Перегляд за автором "Livshits, L.A."

Результати 1-19 з 19

Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine

Hryshchenko, N.V.; Livshits, L.A. (Цитология и генетика, 2009)

Two intercomplementary methods of 17p11.2 duplication/deletion identification have been elaborated: STR allelic variants analysis and direct PMP22 gene dosage measuring by means of quantitative Real Time PCR. It has been ...
Association of IL8 and IL10 gene allelic variants with ischemic stroke risk and prognosis

Kucherenko, A.M.; Shulzhenko, D.V.; Kuznetsova, S.M.; Demydov, S.V.; Livshits, L.A. (Вiopolymers and Cell, 2014)

Aim. Evaluating a role of IL8 gene –781 C/T, and IL10 gene –592C/A polymorphisms as genetic markers of ischemic stroke risk. Methods. A case group consisted of 183 patients with ischemic stroke, which were ...
Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability

Gulkovskyi, R.V.; Livshits, L.A.; Sivolob, A.V. (Вiopolymers and Cell, 2015)

Aim. To investigate a possible association of the EPHA1 gene polymorphism with mild intellectual disability (ID). Methods. The group of patients with mild (IQ score between 50 and 70) idiopathic intellectual disability ...
Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability

Gulkovskyi, R.V.; Volkova, L.S.; Livshits, L.A. (2015)

Aim. To investigate the possible association of LIF gene polymorphism rs929271 with mild intellectual disability (ID). Methods. The group of patients with mild (IQ score between 50 and 70) idiopathic intellectual disability ...
Development of ARMS PCR tests for detection of common CFTR gene mutations

Soloviov, O.O.; Pampukha, V.M.; Livshits, L.A. (Вiopolymers and Cell, 2010)

Aim. To develop diagnostic assays, based on the amplification refractory mutation system (ARMS) principle, for detection of common mutations in the CFTR gene using two approaches: standard PCR with further gel-electrophoresis ...
Development of MLPA approach for SNP detection in MTHFR, F5 and F2 genes

Kravchenko, S.A.; Chernushyn, S.Yu.; Kucherenko, A.M.; Soloviov, O.O.; Livshits, L.A. (Вiopolymers and Cell, 2015)

Single nucleotide polymorphism (SNP) is an important and valuable form of DNA variation among individuals. Various methods for SNP genotyping have been developed, but a few are suitable for the flexible and low-cost ...
Distribution of FSHR307 and FSHR680 allelic variants of FSH receptor gene exon 10 in females from Ukraine

Livshyts, G.B.; Podlesnaja, S.S.; Kravchenko, S.A.; Livshits, L.A. (Біополімери і клітина, 2008)

The purpose of this study was to examine the distribution of two distinct follicle-stimulating hormone receptor (FSHR) variants, Asn680Ser and Thr307Ala, in normaly ovulated group of females from Ukraine. The FSHR gene ...
EPHA1 gene SNPs analysis in population of Ukraine

Gulkovskyi, R.V.; Chernushyn, S.Y.; Kravchenko, S.A.; Bychkova, G.M.; Livshits, L.A. (Вiopolymers and Cell, 2013)

Aim. Analysis the EPHA1 gene G1475A and G1891A alleles distribution in the population of Ukraine, and to study the protein secondary structure as the first step in the investigation of EPHA1 gene involvement in intellectual ...
Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis

Livshits, L.A.; Kravchenko, S.A.; Nechyporenko, M.V.; Pampukha, V.M.; Hryshchenko, N.V.; Livshyts, G.B.; Soloviov, O.O.; Tatarskyy, P.F.; Fesai, O.A.; Chernushyn, S.Yu.; Kucherenko, A.M.; Gulkovskyy, R.V. (Вiopolymers and Cell, 2013)

The summarized results of 25-year studies of department of human genomics of IMBG NASU are presented. The investigations were focused on identification of molecular genetic nature of human genome coding and non-coding ...
IFN-l-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860

Pampukha, V.M.; Kravchenko, S.A.; Moroz, L.V.; Livshits, L.A. (Вiopolymers and Cell, 2011)

