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Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
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.
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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The role of post-transcriptional modifications during development.
Hamar R, Varga M.
Hamar R, et al.
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.
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Morphology of the type D influenza virus (Sendai strain).
HAMAR R, ROSENBERG M.
HAMAR R, et al.
Acta Virol. 1958 Jan-Mar;2(1):65-8.
Acta Virol. 1958.
PMID: 13533035
No abstract available.
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