Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n)

Journal of Biological Chemistry

Volumn 274, Issue 18, 1999, Pages 12797-12802

  Fry, Michael ^a   Loeb, Lawrence A ^b  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; DOUBLE STRANDED DNA; HELICASE; MAGNESIUM ION; TRINUCLEOTIDE;

ANIMAL CELL; ARTICLE; BLOOM SYNDROME; CONTROLLED STUDY; DNA METABOLISM; DNA STRUCTURE; ENZYME ACTIVITY; ENZYME SPECIFICITY; FRAGILE X SYNDROME; HUMAN; LEPIDOPTERA; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT; WERNER SYNDROME;

BASE SEQUENCE; DNA; DNA HELICASES; FRAGILE X SYNDROME; HUMANS; NUCLEIC ACID CONFORMATION; TRINUCLEOTIDE REPEATS; WERNER SYNDROME;

ANIMALIA; LEPIDOPTERA;

EID: 0033617316     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.274.18.12797     Document Type: Article

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