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AHCY deficiency is a unique human methylation disorder. Methylation of various cellular compounds such as DNA, RNA, protein, lipid and function of cellular processes including epigenetic, protein processing, signaling and lipid biosynthesis are affected by AHCY deficiency. Disorder of methylation is observed often in other diseases such as cancer and neurodegeneration. Thus, using AHCY deficiency as model should give new clues to DNA and protein methylation in relevant human disorders.
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论文共 61 篇作者统计合作学者相似作者
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Monika Logara Klaric,Tihana Maric,Lucija Zunic,Lovro Trgovec-Greif,Filip Rokic, Ana Fiolic, Ana Merkler Sorgic,Davor Jezek,Oliver Vugrek,Antonia Jakovcevic,Maja Barbalic,Robert Beluzic,Ana Katusic Bojanac
Genesno. 6 (2024): 707-707
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 94-94
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International journal of molecular sciencesno. 22 (2023): 16102-16102
Virusesno. 12 (2023): 2408-2408
BIOMOLECULESno. 8 (2023)
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#Papers: 61
#Citation: 1311
H-Index: 17
G-Index: 36
Sociability: 6
Diversity: 3
Activity: 8
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