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
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 polymorphic variants of genes were analyzed by PCR and RFLP i...
Saved in:
| Published in: | Вiopolymers and Cell |
|---|---|
| Date: | 2011 |
| Main Authors: | Gorovenko, N.G., Kyryachenko, S.P., Rossokha, Z.I. |
| Format: | Article |
| Language: | English |
| Published: |
Інститут молекулярної біології і генетики НАН України
2011
|
| Subjects: | |
| Online Access: | https://nasplib.isofts.kiev.ua/handle/123456789/156340 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Journal Title: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Cite this: | 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 / N.G. Gorovenko, S.P. Kyryachenko, Z.I. Rossokha // Вiopolymers and Cell. — 2011. — Т. 27, № 3. — С. 206-213. — Бібліогр.: 14 назв. — англ., рос. |
Institution
Digital Library of Periodicals of National Academy of Sciences of UkraineSimilar Items
Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants
by: Tatarskyy, P.F., et al.
Published: (2010)
by: Tatarskyy, P.F., et al.
Published: (2010)
Analysis of polymorphic variants S677T and A1298C of MTHFR gene in patients with psoriasis
by: A. M. Fedota, et al.
Published: (2015)
by: A. M. Fedota, et al.
Published: (2015)
Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability
by: Gulkovskyi, R.V., et al.
Published: (2015)
by: Gulkovskyi, R.V., et al.
Published: (2015)
Specificities of Sanfilippo A syndrome laboratory diagnostics
by: Trofimova, N.S., et al.
Published: (2014)
by: Trofimova, N.S., et al.
Published: (2014)
Association of genotypes by polymorphic variant C-108T of PON1 gene with the risk of developing breast cancer and hypertensive disease in women
by: Fishchuk, L.Ye.
Published: (2014)
by: Fishchuk, L.Ye.
Published: (2014)
Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease
by: Mytsyk, N.Y., et al.
Published: (2016)
by: Mytsyk, N.Y., et al.
Published: (2016)
Cisplatin treatment of C6 rat glioma in vivo did not influence copy number alterations and growth pattern of tumor-derived resistant cells
by: Stepanenko, A.A., et al.
Published: (2015)
by: Stepanenko, A.A., et al.
Published: (2015)
T-138C polymorphism of MGP gene is associated with blood plasma cholesterol levels but not related to other risk factors of atherosclerosis in patients with ischemic stroke
by: Garbuzova, V.Yu., et al.
Published: (2014)
by: Garbuzova, V.Yu., et al.
Published: (2014)
The role of genetic determinant in the development of severe perinatal asphyxia
by: Gorovenko, N.G., et al.
Published: (2010)
by: Gorovenko, N.G., et al.
Published: (2010)
Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene
by: Trofimova, N.S., et al.
Published: (2016)
by: Trofimova, N.S., et al.
Published: (2016)
Spectrum of mutations in patients with organic acidurias from Ukraine
by: Barvinska, O.I., et al.
Published: (2018)
by: Barvinska, O.I., et al.
Published: (2018)
MiR-137 expression in neuroblastoma: a role in clinical course and outcome
by: Inomistova, M.V., et al.
Published: (2016)
by: Inomistova, M.V., et al.
Published: (2016)
Analysis of mutations in GBA gene in Ukrainian patients with Gaucher disease
by: Olkhovych, N.V., et al.
Published: (2017)
by: Olkhovych, N.V., et al.
Published: (2017)
Efficiency of application of different DNA probes in identifying marker chromosomes
by: Tavokina, L.V., et al.
Published: (2016)
by: Tavokina, L.V., et al.
Published: (2016)
Metabolic syndrome is inversely related to soluble receptor for advanced glycation end products: a study in mother-infant pairs
by: Klenovicsova, K., et al.
Published: (2011)
by: Klenovicsova, K., et al.
Published: (2011)
The influence of GSTP1 A313G polymorphism on susceptibility, chemotherapy-related toxicity and prognosis of Hodgkin’s lymphoma in Ukrainian patients
by: Kriachok, I.A., et al.
Published: (2012)
by: Kriachok, I.A., et al.
Published: (2012)
Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children
by: Tatarskyy, P.F., et al.
Published: (2011)
by: Tatarskyy, P.F., et al.
Published: (2011)
Анализ полиморфных вариантов С677Т и А1298С гена MTHFR у больных псориазом
by: Федота, А.М., et al.
Published: (2015)
by: Федота, А.М., et al.
Published: (2015)
Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses
by: Tkach, I.R., et al.
Published: (2015)
by: Tkach, I.R., et al.
Published: (2015)
Suppression of tumorigenicity and metastatic potential of melanoma cells by transduction of interferon gene
by: Lykhova, A.A., et al.
Published: (2014)
by: Lykhova, A.A., et al.
