Перегляд за автором "Gorovenko, N.G."

Результати 1-11 з 11

Association of polymorphic G1934A variant (allele *4) of CYP2D6 gene with increased risk of breast cancer development in Ukrainian women

Levkovich, N.N.; Gorovenko, N.G.; Myasoedov, D.V. (Experimental Oncology, 2011)

Institute of Genetic and Regenerative Medicine of the Ukrainian Academy of Medical Sciences”, Kiev, 03150, UkraineBackground: Breast cancer (BC) is among the most common oncologic pathology in economically developed countries ...
Breast cancer immunohistochemical features in young women with BRCA1/2 mutations

Zakhartseva, L.M.; Gorovenko, N.G.; Podolskaya, S.V.; Anikusko, N.F.; Lobanova, O.E.; Pekur, K.A.; Kropelnytskyi, V.A.; Shurygina, O.V. (Experimental Oncology, 2009)

Breast cancer among young women is a rare pathology. In most studies published so far, this patients group is not being analyzed separately. Particularities of this pathology require an additional examination of the ...
Breast cancer immunohistochemical features in young women with BRCA1/2 mutations

Zakhartseva, L.M.; Gorovenko, N.G.; Podolskaya, S.V.; Anikusko, N.F.; Lobanova, O.E.; Pekur, K.A.; Kropelnytskyi, V.A.; Shurygina, O.V. (Experimental Oncology, 2009)

Breast cancer among young women is a rare pathology. In most studies published so far, this patients group is not being analyzed separately. Particularities of this pathology require an additional examination of the ...
Efficiency of application of different DNA probes in identifying marker chromosomes

Tavokina, L.V.; Brovko, A.O.; Baronova, E.V.; Moskalenko, E.P.; Gorovenko, N.G. (Вiopolymers and Cell, 2016)

The presence of marker chromosomes in the human karyotype always requires a special diagnostic approach. Determination of the marker chromosome type and structure is of great diagnostic and prognostic importance. There are ...
Genetic polymorphisms of the renin-angiotensin system in breast cancer patients

Fishchuk, L.E.; Gorovenko, N.G. (Experimental Oncology, 2013)

Background: breast cancer (BC) is one of the most common cancer pathologies in women. Genetic polymorphism of genes of reninangiotensin system (RAS) is considered to be associated with cancer development, in particular, ...
Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease

Mytsyk, N.Y.; Gorovenko, N.G. (Вiopolymers and Cell, 2016)

GM1-gangliosidosis (MIM# 230500) and mucopolysaccharidosis IV (Morquio B, MIM# 230500) are autosomal-recessive diseases, which belong to the group of lysosomal storage disorders and are caused by changes in the structure ...
Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene

Trofimova, N.S.; Olkhovich, N.V.; Gorovenko, N.G. (Вiopolymers and Cell, 2016)

Mucopolysaccharidosis type III or Sanfilippo syndrome (MIM # 252900) is a rare hereditary autosomal-recessive metabolic disorder, which occurs due to the deficiency of heparan-N-sulfatase enzyme (EC 3.10.1.1). Aim. To ...
Specificities of Sanfilippo A syndrome laboratory diagnostics

Trofimova, N.S.; Olkhovich, N.V.; Gorovenko, N.G. (Вiopolymers and Cell, 2014)

Mucopolysaccharidosis type IIIA (MPS IIIA) occurs due to the deficiency of lysosomal enzyme heparan-N-sulfatase (sulfamidase), which is caused by mutations in the SGSH gene. Aim. To identify the characteristics of biochemical ...
Spectrum of mutations in patients with organic acidurias from Ukraine

Barvinska, O.I.; Olkhovych, N.V.; Shkurko, T.O.; Gorovenko, N.G. (Вiopolymers and Cell, 2018)

Aim. To identify mutations in patients from Ukraine with glutaric aciduria I, isolated methylmalonic aciduria, and isovaleric aciduria. Methods. Sanger sequencing. Results. We have identified 37.5 % of alleles (3/8) in ...
Study on association of the polymorphic variants of ACE (I/D), AT2R1 (A1166C), TNF-a (G308A), MTHFR (C677T) genes and their combinations with the risk of development of perinatal pathology and gestation reduction

Gorovenko, N.G.; Kyryachenko, S.P.; Rossokha, Z.I. (Вiopolymers and Cell, 2011)

Aim. To study the association of the polymorphic variants of ACE (I/D), AT2R1 (A1166C), TNF-á (G308A), MTHFR (C677T) genes and their combinations with the risk of perinatal pathology and gestation reduction. Methods. The ...
The role of genetic determinant in the development of severe perinatal asphyxia

Gorovenko, N.G.; Rossokha, Z.I.; Podolskaya, S.V.; Pokhylko, V.I.; Lundberg, G.A. (Цитология и генетика, 2010)

The frequency of GSTT1 and GSTM1 gene deletion polymorphism was determined in a case-control study of full-term Ukrainian newborns including patients with perinatal asphyxia. Multiplex polymerase chain reaction was used ...

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Перегляд за автором "Gorovenko, N.G."

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