MPS1-dependent mitotic BLM phosphorylation is important for chromosome stability

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 31, 2006, Pages 11485-11490

  Leng, Mai ^a   Chan, Doug W ^a,b   Luo, Hao ^a   Zhu, Cihui ^a   Qin, Jun ^a   Wang, Yi ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Bloom syndrome; Spindle assembly checkpoint

Indexed keywords

GENE PRODUCT; PHOSPHOSERINE; PHOSPHOTRANSFERASE; PROTEIN BLM; PROTEIN MPS1; RECQ HELICASE; THREONINE; UNCLASSIFIED DRUG;

ARTICLE; BLOOM SYNDROME; CANCER SUSCEPTIBILITY; CHROMOSOMAL INSTABILITY; CHROMOSOME BREAKAGE; CHROMOSOME SEGREGATION; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; ENZYME ACTIVATION; GENETIC PREDISPOSITION; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MITOSIS; MITOSIS INHIBITION; MITOSIS SPINDLE; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN DOMAIN; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; SISTER CHROMATID EXCHANGE;

ADENOSINE TRIPHOSPHATASES; ANIMALS; ANTINEOPLASTIC AGENTS; BLOOM SYNDROME; CELL CYCLE PROTEINS; CHROMOSOMAL INSTABILITY; CHROMOSOME SEGREGATION; DNA HELICASES; DNA REPAIR; ENZYME ACTIVATION; HELA CELLS; HUMANS; MITOSIS; MITOTIC SPINDLE APPARATUS; NOCODAZOLE; PHOSPHORYLATION; PROTEIN-SERINE-THREONINE KINASES; PROTO-ONCOGENE PROTEINS; RECOMBINANT FUSION PROTEINS; RNA, SMALL INTERFERING; SISTER CHROMATID EXCHANGE;

EID: 33746841515     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0601828103     Document Type: Article

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