Transmethylation in humans: lessons from inherited metabolic disorders (CROSBI ID 550213)
Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | domaća recenzija
Podaci o odgovornosti
Barić, Ivo
engleski
Transmethylation in humans: lessons from inherited metabolic disorders
Transmethylation, i.e. transfer of methyl group from methionine wia adenosylmethionine to numerous acceptors of very variable function is a crucial function of metabolic reaction between methionine and homocysteine. The fact that transmethylation occurs in all mammalian tissues and cells also reflects its significance. The large list of acceptors of methyl groups transferred by numerous methyltransferases includes important molecules such as DNA, RNA, lipids, proteins and guanidinoacetate. Therefore, the disorder which disturb transmethylation affects numerous tissues and organs.
transmethylation; inborn errors of metabolism
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Podaci o prilogu
54-54.
2009.
nije evidentirano
objavljeno
Podaci o matičnoj publikaciji
Paediatria Croatica. Supplement
Barišić, Ingeborg
Zagreb: Denona
1330-724X
Podaci o skupu
8th Balkan Meeting on Human Genetics
pozvano predavanje
15.05.2009-17.05.2009
Cavtat, Hrvatska