Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells

Human Molecular Genetics

Volumn 9, Issue 19, 2000, Pages 2799-2809

  Trettel, Flavia ^a   Rigamonti, Dorotea ^b   Hilditch Maguire, Paige ^a   Wheeler, Vanessa C ^a   Sharp, Alan H ^c   Persichetti, Francesca ^a   Cattaneo, Elena ^b   MacDonald, Marcy E ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b UNIVERSITY OF MILAN   (Italy)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EPITOPE; GLUTAMINE; HUNTINGTIN; PROTEIN P53; RNA;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; BRAIN NERVE CELL; CELL MEMBRANE TRANSPORT; CELL NUCLEUS; CELL ORGANELLE; CELL STRAIN; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CORPUS STRIATUM; EMBRYO; ENDOPLASMIC RETICULUM; GENE MUTATION; HUNTINGTON CHOREA; HYPOXIA; MOUSE; MOUSE MUTANT; NERVE DEGENERATION; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN DETERMINATION; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; RNA SYNTHESIS; STRESS;

ANIMALIA;

EID: 0034703869     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.19.2799     Document Type: Article

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