Zobrazeno 1 - 10
of 43
pro vyhledávání: '"E V, Shakhtshneider"'
Publikováno v:
Российский кардиологический журнал, Vol 29, Iss 8 (2024)
Among the various dyslipidemia types, familial combined hyperlipidemia (FCH) is the most common genetic disorder, which is characterized by at least two different forms of lipid disorders: hypercholesterolemia and hypertriglyceridemia. In FCH, the
Externí odkaz:
https://doaj.org/article/e4963dfdb74847bdbd6e9dadcef650c6
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 27, Iss 5, Pp 522-529 (2023)
One of the most common congenital metabolic disorders is familial hypercholesterolemia. Familial hyper-cholesterolemia is a condition caused by a type of genetic defect leading to a decreased rate of removal of low-density lipoproteins from the blood
Externí odkaz:
https://doaj.org/article/ea71e6866cde4052bdb646221d3a7b0b
Autor:
S. V. Mikhailova, D. E. Ivanoshchuk, P. S. Orlov, L. D. Latyntseva, E. V. Kashtanova, Ya. V. Polonskaya, Yu. I. Ragino, E. V. Shakhtshneider
Publikováno v:
Сибирский научный медицинский журнал, Vol 43, Iss 4, Pp 97-109 (2023)
Understanding the molecular mechanisms of atherosclerotic vascular lesions formation is necessary both for assessing the risks of cardiovascular diseases and for finding approaches to their therapy. The task remains relevant, despite the large number
Externí odkaz:
https://doaj.org/article/be3a3dc8ca524b2d87b367c32de1539d
Publikováno v:
Сибирский научный медицинский журнал, Vol 42, Iss 4, Pp 79-86 (2022)
Aim. To study the spectrum of variants in the PRL, PRLR, PRLHR genes in women of reproductive age with non-tumor hyperprolactinemia. Material and methods. In women with non-tumor hyperprolactinemia (n = 15), targeted high-throughput sequencing of the
Externí odkaz:
https://doaj.org/article/20e3a4883489477c86249e01667ee3e9
Autor:
O. D. Rymar, S. M. Voevoda, E. V. Shakhtshneider, E. M. Stakhneva, S. V. Mustafina, L. V. Shcherbakova
Publikováno v:
Ожирение и метаболизм, Vol 18, Iss 2, Pp 180-189 (2021)
Background: Hyperprolactinemia is one of the most common hypothalamic-pituitary-endocrine disorders in women of reproductive age, with the highest frequency at the age of 25–44 years. In addition to influencing the reproductive system, it is import
Externí odkaz:
https://doaj.org/article/e9aec3b0bbd34f8f9f0e12a182d87cad
Publikováno v:
Сахарный диабет, Vol 24, Iss 2, Pp 133-140 (2021)
Most young patients with hyperglycemia have type 1 diabetes and type 2 diabetes but up to 10% of all cases of the disease occur in MODY (Maturity Onset Diabetes of the Young). Published abstracts show features of the debut, laboratory and genetic cha
Externí odkaz:
https://doaj.org/article/25c877c8b33c4e0683edfbac50ee1d08
Autor:
E. V. Kashtanova, E. V. Shakhtshneider, M. V. Kruchinina, I. I. Logvinenko, E. V. Striukova, Yu. I. Ragino
Publikováno v:
Бюллетень сибирской медицины, Vol 20, Iss 1, Pp 147-157 (2021)
The 2020 coronavirus infection pandemic has potentiated a large number of studies in the world on the etiopathogenesis, clinical and morphological manifestations of COVID-2019 infection. This review presents biochemical, molecular genetic and clinica
Externí odkaz:
https://doaj.org/article/8156dec0d4604e958568fcc18ddd0d01
Autor:
E. V. Striukova, E. V. Shakhtshneider, D. E. Ivanoshchuk, Yu. I. Ragino, Ya. V. Polonskaya, I. S. Murashov, A. M. Volkov, A. V. Kurguzov, A. M. Chernyavsky, E. S. Valeev, V. N. Maksimov, E. V. Kashtanova
Publikováno v:
Атеросклероз, Vol 17, Iss 1, Pp 29-37 (2021)
Factor V, encoded by the F5 gene, is a procoagulant blood clotting factor that increases the production of thrombin, the central enzyme that converts fibrinogen to fibrin, which leads to the formation of a blood clot. The F5 gene is localized to 1q24
Externí odkaz:
https://doaj.org/article/8aff56ce67424483891b89c6b8715268
Autor:
O. V. Timoshchenko, S. E. Semaev, D. E. Ivanoshchuk, E. M. Stakhneva, Yu. P. Nikitin, E. V. Shakhtshneider, Yu. I. Ragino
Publikováno v:
Атеросклероз, Vol 16, Iss 4, Pp 61-69 (2020)
Purpose of the study. To determine the frequency of the rs9536314 (F325V) polymorphism of the KL gene and the association of this variant with a number of biochemical and anthropometric parameters in men of the study group and in the Caucasian popula
Externí odkaz:
https://doaj.org/article/4b011092cb3c4205a98ea980913451e3
Autor:
D. E. Ivanoshchuk, S. V. Mikhailova, O. G. Fenkova, E. V. Shakhtshneider, A. Z. Fursova, I. V. Bychkov, M. I. Voevoda
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 24, Iss 8, Pp 861-867 (2020)
Primary congenital glaucoma (PСG) is a visual organ pathology that leads to progressive blindness and poor vision in children. Its main cause is an anomaly of the anterior chamber angle. Most cases of PСG are sporadic, but familial cases with an au
Externí odkaz:
https://doaj.org/article/dcf618ea9be5493a9bb9c336173aefee