Aim. The goal of our study was to develop an accurate detection of the SNP rs12979860 by RFLP-based method and to evaluate the polymorphic genotype distribution forthis SNP among individuals with unknown HCV status from ...
IL1β, IL6 and IL8 gene polymorphisms involvement in recurrent corneal erosion in patients with hereditary stromal corneal dystrophies

Kucherenko, A.M.; Pampukha, V.M.; Drozhyna, G.I.; Livshits, L.A. (Цитология и генетика, 2013)

TGFBI gene mutations cause corneal stromal dystrophies of autosomal dominant inheritance. The most frequent complication of stromal dystrophies is recurrent corneal erosion with varying degree of accompanying inflammation. ...
Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy

Soloviov, O.O.; Livshits, G.B.; Podlesnaya, S.S.; Livshits, L.A. (Вiopolymers and Cell, 2010)

Aim. To develop an easy and reliable assay for quantitative analysis of the SMN1 gene exon 7 copy number with Real-Time PCR and a SYBR Green dye which can be used as a test-system for spinal muscular atrophy (SMA) diagnostics. ...
Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants

Tatarskyy, P.F.; Kucherenko, A.M.; Kravchenko, S.A.; Shulzhenko, D.V.; Kuznetsova, S.M.; Livshits, L.A. (Вiopolymers and Cell, 2010)

Aim. To evaluate a possible involvement of the F2, F5, MTHFR gene variants into ischemic stroke pathogenesis in population of Ukraine. Methods. Polymorphic variants were analyzed in unrelated 183 stroke patients, 100 ...
Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability

Gulkovskyi, R.V.; Chernushyn, S.Y.; Livshits, L.A. (Вiopolymers and Cell, 2015)

Aim. To evaluate a possible role of a novel c.A212G substitution in the PUS3 gene at intellectual disability (ID). Methods. The observed group consisted of the ID Ukrainian family members (parents and two affected children) ...
Polymorphic short tandem repeats for PCR-based diagnosis of the Charcot-Marie-Tooth 1A duplication in Ukraine

Hryshchenko, N.V.; Kravchenko, S.A.; Livshits, L.A. (Цитология и генетика, 2005)

Charcot-Marie-Tooth neuropathy (CMT) is one of the most common hereditary disorders, affecting 1 : 2500 individuals. The major mutation – microduplication of 1.4 megabases in 17р11.2 region, which is responsible for 68–90 ...
Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure

Fesai, O.A.; Kravchenko, S.A.; Zinchenko, V.M.; Livshits, L.A. (Вiopolymers and Cell, 2010)

Aim. To study the IVS8-5T allele of the CFTR gene and it is involvement in spermatogenesis failure in men with azoospermia and oligozoospermia. Methods. The IVS8-nT polymorphism was analyzed by PCR followed by «A.L.F.-express» ...
Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children

Tatarskyy, P.F.; Chumachenko, N.G.; Kucherenko, A.M.; Gulkovskyi, R.V.; Arabskaya, L.P.; Smirnova, O.A.; Tolkach, S.I.; Antipkin, Yu.G.; Livshits, L.A. (Вiopolymers and Cell, 2011)

Aim. To study the association of polymorphisms of the enzymes genes CYP1A1 (T6235C), first phase, and NAT2 (Ñ481Ò, G590A, G857A), GSTM1 («0»), GSTT1 («0») and GSTP1 (A313G), second phase of the detoxication system, as ...
Study on the IFNL4 gene ss469415590 variant in Ukrainian population

Kucherenko, A.M.; Pampukha, V.M.; Livshits, L.A. (Вiopolymers and Cell, 2014)

Aim. To determine genotype and allele disribution for the IFNL4 gene ss469415590 and examine it for linkage with the IL28B gene rs12979860 in Ukrainian population. Methods. The studied group consisted of 100 unrelated ...
The role of IL6 and ESR1 gene polymorphisms as immunological factors of pregnancy maintenance

Kucherenko, A.M.; Vorobiova, I.I.; Rudakova, N.V.; Livshits, L.A. (Вiopolymers and Cell, 2013)

Aim. The study is aimed at the evaluation of the association of IL6 gene -174G/C polymorphism and ESR1 gene -397C/T polymorphism with recurrent pregnancy loss (RPL) pathogenesis and at the investigation of the ESR1 gene ...

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Перегляд за автором "Livshits, L.A."

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