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693 results

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A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.
Kohsaka S, Shukla N, Ameur N, Ito T, Ng CK, Wang L, Lim D, Marchetti A, Viale A, Pirun M, Socci ND, Qin LX, Sciot R, Bridge J, Singer S, Meyers P, Wexler LH, Barr FG, Dogan S, Fletcher JA, Reis-Filho JS, Ladanyi M. Kohsaka S, et al. Among authors: bridge j. Nat Genet. 2014 Jun;46(6):595-600. doi: 10.1038/ng.2969. Epub 2014 May 4. Nat Genet. 2014. PMID: 24793135 Free PMC article.
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data.
Wang L, Motoi T, Khanin R, Olshen A, Mertens F, Bridge J, Dal Cin P, Antonescu CR, Singer S, Hameed M, Bovee JV, Hogendoorn PC, Socci N, Ladanyi M. Wang L, et al. Among authors: bridge j. Genes Chromosomes Cancer. 2012 Feb;51(2):127-39. doi: 10.1002/gcc.20937. Epub 2011 Oct 27. Genes Chromosomes Cancer. 2012. PMID: 22034177 Free PMC article.
Myogenin, AP2β, NOS-1, and HMGA2 are surrogate markers of fusion status in rhabdomyosarcoma: a report from the soft tissue sarcoma committee of the children's oncology group.
Rudzinski ER, Anderson JR, Lyden ER, Bridge JA, Barr FG, Gastier-Foster JM, Bachmeyer K, Skapek SX, Hawkins DS, Teot LA, Parham DM. Rudzinski ER, et al. Am J Surg Pathol. 2014 May;38(5):654-9. doi: 10.1097/PAS.0000000000000195. Am J Surg Pathol. 2014. PMID: 24618610 Free PMC article.
Impact of SYT-SSX fusion type on the clinical behavior of synovial sarcoma: a multi-institutional retrospective study of 243 patients.
Ladanyi M, Antonescu CR, Leung DH, Woodruff JM, Kawai A, Healey JH, Brennan MF, Bridge JA, Neff JR, Barr FG, Goldsmith JD, Brooks JS, Goldblum JR, Ali SZ, Shipley J, Cooper CS, Fisher C, Skytting B, Larsson O. Ladanyi M, et al. Among authors: bridge ja. Cancer Res. 2002 Jan 1;62(1):135-40. Cancer Res. 2002. PMID: 11782370
Sclerosing rhabdomyosarcomas in children and adolescents: a clinicopathologic review of 13 cases from the Intergroup Rhabdomyosarcoma Study Group and Children's Oncology Group.
Chiles MC, Parham DM, Qualman SJ, Teot LA, Bridge JA, Ullrich F, Barr FG, Meyer WH; Soft Tissue Sarcoma Committee of Children's Oncology Group. Chiles MC, et al. Among authors: bridge ja. Pediatr Dev Pathol. 2005 Jan-Feb;8(1):141. doi: 10.1007/s10024-005-1550-1. Pediatr Dev Pathol. 2005. PMID: 15803220 No abstract available.
Embryonal rhabdomyosarcoma with a der(16)t(1;16) translocation.
Kapels KM, Nishio J, Zhou M, Qualman SJ, Bridge JA. Kapels KM, et al. Among authors: bridge ja. Cancer Genet Cytogenet. 2007 Apr 1;174(1):68-73. doi: 10.1016/j.cancergencyto.2006.11.013. Cancer Genet Cytogenet. 2007. PMID: 17350470
Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study.
Bridge JA, Liu J, Weibolt V, Baker KS, Perry D, Kruger R, Qualman S, Barr F, Sorensen P, Triche T, Suijkerbuijk R. Bridge JA, et al. Genes Chromosomes Cancer. 2000 Apr;27(4):337-44. doi: 10.1002/(sici)1098-2264(200004)27:4<337::aid-gcc1>3.0.co;2-1. Genes Chromosomes Cancer. 2000. PMID: 10719362
693 results