408(1-2): 171-179.LiWWenCLiWWangHGuanXZhangWThe tRNA(Gly) T10003C mutation in mitochondrial haplogroup M11b in a Chinese family with diabetes decreases the steady-state level of tRNA(Gly), increases aberrant reactive oxygen species production, and reduces mitochondrial membrane potentialMol Cell Biochem20154081-2171–17910.1007/s11010-015-2493-0Search in Google Scholar
Liu H, Li R, Li W, Wang M, Ji J, Zheng J, et al. Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene. Mitochondrion. 2015; 21: 49-57.LiuHLiRLiWWangMJiJZhengJMaternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) geneMitochondrion20152149–5710.1016/j.mito.2015.01.004Search in Google Scholar
Wittenhagen LM, Kelley SO. Dimerization of a pathogenic human mitochondrial tRNA. Nat Struct Biol. 2002; 9(8): 586-590.WittenhagenLMKelleySODimerization of a pathogenic human mitochondrial tRNANat Struct Biol200298586–59010.1038/nsb820Search in Google Scholar
Janssen GM, Maassen JA, van Den Ouweland JM. The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate. J Biol Chem. 1999; 274(42): 29744-29748.JanssenGMMaassenJAvanDen Ouweland JMThe diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rateJ Biol Chem19992744229744–2974810.1074/jbc.274.42.29744Search 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 tRNA mutations. Hum Mutat. 2011; 32(11): 1319-1325.YarhamJWAl-DosaryMBlakelyELAlstonCLTaylorRWElsonJLA comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutationsHum Mutat201132111319–132510.1002/humu.21575Search in Google Scholar
Yoon KL, Aprille JR, Ernst SG. Mitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiency. Biochem Biophys Res Commun. 1991; 173(6): 1112-1115.YoonKLAprilleJRErnstSGMitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiencyBiochem Biophys Res Commun199117361112–111510.1016/0006-291X(91)90399-RSearch in Google Scholar
Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX. Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. Biochem Biophys Res Commun. 2004; 325(4): 1503-1508.ZhaoLYoungWYLiRWangQQianYGuanMXClinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutationBiochem Biophys Res Commun200432541503–150810.1016/j.bbrc.2004.10.199Search in Google Scholar
Zhu Y, Gu X, Xu C. A Mitochondrial DNA A8701G mutation associated with maternally inherited hypertension and dilated cardiomyopathy in a Chinese pedigree of a consanguineous marriage. Chin Med J (Engl). 2016; 129(3): 259-266.ZhuYGuXXuCA Mitochondrial DNA A8701G mutation associated with maternally inherited hypertension and dilated cardiomyopathy in a Chinese pedigree of a consanguineous marriageChin Med J (Engl)20161293259–26610.4103/0366-6999.174491Search in Google Scholar
