Boulton A.J. 2001. Treatments for diabetic neuropathy. Curr. Diab. Rep.
1, 127–132.
PubMed
Article
CAS
Google Scholar
IDF Diabetes Atlas. Edition 2003. Available on http://www.eatlas.idf.org/Complications/Prevalence/index
Zotova, E.V., Chistyakov, D.A., Savost’yanov, K.V., Bursa T.R., Galeev I.V., Strokov I.A., Nosikov V.V. 2003. Association of the SOD2 Ala(−9)Val and SOD3 Arg213Gly polymorphisms with diabetic polyneuropathy in diabetes mellitus type 1. Mol. Biol.
37, 345–348.
Article
CAS
Google Scholar
Zotova E.V., Savost’yanov K.V., Chistyakov D.A., Bursa T.R., Galeev I.V., Strokov I.A., Nosikov V.V. 2004. Association of polymorphic markers of the antioxidant enzyme genes with diabetic polyneuropathy in type 1 diabetes mellitus. Mol. Biol.
38, 244–249.
Article
CAS
Google Scholar
Stevens M.J., Obrosova I., Cao X., et al. 2000. Effects of DL-alpha-lipoic acid on peripheral nerve conduction, blood flow, energy metabolism, and oxidative stress in experimental diabetic neuropathy. Diabetes. 49, 1006–1015.
PubMed
Article
CAS
Google Scholar
Spitsina E.V., Yakunina N.Ya., Chudakova D.A., Nikitin A.G., Svetlova G.N., Soluyanova T.N., Strokov I.A., Nosikov V.V. 2007. The association of the TP53 polymorphisms Pro72Arg and C(−594)CC with diabetic polyneuropathy in Russian Muscovites with type 1 diabetes mellitus. Mol. Biol.
41, 989–993.
Article
CAS
Google Scholar
Kastan M.B., Onyekwere O., Sidransky D., et al. 1991. Participation of p53 protein in the cellular response to DNA damage. Cancer Res.
51, 6304–6311.
PubMed
CAS
Google Scholar
Keim A.L., Chi M.M., Moley K.H. 2001. Hyperglycemia-induced apoptotic cell death in the mouse blastocystis dependent on expression of p53. Mol. Reprod. Dev.
60, 214–224.
PubMed
Article
CAS
Google Scholar
Vincent A.M., Brownlee M., Russell J.W. 2002. Oxidative stress and programmed cell death in diabetic neuropathy. Ann. N.Y. Acad. Sci.
959, 368–383.
PubMed
CAS
Article
Google Scholar
DiMauro S., Schon E.A. 2003. Mitochondrial respiratory-chain diseases. N. Engl. J. Med.
348, 2656–2668.
PubMed
Article
CAS
Google Scholar
van Houten B., Woshner V., Santos J.H. 2006. Role of mitochondrial DNA in toxic responses to oxidative stress. DNA Repair. 5, 145–152.
PubMed
Article
CAS
Google Scholar
Hudson G., Chinnery P.F. 2006. Mitochondrial DNA polymerase-gamma and human disease. Hum. Mol. Genet.
15, 244–252.
Article
CAS
Google Scholar
Zheng W., Khrapko K., Coller H., et al. 2006. Origins of human mitochondrial point mutations as DNA polymerase gamma-mediated errors. Mutat. Res.
599, 11–20.
PubMed
CAS
Google Scholar
Graziewicz M.A., Longley M.J. Copeland W.C. 2006. DNA polymerase gamma in mitochondrial DNA replication and repair. Chem. Rev.
106, 383–405.
PubMed
Article
CAS
Google Scholar
Lee W.S., Sokol R.J. 2007. Mitochondrial hepatopathies: Advances in genetics and pathogenesis. Hepatology. 45, 1555–1565.
PubMed
Article
CAS
Google Scholar
Longley M.J., Ropp P.A., Lim S.E., et al. 1998. Characterization of the native and recombinant catalytic subunit of human DNA polymerase gamma: identification of residues critical for exonuclease activity and dideoxynucleotide sensitivity. Biochemistry. 37, 10529–10539.
PubMed
Article
CAS
Google Scholar
Kaguni L.S. 2004. DNA polymerase gamma, the mitochondrial replicase. Annu. Rev. Biochem.
73, 293–320.
PubMed
Article
CAS
Google Scholar
Longley M.J., Graziewicz M.A., Bienstock R.J., Copeland W.C. 2005. Consequences of mutations in human DNA polymerase gamma. Gene.
354, 125–131.
PubMed
Article
CAS
Google Scholar
Luoma P.T., Eerola J., Ahola S., et al. 2007. Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Neurology. 69, 1152–1159.
PubMed
Article
CAS
Google Scholar
Tiangyou W., Hudson G., Ghezzi D., et al. 2006. POLG1 in idiopathic Parkinson disease. Neurology. 67, 1698–1700.
PubMed
Article
CAS
Google Scholar
Ferrari G., Lamantea E., Donati A., et al. 2005. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gamma A. Brain. 128, 723–731.
