Cristin-person-ID: 754843
Person

Nikolina Sekulic

  • Stilling:
    Forsker
    ved Nikolina Sekulic Group - Structural Biology and Chromatin ved Universitetet i Oslo

Resultater Resultater

Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy.

Brugger, Melanie; Lauri, Antonella; Zhen, Yan; Gramegna, Laura L.; Zott, Benedikt; Sekulic, Nikolina; Fasano, Giulia; Kopajtich, Robert; Cordeddu, Viviana; Radio, Francesca Clementina mfl.. 2024, American Journal of Human Genetics. LM, HHB, ISS, NTNU, ISRAEL, UCDSC, OUS, TUM, UNIBO, HELMOLTZ, UL, UIO, TYSKLAND, ITALIAVitenskapelig artikkel

UiO structural biology core facilities.

Montserrat Canals, Mateu; Sekulic, Nikolina; Krengel, Ute. 2024, NBS Oslo Winter Poster meeting. UIOPoster

CENP-A and CENP-B collaborate to create an open centromeric chromatin state.

Nagpal, Harsh; Ali Ahmad, Ahmad; Hirano, Yasuhiro; Cai, Wei; Halic, Mario; Fukagawa, Tatsuo; Sekulic, Nikolina; Fierz, Beat. 2023, Nature Communications. EPFL, OD, STJ, UIOVitenskapelig artikkel
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