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

Isogenic induced pluripotent stem cell line ICGi036-A-1 from a patient with familial hypercholesterolaemia, derived by correcting a pathogenic variant of the gene LDLR c.530C>T

从一名家族性高胆固醇血症患者中获得的同源诱导多能干细胞系ICGi036-A-1,是通过纠正LDLR基因c.530C>T的致病性变异而获得的。

Zueva, A S; Shevchenko, A I; Medvedev, S P; Elisaphenko, E A; Sleptcov, A A; Nazarenko, M S; Tmoyan, N A; Zakian, S M; Zakharova, I S

Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION

使用 Oxford Nanopore MinION 进行 LDLR 基因单核苷酸和结构变体的调用和定相

Maria S Nazarenko, Aleksei A Sleptcov, Aleksei A Zarubin, Ramil R Salakhov, Alexander I Shevchenko, Narek A Tmoyan, Eugeny A Elisaphenko, Ekaterina S Zubkova, Nina V Zheltysheva, Marat V Ezhov, Valery V Kukharchuk, Yelena V Parfyonova, Suren M Zakian, Irina S Zakharova

The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing

利用综合细胞基因组分析、多色显带和单拷贝染色体测序技术对10q22.2q23.3臂间倒位进行精确断点定位

Tatyana V Karamysheva ,Tatyana A Gayner ,Eugeny A Elisaphenko ,Vladimir A Trifonov ,Elvira G Zakirova ,Konstantin E Orishchenko ,Mariya A Prokhorovich ,Maria E Lopatkina ,Nikolay A Skryabin ,Igor N Lebedev ,Nikolay B Rubtsov

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

利用基于芯片的比较基因组杂交和显微切割染色体测序技术进行10号染色体小超数标记的产前诊断

Igor N Lebedev ,Tatyana V Karamysheva ,Eugeny A Elisaphenko ,Alexey I Makunin ,Daria I Zhigalina ,Maria E Lopatkina ,Gleb V Drozdov ,Aleksander D Cheremnykh ,Natalia B Torkhova ,Gulnara N Seitova ,Stanislav A Vasilyev ,Anna A Kashevarova ,Ludmila P Nazarenko ,Nikolay B Rubtsov

Genome-wide profiling and differential expression of microRNA in rat pluripotent stem cells

大鼠多能干细胞中microRNA的全基因组分析和差异表达

Sherstyuk, Vladimir V; Medvedev, Sergey P; Elisaphenko, Evgeniy A; Vaskova, Evgeniya A; Ri, Maxim T; Vyatkin, Yuri V; Saik, Olga V; Shtokalo, Dmitry N; Pokushalov, Evgeniy A; Zakian, Suren M

Variability of sequence surrounding the Xist gene in rodents suggests taxon-specific regulation of X chromosome inactivation

啮齿动物Xist基因周围序列的变异性表明X染色体失活存在分类群特异性调控。

Shevchenko, Alexander I; Malakhova, Anastasia A; Elisaphenko, Eugeny A; Mazurok, Nina A; Nesterova, Tatyana B; Brockdorff, Neil; Zakian, Suren M

FGF4 independent derivation of trophoblast stem cells from the common vole

普通田鼠滋养层干细胞的FGF4非依赖性来源

Grigor'eva, Elena V; Shevchenko, Alexander I; Mazurok, Nina A; Elisaphenko, Eugeny A; Zhelezova, Antonina I; Shilov, Alexander G; Dyban, Pavel A; Dyban, Andrey P; Noniashvili, Ekaterina M; Slobodyanyuk, Sergey Ya; Nesterova, Tatyana B; Brockdorff, Neil; Zakian, Suren M

Structure and expression pattern of Oct4 gene are conserved in vole Microtus rossiaemeridionalis

Oct4基因的结构和表达模式在田鼠(Microtus rossiaemeridionalis)中是保守的。

Medvedev, Sergey P; Shevchenko, Alexander I; Elisaphenko, Eugene A; Nesterova, Tatyana B; Brockdorff, Neil; Zakian, Suren M

A dual origin of the Xist gene from a protein-coding gene and a set of transposable elements

Xist基因的双重起源:一个是蛋白质编码基因,另一个是一组转座元件。

Elisaphenko, Eugeny A; Kolesnikov, Nikolay N; Shevchenko, Alexander I; Rogozin, Igor B; Nesterova, Tatyana B; Brockdorff, Neil; Zakian, Suren M

Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials

在小鼠和人类中,Xist基因两侧的基因在美洲有袋动物的X染色体上是分开的。

Shevchenko, Alexander I; Zakharova, Irina S; Elisaphenko, Eugeny A; Kolesnikov, Nicolay N; Whitehead, Siobhan; Bird, Christine; Ross, Mark; Weidman, Jennifer R; Jirtle, Randy L; Karamysheva, Tatiana V; Rubtsov, Nicolay B; VandeBerg, John L; Mazurok, Nina A; Nesterova, Tatyana B; Brockdorff, Neil; Zakian, Suren M