日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Mining Differentially Expressed Genes in the Marine Free-Living Flatworm Macrostomum lignano Under Aneuploidy-Driven Ploidy Changes

在非整倍体驱动的倍性变化下,挖掘海洋自由生活扁形动物 Macrostomum lignano 中的差异表达基因

Zadesenets, Kira S; Ershov, Nikita I; Bondar, Natalya P; Orishchenko, Konstantin E; Rubtsov, Nikolay B

Transcriptomic Analysis of TDP1-Knockout HEK293A Cells Treated with the TDP1 Inhibitor (Usnic Acid Derivative)

用TDP1抑制剂(乌斯尼酸衍生物)处理TDP1敲除HEK293A细胞的转录组分析

Zakharenko, Alexandra L; Dyrkheeva, Nadezhda S; Markov, Andrey V; Kleshchev, Maxim A; Ryabchikova, Elena I; Malakhova, Anastasia A; Orishchenko, Konstantin E; Okorokova, Larisa S; Shtokalo, Dmitriy N; Medvedev, Sergey P; Zakian, Suren M; Tupikin, Alexey A; Kabilov, Marsel R; Luzina, Olga A; Deyev, Sergey M; Lavrik, Olga I

Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay

利用微基因检测评估听力损失患者中发现的SLC26A4基因新型和罕见变异的功能意义

Danilchenko, Valeriia Yu; Panina, Ekaterina A; Zytzar, Marina V; Orishchenko, Konstantin E; Posukh, Olga L

Validating TDP1 as an Inhibition Target for Lipophilic Nucleoside Derivative in Human Cells

验证TDP1作为亲脂性核苷衍生物在人细胞中的抑制靶点

Chernyshova, Irina A; Kornienko, Tatyana E; Dyrkheeva, Nadezhda S; Zakharenko, Alexandra L; Chepanova, Arina A; Orishchenko, Konstantin E; Kurochkin, Nikolay N; Drenichev, Mikhail S; Lavrik, Olga I

The Single Nucleotide Substitution T → A rs2072580 Damages the CREB1 Binding Site in the Bidirectional SART3/ISCU Promoter

单核苷酸替换 T → A rs2072580 会破坏双向 SART3/ISCU 启动子中的 CREB1 结合位点

Degtyareva, Arina; Antontseva, Elena; Evseenko, Anastasia; Orishchenko, Konstantin; Merkulova, Tatiana

Comparative analysis of haplotypes carrying pathogenic variants c.1545T>G, c.2027T>A and c.919-2A>G of the SLC26A4 gene in patients with hearing loss from the Tyva Republic (Southern Siberia)

对来自图瓦共和国(西伯利亚南部)听力损失患者的 SLC26A4 基因致病变异 c.1545T>G、c.2027T>A 和 c.919-2A>G 的单倍型进行比较分析

Danilchenko, V Yu; Zytsar, M V; Panina, E A; Orishchenko, K E; Posukh, O L

A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

一例伴有罕见嵌合型超数标记染色体12和12p13.1-p12.1间质重复的Pallister-Killian综合征病例报告

T V Karamysheva # ,I N Lebedev # ,L I Minaycheva ,L P Nazarenko ,A A Kashevarova ,D A Fedotov ,N A Skryabin ,M E Lopatkina ,A D Cheremnykh ,E A Fonova ,T V Nikitina ,E A Sazhenova ,M M Skleimova ,N A Kolesnikov ,G V Drozdov ,Y S Yakovleva ,G N Seitova ,K E Orishchenko ,N B Rubtsov

Crosstalk between BER and NHEJ in XRCC4-Deficient Cells Depending on hTERT Overexpression

XRCC4 缺陷细胞中 BER 与 NHEJ 之间的串扰取决于 hTERT 过表达

Svetlana V Sergeeva, Polina S Loshchenova, Dmitry Yu Oshchepkov, Konstantin E Orishchenko

Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

位于不同Cx26结构域的GJB2基因(Cx26)致病变异的功能后果

Posukh, Olga L; Maslova, Ekaterina A; Danilchenko, Valeriia Yu; Zytsar, Marina V; Orishchenko, Konstantin E

Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia)

深入了解与听力损失相关的 SLC26A4 基因致病变异 c.919-2A>G 的自然史:其起源于俄罗斯西伯利亚南部的证据

Danilchenko, Valeriia Yu; Zytsar, Marina V; Maslova, Ekaterina A; Orishchenko, Konstantin E; Posukh, Olga L