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

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.

包括 lncRNA 基因在内的小型非编码差异甲基化拷贝数变异会导致致命的肺部发育障碍

Szafranski Przemyslaw, Dharmadhikari Avinash V, Brosens Erwin, Gurha Priyatansh, Kolodziejska Katarzyna E, Zhishuo Ou, Dittwald Piotr, Majewski Tadeusz, Mohan K Naga, Chen Bo, Person Richard E, Tibboel Dick, de Klein Annelies, Pinner Jason, Chopra Maya, Malcolm Girvan, Peters Gregory, Arbuckle Susan, Guiang Sixto F 3rd, Hustead Virginia A, Jessurun Jose, Hirsch Russel, Witte David P, Maystadt Isabelle, Sebire Neil, Fisher Richard, Langston Claire, Sen Partha, Stankiewicz Paweł

Novel selective inhibitors of nuclear export CRM1 antagonists for therapy in mantle cell lymphoma

新型选择性核输出 CRM1 抑制剂用于治疗套细胞淋巴瘤

Kejie Zhang, Michael Wang, Archito T Tamayo, Sharon Shacham, Michael Kauffman, John Lee, Liang Zhang, Zhishuo Ou, Changping Li, Luhong Sun, Richard J Ford, Lan V Pham

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

利用阵列比较基因组杂交(array CGH)技术检测自闭症家族基因组中外显子拷贝数变异,发现TMLHE基因存在一个新的缺失。

Patricia B S Celestino-Soper ,Chad A Shaw, Stephan J Sanders, Jian Li, Michael T Murtha, A Gulhan Ercan-Sencicek, Lea Davis, Susanne Thomson, Tomasz Gambin, A Craig Chinault, Zhishuo Ou, Jennifer R German, Aleksandar Milosavljevic, James S Sutcliffe, Edwin H Cook Jr, Pawel Stankiewicz, Matthew W State, Arthur L Beaudet