M
Malia B. Potts
Researcher at University of Texas Southwestern Medical Center
Publications - 15
Citations - 613
Malia B. Potts is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Signal transduction & Receptor tyrosine kinase. The author has an hindex of 9, co-authored 13 publications receiving 516 citations.
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Journal ArticleDOI
Degradation of AMPK by a Cancer-Specific Ubiquitin Ligase
Carlos T. Pineda,Saumya Ramanathan,Klementina Fon Tacer,Jenny L. Weon,Malia B. Potts,Yi Hung Ou,Michael A. White,Patrick Ryan Potts +7 more
TL;DR: A germline mechanism commonly hijacked in cancer to suppress AMPK through its ubiquitination and degradation by the cancer-specific MAGE-A3/6-TRIM28 ubiquitin ligase is described.
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Using Functional Signature Ontology (FUSION) to Identify Mechanisms of Action for Natural Products
Malia B. Potts,Hyun Seok Kim,Kurt W. Fisher,Youcai Hu,Yazmin P. Carrasco,Gamze B. Bulut,Yi Hung Ou,Mireya L. Herrera-Herrera,Federico Cubillos,Saurabh Mendiratta,Guanghua Xiao,Matan Hofree,Trey Ideker,Yang Xie,Lily Jun Shen Huang,Robert E. Lewis,John B. MacMillan,Michael A. White +17 more
TL;DR: This approach identified gene products and natural product compounds that regulated processes as diverse as the breakdown of intracellular components, directed cell migration, and survival signaling, and holds promise for facilitating future drug discovery.
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Direct regulation of egl-1 and of programmed cell death by the Hox protein MAB-5 and by CEH-20, a C. elegans homolog of Pbx1
TL;DR: In the nematode C. elegans, the Hox gene mab-5 is required for the programmed cell deaths of two lineally related cells generated in the P11 and P12 lineages, and a complex between MAB-5 and the Pbx homolog CEH-20 directly regulates transcription of the BH3 domain gene egl-1 to initiate programmed cell death.
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Discoipyrroles A–D: isolation, structure determination, and synthesis of potent migration inhibitors from Bacillus hunanensis
Youcai Hu,Malia B. Potts,Dominic A. Colosimo,Mireya L. Herrera-Herrera,Aaron G. Legako,Muhammed Yousufuddin,Michael A. White,John B. MacMillan +7 more
TL;DR: In this paper, the authors identified a family of alkaloid natural products, Discoipyrroles A-D (1−4), from Bacillus hunanensis that inhibit the DDR2 signaling pathway.
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Mode of action and pharmacogenomic biomarkers for exceptional responders to didemnin B
Malia B. Potts,Elizabeth A. McMillan,Tracy I. Rosales,Hyun Seok Kim,Yi Hung Ou,Jason E. Toombs,Rolf A. Brekken,Mark D. Minden,John B. MacMillan,Michael A. White +9 more
TL;DR: It is found that didemnin B selectively induces rapid and wholesale apoptosis through dual inhibition of PPT1 and EEF1A1 and this may facilitate patient selection that could enhance and expand therapeutic application of didem nin B against neoplastic disease.