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Jasmine Miller-Kleinhenz

Researcher at Emory University

Publications -  18
Citations -  286

Jasmine Miller-Kleinhenz is an academic researcher from Emory University. The author has contributed to research in topics: Breast cancer & Medicine. The author has an hindex of 5, co-authored 10 publications receiving 119 citations.

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Neighborhood-Level Redlining and Lending Bias Are Associated with Breast Cancer Mortality in a Large and Diverse Metropolitan Area.

TL;DR: These findings underscore the role of ecologic measures of structural racism on cancer outcomes, and place-based measures are important contributors to health outcomes, an important unexplored area that offers potential interventions to address disparities.
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Dual-targeting Wnt and uPA receptors using peptide conjugated ultra-small nanoparticle drug carriers inhibited cancer stem-cell phenotype in chemo-resistant breast cancer.

TL;DR: This study developed an ultra-small magnetic iron oxide nanoparticle (IONP) drug carrier conjugated with peptides that are dually targeted to Wnt/LRP5/6 and urokinase plasminogen activator receptor (uPAR) to effectively treat resistant tumors.
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Targeted nanoparticles for image-guided treatment of triple-negative breast cancer: clinical significance and technological advances.

TL;DR: The current status of nanotherapeutic options for TNBC patients, identification of promising molecular targets, challenges associated with the development of targeted Nanotherapeutics, the research done by the group as well as by others, and future perspectives on the nanomedicine field and ways to translate current preclinical studies into the clinic are outlined.
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Theranostic Hyaluronic Acid-Iron Micellar Nanoparticles for Magnetic-Field-Enhanced in vivo Cancer Chemotherapy.

TL;DR: HI showed remarkable tumor ablation efficiency, with magnetic targeting after 3 mg kg−1 intravenous administration (equivalent dose of free HCPT), and the tumors almost disappeared after treatment, suggesting that HIH is a promising theranostic nanocomplex with great translational potency.