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

Customizable virus-like particles deliver CRISPR-Cas9 ribonucleoprotein for effective ocular neovascular and Huntington's disease gene therapy.

可定制的病毒样颗粒递送 CRISPR-Cas9 核糖核蛋白,用于有效的眼部新生血管和亨廷顿病基因治疗

Ling Sikai, Zhang Xue, Dai Yao, Jiang Zhuofan, Zhou Xujiao, Lu Sicong, Qian Xiaoqing, Liu Jianping, Selfjord Niklas, Satir Tugce Munise, Lundin Anders, Touza Julia Liz, Firth Mike, Van Zuydam Natalie, Bilican Bilada, Akcakaya Pinar, Hong Jiaxu, Cai Yujia

VHL Gene Restoration Supports RCC Reprogramming to iPSCs but Does Not Ensure Line Stability.

VHL基因恢复支持RCC重编程为iPSC,但不能保证细胞系稳定性。

Lichner Zsuzsanna, Shamshirgaran Yasaman, Pieczonka Katarzyna, Jonebring Anna, Kibschull Mark, Shynlova Oksana, Meens Jalna, Kim Raymond H, Ailles Laurie, Bilican Bilada, Hicks Ryan, Rogers Ian M

Correction: Human iPSC and CRISPR targeted gene knock-in strategy for studying the somatic TIE2L914F mutation in endothelial cells

更正:利用人诱导多能干细胞和CRISPR靶向基因敲入策略研究内皮细胞中的体细胞TIE2L914F突变

Lazovic, Bojana; Nguyen, Hoang-Tuan; Ansarizadeh, Mohammadhassan; Wigge, Leif; Kohl, Franziska; Li, Songyuan; Carracedo, Miguel; Kettunen, Jere; Krimpenfort, Luc; Elgendy, Ramy; Richter, Kati; De Silva, Laknee; Bilican, Bilada; Singh, Prateek; Saxena, Pratik; Jakobsson, Lars; Hong, Xuechong; Eklund, Lauri; Hicks, Ryan

Human iPSC and CRISPR targeted gene knock-in strategy for studying the somatic TIE2L914F mutation in endothelial cells

人类 iPSC 和 CRISPR 靶向基因敲入策略用于研究内皮细胞体细胞 TIE2L914F 突变

Bojana Lazovic, Hoang-Tuan Nguyen, Mohammadhassan Ansarizadeh, Leif Wigge, Franziska Kohl, Songyuan Li, Miguel Carracedo, Jere Kettunen, Luc Krimpenfort, Ramy Elgendy, Kati Richter, Laknee De Silva, Bilada Bilican, Prateek Singh, Pratik Saxena, Lars Jakobsson, Xuechong Hong, Lauri Eklund, Ryan Hicks

A proteogenomic view of Parkinson's disease causality and heterogeneity

从蛋白质基因组学角度探讨帕金森病的病因和异质性

Kaiser, Sergio; Zhang, Luqing; Mollenhauer, Brit; Jacob, Jaison; Longerich, Simonne; Del-Aguila, Jorge; Marcus, Jacob; Raghavan, Neha; Stone, David; Fagboyegun, Olumide; Galasko, Douglas; Dakna, Mohammed; Bilican, Bilada; Dovlatyan, Mary; Kostikova, Anna; Li, Jingyao; Peterson, Brant; Rotte, Michael; Sanz, Vinicius; Foroud, Tatiana; Hutten, Samantha J; Frasier, Mark; Iwaki, Hirotaka; Singleton, Andrew; Marek, Ken; Crawford, Karen; Elwood, Fiona; Messa, Mirko; Serrano-Fernandez, Pablo

Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes

人类遗传学发现MAP3K15是糖尿病的一种与肥胖无关的治疗靶点。

Nag, Abhishek; Dhindsa, Ryan S; Mitchell, Jonathan; Vasavda, Chirag; Harper, Andrew R; Vitsios, Dimitrios; Ahnmark, Andrea; Bilican, Bilada; Madeyski-Bengtson, Katja; Zarrouki, Bader; Zoghbi, Anthony W; Wang, Quanli; Smith, Katherine R; Alegre-Díaz, Jesus; Kuri-Morales, Pablo; Berumen, Jaime; Tapia-Conyer, Roberto; Emberson, Jonathan; Torres, Jason M; Collins, Rory; Smith, David M; Challis, Benjamin; Paul, Dirk S; Bohlooly-Y, Mohammad; Snowden, Mike; Baker, David; Fritsche-Danielson, Regina; Pangalos, Menelas N; Petrovski, Slavé

CellSIUS provides sensitive and specific detection of rare cell populations from complex single-cell RNA-seq data

CellSIUS能够从复杂的单细胞RNA测序数据中灵敏且特异地检测稀有细胞群。

Rebekka Wegmann ,Marilisa Neri ,Sven Schuierer ,Bilada Bilican ,Huyen Hartkopf ,Florian Nigsch ,Felipa Mapa ,Annick Waldt ,Rachel Cuttat ,Max R Salick ,Joe Raymond ,Ajamete Kaykas ,Guglielmo Roma ,Caroline Gubser Keller

Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons

发育神经元中活动依赖性基因表达进化分化的证据

Jing Qiu, Jamie McQueen, Bilada Bilican, Owen Dando, Dario Magnani, Karolina Punovuori, Bhuvaneish T Selvaraj, Matthew Livesey, Ghazal Haghi, Samuel Heron, Karen Burr, Rickie Patani, Rinku Rajan, Olivia Sheppard, Peter C Kind, T Ian Simpson, Victor Lj Tybulewicz, David Ja Wyllie, Elizabeth Mc Fisher

Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2

由于 Nrf2 的表观遗传抑制,内在抗氧化防御能力减弱,促进了神经元的发育

Karen F S Bell, Bashayer Al-Mubarak, Marc-André Martel, Sean McKay, Nicola Wheelan, Philip Hasel, Nóra M Márkus, Paul Baxter, Ruth F Deighton, Andrea Serio, Bilada Bilican, Sudhir Chowdhry, Paul J Meakin, Michael L J Ashford, David J A Wyllie, Robert H Scannevin, Siddharthan Chandran, John D Hayes, 

Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations

TDP-43 mRNA 颗粒的轴突运输因 ALS 致病突变而受损

Nael H Alami #, Rebecca B Smith #, Monica A Carrasco, Luis A Williams, Christina S Winborn, Steve S W Han, Evangelos Kiskinis, Brett Winborn, Brian D Freibaum, Anderson Kanagaraj, Alison J Clare, Nisha M Badders, Bilada Bilican, Edward Chaum, Siddharthan Chandran, Christopher E Shaw, Kevin C Eggan,