RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway

Human Molecular Genetics

Volumn 13, Issue 20, 2004, Pages 2421-2430

  Yin, Jinhu ^a   Kwon, Yong Tae ^b   Varshavsky, Alexander ^c   Wang, Weidong ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b UNIVERSITY OF PITTSBURGH   (United States)

^c CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CARRIER PROTEIN; CELL EXTRACT; DNA; ENZYME ANTIBODY; HELICASE; PROTEIN; UBIQUITIN PROTEIN LIGASE;

AMINO TERMINAL SEQUENCE; ANGIOGENESIS; APOPTOSIS; ARTICLE; BLOOM SYNDROME; BONE DEFECT; CANCER SUSCEPTIBILITY; CELL ISOLATION; CELL NUCLEUS; CELL TRANSFORMATION; CHROMOSOME; COMPLEX FORMATION; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME LOCALIZATION; ENZYME SUBSTRATE; GENE MUTATION; GENETIC STABILITY; GROWTH RETARDATION; HEART DEVELOPMENT; HELA CELL; HUMAN; HUMAN CELL; IN VIVO STUDY; MEIOSIS; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; PROTEIN TRANSPORT; ROTHMUND THOMSON SYNDROME; SKIN DEFECT; UBIQUITINATION;

ADENOSINE TRIPHOSPHATASES; CELL NUCLEUS; CYTOPLASM; DNA HELICASES; HELA CELLS; HUMANS; IMMUNOPRECIPITATION; MUTATION; RECQ HELICASES; ROTHMUND-THOMSON SYNDROME; SYNDROME; UBIQUITIN; UBIQUITIN-PROTEIN LIGASES;

EID: 19544366597     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddh269     Document Type: Article

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