Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Petr A. Slominsky"'
Autor:
Marina V. Shulskaya, Ekaterina I. Semenova, Margarita M. Rudenok, Suzanna A. Partevian, Maria V. Lukashevich, Alexei V. Karabanov, Ekaterina Yu. Fedotova, Sergey N. Illarioshkin, Petr A. Slominsky, Maria I. Shadrina, Anelya Kh. Alieva
Publikováno v:
Biomedicines, Vol 12, Iss 7, p 1391 (2024)
Parkinson’s disease (PD) is one of the most common human neurodegenerative diseases. Belated diagnoses of PD and late treatment are caused by its elongated prodromal phase. Thus, searching for new candidate genes participating in the development of
Externí odkaz:
https://doaj.org/article/b318e57eae254aceaa4a8bb8ef4f77ef
Autor:
Karine Yu. Sarkisova, Ekaterina A. Fedosova, Alla B. Shatskova, Margarita M. Rudenok, Vera A. Stanishevskaya, Petr A. Slominsky
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 398 (2023)
The reduced expression of the HCN1 ion channel in the somatosensory cortex (SSC) and mesolimbic dopamine deficiency are thought to be associated with the genesis of spike-wave discharges (SWDs) and comorbid depression in the WAG/Rij rat model of abse
Externí odkaz:
https://doaj.org/article/4a08d873bfe24d65bd60fee5b5e12fb2
Autor:
Elena V. Filatova, Natalia S. Krylova, Ivan N. Vlasov, Maria S. Maslova, Natalia G. Poteshkina, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Hypertrophic cardiomyopathy (HCM), described as the presence of hypertrophy of left ventricular, is the most prevalent heritable cardiovascular disease with predominantly an autosomal dominant type of inheritance. However, pathoge
Externí odkaz:
https://doaj.org/article/2e3c0cb32a2d42dabacb2b2e3626ff14
Autor:
Ekaterina I. Semenova, Ivan N. Vlasov, Suzanna A. Partevian, Anna V. Rosinskaya, Ivan N. Rybolovlev, Petr A. Slominsky, Maria I. Shadrina, Anelya Kh. Alieva
Publikováno v:
Cells, Vol 11, Iss 16, p 2599 (2022)
Parkinson’s disease (PD) is one of the most common neurodegenerative diseases. Investigating individuals with the most identical genetic background is optimal for minimizing the genetic contribution to gene expression. These individuals include mon
Externí odkaz:
https://doaj.org/article/6bbde47c4a0b41de95b91dc26dc7d5fd
Autor:
Margarita M. Rudenok, Maria I. Shadrina, Elena V. Filatova, Ivan N. Rybolovlev, Maxim S. Nesterov, Denis A. Abaimov, Ruslan A. Ageldinov, Anna A. Kolacheva, Michael V. Ugrumov, Petr A. Slominsky, Anelya Kh. Alieva
Publikováno v:
Life, Vol 12, Iss 5, p 751 (2022)
Processes of intracellular and extracellular transport play one of the most important roles in the functioning of cells. Changes to transport mechanisms in a neuron can lead to the disruption of many cellular processes and even to cell death. It was
Externí odkaz:
https://doaj.org/article/ee6d332f92ee437e851a8eb73244f36d
Autor:
Anelya Kh. Alieva, Elena V. Filatova, Margarita M. Rudenok, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Cells, Vol 10, Iss 9, p 2252 (2021)
A critical aspect of real-time PCR is the presence of housekeeping genes (HKGs) as an internal control for the normalization of expression data for genes of interest. It is necessary to select correct HKGs in the investigation of various pathologies.
Externí odkaz:
https://doaj.org/article/18c0eef5621d4784b638a2cd6f584fbb
Publikováno v:
Cells, Vol 10, Iss 6, p 1283 (2021)
Major depressive disorder (MDD) is a heterogeneous disease affecting one out of five individuals and is the leading cause of disability worldwide. Presently, MDD is considered a multifactorial disease with various causes such as genetic susceptibilit
Externí odkaz:
https://doaj.org/article/31a5acfa8ea54251b04592c0d87ab845
Publikováno v:
Frontiers in Psychiatry, Vol 9 (2018)
Depressive disorders (DDs) are one of the most widespread forms of psychiatric pathology. According to the World Health Organization, about 350 million people in the world are affected by this condition. Family and twin studies have demonstrated that
Externí odkaz:
https://doaj.org/article/be1b98ad280345388d8c3b02f71f9a83
Autor:
Marina V. Shulskaya, Anelya Kh. Alieva, Ivan N. Vlasov, Vladimir V. Zyrin, Ekaterina Yu. Fedotova, Natalia Yu. Abramycheva, Tatiana S. Usenko, Andrei F. Yakimovsky, Anton K. Emelyanov, Sofya N. Pchelina, Sergei N. Illarioshkin, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Frontiers in Aging Neuroscience, Vol 10 (2018)
Background: Parkinson’s disease (PD) is a complex disease with its monogenic forms accounting for less than 10% of all cases. Whole-exome sequencing (WES) technology has been used successfully to find mutations in large families. However, because o
Externí odkaz:
https://doaj.org/article/060d9b909e7946ffb39f93050ede2a8d
Autor:
Anelya Kh. Alieva, Elena V. Filatova, Aleksey V. Karabanov, Sergey N. Illarioshkin, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Parkinson's Disease, Vol 2015 (2015)
Parkinson’s disease (PD) is a widespread neurodegenerative disorder. Despite the intensive studies of this pathology, in general, the picture of the etiopathogenesis has still not been clarified fully. To understand better the mechanisms underlying
Externí odkaz:
https://doaj.org/article/ca469d9fbe4b42b0ab650a0c46e5de93