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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Attempt to identify a molecular basis (mutation) of a new hereditary hemolytic anemia associated with the lack of MPP1 palmitoylation.

2012/05/B/NZ5/01464

Keywords:

hereditary hemolytic anemia protein palmitoylation red blood cell membrane acyltransferases membrane microdomains (rafts)

Descriptors:

  • NZ5_1: Etiology of human diseases

Panel:

NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)

Host institution :

Uniwersytet Zielonogórski, Wydział Nauk Biologicznych

woj. lubuskie

Other projects carried out by the institution 

Principal investigator (from the host institution):

dr Dżamila Bogusławska 

Number of co-investigators in the project: 5

Call: OPUS 3 - announced on 2012-03-15

Amount awarded: 594 000 PLN

Project start date (Y-m-d): 2013-02-20

Project end date (Y-m-d): 2017-02-19

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

Project status: Project settled

Equipment purchased [PL]

  1. Termocykler.

Information in the final report

  • Publication in academic press/journals (3)
  • Articles in post-conference publications (1)
  1. A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis
    Authors:
    Dżamila M. Bogusławska, Elżbieta Heger, Beata Machnicka, Michał Skulski, Kazimierz Kuliczkowski, Aleksander F. Sikorski
    Academic press:
    Annals of Hematology (rok: 2017, tom: 96, strony: 163-165), Wydawca: Springer
    Status:
    Published
    DOI:
    10.1007/s00277-016-2838-0 - link to the publication
  2. Efficient method for isolation of reticulocyte RNA from healthy individuals and hemolytic anemia patients
    Authors:
    Michał Skulski, Rafał Bartoszewski, Michał Majkowski, Beata Machnicka, Kazimierz Kuliczkowski, Aleksander F. Sikorski, Dżamila M. Bogusławska
    Academic press:
    Journal of Cellular and Molecular Medicine (rok: 2018, ), Wydawca: Wiley Online Library
    Status:
    Accepted for publication
    DOI:
    10.1111/jcmm.13951 - link to the publication
  3. A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
    Authors:
    Dżamila M. Bogusławska, Elżbieta Heger, Marcin Listowski, Dariusz Wasiński, Kazimierz Kuliczkowski, Beata Machnicka, Aleksander F. Sikorski
    Academic press:
    British Journal of Haematology (rok: 2014, tom: 167(2), strony: 269-71), Wydawca: Wiley
    Status:
    Published
    DOI:
    10.1111/bjh.12960 - link to the publication
  1. A novel mutation of the SPTB gene: a truncated beta-chain responsible for dominant hereditary spherocytosis
    Authors:
    Dżamila M. Bogusławska, Elżbieta Heger, Beata Machnicka, Michał Skulski, Kazimierz Kuliczkowski, Aleksander F. Sikorski
    Conference:
    BIO 2016 Congress - "Epanding beyond the limits", Wrocław, Poland, September 13th–16th 2016 (rok: 2016, ), Wydawca: Acta Biochimica Polonica
    Data:
    konferencja 13-16.09.2016
    Status:
    Published
    DOI:
    link to the publication

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