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Page 1
The role of post-transcriptional modifications during development.
Biol Futur. 2023 Jun;74(1-2):45-59. doi: 10.1007/s42977-022-00142-3. Epub 2022 Dec 8.
Biol Futur. 2023.
PMID: 36481986
Review.
Zebrafish Models of Rare Hereditary Pediatric Diseases.
Varga M, Ralbovszki D, Balogh E, Hamar R, Keszthelyi M, Tory K.
Varga M, et al. Among authors: hamar r.
Diseases. 2018 May 22;6(2):43. doi: 10.3390/diseases6020043.
Diseases. 2018.
PMID: 29789451
Free PMC article.
Review.
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Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Balogh E, Chandler JC, Varga M, Tahoun M, Menyhárd DK, Schay G, Goncalves T, Hamar R, Légrádi R, Szekeres Á, Gribouval O, Kleta R, Stanescu H, Bockenhauer D, Kerti A, Williams H, Kinsler V, Di WL, Curtis D, Kolatsi-Joannou M, Hammid H, Szőcs A, Perczel K, Maka E, Toldi G, Sava F, Arrondel C, Kardos M, Fintha A, Hossain A, D'Arco F, Kaliakatsos M, Koeglmeier J, Mifsud W, Moosajee M, Faro A, Jávorszky E, Rudas G, Saied MH, Marzouk S, Kelen K, Götze J, Reusz G, Tulassay T, Dragon F, Mollet G, Motameny S, Thiele H, Dorval G, Nürnberg P, Perczel A, Szabó AJ, Long DA, Tomita K, Antignac C, Waters AM, Tory K.
Balogh E, et al. Among authors: hamar r.
Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15137-15147. doi: 10.1073/pnas.2002328117. Epub 2020 Jun 17.
Proc Natl Acad Sci U S A. 2020.
PMID: 32554502
Free PMC article.
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