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Craig R. Braun

Researcher at Harvard University

Publications -  16
Citations -  1047

Craig R. Braun is an academic researcher from Harvard University. The author has contributed to research in topics: Bcl-2-associated X protein & Amide. The author has an hindex of 13, co-authored 16 publications receiving 896 citations. Previous affiliations of Craig R. Braun include University of Manitoba.

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Differential Glutamate Metabolism in Proliferating and Quiescent Mammary Epithelial Cells.

TL;DR: A competitive and partially redundant relationship between transaminases and GLUD is described, and they reveal how coupling of glutamate-derived carbon and nitrogen metabolism can be regulated to support cell proliferation.
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Direct activation of full-length proapoptotic BAK

TL;DR: Production of full-length, monomeric BAK by mutagenesis-based solubilization of its C-terminal α-helical surface is reported, providing opportunities for developing proapoptotic agents that activate the death pathway through direct but differential engagement of BAK and BAX.
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Inhibition of Pro-Apoptotic BAX by a Noncanonical Interaction Mechanism

TL;DR: Data reveal a previously unappreciated binding site for targeted inhibition of BAX and suggest that the BCL-2 BH4 domain may participate in apoptosis blockade by a noncanonical interaction mechanism.
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A Strategy to Combine Sample Multiplexing with Targeted Proteomics Assays for High-Throughput Protein Signature Characterization

TL;DR: A two-dimensional multiplexing workflow is presented that utilizes synthetic peptides for each protein to prompt the simultaneous quantification of >100 peptides from up to ten mixed sample conditions and elucidated a correlation between the expression of key proteins and their cellular response to drug treatment.
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Post-transcriptional regulation of meiotic genes by a nuclear RNA silencing complex

TL;DR: It is demonstrated that Red1 partners with other proteins to silence meiotic gene expression at the post-transcriptional level and Conservation of a NURS-like complex in human cells suggests that this pathway plays an ancient and fundamental role in RNA silencing.