Histone deacetylase inhibitors prevent oxidative neuronal death independent of expanded polyglutamine repeats via an Sp1-dependent pathway

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue 7, 2003, Pages 4281-4286

  Ryu, Hoon ^a,b,f   Lee, Junghee ^a,b   Olofsson, Beatrix A ^c   Mwidau, Aziza ^a,b   Deodoglu, Alpaslan ^d   Escudero, Maria ^e   Flemington, Erik ^e   Azizkhan Clifford, Jane ^c   Ferrante, Robert J ^d   Ratan, Rajiv R ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b HARVARD INSTITUTES OF MEDICINE   (United States)

^c DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

^d BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HISTONE DEACETYLASE INHIBITOR; POLYGLUTAMINE; TRANSCRIPTION FACTOR SP1; ANTISENSE OLIGODEOXYNUCLEOTIDE; ENZYME INHIBITOR; HISTONE DEACETYLASE; MESSENGER RNA; PEPTIDE;

ACETYLATION; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; GENE ACTIVATION; GENE EXPRESSION; NERVE CELL NECROSIS; NERVE DEGENERATION; NEUROPROTECTION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN DNA BINDING; RAT; ANIMAL; BRAIN CORTEX; CELL CULTURE; CELL DEATH; CYTOLOGY; DRUG ANTAGONISM; DRUG EFFECT; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; NERVE CELL; NUCLEOTIDE SEQUENCE; PHYSIOLOGY; SPRAGUE DAWLEY RAT;

ANIMALIA;

ACETYLATION; ANIMALS; BASE SEQUENCE; CELL DEATH; CELLS, CULTURED; CEREBRAL CORTEX; ENZYME INHIBITORS; GENE EXPRESSION REGULATION; HISTONE DEACETYLASES; NEURONS; OLIGODEOXYRIBONUCLEOTIDES, ANTISENSE; OXIDATIVE STRESS; PEPTIDES; RATS; RATS, SPRAGUE-DAWLEY; RNA, MESSENGER; SP1 TRANSCRIPTION FACTOR;

EID: 0037386621     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0737363100     Document Type: Article

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