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David E. Golan

Researcher at Stanford University

Publications -  170
Citations -  16667

David E. Golan is an academic researcher from Stanford University. The author has contributed to research in topics: Band 3 & T cell. The author has an hindex of 59, co-authored 168 publications receiving 15221 citations. Previous affiliations of David E. Golan include University of Illinois at Chicago & Brigham and Women's Hospital.

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Protein therapeutics: a summary and pharmacological classification

TL;DR: Some of the key characteristics of protein therapeutics are overviewed, a new classification of these proteins according to their pharmacological action is suggested and this article summarizes the more than 130 protein therapeuticals used currently and suggests a new classifications.
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Stress granules and processing bodies are dynamically linked sites of mRNP remodeling

TL;DR: It is proposed that mRNA released from disassembled polysomes is sorted and remodeled at SGs, from which selected transcripts are delivered to PBs for degradation, an interaction that is promoted by the related mRNA decay factors TTP and BRF1.
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Identifying personal genomes by surname inference.

TL;DR: It is reported that surnames can be recovered from personal genomes by profiling short tandem repeats on the Y chromosome (Y-STRs) and querying recreational genetic genealogy databases and it is shown that a combination of a surname with other types of metadata, such as age and state, can be used to triangulate the identity of the target.
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Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules.

TL;DR: Fluorescence recovery after photobleaching shows that both TIA-1 and PABP-I rapidly and continuously shuttle in and out ofSGs, indicating that the assembly of SGs is a highly dynamic process, and proposes that mammalian SGs are sites at which untranslated mRNAs are sorted and processed for either reinitiation, degradation, or packaging into stable nonpolysomal mRNP complexes.
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RNA splicing is a primary link between genetic variation and disease

TL;DR: This study quantified the contribution of cis-acting genetic effects at all major stages of gene regulation from chromatin to proteins, in Yoruba lymphoblastoid cell lines (LCLs), and provides a comprehensive view of the mechanisms linking genetic variation to variation in human gene regulation.