Výsledky vyhledávání - "M. Ya. Tyrkus"

Akademický článek

Association between Val158Met polymorphism in the COMT gene with anxiety and heart rate variability in children with irritable bowel syndrome

Autor: M. O. Semen, O. L. Lychkovska, M. Ya. Tyrkus, D. V. Kaminskyy, O. P. Yelisyeyeva

Publikováno v: Zaporožskij Medicinskij Žurnal, Vol 25, Iss 5, Pp 439-446 (2023)

The aim of this study was to examine the peculiarities of trait anxiety and heart rate variability parameters as well as their relationship depending on the catechol O-methyltransferase (COMT) gene Val158Met polymorphism in children with irritable bo

Externí odkaz: https://doaj.org/article/48ce32381d6348c895da2962fa3d3791

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Determining the Number of TREC and KREC Copies for Screening of Inborn Errors of Immunity

Autor: H. V. Makukh, O. R. Boyarchuk, V. S. Kravets, N. M. Yarema, I. E. Shimanska, M. I. Kinash, M. Ya. Tyrkus, O. M. Shulhai

Publikováno v: Cytology and Genetics. 57:12-18

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e636e7bd0f72ed7a8d24dc7c55d00552
https://doi.org/10.3103/s009545272301005x

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Analysis of the PAH Gene Mutations in the Ukrainian Population: A Report from the West Ukrainian Region

Autor: Ye. O. Poliakova, Halyna Makukh, M. Ya. Tyrkus, A. Y. Malakhova, V. I. Shuvarska, L. B. Chorna, H. R. Akopyan

Publikováno v: Cytology and Genetics. 55:414-419

Phenylketonuria (PKU) is one of the most frequent autosomal recessive diseases caused by inherited deficiency of phenylalanine hydroxylase (PAH), which is accompanied by intellectual disability. The PAH gene mutations lead to a complete or partial lo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9e6dfa2631c8bf4f32da6e4d0eb3655e
https://doi.org/10.3103/s0095452721050066

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CAG polymorphism of the androgen receptor gene in azoospermic and oligozoospermic men from Ukraine

Autor: G. V. Makuh, M. Ya. Tyrkus, V. M. Zinchenko, G. V. Strelko, O. A. Fesai, S. A. Kravchenko, L. A. Livshits

Publikováno v: Cytology and Genetics. 43:401-405

An analysis of the number of CAG repeats in exon 1 of the gene was conducted in a group of 228 infertile males with azoospermia (n = 68) and oligozoospermia (n = 160), and in a control group (124 proven fathers) by means of polymerase chain reaction

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ac9d85b74eacbcc698907843b9a34867
https://doi.org/10.3103/s0095452709060061

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Microdeletions in the Y chromosome as a predictive marker of infertility in males

Autor: N. L. Guleiok, M. Ya. Tyrkus, Danuta Zastavna, A. Y. Nakonechnyy, B. R. Stoyka, G. V. Makukh

Publikováno v: Cytology and Genetics. 42:111-115

Results of a molecular-genetics study of microdeletions in the Y chromosome among males with disturbances in spermatogenesis and among patients with cryptorchism are presented. A study of subregions AZFa, AZFb and AZFc with the use of DNA analysis in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a2356e5969257b4b4ee189bb2e82e2d
https://doi.org/10.1007/s11956-008-2008-y

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The frequency of terminal deletions sY160 among men with microdeletions of AZFc region Y-chromosome

Autor: M. Ya. Tyrkus, Halyna Makukh, I. Ye. Haiboniuk

Publikováno v: Faktori eksperimental'noi evolucii organizmiv. 21:301-305

Aim. Determine the frequency of absence marker terminal deletions sY160 among men with microdeletions of AZFc region Y-chromosome. Methods. DNA from probands blood samples was isolated using a modified salting out method. Microdeletions of Y chromoso

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::da8f233d5ac3361e8034c3426bc0dab6
https://doi.org/10.7124/feeo.v21.856

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