DNA damage-induced RPA focalization is independent of γ-H2AX and RPA hyper-phosphorylation

Journal of Cellular Biochemistry

Volumn 99, Issue 5, 2006, Pages 1452-1462

  Liu, Jen Sing ^a,b   Kuo, Shu Ru ^a   Melendy, Thomas ^a  

^a UNIVERSITY AT BUFFALO   (United States)

^b SCOTT AND WHITE MEMORIAL HOSPITAL   (United States)

Author keywords

H2AX; DNA damage; GFP; PI3 kinase; Replication protein A (RPA); Replicational stress

Indexed keywords

CHECKPOINT KINASE 1; DNA BINDING PROTEIN; GREEN FLUORESCENT PROTEIN; HISTONE; HISTONE H2AX; INOSITOL PHOSPHATE; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHOTRANSFERASE; PROTEIN KINASE; PROTEIN SUBUNIT; REPLICATION PROTEIN A;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DNA DAMAGE; DNA RECOMBINATION; DNA REPAIR; DNA REPLICATION; EUKARYOTE; HUMAN; HUMAN CELL; MOLECULAR MECHANICS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN DNA INTERACTION; PROTEIN FUNCTION; PROTEIN INDUCTION; PROTEIN PHOSPHORYLATION; PROTEIN TRANSPORT;

1-PHOSPHATIDYLINOSITOL 3-KINASE; AMINOGLYCOSIDES; ANDROSTADIENES; ANIMALS; ANTIBIOTICS, ANTINEOPLASTIC; ANTINEOPLASTIC AGENTS, ALKYLATING; CELL LINE; CYCLOHEXANECARBOXYLIC ACIDS; CYCLOHEXENES; DNA DAMAGE; ENEDIYNES; HISTONES; HUMANS; INDOLES; MICE; PROTEIN KINASE INHIBITORS; RECOMBINANT FUSION PROTEINS; REPLICATION PROTEIN A;

EUKARYOTA;

EID: 33751187885     PISSN: 07302312     EISSN: 10974644     Source Type: Journal    
DOI: 10.1002/jcb.21066     Document Type: Article

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