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

Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing

通过基于 CRISPR 的表观基因组编辑激活印迹普拉德-威利综合征基因座

Dahlia Rohm, Joshua B Black, Sean R McCutcheon, Alejandro Barrera, Shanté S Berry, Daniel J Morone, Xander Nuttle, Celine E de Esch, Derek J C Tai, Michael E Talkowski, Nahid Iglesias, Charles A Gersbach

Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries

使用 piggyBac 转座子传递 CRISPR 文库对突变模型进行并行工程设计

Xander Nuttle, Nicholas D Burt, Benjamin Currall, Mariana Moysés-Oliveira, Kiana Mohajeri, Riya Bhavsar, Diane Lucente, Rachita Yadav, Derek J C Tai, James F Gusella, Michael E Talkowski

Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing

通过基于 CRISPR 的表观基因组编辑激活印迹普拉德-威利综合征基因座

Dahlia Rohm, Joshua B Black, Sean R McCutcheon, Alejandro Barrera, Daniel J Morone, Xander Nuttle, Celine E de Esch, Derek J C Tai, Michael E Talkowski, Nahid Iglesias, Charles A Gersbach

Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

自闭症相关基因的趋同共表达表明,一些新的风险基因可能无法在大规模遗传研究中检测到

Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li, Alex Yu, Nicholas D Burt, Serkan Erdin, Jack M Fu, Minghui Wang, Theodore Morley, Lide Han; CommonMind Consortium; Patrick A Dion, Guy A Rouleau, Bin Zhang, Kristen J Brennand, Michael E Talkowski, Doug

Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models

小鼠脑和人类神经元模型中16p11.2相互基因组紊乱的组织和细胞类型特异性分子和功能特征

Derek J C Tai ,Parisa Razaz ,Serkan Erdin ,Dadi Gao ,Jennifer Wang ,Xander Nuttle ,Celine E de Esch ,Ryan L Collins ,Benjamin B Currall ,Kathryn O'Keefe ,Nicholas D Burt ,Rachita Yadav ,Lily Wang ,Kiana Mohajeri ,Tatsiana Aneichyk ,Ashok Ragavendran ,Alexei Stortchevoi ,Elisabetta Morini ,Weiyuan Ma ,Diane Lucente ,Alex Hastie ,Raymond J Kelleher ,Roy H Perlis ,Michael E Talkowski ,James F Gusella

Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

智人特有基因家族的出现和 16p11.2 染色体 CNV 易感性

Xander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, Joshua G Schraiber, Iñigo Narvaiza, Peter H Sudmant, Osnat Penn, Giorgia Chiatante, Maika Malig, John Huddleston, Chris Benner, Francesca Camponeschi, Simone Ciofi-Baffoni, Holly A F Stessman, Maria C N Marchetto, Laura Denman, Lana Harshman, Car

Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencing

使用大规模并行测序解决片段 DNA 重复中与基因组疾病相关的断点

Xander Nuttle, Andy Itsara, Jay Shendure, Evan E Eichler