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Detailed analysis of the molecular background of the severe developmental disorder, Exon38/39 missense syndrome
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Details of project
Identifier
142851
Type
K
Principal investigator
Tantos, Ágnes
Title in Hungarian
A súlyos fejlődési rendellenességet okozó Exon 38/39 misszensz szindróma molekuláris hátterének részletes vizsgálata
Title in English
Detailed analysis of the molecular background of the severe developmental disorder, Exon38/39 missense syndrome
Keywords in Hungarian
KMT2D, hisztin metiltrtnszferáz, fehérje-RNS interakció, fázisátmenet, nukleáris testek
Keywords in English
KMT2D, histone methyltransferase, protein-RNA interaction, phase separation, nuclear bodies
Discipline
Molecular biology (Council of Medical and Biological Sciences)
80 %
Epigenetics and gene regulation (Council of Medical and Biological Sciences)
20 %
Panel
Molecular and Structural Biology and Biochemistry
Department or equivalent
Institute of Molecular Life Sciences (Research Center of Natural Sciences)
Participants
Apáti, Ágota
Bodor, Andrea
Kardos, József
Micsonai, András
Murvai, Nikoletta
Neha, Singh
Némethné Szabó, Beáta
Rawan K. I., Abukhairan
Schád, Éva
Starting date
2022-09-01
Closing date
2026-08-31
Funding (in million HUF)
47.952
FTE (full time equivalent)
13.83
state
running project
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