Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes

Cerebellum

Volumn 7, Issue 2, 2008, Pages 150-158

  Ikeda, Yoshio ^a   Daughters, Randy S ^a   Ranum, Laura P W ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

BAC transgenic mouse; Bidirectional expression; CTG CAG repeat expansion; Polyglutamine; Spinocerebellar ataxia type 8

Indexed keywords

ATAXIN 7; ATAXIN 8; DNA; MICROSATELLITE DNA; POLYGLUTAMINE; RNA; UNCLASSIFIED DRUG; ATAXIN 8 PROTEIN, HUMAN; COMPLEMENTARY DNA; NERVE PROTEIN; PEPTIDE; SCA8 PROTEIN, HUMAN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; CELL NUCLEUS INCLUSION BODY; CHROMOSOME 13Q; CONTROLLED STUDY; GENE EXPRESSION; GENE ISOLATION; GENE MUTATION; GENE SEGREGATION; GENETIC CODE; GENETIC LINKAGE; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; MICROSATELLITE INSTABILITY; MOLECULAR CLONING; MOUSE; NERVE CELL; NONHUMAN; PATHOGENICITY; PENETRANCE; PHENOTYPE; PRIORITY JOURNAL; PURKINJE CELL; RECESSIVE INHERITANCE; REVIEW; SPINOCEREBELLAR DEGENERATION; ANIMAL; ARTICLE; BRAIN; CHROMOSOME MAP; DOMINANT GENE; GENETICS; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PHYSIOLOGY; REFERENCE VALUE; TRINUCLEOTIDE REPEAT;

ANIMALS; BRAIN; CHROMOSOME MAPPING; DNA, COMPLEMENTARY; GENES, DOMINANT; HUMANS; MAGNETIC RESONANCE IMAGING; MICE; MUTATION; NERVE TISSUE PROTEINS; NEURONS; PEPTIDES; REFERENCE VALUES; SPINOCEREBELLAR ATAXIAS; TRANSCRIPTION, GENETIC; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 61449238441     PISSN: 14734222     EISSN: 14734230     Source Type: Journal    
DOI: 10.1007/s12311-008-0010-7     Document Type: Review

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