Concurrent Session
Concurrent Group III
The concurrent sessions cover topics from across the spectrum of stem cell research. Each session, framed by a brief topic overview, includes one or two invited speakers whose work highlights leading research in the field. The session is rounded out with four or more abstract-selected speakers who, combined with the invited talks, give an excellent snapshot of the most current work on the topic. The five concurrent sessions run in parallel and attendees are encouraged to move between sessions to hear talks of interest. Concurrent sessions are held Thursday, Friday, and Saturday afternoons.
Concurrent IIID: Hematopoiesis
6/22/2018
13:15 - 15:15
Session Chair/Presenter(s)
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Concurrent Speaker(s)
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Oral Abstract Presenter(s)
VL
Vanessa Lundin
Boston Children’s Hospital and Dana-Farber Cancer Institute, MA, United States
LD
Lei Ding
Columbia University Medical Center, NY, United States
KP
Kathryn Potts
Albert Einstein College of Medicine, NY, United States
LP
ST
Presentations:
13:15 - 13:20
TOPIC OVERVIEW BY CHAIR
13:20 - 13:45
MODELING NORMAL AND MALIGNANT HAEMATOPOIESIS USING HUMAN PLURIPOTENT STEM CELLS
13:45 - 14:00
YAP REGULATES HEMATOPOIETIC STEM CELL FORMATION IN RESPONSE TO THE BIOPHYSICAL FORCES OF BLOOD FLOW
14:00 - 14:15
LIVER-DERIVED SYSTEMIC THROMBOPOIETIN IS REQUIRED FOR BONE MARROW HEMATOPOIETIC STEM CELL MAINTENANCE
14:15 - 14:30
THE SPLICEOSOMAL COMPONENT SF3B1 IS ESSENTIAL FOR ZEBRAFISH HEMATOPOIETIC STEM CELL FORMATION THROUGH REGULATION OF THE JAK/STAT SIGNALING PATHWAY
14:30 - 14:45
ROS SUPRESSION THROUGH P53 ACTIVITY AND A REMODELED MITOCHONDRIAL NETWORK DETERMINES THE FATE OF FUNCTIONAL HUMAN HEMATOPOETIC STEM CELLS DURING EX-VIVO EXPANSION
14:45 - 15:00
CONSTITUTIVE DELETION OF AP2A2 RESULTS IN FETAL LIVER HAEMATOPOEISIS EXHAUSTION DUE TO LOSS OF HSC QUIESCENCE AND PERTURBED ASYMMETRICAL:SYMMETRICAL HSC FATE