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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Molecular basis of skeletal development

2013/11/B/NZ4/03660

Keywords:

bone cartilage limb development skeletal malformations genetics chick

Descriptors:

  • NZ4_12: Other related subjects

Panel:

NZ4 - Biology of tissues, organs and organisms: morphology and functions of animal's and human's systems, organs and organisms, experimental medicine, basics of neurology

Host institution :

Uniwersytet Medyczny w Lublinie, II Wydział Lekarski z Oddziałem Anglojęzycznym

woj. lubelskie

Other projects carried out by the institution 

Principal investigator (from the host institution):

prof. Przemyslaw Tylzanowski 

Number of co-investigators in the project: 5

Call: OPUS 6 - announced on 2013-09-16

Amount awarded: 1 028 232 PLN

Project start date (Y-m-d): 2014-09-08

Project end date (Y-m-d): 2019-03-07

Project duration:: 54 months (the same as in the proposal)

Project status: Project settled

Equipment purchased [PL]

  1. Program komputerowy Express Static Acad.
  2. Stereo Mikroskop z fluorescencjaZEISS V8 lub rownowazny (130 000 PLN)
  3. Wirówka VWR 2 Micro Star.
  4. Łaźnia wodna VWB 2.

Information in the final report

  • Publication in academic press/journals (4)
  1. Cleidocranial dysplasia and RUNX2- clinical phenotype genotype correlation
    Authors:
    Anna Jaruga, Ewa Hordyjewska, Grzegorz Kandzierski, Przemko Tylzanowski
    Academic press:
    Clinical Genetics (rok: 2016, tom: 90, strony: 393-402), Wydawca: Wiley
    Status:
    Published
    DOI:
    10.1111/cge.12812 - link to the publication
  2. Mutations in gene regulatory elements linked to human limb malformations
    Authors:
    Karol Nowosad, Ewa Hordyjewska-Kowalczyk, Przemko Tylżanowski
    Academic press:
    Journal of Medical Genetics (rok: 2019, ), Wydawca: BMJ Journals
    Status:
    Published
    DOI:
    10.1136/jmedgenet-2019-106369 - link to the publication
  3. Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia
    Authors:
    Ewa Hordyjewska, Anna Jaruga, Grzegorz Kandzierski, Przemko Tylzanowski
    Academic press:
    Molecular Syndromology (rok: 2017, tom: 8, strony: 253-260), Wydawca: KARGER
    Status:
    Published
    DOI:
    10.1159/000477307 - link to the publication
  4. Gollop–Wolfgang Complex is Associated with a Monoallelic Variation in WNT11
    Authors:
    Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemysław Tylżanowski
    Academic press:
    Genes (rok: 2024, tom: 15, strony: 129), Wydawca: MDPI
    Status:
    Published
    DOI:
    10.3390/genes15010129 - link to the publication

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