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• W2893204064 endingPage "210" @default.
• W2893204064 startingPage "191" @default.
• W2893204064 abstract "Abstract Double-stranded DNA and RNA, and DNA/RNA hybrids form naturally in cells between two nucleic acid strands containing complementary sequences. However, these double-stranded nucleic acid structures need to be separated for DNA replication, RNA transcription, RNA processing, and DNA repair. These cellular processes are vital for normal cell growth and efficient recovery from environmental insults that damage DNA. Normally during these processes, DNA and RNA helicases unwind the double-stranded nucleic acid structures. Thus dysfunctions in these helicases contribute to a variety of clinical symptoms, including developmental abnormalities, mental retardation, neuromuscular degeneration, premature aging, and cancer predisposition. This review surveys the human diseases that have been linked to mutations in the helicase genes ATRX, BLM, CSA/B, DDX11, FANCJ/M, IFIH1, IGHMBP2, MCM4/5, RECQ4, RTEL1, SETX, TWINKLE, WRN, and XPB/D. The molecular functions of these helicases are also discussed." @default.
• W2893204064 created "2018-10-05" @default.
• W2893204064 creator A5027417887 @default.
• W2893204064 creator A5034411468 @default.
• W2893204064 creator A5052024256 @default.
• W2893204064 creator A5080799796 @default.
• W2893204064 date "2019-01-01" @default.
• W2893204064 modified "2023-09-25" @default.
• W2893204064 title "Helicase Dysfunctions in Human Diseases" @default.
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