SMARCA2 and THAP11: Potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies

Journal of Human Genetics

Volumn 49, Issue 11, 2004, Pages 596-602

  Pandey, Neeraj ^a   Mittal, Uma ^a   Srivastava, Achal K ^b   Mukerji, Mitali ^a  

^a CSIR INSTITUTE OF GENOMICS AND INTEGRATIVE BIOLOGY   (India)

^b ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

CTG B43a; hBRM; Natively unfolded protein; Polyglutamine; SMARCA2; Spinocerebellar ataxia; THAP11; Triplet repeats

Indexed keywords

ADENINE; CYTOSINE; GLUTAMINE; GUANINE; POLYGLUTAMINE; REPETITIVE DNA;

ARTICLE; ATAXIA; BRAIN; CELL HETEROGENEITY; CONTROLLED STUDY; DNA POLYMORPHISM; GENE EXPRESSION; GENE LOCUS; GENE SEQUENCE; GENETIC ANALYSIS; GENOME; HUMAN; INDIA; MAJOR CLINICAL STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; POPULATION RESEARCH; PREVALENCE; PROTEIN FOLDING;

ANIMALS; BASE SEQUENCE; BRAIN; COMPUTER SIMULATION; DNA PRIMERS; DNA-BINDING PROTEINS; HUMANS; INDIA; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; PEPTIDES; POLYMORPHISM, GENETIC; PRIMATES; PROTEIN FOLDING; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE ANALYSIS, DNA; SPINOCEREBELLAR ATAXIAS; TRANSCRIPTION FACTORS;

ATAXIA;

EID: 15244348259     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-004-0194-8     Document Type: Article

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