Bruce Sun
New York Stem Cell Foundation
12 Papers
18 Citations
Bruce Sun is an academic researcher from New York Stem Cell Foundation. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 7, co-authored 10 publications. Previous affiliations of Bruce Sun include City University of New York.
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Papers
Directed Differentiation of Human Pluripotent Stem Cells to Microglia.
Panagiotis Douvaras,Bruce Sun,Minghui Wang,I. A. Kruglikov,Gregory Lallos,Matthew Zimmer,Cecile Terrenoire,Bin Zhang,Sam Gandy,Eric E. Schadt,Donald O. Freytes,Scott Noggle,Valentina Fossati +12 more
TL;DR: iPSC-MG were able to phagocytose and responded to ADP by producing intracellular Ca2+ transients, whereas macrophages lacked such response, and the differentiation protocol was highly reproducible across several pluripotent stem cell lines.
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Automated, high-throughput derivation, characterization and differentiation of induced pluripotent stem cells.
Daniel Paull,Ana Sevilla,Hongyan Zhou,Aana Kim Hahn,Hesed Kim,Christopher Napolitano,Alexander M. Tsankov,Alexander M. Tsankov,Linshan Shang,Katie Krumholz,Premlatha Jagadeesan,Chris M. Woodard,Bruce Sun,Thierry Vilboux,Thierry Vilboux,Matthew Zimmer,Eliana Forero,Dorota N. Moroziewicz,Hector Martinez,May Christine V. Malicdan,Keren A. Weiss,Keren A. Weiss,Lauren B Vensand,Carmen R Dusenberry,Hannah Polus,Karla Therese L Sy,David J. Kahler,David J. Kahler,William A. Gahl,Susan L. Solomon,Stephen Chang,Alexander Meissner,Alexander Meissner,Kevin Eggan,Scott Noggle +34 more
TL;DR: It is demonstrated that automated reprogramming and the pooled selection of polyclonal pluripotent cells results in high-quality, stable iPSCs, which display less line-to-line variation than either manually produced lines or lines produced through automation followed by single-colony subcloning.
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Genetic Drift Can Compromise Mitochondrial Replacement by Nuclear Transfer in Human Oocytes
Mitsutoshi Yamada,Valentina Emmanuele,Maria J. Sanchez-Quintero,Bruce Sun,Gregory Lallos,Daniel Paull,Matthew Zimmer,Shardonay Pagett,Robert W. Prosser,Mark V. Sauer,Michio Hirano,Dieter Egli,Dieter Egli +12 more
TL;DR: Using human mitochondrial replacement stem cell lines, it is shown that, even though the low levels of heteroplasmy introduced into human oocytes by mitochondrial carryover during nuclear transfer often vanish, they can sometimes instead result in mtDNA genotypic drift and reversion to the original genotype.
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Modeling gene × environment interactions in PTSD using human neurons reveals diagnosis-specific glucocorticoid-induced gene expression
Carina Seah,Michael S. Breen,Tomasz Rusielewicz,Heather N. Bader,Changxin Xu,Christopher J. Hunter,Barry McCarthy,P. M. Deans,Mitali Chattopadhyay,Jordan Goldberg,Frank Desarnaud,Iouri Makotkine,Janine D. Flory,Linda M. Bierer,Migle Staniskyte,Lauren Bauer,Katie Brenner,Geoff Buckley-Herd,Sean DesMarteau,Patrick Fenton,Peter Ferrarotto,Jenna Hall,Selwyn Jacob,Travis Kroeker,Gregory Lallos,H. Martínez,Paull McCoy,Frederick J. Monsma,Dorota Moroziewicz,Reid Otto,Kathryn S. Reggio,Bruce Sun,Rebecca Tibbets,Dong-Woo Shin,Hongyan Zhou,Matthew Zimmer,Scott Noggle,Laura M. Huckins,Daniel Paull,Kristen J. Brennand,Rachel Yehuda +40 more
TL;DR: This article found evidence of a coregulated network of transcription factors that mediates glucocorticoid hyper-responsivity in post-traumatic stress disorder (PTSD) using human induced pluripotent stem cell (hiPSC)-derived glutamatergic neurons and peripheral blood mononuclear cells (PBMCs).
Characterization of a subpopulation of developing cortical interneurons from human iPSCs within serum-free embryoid bodies
Michael W. Nestor,Samson T. Jacob,Bruce Sun,Deborah Pre,Andrew A. Sproul,Seong Im Hong,Chris M. Woodard,Matthew Zimmer,Vorapin Chinchalongporn,Vorapin Chinchalongporn,Ottavio Arancio,Scott Noggle +11 more
TL;DR: Using serum-free embryoid bodies generated from human inducible pluripotent stem cells (iPSCs), it is demonstrated that these interneuron progenitors exhibit morphological, immunocytochemical, and electrophysiological hallmarks of developing cortical interneurons.
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