IoO Seminar Series
26 January 2022, 2:30 pm–5:00 pm
Speaker: Seth Blackshaw from the Solomon H. Snyder Department of Neuroscience, Johns Hopkins University.
Event Information
Open to
- All | UCL staff | UCL students
Availability
- Yes
Organiser
-
Trudy Muggridge
Programme
14:30-15:30 Seminar and questions
15:30-16:00 Postdoc/PhD student discussion
16:00 -1700 PI roundtable discussion
About the Speaker
Seth Blackshaw
at UCL Institute of Ophthalmology
Professor Seth Blackshaw is a professor of neuroscience, neurology and ophthalmology at the Johns Hopkins University School of Medicine. Additionally, he serves as an investigator in both the High Throughput Biology Center and the Institute for Cell Engineering at Johns Hopkins. Dr Blackshaw received a B.A. in biology and an M.S. in biochemistry from the University of Chicago in 1991. He completed his PhD in neurosciences at Johns Hopkins in 1997 and subsequently conducted postdoctoral work in genetics at the Harvard University Medical School. He joined the Hopkins faculty in 2004. Dr Blackshaw has authored or co-authored more than 110 peer-reviewed publications and holds several patents and copyrights. His laboratory aims to identify genes that pattern progenitors in time and regulate their ability to proliferate and give rise to specific types of retinal cells at different stages during the course of neurogenesis.
Website: https://blackshawlab.com
Recent publications:
- Lyu et al. 2021. Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina. Cell Reports. 10.1016/j.celrep.2021.109994
- Weir et al. 2021. Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility using scRNA-Seq and scATAC-Seq. J Vis Exp. 10.3791/62239
- Hoang and Wang et al. 2020. Gene regulatory networks controlling vertebrate retinal regeneration. Science. 10.1126/science.abb8598
- Clark et al. 2019. Single-Cell RNA-Seq Analysis of Retinal Development Identifies NFI Factors as Regulating Mitotic Exit and Late-Born Cell Specification. Neuron. 10.1016/j.neuron.2019.04.010