Harvey F. Lodish

Affiliations: 
Biology Massachusetts Institute of Technology, Cambridge, MA, United States 
Area:
Cell biology, hematology, endocrinology
Website:
http://lodishlab.wi.mit.edu/people/profiles/HarveyProfile.html
Google:
"Harvey F. Lodish"
Bio:

http://wi.mit.edu/about/history/founders
https://biology.mit.edu/people/harvey_lodish

Cross-listing: Cell Biology Tree - Chemistry Tree

Parents

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Norton D. Zinder grad student 1962-1966 Rockefeller (Chemistry Tree)
Sydney Brenner post-doc 1966-1968 MRC-LMB (Neurotree)
Francis Harry Compton Crick post-doc 1966-1968 MRC-LMB (Neurotree)

Children

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Sondra G. Lazarowitz research assistant MIT (Cell Biology Tree)
Michael Murrell research assistant MIT (BME Tree)
Cameron Sadegh research assistant 2003-2006 MIT (Neurotree)
Gregory Longmore grad student (Cell Biology Tree)
Charles S. Zuker grad student MIT
Lydia Villa-Komaroff grad student 1975 MIT (Cell Biology Tree)
Jonathan S. Bogan post-doc Harvard & MIT (Cell Biology Tree)
Aaron Ciechanover post-doc MIT (Chemistry Tree)
Stephen Cohen post-doc
Richard Firtel post-doc (Neurotree)
David Housman post-doc (Neurotree)
Allan Jacobson post-doc (Neurotree)
Ron Kopito post-doc (Neurotree)
John Kenneth Rose post-doc MIT (Chemistry Tree)
Jean E. Schaffer post-doc MIT (Cell Biology Tree)
Alan M. Weiner post-doc 1974-1976 MIT (Chemistry Tree)
Randall L. Dimond post-doc 1975-1977 MIT (Cell Biology Tree)
James E. Rothman post-doc 1976-1978 MIT (Cell Biology Tree)
Akhilesh Pandey post-doc 1996-1999 MIT (Chemistry Tree)
Xiaofei Gao post-doc 2012-2017 MIT (Microtree)
Georgios I Karras post-doc 2016-2018 Whitehead Institute (MIT) (Chemistry Tree)
BETA: Related publications

Publications

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Jiang M, Chavarria TE, Yuan B, et al. (2020) Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis. Proceedings of the National Academy of Sciences of the United States of America
Li H, Natarajan A, Ezike J, et al. (2019) Rate of Progression through a Continuum of Transit-Amplifying Progenitor Cell States Regulates Blood Cell Production. Developmental Cell
Yien YY, Shi J, Chen C, et al. (2018) FAM210B is an erythropoietin target and regulates erythroid heme synthesis by controlling mitochondrial iron import and ferrochelatase activity. The Journal of Biological Chemistry
Li H, Lodish HF, Sieff CA. (2018) Critical Issues in Diamond-Blackfan Anemia and Prospects for Novel Treatment. Hematology/Oncology Clinics of North America. 32: 701-712
Huang NJ, Lin YC, Lin CY, et al. (2018) Enhanced phosphocholine metabolism is essential for terminal erythropoiesis. Blood
Huang NJ, Pishesha N, Mukherjee J, et al. (2017) Genetically engineered red cells expressing single domain camelid antibodies confer long-term protection against botulinum neurotoxin. Nature Communications. 8: 423
Gao X, Lee HY, Li W, et al. (2017) Thyroid hormone receptor beta and NCOA4 regulate terminal erythrocyte differentiation. Proceedings of the National Academy of Sciences of the United States of America
Pishesha N, Bilate AM, Wibowo MC, et al. (2017) Engineered erythrocytes covalently linked to antigenic peptides can protect against autoimmune disease. Proceedings of the National Academy of Sciences of the United States of America
Doulatov S, Vo LT, Macari ER, et al. (2017) Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors. Science Translational Medicine. 9
Gao X, Lee HY, da Rocha EL, et al. (2016) TGF-β inhibitors stimulate red blood cell production by enhancing self-renewal of BFU-E erythroid progenitors. Blood
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