Induced Pluripotent Stem Cell Differentiation Enables Functional Validation of GWAS Variants in Metabolic Disease
Curtis R. Warren, John F. O’Sullivan, Max Friesen, Caroline E. Becker, Xiaoling Zhang, Poching Liu, Yoshiyuki Wakabayashi, Jordan E. Morningstar, Xu Shi, Jihoon Choi, Fang Xia, Derek T. Peters, Mary H.C. Florido, Alexander M. Tsankov, Eilene Duberow, Lauren Comisar, Jennifer Shay, Xin Jiang, Alexander Meissner, Kiran Musunuru, Sekar Kathiresan, Laurence Daheron, Jun Zhu, Robert E. Gerszten, Rahul C. Deo, Ramachandran S. Vasan, Christopher J. O’Donnell, Chad A. Cowan
Index: 10.1016/j.stem.2017.01.010
Full Text: HTML
Abstract
As part of the NHLBI NextGen consortium, Warren et al. show that analyzing the cellular pathophysiology of cells differentiated from multiple lines of an iPSC library is a promising complementary approach in the functional analysis of GWAS variants.
Latest Articles:
2017-07-13
[10.1016/j.stem.2017.06.004]
Lineage Tracing: Papers and Progress
2017-07-06
[10.1016/j.stem.2017.06.015]
Intestinal Enteroendocrine Lineage Cells Possess Homeostatic and Injury-Inducible Stem Cell Activity
2017-07-06
[10.1016/j.stem.2017.06.014]
Direct Neuronal Reprogramming: Achievements, Hurdles, and New Roads to Success
2017-07-06
[10.1016/j.stem.2017.06.011]
Making HSCs on Demand: Looking Ahead
2017-07-06
[10.1016/j.stem.2017.06.010]