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William Jeremy Blake
Researcher at Boston University
Publications - 24
Citations - 5623
William Jeremy Blake is an academic researcher from Boston University. The author has contributed to research in topics: Gene & Gene expression. The author has an hindex of 13, co-authored 24 publications receiving 5328 citations.
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Journal ArticleDOI
Stochasticity in gene expression: from theories to phenotypes
TL;DR: Stochasticity in gene expression can provide the flexibility needed by cells to adapt to fluctuating environments or respond to sudden stresses, and a mechanism by which population heterogeneity can be established during cellular differentiation and development.
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Noise in eukaryotic gene expression
TL;DR: It is shown that stochasticity (noise) arising from transcription contributes significantly to the level of heterogeneity within a eukaryotic clonal population, in contrast to observations in prokaryotes, and that such noise can be modulated at the translational level.
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Phenotypic consequences of promoter-mediated transcriptional noise.
William Jeremy Blake,Gábor Balázsi,Michael A. Kohanski,Farren J. Isaacs,Kevin F. Murphy,Yina Kuang,Charles R. Cantor,David R. Walt,James J. Collins +8 more
TL;DR: It is shown that increased variability in gene expression, affected by the sequence of the TATA box, can be beneficial after an acute change in environmental conditions.
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Synthetic chromosome arms function in yeast and generate phenotypic diversity by design
Jessica S. Dymond,Sarah M. Richardson,Candice E. Coombes,Timothy D. Babatz,Héloïse Muller,Narayana Annaluru,William Jeremy Blake,Joy Wu Schwerzmann,Joy Wu Schwerzmann,Junbiao Dai,Junbiao Dai,Derek L. Lindstrom,Derek L. Lindstrom,Annabel C. Boeke,Annabel C. Boeke,Daniel E. Gottschling,Srinivasan Chandrasegaran,Joel S. Bader,Jef D. Boeke +18 more
TL;DR: This work describes a synthetic yeast genome project, Sc2.0, and the first partially synthetic eukaryotic chromosomes, Saccharomyces cerevisiae chromosome synIXR, and semi-synVIL, and shows the utility of SCRaMbLE as a novel method of combinatorial mutagenesis, capable of generating complex genotypes and a broad variety of phenotypes.
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The engineering of gene regulatory networks.
TL;DR: How networks with increased complexity are being constructed from simple modular components and how quantitative deterministic and stochastic modeling of these modules may provide the foundation for accurate in silico representations of gene regulatory network function in vivo are discussed.