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  1. Article ; Online: Variant Polycomb complexes in

    Kang, Hyuckjoon / Cabrera, Janel R / Zee, Barry M / Kang, Heather A / Jobe, Jenny Marie / Hegarty, Maeve B / Barry, Aurelie E / Glotov, Alexander / Schwartz, Yuri B / Kuroda, Mitzi I

    Science advances

    2022  Volume 8, Issue 36, Page(s) eadd0103

    Abstract: Polycomb group (PcG) mutants were first identified ... ...

    Abstract Polycomb group (PcG) mutants were first identified in
    Language English
    Publishing date 2022-09-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.add0103
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Convergence of coronary artery disease genes onto endothelial cell programs.

    Schnitzler, Gavin R / Kang, Helen / Fang, Shi / Angom, Ramcharan S / Lee-Kim, Vivian S / Ma, X Rosa / Zhou, Ronghao / Zeng, Tony / Guo, Katherine / Taylor, Martin S / Vellarikkal, Shamsudheen K / Barry, Aurelie E / Sias-Garcia, Oscar / Bloemendal, Alex / Munson, Glen / Guckelberger, Philine / Nguyen, Tung H / Bergman, Drew T / Hinshaw, Stephen /
    Cheng, Nathan / Cleary, Brian / Aragam, Krishna / Lander, Eric S / Finucane, Hilary K / Mukhopadhyay, Debabrata / Gupta, Rajat M / Engreitz, Jesse M

    Nature

    2024  Volume 626, Issue 8000, Page(s) 799–807

    Abstract: Linking variants from genome-wide association studies (GWAS) to underlying mechanisms of disease remains a ... ...

    Abstract Linking variants from genome-wide association studies (GWAS) to underlying mechanisms of disease remains a challenge
    MeSH term(s) Humans ; Coronary Artery Disease/genetics ; Coronary Artery Disease/pathology ; Endothelial Cells/metabolism ; Endothelial Cells/pathology ; Genetic Predisposition to Disease/genetics ; Genome-Wide Association Study ; Hemangioma, Cavernous, Central Nervous System/genetics ; Hemangioma, Cavernous, Central Nervous System/pathology ; Polymorphism, Single Nucleotide ; Epigenomics ; Signal Transduction/genetics ; Multifactorial Inheritance
    Chemical Substances CCM2 protein, human ; TLNRD1 protein, human
    Language English
    Publishing date 2024-02-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-024-07022-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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