Ribosomal protein S3, a new substrate of Akt, serves as a signal mediator between neuronal apoptosis and DNA repair

Journal of Biological Chemistry

Volumn 285, Issue 38, 2010, Pages 29457-29468

  Lee, Sang Bae ^a   Kwon, Il Sun ^a   Park, Jihye ^a   Lee, Kyung Hoon ^a   Ahn, Younghee ^b   Lee, Cheolju ^b   Kim, Joon ^c   Choi, Soo Young ^d   Cho, Sung Woo ^e   Ahn, Jee Yin ^a  

^a Sungkyunkwan University School of Medicine   (South Korea)

^b Korea Institute of Science and Technology   (South Korea)

^c Korea University   (South Korea)

^d Hallym University   (South Korea)

^e University of Ulsan College of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DEATH; DNA; GENES; PHOSPHATASES; PROTEINS; REPAIR;

APOPTOTIC; APOPTOTIC CELL DEATH; DNA REPAIR; ENDONUCLEASES; MOLECULAR SWITCHES; NEURONAL APOPTOSIS; NEURONAL SURVIVAL; NUCLEAR ACCUMULATION; NUCLEAR TRANSLOCATIONS; PRO-APOPTOTIC FUNCTION; RIBOSOMAL PROTEINS; RIBOSOME BIOGENESIS;

PHOSPHORYLATION;

BIM PROTEIN; DNA; ENDONUCLEASE; NERVE GROWTH FACTOR; PROTEIN KINASE B; PROTEIN S3; RIBOSOME PROTEIN; TRANSCRIPTION FACTOR E2F1; UNCLASSIFIED DRUG; PROTEIN BINDING; RIBOSOMAL PROTEIN S3;

ANIMAL CELL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL DEATH; CONTROLLED STUDY; DNA REPAIR; ENZYME SUBSTRATE; MUTAGENESIS; NERVE CELL NECROSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN PHOSPHORYLATION; PROTEIN TARGETING; RAT; SIGNAL TRANSDUCTION; UPREGULATION; ANIMAL; CELL CULTURE; DNA FRAGMENTATION; DRUG EFFECTS; GENETICS; IMMUNOPRECIPITATION; METABOLISM; PC12 CELL LINE; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SPRAGUE DAWLEY RAT;

EUKARYOTA;

ANIMALS; APOPTOSIS; CELLS, CULTURED; DNA FRAGMENTATION; DNA REPAIR; IMMUNOPRECIPITATION; NERVE GROWTH FACTOR; PC12 CELLS; PROTEIN BINDING; PROTO-ONCOGENE PROTEINS C-AKT; RATS; RATS, SPRAGUE-DAWLEY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RIBOSOMAL PROTEINS;

EID: 77956510397     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.131367     Document Type: Article

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