S
Stuart S. Levine
Researcher at Massachusetts Institute of Technology
Publications - 74
Citations - 23036
Stuart S. Levine is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Chromatin & Cellular differentiation. The author has an hindex of 35, co-authored 68 publications receiving 21221 citations. Previous affiliations of Stuart S. Levine include Harvard University.
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Journal ArticleDOI
Monitoring Error Rates In Illumina Sequencing.
TL;DR: The PPR's unique capabilities as a cross-instrument comparison device, as a troubleshooting tool, and as a tool for monitoring instrument performance can provide an increase in clarity over SAV metrics that is often crucial for maintaining instrument health.
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H2A.Z acidic patch couples chromatin dynamics to regulation of gene expression programs during ESC differentiation.
Vidya Subramanian,Aprotim Mazumder,Lauren E. Surface,Vincent L. Butty,Paul A. Fields,Allison Alwan,Lillian Torrey,Kevin K. Thai,Stuart S. Levine,Mark Bathe,Laurie A. Boyer +10 more
TL;DR: This work suggests that the divergent residues in the H2A.Z acidic patch comprise a unique domain that couples control of chromatin dynamics to the regulation of developmental gene expression patterns during lineage commitment.
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HRI coordinates translation necessary for protein homeostasis and mitochondrial function in erythropoiesis
Shuping Zhang,Alejandra Macias-Garcia,Jacob C. Ulirsch,Jason Velazquez,Vincent L. Butty,Stuart S. Levine,Vijay G. Sankaran,Vijay G. Sankaran,Vijay G. Sankaran,Jane-Jane Chen +9 more
TL;DR: The known role of HRI-mediated translational stimulation of integratedstressresponse mRNAs during iron deficiency in vivo is validated and GRB10 is identified as a previously unappreciated regulator of terminal erythropoiesis.
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Global transcriptional regulation of innate immunity by ATF-7 in C. elegans.
TL;DR: A genomic analysis of the transcriptional response of C. elegans to infection by Pseudomonas aeruginosa reveals a striking level of control over the innate immune response to infection through a single transcriptional regulator.
Journal ArticleDOI
Vasopressin regulated trafficking of a green fluorescent protein-aquaporin 2 chimera in LLC-PK1 cells.
Corinne E. Gustafson,Stuart S. Levine,Toshiya Katsura,Margaret McLaughlin,Maria Deize Aleixo,B. K. Tamarappoo,Alan S. Verkman,Dennis Brown +7 more
TL;DR: The abnormal, constitutive membrane localization of the GFP-AQP2(NT) chimera suggests that one or more trafficking signals exist on the carboxyl-terminus of the AQP2 protein.