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Aktivacija supresora tumora p53 pogreškama u sintezi ribosoma: uloga u patogenezi bolesti
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Naziv
Akcije
Mihalek, Ivana
Metode visoke propusnosti u medicinskoj dijagnostici 2021. Rijeka: (bez nakladnika), 2021. 8..
Mihalek, Ivana
Indel game. Rijeka: (bez nakladnika), 2021. 1..
Oršolić, Ines ; Bursać, Slađana ; Jurada, Deana ; Drmić Hofman, Irena ; Dembić, Zlatko ; Bartek, Jiri ; Mihalek, Ivana ; Volarević, Siniša
Cancer-associated mutations in the ribosomal protein L5 gene dysregulate the HDM2/p53-mediated ribosome biogenesis checkpoint // Oncogene, 39 (2020), 3443-3457. doi: 10.1038/s41388-020-1231-6
Kelly, McKenna ; Park, Meredith ; Mihalek, Ivana ; Rochtus, Anne ; Gramm, Marie ; Pérez-Palma, Eduardo ; Axeen, Erika Takle ; Hung, Christina Y. ; Olson, Heather ; Swanson, Lindsay et al.
Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region // Epilepsia (Copenhagen), 60 (2019), 3; 406-418. doi: 10.1111/epi.14653
Mihalek, Ivana
High throughput methods in medical diagnostics 2019. Rijeka: (bez nakladnika), 2019. 8..
Hung, Christina Y. ; Rodriguez, Mario ; Roberts, Abra ; Bauer, Mislen ; Mihalek, Ivana ; Bodamer, Olaf
A novel FAM20C mutation causes a rare form of neonatal lethal Raine syndrome // American journal of medical genetics. Part A, 179 (2019), 1866-1871. doi: 10.1002/ajmg.a.61291
Mihalek, Ivana
Exome dashoard: emulator platforme za analizu exoma u dijagnostici rijetkih genetskih bolesti. Rijeka: (bez nakladnika), 2019. 1..
Nelson, Nya D. ; Dodson, Lois M. ; Escudero, Laura ; Sukumar, Ann T. ; Williams, Christopher L. ; Mihalek, Ivana ; Baldan, Alessandro ; Baird, Duncan M. ; Bertuch, Alison A.
The C-terminal extension unique to the long isoform of the shelterin component TIN2 enhances its interaction with TRF2 in a phosphorylation- and dyskeratosis congenita cluster-dependent fashion // Molecular and cellular biology, 38 (2018), 12; e00025, 18. doi: 10.1128/mcb.00025-18
Mihalek, Ivana
Gunshot sequencing game. Rijeka: (bez nakladnika), 2018. 1..
Mihalek, Ivana ; Bodamer, Olaf
Estimating incidence of inborn errors of metabolism from the frequency of variants in general population.. 2017. str. 473-473
