Zobrazeno 1 - 10
of 20
pro vyhledávání: '"M. O. Ryznychuk"'
Publikováno v:
Regulatory Mechanisms in Biosystems, Vol 9, Iss 1, Pp 41-46 (2018)
Tubulopathy is a heterogeneous group of diseases combined by the nephron functions disorders of one or more enzyme proteins in the tubular epithelium that cease to function as a reabsorption of one or several substances filtered from the blood throug
Externí odkaz:
https://doaj.org/article/7c1017a7a28e493b998a29a742df5a1b
Autor:
M. O. Ryznychuk, V. P. Pishak
Publikováno v:
Regulatory Mechanisms in Biosystems, Vol 8, Iss 1, Pp 23-29 (2017)
The article highlights the role of desynchronosis and certain genetic factors in the development of obesity. Some pathogenetic links of obesity and the influence of melatonin on them are analyzed.Desynchronosis is one of the causes of obesity as a re
Externí odkaz:
https://doaj.org/article/8a30eb8c5ecc4f6e86179407ccfd0518
Autor:
V. P. Pishak, M. O. Ryznychuk
Publikováno v:
Неонатологія, хірургія та перинатальна медицина, Vol 7, Iss 3(25) (2017)
Резюме. В огляді розглянута роль мікроРНК на ранній етапах онтогенезу. Початок третього тисячоліття ознаменований революційним відкри
Externí odkaz:
https://doaj.org/article/3453f91e482a40a6aec11ee95f4341d1
Publikováno v:
Морфологія, Vol 10, Iss 3, Pp 196-198 (2016)
Background. Beta-blockers, including propranolol, are widely used in clinical practice as effective heart medicines. By the spectrum of action, some of them are selectively blocking beta-blockers, which are located in the heart muscle, and called car
Externí odkaz:
https://doaj.org/article/088a7df7f75c47efa3d487fef1ee40d7
Publikováno v:
Неонатологія, хірургія та перинатальна медицина, Vol 7, Iss 1(23) (2017)
У статті розглянуті генетичні форми недостатності гормону росту в дітей. Аналіз генів, дефекти яких можуть призводити до вираженої затр
Externí odkaz:
https://doaj.org/article/f2c5657c2b54468286fc07eb2facb597
Publikováno v:
Regulatory Mechanisms in Biosystems. 12:445-451
Tubulopathies are a group of heterogeneous diseases that are manifested in the malfunction of the renal tubules. This review addresses tubulopathies associated with polyuria syndrome, namely renal glucosuria syndrome, nephrogenic diabetes insipidus a
Autor:
N. B. Kuzniak, M. O. Ryznychuk, S. O. Batranovska, S. P. Melnychuk, I. I. Zamorskii, T. V. Khmara
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 6:71-77
Congenital abnormalities occur in 2-3% of all children and about 1% have hereditary syndromes or multiple malformations. About 30% of all cases have a cleft lip or palate. Genetic factors such as chromosomal abnormalities and gene mutations cause abo
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 6:20-30
Annually severe congenital abnormalities occur in 1 of 33 newborns or about 125.000 live births in the United States and are the leading cause of infant mortality. Craniofacial anomalies account for about one-third of all abnormalities. The prevalenc
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 5:61-70
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 5:98-106