FRAP reveals that mobility of oestrogen receptor-α is ligand- and proteasome-dependent

Nature Cell Biology

Volumn 3, Issue 1, 2001, Pages 15-23

  Stenoien, D L ^a   Patel, K ^a   Mancini, M G ^a   Dutertre, M ^a   Smith, C L ^a   O'Malley, B W ^a   Mancini, M A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXYTAMOXIFEN; ESTROGEN RECEPTOR; PROTEASOME;

ARTICLE; BLEACHING; CONFORMATIONAL TRANSITION; GENE TARGETING; HUMAN; HUMAN CELL; IMMOBILIZED CELL; LIFE CYCLE; LIGAND BINDING; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN METABOLISM; RECEPTOR UPREGULATION; TRANSACTIVATION; TRANSCRIPTION REGULATION;

BACTERIAL PROTEINS; BIOLOGICAL TRANSPORT; CYSTEINE ENDOPEPTIDASES; CYSTEINE PROTEINASE INHIBITORS; DACTINOMYCIN; ESTRADIOL; ESTROGEN ANTAGONISTS; ESTROGEN RECEPTOR ALPHA; HELA CELLS; HISTONE ACETYLTRANSFERASES; HUMANS; LEUPEPTINS; LIGANDS; LUMINESCENT PROTEINS; MICROSCOPY, FLUORESCENCE; MULTIENZYME COMPLEXES; NUCLEAR MATRIX; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, ESTROGEN; TAMOXIFEN; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC;

EID: 0035141041     PISSN: 14657392     EISSN: None     Source Type: Journal    
DOI: 10.1038/35050515     Document Type: Article

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