NLM DIR Seminar Schedule
UPCOMING SEMINARS
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Jan. 22, 2026 Mario Flores
AI Pipeline for Characterization of the Tumor Microenvironment -
Jan. 27, 2026 Zhaohui Liang
Heterogeneous Graph Re-ranking for CLIP-based Medical Cross-modal Retrieval -
Jan. 29, 2026 Mehdi Bagheri Hamaneh
FastSpel: A simple peptide spectrum predictor that achieves deep learning-level performance at a fraction of the computational cost -
Feb. 3, 2026 Matthew Diller
TBD -
Feb. 5, 2026 Lana Yeganova
From Algorithms to Insights: Bridging AI and Topic Discovery for Large-Scale Biomedical Literature Analysis.
RECENT SEMINARS
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Jan. 20, 2026 Anastasia Gulyaeva
Diversity and evolution of the ribovirus class Stelpaviricetes -
Jan. 8, 2026 Won Gyu Kim
LitSense 2.0: AI-powered biomedical information retrieval with sentence and passage level knowledge discovery -
Dec. 16, 2025 Sarvesh Soni
ArchEHR-QA: A Dataset and Shared Task for Grounded Question Answering from Electronic Health Records -
Dec. 2, 2025 Qingqing Zhu
CT-Bench & CARE-CT: Building Reliable Multimodal AI for Lesion Analysis in Computed Tomography -
Nov. 25, 2025 Jing Wang
MIMIC-EXT-TE: Millions Clinical Temporal Event Time-Series Dataset
Scheduled Seminars on March 11, 2025
In-person: Building 38A/B2N14 NCBI Library or Meeting Link
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
Bacterial defense systems against phages are diverse, yet mechanisms involving membrane-associated components remain largely unexplored. Here, I will characterize Tmn, a member of the KAP NTPase family, as a membrane-associated defense system that targets phage infection through reversible plasmolysis. Tmn activation requires direct interactions with phage proteins expressed during infection. Upon activation, Tmn manipulates potassium export to induce plasmolysis, disrupting phage maturation at a stage where host chromosome degradation is avoided. These findings reveal that Tmn provides an elegant strategy to disrupt phage replication while enabling host cell recovery, underscoring the diverse adaptations of membrane-targeting bacterial defense systems.