|
Shaikh, Tamim H; O'Connor, Ronald J; Pierpont, Mary Ella et al. (2007) Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms. Genome Res 17:482-91
|
|
Saitta, Sulagna C; Harris, Stacy E; McDonald-McGinn, Donna M et al. (2004) Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome. Am J Med Genet A 124A:313-7
|
|
Saitta, Sulagna C; Harris, Stacy E; Gaeth, Ann P et al. (2004) Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion. Hum Mol Genet 13:417-28
|
|
Cron, Randy Q (2003) CD154 transcriptional regulation in primary human CD4 T cells. Immunol Res 27:185-202
|
|
Ming, J E; Elkan, M; Tang, K et al. (2002) Type I bone morphogenetic protein receptors are expressed on cerebellar granular neurons and a constitutively active form of the type IA receptor induces cerebellar abnormalities. Neuroscience 114:849-57
|
|
Maris, J M; Guo, C; White, P S et al. (2001) Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma. Med Pediatr Oncol 36:24-7
|
|
Maris, J M; Guo, C; Blake, D et al. (2001) Comprehensive analysis of chromosome 1p deletions in neuroblastoma. Med Pediatr Oncol 36:32-6
|
|
McVeigh, K E; Mallee, J J; Lucente, A et al. (2000) Murine chromosome 16 telomeric region, homologous with human chromosome 21q22, contains the osmoregulatory Na(+)/myo-inositol cotransporter (SLC5A3) gene. Cytogenet Cell Genet 88:153-8
|
|
Korimilli, A; Gonzales, L W; Guttentag, S H (2000) Intracellular localization of processing events in human surfactant protein B biosynthesis. J Biol Chem 275:8672-9
|
|
Guttentag, S H; Beers, M F; Bieler, B M et al. (1998) Surfactant protein B processing in human fetal lung. Am J Physiol 275:L559-66
|
Showing the most recent 10 out of 39 publications
