Projects funded by the NCN


Information on the principal investigator and host institution

Information of the project and the call

Keywords

Equipment

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Leber Hereditary Optic Neuropathy -why are not all men (and women) created equal?

2014/15/B/NZ2/02272

Keywords:

Leber hereditary optic neuropathy chromosome X sequencing gender differences

Descriptors:

  • NZ2_1: Molecular genetics
  • NZ2_2: Genomics, transcriptomics, epigenomics
  • NZ2_11: Genetic epidemiology

Panel:

NZ2 - Genetics, genomics: molecular genetics, genomics, proteomics, bioinformatics, systems biology, genetic epidemiology

Host institution :

Uniwersytet Warszawski, Wydział Biologii

woj. mazowieckie

Other projects carried out by the institution 

Principal investigator (from the host institution):

prof. Ewa Bartnik 

Number of co-investigators in the project: 11

Call: OPUS 8 - announced on 2014-09-15

Amount awarded: 1 367 393 PLN

Project start date (Y-m-d): 2015-07-16

Project end date (Y-m-d): 2019-07-15

Project duration:: 48 months (the same as in the proposal)

Project status: Project settled

Equipment purchased [PL]

  1. Pojemnik Dewara (5 000 PLN)
  2. Wytrząsarka kołyskowa (5 000 PLN)
  3. stacja do wstępnej obróbki danych (15 000 PLN)

Information in the final report

  • Publication in academic press/journals (6)
  1. Choroby mitochondrialne
    Authors:
    Piotrowska A, Jankauskaite E, Bartnik E
    Academic press:
    Postępy Biochemii (rok: 2016, tom: 62, strony: 111-115), Wydawca: Polskie Towarzystwo Biochemiczne
    Status:
    Published
  2. Analysis of BNIP3 and BNIP3L/Nix expression in cybrid cell lines harboring two LHON-associated mutations
    Authors:
    Kodron A., Hajieva P., Kulicka A, Paterczyk B, Jankauskaite E, Bartnik E.
    Academic press:
    Acta Biochimica Polonica (rok: 2019, tom: 66, strony: 427-435), Wydawca: Polskie Towarzystwo Biochemiczne
    Status:
    Published
    DOI:
    10.18388/abp.2019_2837 - link to the publication
  3. Mitochondrial genome variation in male LHON patients with the m.11778G>A mutation
    Authors:
    Agnieszka Piotrowska-Nowak, Maciej R. Krawczyński, Ewa Kosior-Jarecka, Anna M. Ambroziak, Magdalena Korwin, Monika Ołdak, Katarzyna Tońska, Ewa Bartnik
    Academic press:
    Metabolic Brain Disease (rok: 2020, tom: 35, strony: 1317-1327), Wydawca: Springer
    Status:
    Published
    DOI:
    10.0007/s1011-020-00605-3 - link to the publication
  4. Testosterone increases apoptotic cell death and decreases mitophagy in Leber's hereditary optic neuropathy cells
    Authors:
    Elona Jankauskaitė, Anna Maria Ambroziak, Parvana Hajieva, Monika Ołdak, Katarzyna Tońska, Magdalena Korwin, Ewa Bartnik, Agata Kodroń
    Academic press:
    Journal of Applied Genetics (rok: 2020, tom: 61, strony: 195-203), Wydawca: Springer
    Status:
    Published
    DOI:
    10.007/s13353-020-00550-y - link to the publication
  5. Choroby mitochondrialne, postęp w badaniu i leczeniu
    Authors:
    Katarzyna Tońska, Joanna Rusecka, Ewa Bartnik
    Academic press:
    Postępy Biochemii (rok: 2018, tom: 64, strony: 300-303), Wydawca: Polskie Towarzystwo Biochemiczne
    Status:
    Published
    DOI:
    10.18388/pb.2018_143. - link to the publication
  6. Investigating Leber's Hereditary Optic Neuropathy: Cell Models and Future Perspectives
    Authors:
    Jankauskaite E, Bartnik E, Kodroń A
    Academic press:
    Mitochondrion (rok: 2017, tom: 32, strony: 19-26), Wydawca: Mitochondria Research Society, Elsevier
    Status:
    Published
    DOI:
    10.16/j.mito.2016.11.006 - link to the publication