Associated Papers
Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.
Shi J et al.
Laboratory Medicine, 2023
A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.
Zhang D et al.
Annals of Human Genetics, 2022
Human catalase, its polymorphisms, regulation and changes of its activity in different diseases.
Kodydková J et al.
Folia Biologica, 2014
Polymorphisms of antioxidant enzymes, blood pressure and risk of hypertension.
Mansego ML et al.
Journal of Hypertension, 2011
[Role of polymorphic markers of antioxidants (NQO1, GSTP1, GPX1) genes in adaptive response to hazardous work conditions in workers].
Kochetova OV et al.
Meditsina Truda I Promyshlennaia Ekologiia, 2010
[Polymorphism of the genes for antioxidant defense enzymes and their association with the development of chronic obstructive pulmonary disease in the population of Bashkortostan].
Korytina GF et al.
Genetika, 2009
The 262T>C promoter polymorphism of the catalase gene is associated with diabetic neuropathy in type 1 diabetic Russian patients.
Chistiakov DA et al.
Diabetes & Metabolism, 2006
Catalase enzyme mutations and their association with diseases.
Góth L et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology, 2004
[Associative analysis of the connection between mutation C1167T in the catalase gene and polymorphic marker D6S392 nearby the Mn-dependent superoxide dismutase gene with diabetic microangiopathies].
Chistiakov DA et al.
Terapevticheskii Arkhiv, 2002
[Analysis of polymorphism of the D11S2008 locus of the catalase gene in patients with hypertension and ischemic heart disease in non-insulin-dependent diabetes mellitus in the Muscovite population].
Chistiakov DA et al.
Genetika, 2000
[Polymorphism of angiotensinogen T174M gene and cardiovascular diseases in the Moscow population].
Chistiakov DA et al.
Genetika, 1999
[Allelic polymorphism of short tandemly repeating sequences of the HUMF13A01 and HUMCD4 loci in Russian populations from Moscow and Tomsk].
Turakulov RI et al.
Genetika, 1997
[Distribution of alleles of microsatellite loci HUMCYAR04 and D19S253 in population samples of two Russian cities].
Chistiakov DA et al.
Genetika, 1997
[T174M polymorphism of angiotensinogen gene in Moscow population is associated with hypertension].
Chistiakov DA et al.
Molekuliarnaia Biologiia, 0
[Association of the SOD2 Ala(-9)Val and SOD3 Arg213Gly polymorphisms with diabetic polyneuropathy in patients with diabetes mellitus type 1].
Zotova EV et al.
Molekuliarnaia Biologiia, 0
[Genomics of type I diabetes mellitus and its late complications].
Nosikov VV
Molekuliarnaia Biologiia, 0
A new type 1 diabetes susceptibility locus containing the catalase gene (chromosome 11p13) in a Russian population.
Chistiakov DA et al.
Diabetes/metabolism Research and Reviews, 0
[Lymphocyte metabolism in patients with acute pancreatitis with different genotypes of GSTM1 and GSTT1 genes].
Markova EV et al.
Biomeditsinskaia Khimiia, 0
[DIO2, TPO, CYP1A1 AND CYP1A2 gene polymorphism in women with thyroid disease].
Kochetova OV et al.
Gigiena I Sanitariia, 0
[Analysis of the distribution of alleles of four hypervariable tandem repeats among unrelated Russian individuals living in Moscow, using the polymerase chain reaction].
Chistiakov DA et al.
Molekuliarnaia Biologiia, 0
[Analysis of allelic polymorphism of two tetranucleotide tandem repeats in two urban populations in Russia].
Chistiakov DA et al.
Molekuliarnaia Biologiia, 0