Qing Dong, PhD

Title(s)Assistant Researcher, Pathology
SchoolSchool of Medicine
Address513 Parnassus Avenue, HSW, #425
San Francisco CA 94143
Phone415-476-8734
PronounsShe/Her/Hers
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    Other Positions
    Title(s)UCSF Weill Institute for Neurosciences


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    Collapse awards and honors
    Weill Neurohub2023  - 2025Weill Neurohub Fellowship

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    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Mutant β1-adrenergic receptor improves REM sleep and ameliorates tau accumulation in a mouse model of tauopathy. Proc Natl Acad Sci U S A. 2023 04 11; 120(15):e2221686120. Dong Q, Ptácek LJ, Fu YH. PMID: 37014857; PMCID: PMC10104526.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
    2. Familial natural short sleep mutations reduce Alzheimer pathology in mice. iScience. 2022 Apr 15; 25(4):103964. Dong Q, Gentry NW, McMahon T, Yamazaki M, Benitez-Rivera L, Wang T, Gan L, Ptácek L, Fu YH. PMID: 35496999; PMCID: PMC9042888.
      View in: PubMed   Mentions: 9  
    3. NC2 complex is a key factor for the activation of catalase-3 transcription by regulating H2A.Z deposition. Nucleic Acids Res. 2020 09 04; 48(15):8332-8348. Cui G, Dong Q, Duan J, Zhang C, Liu X, He Q. PMID: 32633757; PMCID: PMC7470962.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    4. Histone variant H2A.Z antagonizes the positive effect of the transcriptional activator CPC1 to regulate catalase-3 expression under normal and oxidative stress conditions. Free Radic Biol Med. 2018 06; 121:136-148. Dong Q, Wang Y, Qi S, Gai K, He Q, Wang Y. PMID: 29738831.
      View in: PubMed   Mentions: 12     Fields:    Translation:AnimalsCells
    5. Cross-pathway control gene CPC1/GCN4 coordinates with histone acetyltransferase GCN5 to regulate catalase-3 expression under oxidative stress in Neurospora crassa. Free Radic Biol Med. 2018 03; 117:218-227. Qi S, He L, Zhang Q, Dong Q, Wang Y, Yang Q, Tian C, He Q, Wang Y. PMID: 29421311.
      View in: PubMed   Mentions: 13     Fields:    Translation:Animals
    6. Transcriptional repression of frequency by the IEC-1-INO80 complex is required for normal Neurospora circadian clock function. PLoS Genet. 2017 04; 13(4):e1006732. Gai K, Cao X, Dong Q, Ding Z, Wei Y, Liu Y, Liu X, He Q. PMID: 28403234; PMCID: PMC5406019.
      View in: PubMed   Mentions: 8     Fields:    Translation:AnimalsCells
    7. Regulation of Neurospora Catalase-3 by global heterochromatin formation and its proximal heterochromatin region. Free Radic Biol Med. 2016 10; 99:139-152. Wang Y, Dong Q, Ding Z, Gai K, Han X, Kaleri FN, He Q, Wang Y. PMID: 27458122.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
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