Ehrlich / New York / Oxford / Madison / Durham / /
Company
SSB / Macmillan Magazines Ltd / /
Country
United States / United Kingdom / /
Event
Product Issues / /
Facility
University of Oxford / University of Southern California / Memorial Sloan-Kettering Cancer Center / University of Massachusetts / Duke University Medical Center / University of Wisconsin-Madison / /
IndustryTerm
replication machinery / detrimental side products / homologous recombination systems / dimeric chromosomal products / bacterial systems / similar systems / repair systems / fork reactivation systems / umuDC gene products / enzymatic systems / checkpoint systems / dif resolvase site / viral systems / recombination systems / /
OperatingSystem
Fork / /
Organization
University of Southern California / Los Angeles / University of Massachusetts / Amherst / University of Oxford / Division of Molecular Genetics / Department of Microbiology / Department of Biochemistry / Memorial Sloan-Kettering Cancer Center / Duke University Medical Center / University of Wisconsin / /
Person
Kenneth N. Kreuzer / Michael M. Cox / Kenneth J. Marians / Myron F. Goodman / Genet / David J. Sherratt / Kuempel / Steven J. Sandlerk / /
Position
D. J. / Walker / General / Nurse / representative / /
Product
XerCD / respectively30 / 49 / DNA / /
ProvinceOrState
Wisconsin / Southern California / New York / South Dakota / South Carolina / North Carolina / California / Massachusetts / /
Region
Southern California / /
Technology
DNA synthesis / recombination system / recombination / /
progress The importance of repairing stalled replication forks Michael M. Cox*, Myron F. Goodman², Kenneth N. Kreuzer³, David J. Sherratt§, Steven J. Sandlerk & Kenneth J. Marians¶ * Department of Biochemistry, Univ