Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

EMBO Journal

Volumn 19, Issue 17, 2000, Pages 4439-4448

  Miller, Jill W ^a   Urbinati, Carl R ^a   Teng Umnuay, Patana ^a   Stenberg, Myrna G ^a   Byrne, Barry J ^a   Thornton, Charles A ^b   Swanson, Maurice S ^a  

^a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

Author keywords

DM1; EXP proteins; Muscleblind; Myotonic dystrophy; RNA dominance

Indexed keywords

MUSCLE PROTEIN; PROTEIN KINASE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL DIFFERENTIATION; DYSTROPHY; FRAGILE X SYNDROME; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; HUMAN TISSUE; IN SITU HYBRIDIZATION; MAMMAL; MYOBLAST; MYOTONIC DYSTROPHY; NEUROMUSCULAR DISEASE; NUCLEOTIDE SEQUENCE; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN BINDING;

EID: 0034282958     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/19.17.4439     Document Type: Article

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