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

RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease

在散发性CDA III病例中发现的RACGAP1变异提示中心纺锤体蛋白功能障碍是该疾病的病因。

Wontakal, Sandeep N; Britto, Mishan; Zhang, Huan; Han, Yongshuai; Gao, Chengjie; Tannenbaum, Sarah; Durham, Benjamin H; Lee, Margaret T; An, Xiuli; Mishima, Masanori

Approaching the Interpretation of Discordances in SARS-CoV-2 Testing

SARS-CoV-2检测结果不一致的解读方法

Wontakal, Sandeep N; Bortz, Robert H 3rd; Lin, Wen-Hsuan W; Gendlina, Inessa; Fox, Amy S; Hod, Eldad A; Chandran, Kartik; Prystowsky, Michael B; Weiss, Louis M; Spitalnik, Steven L

Diagnosis of a rare fetal haemoglobinopathy in the age of next-generation sequencing

在下一代测序技术时代诊断一种罕见的胎儿血红蛋白病

Hooven, Thomas A; Hooper, Ellen M; Wontakal, Sandeep N; Francis, Richard O; Sahni, Rakesh; Lee, Margaret T

PU.1 directly regulates cdk6 gene expression, linking the cell proliferation and differentiation programs in erythroid cells.

PU.1 直接调控 cdk6 基因表达,将红系细胞的增殖和分化程序联系起来

Choe Kevin S, Ujhelly Olga, Wontakal Sandeep N, Skoultchi Arthur I