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  1. Article: Evaluating Large Language Models in Extracting Cognitive Exam Dates and Scores.

    Zhang, Hao / Jethani, Neil / Jones, Simon / Genes, Nicholas / Major, Vincent J / Jaffe, Ian S / Cardillo, Anthony B / Heilenbach, Noah / Ali, Nadia Fazal / Bonanni, Luke J / Clayburn, Andrew J / Khera, Zain / Sadler, Erica C / Prasad, Jaideep / Schlacter, Jamie / Liu, Kevin / Silva, Benjamin / Montgomery, Sophie / Kim, Eric J /
    Lester, Jacob / Hill, Theodore M / Avoricani, Alba / Chervonski, Ethan / Davydov, James / Small, William / Chakravartty, Eesha / Grover, Himanshu / Dodson, John A / Brody, Abraham A / Aphinyanaphongs, Yindalon / Masurkar, Arjun / Razavian, Narges

    medRxiv : the preprint server for health sciences

    2024  

    Abstract: Importance: Large language models (LLMs) are crucial for medical tasks. Ensuring their reliability is vital to avoid false results. Our study assesses two state-of-the-art LLMs (ChatGPT and LlaMA-2) for extracting clinical information, focusing on ... ...

    Abstract Importance: Large language models (LLMs) are crucial for medical tasks. Ensuring their reliability is vital to avoid false results. Our study assesses two state-of-the-art LLMs (ChatGPT and LlaMA-2) for extracting clinical information, focusing on cognitive tests like MMSE and CDR.
    Objective: Evaluate ChatGPT and LlaMA-2 performance in extracting MMSE and CDR scores, including their associated dates.
    Methods: Our data consisted of 135,307 clinical notes (Jan 12th, 2010 to May 24th, 2023) mentioning MMSE, CDR, or MoCA. After applying inclusion criteria 34,465 notes remained, of which 765 underwent ChatGPT (GPT-4) and LlaMA-2, and 22 experts reviewed the responses. ChatGPT successfully extracted MMSE and CDR instances with dates from 742 notes. We used 20 notes for fine-tuning and training the reviewers. The remaining 722 were assigned to reviewers, with 309 each assigned to two reviewers simultaneously. Inter-rater-agreement (Fleiss' Kappa), precision, recall, true/false negative rates, and accuracy were calculated. Our study follows TRIPOD reporting guidelines for model validation.
    Results: For MMSE information extraction, ChatGPT (vs. LlaMA-2) achieved accuracy of 83% (vs. 66.4%), sensitivity of 89.7% (vs. 69.9%), true-negative rates of 96% (vs 60.0%), and precision of 82.7% (vs 62.2%). For CDR the results were lower overall, with accuracy of 87.1% (vs. 74.5%), sensitivity of 84.3% (vs. 39.7%), true-negative rates of 99.8% (98.4%), and precision of 48.3% (vs. 16.1%). We qualitatively evaluated the MMSE errors of ChatGPT and LlaMA-2 on double-reviewed notes. LlaMA-2 errors included 27 cases of total hallucination, 19 cases of reporting other scores instead of MMSE, 25 missed scores, and 23 cases of reporting only the wrong date. In comparison, ChatGPT's errors included only 3 cases of total hallucination, 17 cases of wrong test reported instead of MMSE, and 19 cases of reporting a wrong date.
    Conclusions: In this diagnostic/prognostic study of ChatGPT and LlaMA-2 for extracting cognitive exam dates and scores from clinical notes, ChatGPT exhibited high accuracy, with better performance compared to LlaMA-2. The use of LLMs could benefit dementia research and clinical care, by identifying eligible patients for treatments initialization or clinical trial enrollments. Rigorous evaluation of LLMs is crucial to understanding their capabilities and limitations.
    Language English
    Publishing date 2024-02-13
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.07.10.23292373
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle Epithelium.

    Sadler, Erica / Ryals, Matthew M / May, Lindsey A / Martin, Daniel / Welsh, Nora / Boger, Erich T / Morell, Robert J / Hertzano, Ronna / Cunningham, Lisa L

    Frontiers in cellular neuroscience

    2020  Volume 14, Page(s) 123

    Abstract: Sensory epithelia of the inner ear contain mechanosensory hair cells (HCs) and glia-like supporting cells (SCs), both of which are required for hearing and balance functions. Each of these cell types has unique responses to ototoxic and cytoprotective ... ...

    Abstract Sensory epithelia of the inner ear contain mechanosensory hair cells (HCs) and glia-like supporting cells (SCs), both of which are required for hearing and balance functions. Each of these cell types has unique responses to ototoxic and cytoprotective stimuli. Non-lethal heat stress in the mammalian utricle induces heat shock proteins (HSPs) and protects against ototoxic drug-induced hair cell death. Induction of HSPs in the utricle demonstrates cell-type specificity at the protein level, with HSP70 induction occurring primarily in SCs, while HSP32 (also known as heme oxygenase 1, HMOX1) is induced primarily in resident macrophages. Neither of these HSPs are robustly induced in HCs, suggesting that HCs may have little capacity for induction of stress-induced protective responses. To determine the transcriptional responses to heat shock of these different cell types, we performed cell-type-specific transcriptional profiling using the RiboTag method, which allows for immunoprecipitation (IP) of actively translating mRNAs from specific cell types. RNA-Seq differential gene expression analyses demonstrated that the RiboTag method identified known cell type-specific markers as well as new markers for HCs and SCs. Gene expression differences suggest that HCs and SCs exhibit differential transcriptional heat shock responses. The chaperonin family member
    Language English
    Publishing date 2020-05-15
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2452963-1
    ISSN 1662-5102
    ISSN 1662-5102
    DOI 10.3389/fncel.2020.00123
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: A Pliable Mediator Acts as a Functional Rather Than an Architectural Bridge between Promoters and Enhancers

