Seckel syndrome (SS) is a rare spectrum of congenital severe microcephaly and dwarfism. One SS-causative gene is Ataxia Telangiectasia and Rad3-Related Protein (ATR), and ATR (c.2101 A>G) mutation cau
Many stem cells utilize asymmetric cell division (ACD) to produce a self-renewed stem cell and a differentiating daughter cell. How non-genic information could be inherited differentially to establish
We aimed to generate human induced pluripotent stem cell (iPSC) lines from New Zealand donors. These lines are the first to be generated in New Zealand. Human dermal fibroblasts were collected from tw
Representative confocal line scan data and kymographs for an isogenic trio of c.MYH7C9123T R-GECO1.0 expressing hiPSC-CMs at day 30 and an isogenic pair of c.ACTC1G301A R-GECO1.0 expressing hiPSC-CMs
