Natalia Semenova
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Explore the profile of Natalia Semenova including associated specialties, affiliations and a list of published articles.
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20
Citations
706
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Recent Articles
1.
Bostanova F, Levchenko O, Sharova M, Semenova N
Clin Pract
. 2024 May;
14(3):928-933.
PMID: 38804405
Tatton-Brown-Rahman syndrome is a rare autosomal dominant hereditary disease caused by pathogenic variants in the gene, which is an important participant in epigenetic regulation, especially during embryonic development, and is...
2.
Lenz D, Schlieben L, Shimura M, Bianzano A, Smirnov D, Kopajtich R, et al.
Hepatology
. 2023 Nov;
79(5):1075-1087.
PMID: 37976411
Background And Aims: Pediatric acute liver failure (PALF) is a life-threatening condition. In Europe, the main causes are viral infections (12%-16%) and inherited metabolic diseases (14%-28%). Yet, in up to...
3.
Yakovlev A, Gritskova A, Manzhurtsev A, Ublinskiy M, Menshchikov P, Vanin A, et al.
MAGMA
. 2023 Sep;
37(1):39-51.
PMID: 37715877
Objective: To find a possible quantitative relation between activation-induced fast (< 10 s) changes in the γ-aminobutyric acid (GABA) level and the amplitude of a blood oxygen level-dependent contrast (BOLD)...
4.
Semenova N, Kamenets E, Annenkova E, Marakhonov A, Gusarova E, Demina N, et al.
Int J Mol Sci
. 2023 Jul;
24(14).
PMID: 37511516
Alagille syndrome (ALGS) is a multisystem condition characterized by cholestasis and bile duct paucity on liver biopsy and variable involvement of the heart, skeleton, eyes, kidneys, and face and caused...
5.
Semenova N, Shatokhina O, Shchagina O, Kamenec E, Marakhonov A, Degtyareva A, et al.
Int J Mol Sci
. 2023 Apr;
24(8).
PMID: 37108612
The congenital disorder of glycosylation type IIs (ATP6AP1-CDG; OMIM# 300972) is a rare X-linked recessive complex syndrome characterized by liver dysfunction, recurrent bacterial infections, hypogammaglobulinemia, and defective glycosylation of serum...
6.
Bogdanova E, Sadykov A, Ivanova G, Zubina I, Beresneva O, Semenova N, et al.
Int J Mol Sci
. 2023 Apr;
24(8).
PMID: 37108433
The initial phases of molecular and cellular maladaptive bone responses in early chronic kidney disease (CKD) remain mostly unknown. We induced mild CKD in spontaneously hypertensive rats (SHR) by either...
7.
Semenova N, Marakhonov A, Ampleeva M, Kurkina M, Baydakova G, Skoblov M, et al.
Int J Mol Sci
. 2022 Dec;
23(23).
PMID: 36499355
Hyperammonemia due to carbonic anhydrase VA deficiency (OMIM# 615751) is a rare, life-threatening hereditary disease caused by biallelic mutations in the CA5A gene, presenting as encephalopathic hyperammonemia of unexplained origin...
8.
Pirkis J, Gunnell D, Shin S, Del Pozo-Banos M, Arya V, Aguilar P, et al.
EClinicalMedicine
. 2022 Aug;
51:101573.
PMID: 35935344
Background: Predicted increases in suicide were not generally observed in the early months of the COVID-19 pandemic. However, the picture may be changing and patterns might vary across demographic groups....
9.
Levchenko O, Dadali E, Bessonova L, Demina N, Rudenskaya G, Matyushchenko G, et al.
Int J Mol Sci
. 2022 Jul;
23(14).
PMID: 35887114
Intellectual development disorder (IDD) is characterized by a general deficit in intellectual and adaptive functioning. In recent years, there has been a growing interest in studying the genetic structure of...
10.
Enukashvily N, Semenova N, Chubar A, Ostromyshenskii D, Gushcha E, Gritsaev S, et al.
Int J Mol Sci
. 2022 Mar;
23(6).
PMID: 35328779
Mesenchymal stromal cells (MSC) 'educated' by tumor cells are an essential component of the multiple myeloma (MM) tumor microenvironment (TME) involved in tumor progression. Transcription of tandemly repeated (TR) non-coding...