Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

Martin F. Arlt(University of Michigan), Thomas W. Glover(University of Michigan)

Genes Chromosomes and Cancer

November 8, 2001

10.1002/gcc.10000

Cited by 107

Related Papers

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative RhoRac guanine nucleotide exchange factor

|Cell|1994|297

The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability

|Human Molecular Genetics|2005|281

Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting

|The American Journal of Human Genetics|2011|96

Comparative Study of X-Ray and UV Induced Cytotoxicity, DNA Repair, and Mutagenesis in Down's Syndrome and Normal Fibroblasts

|Pediatric Research|1980|35

Replication stress induces POLQ-mediated structural variant formation throughout common fragile sites after entry into mitosis

|Nature Communications|2024|12