Published: (2014)
Single center study of ESBL-related strains of Enterobacteriaceae collected from clinical specimens of infants with the congenital heart disease using multiplex PCR amplification
by: Filonenko, G.V., et al.
Published: (2017)
by: Filonenko, G.V., et al.
Published: (2017)
Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability
by: Gulkovskyi, R.V., et al.
Published: (2015)
by: Gulkovskyi, R.V., et al.
Published: (2015)
Study of association between polymorphisms in the PSMB5 (rs11543947) and PSMA3 (rs2348071) genes and multiple sclerosis in Latvians
by: Kalnina, J., et al.
Published: (2014)
by: Kalnina, J., et al.
Published: (2014)
Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients
by: Chernushyn, S.Yu., et al.
Published: (2018)
by: Chernushyn, S.Yu., et al.
Published: (2018)
Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability
by: Gulkovskyi, R.V., et al.
Published: (2015)
by: Gulkovskyi, R.V., et al.
Published: (2015)
Familial adenomatous polyposis: age of onset and association with mutations of the APC gene in patients from West Ukraine
by: Lozynska, M.R., et al.
Published: (2017)
by: Lozynska, M.R., et al.
Published: (2017)
Chromosomal aberrations in spontaneously aborted products of conception from Ukraine
by: Tkach, I.R., et al.
Published: (2017)
by: Tkach, I.R., et al.
Published: (2017)
Comparative analysis of epigenetic markers in plasma and tissue of patients with colorectal cancer
by: Kondratov, A.G., et al.
Published: (2014)
by: Kondratov, A.G., et al.
Published: (2014)
Пошук генів – потенційних маркерів агресивності і метастазування раку простати людини
by: Розенберг, Є.Е., et al.
Published: (2013)
by: Розенберг, Є.Е., et al.
Published: (2013)
PPM1M and PRICKLE2 are potential tumor suppressor genes in human clear-cell renal cell carcinoma
by: Rudenko, E.E., et al.
Published: (2014)
by: Rudenko, E.E., et al.
Published: (2014)
The binding properties of some novel ruthenium (III) complexes with human serum transferrin
by: Uivarosi, V., et al.
Published: (2011)
by: Uivarosi, V., et al.
Published: (2011)
Development of ARMS PCR tests for detection of common CFTR gene mutations
by: Soloviov, O.O., et al.
Published: (2010)
by: Soloviov, O.O., et al.
Published: (2010)
Comparison of dual acting drugs and conventional NSAIDs towards parameters of NO-synthase system and oxidative stress in mucosal membrane of large intestine of rats with experimental ulcerative colitis
by: Sklyarov, A.Ya., et al.
Published: (2011)
by: Sklyarov, A.Ya., et al.
Published: (2011)
Effect of anticancer drugs on breast cancer cells sensitive and resistant to doxorubicin: expression of mRNAs of TGF-β and its receptors
by: Chorna, I.V., et al.
Published: (2014)
by: Chorna, I.V., et al.
Published: (2014)
Дослідження можливої ролі поліморфізму генів системи детоксикації та коагуляції крові у патогенезі втрати вагітності
by: Татарський, П.Ф., et al.
Published: (2011)
by: Татарський, П.Ф., et al.
Published: (2011)
Migration of labeled bone marrow MSCs and skin fibroblasts after systemic and local transplantation in rat burn wound model
by: Shchegelskaya, E.A., et al.
Published: (2015)
by: Shchegelskaya, E.A., et al.
Published: (2015)
Аналіз розподілу алельних варіантів генів HLA-DRB1, HLA-DQA1, HLA-DQB1 і HLA-G серед жінок з навиковим невиношуванням вагітності нез’ясованого ґенезу
by: Терпиляк, О.І., et al.
Published: (2013)
by: Терпиляк, О.І., et al.
Published: (2013)
The STAT5 transcription factor in B-cells of patients with chronic lymphocytic leukemia
by: Matvieieva, A.S., et al.
Published: (2019)
by: Matvieieva, A.S., et al.
Published: (2019)
Vitamin, mineral and iron supplementation in pregnancy: cross-sectional study
by: Leppee, M., et al.
Published: (2010)
by: Leppee, M., et al.
Published: (2010)
Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure
by: Fesai, O.A., et al.
Published: (2010)
by: Fesai, O.A., et al.
Published: (2010)
Similar Items
-
Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants
by: Tatarskyy, P.F., et al.
Published: (2010) -
Analysis of polymorphic variants S677T and A1298C of MTHFR gene in patients with psoriasis
by: A. M. Fedota, et al.
Published: (2015) -
Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability
by: Gulkovskyi, R.V., et al.
Published: (2015) -
Specificities of Sanfilippo A syndrome laboratory diagnostics
by: Trofimova, N.S., et al.
Published: (2014) -
Association of genotypes by polymorphic variant C-108T of PON1 gene with the risk of developing breast cancer and hypertensive disease in women
by: Fishchuk, L.Ye.
Published: (2014)