Drosophila linker histone H1 coordinates STAT-dependent organization of heterochromatin and suppresses tumorigenesis caused by hyperactive JAK-STAT signaling

Epigenetics and Chromatin

Volumn 7, Issue 1, 2014, Pages

  Xu, Na ^a   Emelyanov, Alexander V ^a   Fyodorov, Dmitry V ^a   Skoultchi, Arthur I ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Drosophila melanogaster; Heterochromatin; JAK STAT signaling; Linker histone H1; Melanotic tumors; Tumor suppressor

Indexed keywords

GLUTATHIONE TRANSFERASE; HISTONE H1; JANUS KINASE; STAT PROTEIN; STAT92E PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUTOFLUORESCENCE; CARCINOGENESIS; CELL STRUCTURE; CELLULAR DISTRIBUTION; CHROMATIN STRUCTURE; CHROMOSOME STRUCTURE; CONTROLLED STUDY; EXPERIMENT; GENE MUTATION; GENE OVEREXPRESSION; HETEROCHROMATIN; IMMUNOBLOTTING; IMMUNOFLUORESCENCE; IN VITRO STUDY; MOLECULAR INTERACTION; NONHUMAN; POLYTENE CHROMOSOME; PROTEIN DEPLETION; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION; WESTERN BLOTTING;

DROSOPHILA MELANOGASTER;

EID: 84904769747     PISSN: None     EISSN: 17568935     Source Type: Journal    
DOI: 10.1186/1756-8935-7-16     Document Type: Article

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