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Naama Barkai

Researcher at Weizmann Institute of Science

Publications -  148
Citations -  10896

Naama Barkai is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Gene & Morphogen. The author has an hindex of 53, co-authored 141 publications receiving 9828 citations. Previous affiliations of Naama Barkai include University of Minnesota.

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Noise in protein expression scales with natural protein abundance.

TL;DR: Deviation of coexpressed genes from this general trend, including high noise in stress-related genes and low noise in proteasomal genes, may indicate fluctuations in pathway-specific regulators or a differential activation pattern of the underlying gene promoters.
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Robustness of the BMP morphogen gradient in Drosophila embryonic patterning

TL;DR: It is found that the BMP activation gradient itself is robust to changes in gene dosage, and it is shown experimentally that Dpp is widely diffusible in the presence of Sog but tightly localized in its absence, thus validating a central prediction of the theoretical study.
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Iterative signature algorithm for the analysis of large-scale gene expression data.

TL;DR: It is shown analytically that for noisy expression data the proposed approach leads to better classification due to the implementation of the threshold, and argues that the method is in fact a generalization of singular value decomposition, which corresponds to the special case where no threshold is applied.
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Two strategies for gene regulation by promoter nucleosomes

TL;DR: The connection between patterns of nucleosome occupancy and the capacity to modulate gene expression upon changing conditions, i.e., transcriptional plasticity, is examined and two distinct strategies for gene regulation by chromatin are suggested, which are selectively employed by different genes.
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A Yeast Hybrid Provides Insight into the Evolution of Gene Expression Regulation

TL;DR: Compared the allele-specific expression of two yeast species and their hybrid, which allowed us to distinguish changes in regulatory sequences of the gene itself (cis) from changes in upstream regulatory factors (trans), insights are provided on the regulatory changes in cis and trans during the divergence of species and upon hybridization.