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Developmental Disabilities Research Reviews|July 19, 2008
Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsBeverly S EmanuelNature Reviews. Genetics|October 19, 2007
From microscopes to microarrays: dissecting recurrent chromosomal rearrangementsBeverly S Emanuel, Sulagna C SaittaCurrent Opinion in Genetics & Development|March 10, 2012
Chromosomal translocations and palindromic AT-rich repeatsTakema Kato, Hiroki Kurahashi, Beverly S EmanuelJournal of Molecular Biology|December 5, 2006
Mammalian TIMELESS and Tipin are evolutionarily conserved replication fork-associated factorsAnthony L Gotter, Christine Suppa, Beverly S EmanuelAmerican Journal of Human Genetics|January 31, 2003
The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeatsHiroki Kurahashi, Tamim Shaikh, Masayuki Takata, et al.Human Molecular Genetics|September 4, 2003
A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)Manjunath A Nimmakayalu, Anthony L Gotter, Tamim H Shaikh, et al.Prenatal Diagnosis|July 29, 2005
A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancerVaidehi Jobanputra, Wendy K Chung, April M Hacker, et al.DNA Repair|July 11, 2006
Palindrome-mediated chromosomal translocations in humansHiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.Nucleic Acids Research|February 1, 2007
Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeatsHiroshi Kogo, Hidehito Inagaki, Tamae Ohye, et al.Cell Cycle (Georgetown, Tex.)|June 9, 2006
Chromosomal translocations mediated by palindromic DNAHiroki Kurahashi, Hidehito Inagaki, Tamae Ohye, et al.Pageof 14