The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis

[1]  A. Orekhov,et al.  [Study of intima-medial thickness (IMT) of the carotid arteries as an indicator of natural atherosclerosis progress in Moscow population]. , 2012, Patologicheskaia fiziologiia i eksperimental'naia terapiia.

[2]  C. Weber,et al.  The Use of High-Throughput Technologies to Investigate Vascular Inflammation and Atherosclerosis , 2012, Arteriosclerosis, thrombosis, and vascular biology.

[3]  A. Orekhov,et al.  [A new method of quantitative estimation of mutant allele in mitochondrial genome]. , 2011, Patologicheskaia fiziologiia i eksperimental'naia terapiia.

[4]  A. Orekhov,et al.  Corrigendum to Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome [Atherosclerosis 204 (2009) 184―190] , 2010 .

[5]  M. Andreassi Metabolic syndrome, diabetes and atherosclerosis: influence of gene-environment interaction. , 2009, Mutation research.

[6]  A. Orekhov,et al.  Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome. , 2009, Atherosclerosis.

[7]  M. Schwartz,et al.  Late onset of stroke-like episode associated with a 3256C→T point mutation of mitochondrial DNA , 2003, Journal of the Neurological Sciences.

[8]  P. Bénit,et al.  The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency , 2003, Journal of medical genetics.

[9]  P. Oefner,et al.  Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene , 2002, Journal of medical genetics.

[10]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[11]  S. Dimauro,et al.  Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA. , 1999, The New England journal of medicine.

[12]  S. Dimauro,et al.  A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria , 1999, Annals of neurology.

[13]  S. Dimauro,et al.  Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy , 1998, Neurology.

[14]  V. Kalinin,et al.  [Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region]. , 1997, Genetika.

[15]  F. Amosenko,et al.  [TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses]. , 1997, Genetika.

[16]  V. Kalinin,et al.  [Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]. , 1995, Genetika.

[17]  M. Sazonova [Association of mitochondrial genome mutations with lipofibrous plaques in human aortic intima]. , 2015, Patologicheskaia fiziologiia i eksperimental'naia terapiia.

[18]  Cheng-BoHan,et al.  Mutations of mitochondrial 12S rRNA in gastric carcinoma and their significance , 2005 .

[19]  M. Freidin,et al.  Russian Journal of Genetics , 2002 .