PubMed
Article
Google Scholar
Nguyen K.V., Ostergaard E., Ravn S.H., et al. 2005. POLG mutations in Alpers syndrome. Neurology. 65, 1493–1495.
PubMed
Article
CAS
Google Scholar
van Goethem G., Martin J.J., Dermaut B., et al. 2003. Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. Neuromusc. Disord.
13, 133–142.
PubMed
Article
Google Scholar
Korhonen J.A., Gaspari M., Falkenberg M. 2003. TWINKLE has DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein. J. Biol. Chem.
278, 48627–48632.
PubMed
Article
CAS
Google Scholar
Korhonen J.A., Pham X.H., Pellegrini M., et al. 2004. Reconstitution of a minimal mtDNA replisome in vitro. EMBO J.
23, 2423–2429.
PubMed
Article
CAS
Google Scholar
Spelbrink J.N., Toivonen J.M., Hakkaart G.A., et al. 2000. In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells. J. Biol. Chem.
275, 24818–24828.
PubMed
Article
CAS
Google Scholar
Tyynismaa H., Sembongi H., Bokori-Brown M., et al. 2004. Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number. Hum. Mol. Genet.
13, 3219–3227.
PubMed
Article
CAS
Google Scholar
Spelbrink J.N., Li F.-Y., Tiranti V., et al. 2001. Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria. Nature Genet.
28, 223–231.
PubMed
Article
CAS
Google Scholar
Baloh R.H., Salavaggione E., Milbrandt J., et al. 2007. Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle. Arch. Neurol.
64, 998–1000.
PubMed
Article
Google Scholar
Kristal B.S., Matsuda M., Yu B.P. 1996. Abnormalities in the mitochondrial permeability transition in diabetic rats. Biochem. Biophys. Res. Commun.
222, 519–523.
PubMed
Article
CAS
Google Scholar
Halestrap A.P., McStay G.P., Clarke S.J. 2002. The permeability transition pore complex: Another view. Biochimie. 84, 153–166.
PubMed
Article
CAS
Google Scholar
Vyssokikh M.Y., Brdiczka D. 2003. The function of complexes between the outer mitochondrial membrane pore (VDAC) and the adenine nucleotide translocase in regulation of energy metabolism and apoptosis. Acta Biochim. Pol.
50, 389–404.
PubMed
CAS
Google Scholar
Klingenberg M. 1985. The ADP/ATP carrier in mitochondrial membranes. In: The enzymes of Biological Membranes. N.Y.: Plenum Press, vol. 4, pp. 511–553.
Google Scholar
Bottero V., Rossi F., Samson M., et al. 2001. Iκ b-α, the NF-κ B inhibitory subunit, interacts with ANT, the mitochondrial ATP/ADP translocator. J. Biol. Chem.
276, 21317–21324.
PubMed
Article
CAS
Google Scholar
Belzacq A.S., Vieira H.L., Kroemer G., et al. 2002. The adenine nucleotide translocator in apoptosis. Biochimie. 84, 167–176.
PubMed
Article
CAS
Google Scholar
Graham B.H., Waymire K.G., Cottrell B., et al. 1997. A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. Nature Genet.
16, 226–234.
PubMed
Article
CAS
Google Scholar
Lodi T., Bove C., Fontanesi F., et al. 2006. Mutation D104G in ANT1 gene: Complementation study in Saccharomyces cerevisiae as a model system. Biochem. Biophys. Res. Commun.
341, 810–815.
PubMed
Article
CAS
Google Scholar
Ziegler D., Hanefeld M., Ruhnau K.J., et al. 1995. Treatment of symptomatic diabetic peripheral neuropathy with the anti-oxidant alpha-lipoic acid: A 3-week multicentre randomized controlled trial (ALADIN Study). Diabetologia. 38, 1425–1433.
PubMed
Article
CAS
Google Scholar
Strokov I.A., Novosadova M.V., Barinov A.N., Yakhno N.N. 2000. Cliniocal methods for assessing the severity of diabetic polyneuropathy. Neurol. Zh.
5, 14–18.
Google Scholar
Dyck P.J., Melton J.L., O’Brien P.C., Service F.G. 1997. Approaches to improve epidemiological studies of diabetic neuropathy: Insights from the Rochester Diabetic Neuropathy Study. Diabetes. 46, 5–8.
Google Scholar
Komantsev V.N., Zabolotnykh V.A. 2001. Metodicheskie osnovy klinicheskoi elektroneiromiografii. Rukovodstvo dlya vrachei (Methodological Foundations of Clinical Electroneuromyography: A Manual for Doctors). St. Petersburg: Lan’.
Google Scholar
Johns M.B., Paulus-Thomas J.E. 1989. Purification of human genomic DNA from whole blood using perchlorate in place of phenol. Anal. Biochem.
180, 276–278.
PubMed
Article
CAS
Google Scholar
Hudson G., Chinnery P.F. 2006. Mitochondrial DNA polymerase-gamma and human disease. Hum. Mol. Genet.
15, 244–252.
Article
CAS
Google Scholar