Detailed analysis of the molecular background of the severe developmental disorder, Exon38/39 missense syndrome  Page description

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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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