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

Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies

利用短多重聚合序列同源性检测拷贝数变异

Jobanputra, Vaidehi; Andrews, Peter; Felice, Vanessa; Abhyankar, Avinash; Kozon, Lukasz; Robinson, Dino; London, Ferrah; Hakker, Inessa; Wrzeszczynski, Kazimierz; Ronemus, Michael

DNA copy number variations in children with vesicoureteral reflux and urinary tract infections

患有膀胱输尿管反流和尿路感染的儿童的DNA拷贝数变异

Liang, Dong; McHugh, Kirk M; Brophy, Pat D; Shaikh, Nader; Manak, J Robert; Andrews, Peter; Hakker, Inessa; Wang, Zihua; Schwaderer, Andrew L; Hains, David S

Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate Cancer

单细胞基因组学在前列腺癌诊断评估中的应用

Alexander, Joan; Kendall, Jude; McIndoo, Jean; Rodgers, Linda; Aboukhalil, Robert; Levy, Dan; Stepansky, Asya; Sun, Guoli; Chobardjiev, Lubomir; Riggs, Michael; Cox, Hilary; Hakker, Inessa; Nowak, Dawid G; Laze, Juliana; Llukani, Elton; Srivastava, Abhishek; Gruschow, Siobhan; Yadav, Shalini S; Robinson, Brian; Atwal, Gurinder; Trotman, Lloyd C; Lepor, Herbert; Hicks, James; Wigler, Michael; Krasnitz, Alexander

SMASH, a fragmentation and sequencing method for genomic copy number analysis

SMASH,一种用于基因组拷贝数分析的片段化和测序方法

Wang, Zihua; Andrews, Peter; Kendall, Jude; Ma, Beicong; Hakker, Inessa; Rodgers, Linda; Ronemus, Michael; Wigler, Michael; Levy, Dan

The contribution of de novo coding mutations to autism spectrum disorder

新发编码突变对自闭症谱系障碍的贡献

Iossifov, Ivan; O'Roak, Brian J; Sanders, Stephan J; Ronemus, Michael; Krumm, Niklas; Levy, Dan; Stessman, Holly A; Witherspoon, Kali T; Vives, Laura; Patterson, Karynne E; Smith, Joshua D; Paeper, Bryan; Nickerson, Deborah A; Dea, Jeanselle; Dong, Shan; Gonzalez, Luis E; Mandell, Jeffrey D; Mane, Shrikant M; Murtha, Michael T; Sullivan, Catherine A; Walker, Michael F; Waqar, Zainulabedin; Wei, Liping; Willsey, A Jeremy; Yamrom, Boris; Lee, Yoon-ha; Grabowska, Ewa; Dalkic, Ertugrul; Wang, Zihua; Marks, Steven; Andrews, Peter; Leotta, Anthony; Kendall, Jude; Hakker, Inessa; Rosenbaum, Julie; Ma, Beicong; Rodgers, Linda; Troge, Jennifer; Narzisi, Giuseppe; Yoon, Seungtai; Schatz, Michael C; Ye, Kenny; McCombie, W Richard; Shendure, Jay; Eichler, Evan E; State, Matthew W; Wigler, Michael

De novo gene disruptions in children on the autistic spectrum

自闭症谱系儿童的新生基因突变

Iossifov, Ivan; Ronemus, Michael; Levy, Dan; Wang, Zihua; Hakker, Inessa; Rosenbaum, Julie; Yamrom, Boris; Lee, Yoon-Ha; Narzisi, Giuseppe; Leotta, Anthony; Kendall, Jude; Grabowska, Ewa; Ma, Beicong; Marks, Steven; Rodgers, Linda; Stepansky, Asya; Troge, Jennifer; Andrews, Peter; Bekritsky, Mitchell; Pradhan, Kith; Ghiban, Elena; Kramer, Melissa; Parla, Jennifer; Demeter, Ryan; Fulton, Lucinda L; Fulton, Robert S; Magrini, Vincent J; Ye, Kenny; Darnell, Jennifer C; Darnell, Robert B; Mardis, Elaine R; Wilson, Richard K; Schatz, Michael C; McCombie, W Richard; Wigler, Michael

Distinctive roles of different beta-amyloid 42 aggregates in modulation of synaptic functions

不同β-淀粉样蛋白42聚集体在调节突触功能中的不同作用

Chiang, Hsueh-Cheng; Iijima, Koichi; Hakker, Inessa; Zhong, Yi

Overexpression of neprilysin reduces alzheimer amyloid-beta42 (Abeta42)-induced neuron loss and intraneuronal Abeta42 deposits but causes a reduction in cAMP-responsive element-binding protein-mediated transcription, age-dependent axon pathology, and premature death in Drosophila

脑啡肽酶的过表达可减少阿尔茨海默病淀粉样蛋白β42 (Aβ42) 诱导的神经元丢失和神经元内Aβ42沉积,但会导致cAMP反应元件结合蛋白介导的转录减少、年龄依赖性轴突病变以及果蝇过早死亡。

Iijima-Ando, Kanae; Hearn, Stephen A; Granger, Linda; Shenton, Christopher; Gatt, Anthony; Chiang, Hsueh-Cheng; Hakker, Inessa; Zhong, Yi; Iijima, Koichi

Abeta42 mutants with different aggregation profiles induce distinct pathologies in Drosophila

具有不同聚集特征的Aβ42突变体在果蝇中诱发不同的病理

Iijima, Koichi; Chiang, Hsueh-Cheng; Hearn, Stephen A; Hakker, Inessa; Gatt, Anthony; Shenton, Christopher; Granger, Linda; Leung, Amy; Iijima-Ando, Kanae; Zhong, Yi