Stephen Blacklow

Stephen Blacklow, MD, PhD

Gustavus Adolphus Pfeiffer Professor of Biological Chemistry and Molecular Pharmacology, Harvard Medical School

Dr. Blacklow is currently the Gustavus Adolphus Pfeiffer Professor and Chair of the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School, and a member of the Department of Cancer Biology at the Dana Farber Cancer Institute.

Research led by Dr. Blacklow’s team has shown how cell surface receptors can convey a developmental signal directly from one contacting cell surface to the next and then from the membrane to the nucleus. He has elucidated key molecular events in Notch signal transduction, a conserved cell-cell communication system that influences cell fate decisions in all metazoan organisms, and that is frequently hijacked as an oncogenic driver in human leukemia. His research on the Notch pathway has led to the development of new investigational therapies for hematologic malignancies such as T cell acute lymphocytic leukemia (ALL).

Dr. Blacklow was a recipient of the National Cancer Institute’s prestigious Outstanding Investigator Award in 2017, and elected to the Association of American Physicians in 2018. Dr. Blacklow directed the MD-PhD Program in Basic and Translational Sciences at Harvard Medical School and has served on Advisory Committees for pre-clinical departments, graduate programs, and MD-PhD programs at several major research universities and institutions, including Stanford, the University of Pennsylvania, and the Memorial Sloan Kettering Cancer Center.

Dr. Blacklow received his MD and PhD degrees from Harvard University in 1991, completed his residency in Clinical Pathology at Brigham and Women’s Hospital, and carried out postdoctoral research at the Whitehead Institute with Dr. Peter S. Kim.

Notch ankyrin repeat domain variation influences leukemogenesis and Myc transactivation.
Authors: Authors: Aster JC, Bodnar N, Xu L, Karnell F, Milholland JM, Maillard I, Histen G, Nam Y, Blacklow SC, Pear WS.
PLoS One
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Pre-TCR signaling inactivates Notch1 transcription by antagonizing E2A.
Authors: Authors: Yashiro-Ohtani Y, He Y, Ohtani T, Jones ME, Shestova O, Xu L, Fang TC, Chiang MY, Intlekofer AM, Blacklow SC, Zhuang Y, Pear WS.
Genes Dev
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Structure of an LDLR-RAP complex reveals a general mode for ligand recognition by lipoprotein receptors.
Authors: Authors: Fisher C, Beglova N, Blacklow SC.
Mol Cell
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Global defects in the expression and function of the low density lipoprotein receptor (LDLR) associated with two familial hypercholesterolemia mutations resulting in misfolding of the LDLR epidermal growth factor-AB pair.
Authors: Authors: Boswell EJ, Jeon H, Blacklow SC, Downing AK.
J Biol Chem
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Implications for familial hypercholesterolemia from the structure of the LDL receptor YWTD-EGF domain pair.
Authors: Authors: Jeon H, Meng W, Takagi J, Eck MJ, Springer TA, Blacklow SC.
Nat Struct Biol
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Quantitative plasma D-dimer levels among patients undergoing pulmonary angiography for suspected pulmonary embolism.
Authors: Authors: Goldhaber SZ, Simons GR, Elliott CG, Haire WD, Toltzis R, Blacklow SC, Doolittle MH, Weinberg DS.
JAMA
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Domain integration of ADAM family proteins: Emerging themes from structural studies.
Authors: Authors: Seegar TC, Blacklow SC.
Exp Biol Med (Maywood)
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Structural Basis for Regulation of ESCRT-III Complexes by Lgd.
Authors: Authors: McMillan BJ, Tibbe C, Drabek AA, Seegar TCM, Blacklow SC, Klein T.
Cell Rep
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A tail of two sites: a bipartite mechanism for recognition of notch ligands by mind bomb E3 ligases.
Authors: Authors: McMillan BJ, Schnute B, Ohlenhard N, Zimmerman B, Miles L, Beglova N, Klein T, Blacklow SC.
Mol Cell
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Epstein-Barr virus exploits intrinsic B-lymphocyte transcription programs to achieve immortal cell growth.
Authors: Authors: Zhao B, Zou J, Wang H, Johannsen E, Peng CW, Quackenbush J, Mar JC, Morton CC, Freedman ML, Blacklow SC, Aster JC, Bernstein BE, Kieff E.
Proc Natl Acad Sci U S A
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