Linking abnormal Ca2+ signaling and the unfolded protein response with Huntington's disease pathology in both YAC128 mouse model and iPSC-derived neurons from HD patients

2019/33/B/NZ3/02889

Keywords

Descriptors

  • NZ3_005: Neurobiologia molekularna
  • NZ3_006: Neurobiologia komórkowa
  • NZ3_007: Przekaźnictwo sygnału

Panel

NZ3 – Cellular and developmental biology: cell biology, developmental biology, ageing biology, neurobiology

Host institution

Międzynarodowy Instytut Biologii Molekularnej i Komórkowej

Voivodeship: mazowieckie

Other projects carried out by the institution »

Principal investigator (from the host institution)

dr Magdalena Czeredys

Number of co-investigators in the project: 4

Call

OPUS 17 – announced on 2019-03-15

Amount awarded
1 857 550 PLN
Project start date
2020-04-01
Project end date
2024-09-30
Project duration
54 months (the same as in the proposal)
Project status
Project settled

Project description

Download the project description in a pdf file

Note — project descriptions were prepared by the authors of the applications themselves and placed in the system in an unchanged form.

Information in the final report

Publication in academic press/journals (5)

  1. Molecular Components of Store-Operated Calcium Channels in the Regulation of Neural Stem Cell Physiology, Neurogenesis, and the Pathology of Huntington's Disease

    Authors:
    Ewelina Latoszek, Magdalena Czeredys
    Academic press:
    Front. Cell Dev. Biol. (year: 2021, volume: 9:657337), Publisher: Frontiers Media S.A.
    Status:
    Published
    DOI:
    10.3389/fcell.2021.657337 – link to the publication
  2. Dysregulation of Neuronal Calcium Signaling via Store-Operated Channels in Huntington's Disease

    Authors:
    Magdalena Czeredys
    Academic press:
    Front. Cell Dev. Biol. (year: 2020, volume: 8:611735), Publisher: Frontiers Media S.A.
    Status:
    Published
    DOI:
    10.3389/fcell.2020.611735 – link to the publication
  3. Generation of three human iPSC lines from patients with Huntington's disease with different CAG lengths and human control iPSC line from a healthy donor

    Authors:
    Latoszek E, Piechota M, Liszewska E, Hansíková H, Klempíř J, Mühlbäck A, Landwehrmeyer GB, Kuznicki J, Czeredys M.
    Academic press:
    Stem Cell Research (year: 2022, volume: 64, pages: 46027), Publisher: Elsevier
    Status:
    Published
    DOI:
    10.1016/j.scr.2022.102931 – link to the publication
  4. Siah-1-interacting protein regulates mutated huntingtin protein aggregation in Huntington's disease models

    Authors:
    Latoszek E, Wiweger M, Ludwiczak J, Dunin-Horkawicz S, Kuznicki J, Czeredys M.
    Academic press:
    Cell & Bioscience (year: 2022, volume: 0,523611111111111, pages: 46043), Publisher: Springer Nature
    Status:
    Published
    DOI:
    10.1186/s13578-022-00755-0 – link to the publication
  5. Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors.

    Authors:
    Piechota M, Latoszek E, Liszewska E, Hansíková H, Klempíř J, Mühlbäck A, Landwehrmeyer GB, Kuźnicki J, Czeredys M.
    Academic press:
    Stem Cell Research (year: 2023, volume: 71, pages: 46027), Publisher: Elsevier
    Status:
    Published
    DOI:
    10.1016/j.scr.2023.103194 – link to the publication

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