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

G-quadruplexes as potential traps for superenhancer marker BRD4: ligand-sensitive binding and co-separation in vitro

G-四链体作为超级增强子标记物BRD4的潜在捕获物:体外配体敏感结合和共分离

Pavlova, Iuliia I; Ivanova, Olga M; Iudin, Mikhail S; Surdina, Anastasiya V; Barinov, Nikolay A; Bogomiakova, Margarita E; Oreshkov, Sergey D; Shenkarev, Zakhar O; Severov, Vjacheslav V; Klinov, Dmitriy V; Shender, Victoria O; Bogomazova, Alexandra N; Lagarkova, Maria A; Varizhuk, Anna M; Tsvetkov, Vladimir B

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy.

ELFN1 缺陷:一种伴有癫痫的神经发育障碍的机制基础和表型谱

Dore Rhys, Chang Chu-Ting, Declève Amber, Brunori Gloria, Ludlam W Grant, Huang Alden, Movahedinia Mojtaba, Damseh Nadirah S, Anwar Ijaz, Vahidi Mehrjardi Mohammad Yahya, Ny Annelii, Khorrami Mehdi, Kheirollahi Majid, Frederiksen Helen, Eghbal Fatemeh, Mirjalili Mohammad Reza, Dehghani Mohammadreza, Karimiani Ehsan Ghayoor, Oreshkov Sergey, Alves Cesar, Striano Pasquale, Suri Mohnish, Martinez-Agosto Julian, Ansar Muhammad, Zahid Muhammad, Akram Samra, Ansar Muhammad, Nelson Stanley F, Antonarakis Stylianos E, Houlden Henry, Copmans Daniëlle, Martemyanov Kirill A, Maroofian Reza

Relative subsystems and quantum reference frame transformations

相对子系统和量子参考系变换

Castro-Ruiz, Esteban; Oreshkov, Ognyan

Deciphering the Genetic Basis of Degenerative and Developmental Eye Disorders in 50 Pakistani Consanguineous Families Using Whole-Exome Sequencing

利用全外显子组测序技术解析50个巴基斯坦近亲结婚家庭退行性和发育性眼病的遗传基础

Zafar, Ainee; Baig, Ruqia Mehmood; Arshad, Abida; Rashid, Abdur; Oreshkov, Sergey; Frederiksen, Helen Nabiryo; Ansar, Muhammad

A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family

巴基斯坦一个家族中发现一种新的纯合DST变异导致遗传性感觉和自主神经病变。

Munir, Asad; Frederiksen, Helen Nabiryo; Ali, Fawad; Shah, Sabawoon; Rashid, Abdur; Oreshkov, Sergey; Khan, Kashif; Shahzeb, Muhammad; Ullah, Inam; Rahman, Hamid Ur; Ullah, Mukhtar; Ansar, Muhammad; Rehman, Atta Ur

Whole genome sequencing and single-cell transcriptomics identify KMT2D inactivation as a potential new driver for pituitary tumors: a case report

全基因组测序和单细胞转录组学鉴定出KMT2D失活可能是垂体肿瘤的一个潜在新驱动因素:病例报告

Brunner, Maxime; Meylan-Merlini, Jenny; Muriset, Maude; Oreshkov, Sergey; Messina, Andrea; Messerer, Mahmoud; Daniel, Roy; Hewer, Ekkehard; Brouland, Jean Phillipe; Santoni, Federico

When less is more: sketching with minimizers in genomics

少即是多:基因组学中的最小化草图绘制

Ndiaye, Malick; Prieto-Baños, Silvia; Fitzgerald, Lucy M; Yazdizadeh Kharrazi, Ali; Oreshkov, Sergey; Dessimoz, Christophe; Sedlazeck, Fritz J; Glover, Natasha; Majidian, Sina

pyTWMR: transcriptome-wide Mendelian randomization in python

pyTWMR:Python 中的转录组范围孟德尔随机化

Oreshkov, Sergey; Lepik, Kaido; Santoni, Federico

Secondary structure of the human mitochondrial genome affects formation of deletions

人类线粒体基因组的二级结构影响缺失的形成

Shamanskiy, Victor; Mikhailova, Alina A; Tretiakov, Evgenii O; Ushakova, Kristina; Mikhailova, Alina G; Oreshkov, Sergei; Knorre, Dmitry A; Ree, Natalia; Overdevest, Jonathan B; Lukowski, Samuel W; Gostimskaya, Irina; Yurov, Valerian; Liou, Chia-Wei; Lin, Tsu-Kung; Kunz, Wolfram S; Reymond, Alexandre; Mazunin, Ilya; Bazykin, Georgii A; Fellay, Jacques; Tanaka, Masashi; Khrapko, Konstantin; Gunbin, Konstantin; Popadin, Konstantin

Aminooxy Click Modification of a Periodate-Oxidized Immunoglobulin G: A General Approach to Antibody-Drug Conjugates with Dye-Mediated Expeditious Stoichiometry Control

高碘酸氧化免疫球蛋白 G 的氨氧点击修饰:一种利用染料介导的快速化学计量控制抗体-药物结合物的通用方法

Ksenia A Sapozhnikova, Evgeny L Gulyak, Vladimir A Brylev, Vsevolod A Misyurin, Sergey D Oreshkov, Anastasiya V Alexeeva, Dmitry Yu Ryazantsev, Maria A Simonova, Ekaterina V Ryabukhina, Galina P Popova, Nataliya A Tikhonova, Natalia A Lyzhko, Alexander E Barmashov, Andrey V Misyurin, Alexey V Ustino