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.

A new niche for Notch on Deltex?
Authors: Authors: Blacklow SC.
Structure
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The mature avian leukosis virus subgroup A envelope glycoprotein is metastable, and refolding induced by the synergistic effects of receptor binding and low pH is coupled to infection.
Authors: Authors: Smith JG, Mothes W, Blacklow SC, Cunningham JM.
J Virol
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Backbone dynamics of a module pair from the ligand-binding domain of the LDL receptor.
Authors: Authors: Beglova N, North CL, Blacklow SC.
Biochemistry
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How can a catalytic lesion be offset? The energetics of two pseudorevertant triosephosphate isomerases.
Authors: Authors: Blacklow SC, Knowles JR.
Biochemistry
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Bispecific Forkhead Transcription Factor FoxN3 Recognizes Two Distinct Motifs with Different DNA Shapes.
Authors: Authors: Rogers JM, Waters CT, Seegar TCM, Jarrett SM, Hallworth AN, Blacklow SC, Bulyk ML.
Mol Cell
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Genome-wide identification and characterization of Notch transcription complex-binding sequence-paired sites in leukemia cells.
Authors: Authors: Severson E, Arnett KL, Wang H, Zang C, Taing L, Liu H, Pear WS, Shirley Liu X, Blacklow SC, Aster JC.
Sci Signal
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Biased multicomponent reactions to develop novel bromodomain inhibitors.
Authors: Authors: McKeown MR, Shaw DL, Fu H, Liu S, Xu X, Marineau JJ, Huang Y, Zhang X, Buckley DL, Kadam A, Zhang Z, Blacklow SC, Qi J, Zhang W, Bradner JE.
J Med Chem
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Evidence for increased exposure of the Notch1 metalloprotease cleavage site upon conversion to an activated conformation.
Authors: Authors: Tiyanont K, Wales TE, Aste-Amezaga M, Aster JC, Engen JR, Blacklow SC.
Structure
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Modulation of Notch signaling by antibodies specific for the extracellular negative regulatory region of NOTCH3.
Authors: Authors: Li K, Li Y, Wu W, Gordon WR, Chang DW, Lu M, Scoggin S, Fu T, Vien L, Histen G, Zheng J, Martin-Hollister R, Duensing T, Singh S, Blacklow SC, Yao Z, Aster JC, Zhou BB.
J Biol Chem
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De novo genetic codes and pure translation display.
Authors: Authors: Tan Z, Blacklow SC, Cornish VW, Forster AC.
Methods
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