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

Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect

ANO4 中的错义变异会导致散发性脑病或家族性癫痫,并有证据表明存在显性负效应

Fang Yang, Anais Begemann, Nadine Reichhart, Akvile Haeckel, Katharina Steindl, Eyk Schellenberger, Ronja Fini Sturm, Magalie Barth, Sissy Bassani, Paranchai Boonsawat, Thomas Courtin, Bruno Delobel; EuroEPINOMICS-RES Dravet working group; Boudewijn Gunning, Katia Hardies, Mélanie Jennesson, Louis L

Siphophage 0105phi7-2 of Bacillus thuringiensis: Novel Propagation, DNA, and Genome-Implied Assembly

苏云金芽孢杆菌的噬菌体 0105phi7-2:新的繁殖、DNA 和基因组组装

Roberts, Samantha M; Aldis, Miranda; Wright, Elena T; Gonzales, Cara B; Lai, Zhao; Weintraub, Susan T; Hardies, Stephen C; Serwer, Philip

Identification of Structural and Morphogenesis Genes of Sulfitobacter Phage ΦGT1 and Placement within the Evolutionary History of the Podoviruses

亚硫酸杆菌噬菌体 ΦGT1 的结构和形态发生基因的鉴定及其在足病毒进化史中的位置

Stephen C Hardies, Byung Cheol Cho, Gwang Il Jang, Zhiqing Wang, Chung Yeon Hwang

Genomic Analysis of Two Cold-Active Pseudoalteromonas Phages Isolated from the Continental Shelf in the Arctic Ocean

对从北冰洋大陆架分离出的两种耐寒假交替单胞菌噬菌体的基因组分析

Hwang, Chung Yeon; Cho, Byung Cheol; Kang, Jin Kyeong; Park, Jihye; Hardies, Stephen C

Prevalence and correlates of sexual harassment in professional service firms

专业服务公司性骚扰的普遍程度及其相关因素

Hardies, Kris

Nucleic acid binding by SAMHD1 contributes to the antiretroviral activity and is enhanced by the GpsN modification

SAMHD1 的核酸结合有助于抗逆转录病毒活性,并且通过 GpsN 修饰得到增强

Corey H Yu, Akash Bhattacharya #, Mirjana Persaud #, Alexander B Taylor, Zhonghua Wang, Angel Bulnes-Ramos, Joella Xu, Anastasia Selyutina, Alicia Martinez-Lopez, Kristin Cano, Borries Demeler, Baek Kim, Stephen C Hardies, Felipe Diaz-Griffero, Dmitri N Ivanov

Structural Studies of the Phage G Tail Demonstrate an Atypical Tail Contraction

噬菌体G尾部的结构研究表明其尾部收缩方式非典型

González, Brenda; Li, Daoyi; Li, Kunpeng; Wright, Elena T; Hardies, Stephen C; Thomas, Julie A; Serwer, Philip; Jiang, Wen

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

GAD1双等位基因变异会导致新生儿期发病的综合征性发育性癫痫性脑病。

Chatron, Nicolas; Becker, Felicitas; Morsy, Heba; Schmidts, Miriam; Hardies, Katia; Tuysuz, Beyhan; Roselli, Sandra; Najafi, Maryam; Alkaya, Dilek Uludag; Ashrafzadeh, Farah; Nabil, Amira; Omar, Tarek; Maroofian, Reza; Karimiani, Ehsan Ghayoor; Hussien, Haytham; Kok, Fernando; Ramos, Luiza; Gunes, Nilay; Bilguvar, Kaya; Labalme, Audrey; Alix, Eudeline; Sanlaville, Damien; de Bellescize, Julitta; Poulat, Anne-Lise; Moslemi, Ali-Reza; Lerche, Holger; May, Patrick; Lesca, Gaetan; Weckhuysen, Sarah; Tajsharghi, Homa

Complete Genome Sequence of Sulfitobacter Phage ϕGT1, Isolated from a Tidal Flat

从潮滩分离的硫杆菌噬菌体ϕGT1的完整基因组序列

Hwang, Chung Y; Cho, Yirang; Jang, Gwang I; Cho, Byung C; Hardies, Stephen C

Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish

双等位基因 VARS 变异会导致发育性脑病和小头畸形,这种现象在 vars 基因敲除的斑马鱼中重现

Aleksandra Siekierska, Hannah Stamberger, Tine Deconinck, Stephanie N Oprescu, Michèle Partoens, Yifan Zhang, Jo Sourbron, Elias Adriaenssens, Patrick Mullen, Patrick Wiencek, Katia Hardies, Jeong-Soo Lee, Hoi-Khoanh Giong, Felix Distelmaier, Orly Elpeleg, Katherine L Helbig, Joseph Hersh, Sedat Isi