The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage

Cell

Volumn 136, Issue 3, 2009, Pages 420-434

  Stewart, Grant S ^a   Panier, Stephanie ^b,c   Townsend, Kelly ^a   Al Hakim, Abdallah K ^b   Kolas, Nadine K ^b   Miller, Edward S ^a   Nakada, Shinichiro ^b   Ylanko, Jarkko ^b,c   Olivarius, Signe ^b   Mendez, Megan ^b   Oldreive, Ceri ^a   Wildenhain, Jan ^b   Tagliaferro, Andrea ^b   Pelletier, Laurence ^b,c   Taubenheim, Nadine ^d   Durandy, Anne ^d   Byrd, Philip J ^a   Stankovic, Tatjana ^a   Taylor, A Malcolm R ^a   Durocher, Daniel ^b,c  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b MOUNT SINAI HOSPITAL   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

DNA; SIGNALING

Indexed keywords

DNA; HISTONE H2A; UBIQUITIN PROTEIN LIGASE;

ARTICLE; CHROMATIN; CONTROLLED STUDY; DNA DAMAGE; FACE DYSMORPHIA; GENE LOSS; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNE DEFICIENCY; LEARNING DISORDER; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN MODIFICATION; UBIQUITINATION;

ATAXIA TELANGIECTASIA;

EID: 59049103900     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cell.2008.12.042     Document Type: Article

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