    El Khattabi, Laila / Aiden, Erez Lieberman / Asturias, Francisco J / Casellas, Rafael / Chauss, Daniel / Huang, Su-Chen / Jung, Seolkyoung / Kalchschmidt, Jens / Kieffer-Kwon, Kyong-Rim / Kieffer-Kwon, Philippe / Krebs, Jordan / Lopez, Andrea / Nóbrega, Marcelo A / Park, Solji / Pruett, Nathanael / Rao, Suhas S.P / Sadler, Erica / Sakabe, Noboru / Sobreira, Débora R /
    Tripathi, Subhash / Van Blerkom, Peter / Wang, Xiang / Young, Natalie / Zhao, Haiyan

    Cell. 2019 Aug. 22, v. 178, no. 5

    2019  

    Abstract: While Mediator plays a key role in eukaryotic transcription, little is known about its mechanism of action. This study combines CRISPR-Cas9 genetic screens, degron assays, Hi-C, and cryoelectron microscopy (cryo-EM) to dissect the function and structure ... ...

    Abstract While Mediator plays a key role in eukaryotic transcription, little is known about its mechanism of action. This study combines CRISPR-Cas9 genetic screens, degron assays, Hi-C, and cryoelectron microscopy (cryo-EM) to dissect the function and structure of mammalian Mediator (mMED). Deletion analyses in B, T, and embryonic stem cells (ESC) identified a core of essential subunits required for Pol II recruitment genome-wide. Conversely, loss of non-essential subunits mostly affects promoters linked to multiple enhancers. Contrary to current models, however, mMED and Pol II are dispensable to physically tether regulatory DNA, a topological activity requiring architectural proteins. Cryo-EM analysis revealed a conserved core, with non-essential subunits increasing structural complexity of the tail module, a primary transcription factor target. Changes in tail structure markedly increase Pol II and kinase module interactions. We propose that Mediator’s structural pliability enables it to integrate and transmit regulatory signals and act as a functional, rather than an architectural bridge, between promoters and enhancers.
    Keywords CRISPR-Cas systems ; cryo-electron microscopy ; DNA ; embryonic stem cells ; enzymes ; mammals ; mechanism of action ; models ; topology ; transcription factors
    Language English
    Dates of publication 2019-0822
    Size p. 1145-1158.e20.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2019.07.011
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: A Pliable Mediator Acts as a Functional Rather Than an Architectural Bridge between Promoters and Enhancers.

    El Khattabi, Laila / Zhao, Haiyan / Kalchschmidt, Jens / Young, Natalie / Jung, Seolkyoung / Van Blerkom, Peter / Kieffer-Kwon, Philippe / Kieffer-Kwon, Kyong-Rim / Park, Solji / Wang, Xiang / Krebs, Jordan / Tripathi, Subhash / Sakabe, Noboru / Sobreira, Débora R / Huang, Su-Chen / Rao, Suhas S P / Pruett, Nathanael / Chauss, Daniel / Sadler, Erica /
    Lopez, Andrea / Nóbrega, Marcelo A / Aiden, Erez Lieberman / Asturias, Francisco J / Casellas, Rafael

    Cell

    2019  Volume 178, Issue 5, Page(s) 1145–1158.e20

    Abstract: While Mediator plays a key role in eukaryotic transcription, little is known about its mechanism of action. This study combines CRISPR-Cas9 genetic screens, degron assays, Hi-C, and cryoelectron microscopy (cryo-EM) to dissect the function and structure ... ...

    Abstract While Mediator plays a key role in eukaryotic transcription, little is known about its mechanism of action. This study combines CRISPR-Cas9 genetic screens, degron assays, Hi-C, and cryoelectron microscopy (cryo-EM) to dissect the function and structure of mammalian Mediator (mMED). Deletion analyses in B, T, and embryonic stem cells (ESC) identified a core of essential subunits required for Pol II recruitment genome-wide. Conversely, loss of non-essential subunits mostly affects promoters linked to multiple enhancers. Contrary to current models, however, mMED and Pol II are dispensable to physically tether regulatory DNA, a topological activity requiring architectural proteins. Cryo-EM analysis revealed a conserved core, with non-essential subunits increasing structural complexity of the tail module, a primary transcription factor target. Changes in tail structure markedly increase Pol II and kinase module interactions. We propose that Mediator's structural pliability enables it to integrate and transmit regulatory signals and act as a functional, rather than an architectural bridge, between promoters and enhancers.
    MeSH term(s) Animals ; CD4-Positive T-Lymphocytes/cytology ; CD4-Positive T-Lymphocytes/metabolism ; CRISPR-Cas Systems/genetics ; Cell Cycle Proteins/metabolism ; Cells, Cultured ; Chromosomal Proteins, Non-Histone/metabolism ; Cryoelectron Microscopy ; Enhancer Elements, Genetic ; Gene Editing ; Humans ; Male ; Mediator Complex/chemistry ; Mediator Complex/genetics ; Mediator Complex/metabolism ; Mice ; Mice, Inbred C57BL ; Mouse Embryonic Stem Cells/cytology ; Mouse Embryonic Stem Cells/metabolism ; Promoter Regions, Genetic ; Protein Structure, Quaternary ; RNA Polymerase II/genetics ; RNA Polymerase II/metabolism ; Saccharomyces cerevisiae/metabolism ; Saccharomyces cerevisiae Proteins/metabolism ; Cohesins
    Chemical Substances Cell Cycle Proteins ; Chromosomal Proteins, Non-Histone ; Mediator Complex ; Saccharomyces cerevisiae Proteins ; RNA Polymerase II (EC 2.7.7.-)
    Language English
    Publishing date 2019-08-08
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2019.07.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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