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

WNT5A mutations in patients with autosomal dominant Robinow syndrome.

常染色体显性罗宾诺综合征患者的WNT5A基因突变

Person Anthony D, Beiraghi Soraya, Sieben Christine M, Hermanson Spencer, Neumann Ann N, Robu Mara E, Schleiffarth J Robert, Billington Charles J Jr, van Bokhoven Hans, Hoogeboom Jeannette M, Mazzeu Juliana F, Petryk Anna, Schimmenti Lisa A, Brunner Han G, Ekker Stephen C, Lohr Jamie L

p53 activation by knockdown technologies

通过基因敲除技术激活p53

Robu, Mara E; Larson, Jon D; Nasevicius, Aidas; Beiraghi, Soraya; Brenner, Charles; Farber, Steven A; Ekker, Stephen C

Genome-wide reverse genetics framework to identify novel functions of the vertebrate secretome

利用全基因组反向遗传学框架鉴定脊椎动物分泌组的新功能

Pickart, Michael A; Klee, Eric W; Nielsen, Aubrey L; Sivasubbu, Sridhar; Mendenhall, Eric M; Bill, Brent R; Chen, Eleanor; Eckfeldt, Craig E; Knowlton, Michelle; Robu, Mara E; Larson, Jon D; Deng, Yun; Schimmenti, Lisa A; Ellis, Lynda B M; Verfaillie, Catherine M; Hammerschmidt, Matthias; Farber, Steven A; Ekker, Stephen C