Rowe S - Search Results

1

Der(16)t(1;16)(q21;q13) in Wilms' tumor: friend or foe.

Mathew P, Douglass EC, Jones D, Valentine M, Valentine V, Rowe S, Shapiro DN. Mathew P, et al. Among authors: rowe s. Med Pediatr Oncol. 1996 Jul;27(1):3-7. doi: 10.1002/(SICI)1096-911X(199607)27:1<3::AID-MPO2>3.0.CO;2-K. Med Pediatr Oncol. 1996. PMID: 8614388

2

Malignant rhabdoid tumor: a highly malignant childhood tumor with minimal karyotypic changes.

Douglass EC, Valentine M, Rowe ST, Parham DM, Wilimas JA, Sanders JM, Houghton PJ. Douglass EC, et al. Among authors: rowe st. Genes Chromosomes Cancer. 1990 Sep;2(3):210-6. doi: 10.1002/gcc.2870020308. Genes Chromosomes Cancer. 1990. PMID: 1964081

3

A second nonrandom translocation, der(16)t(1;16)(q21;q13), in Ewing sarcoma and peripheral neuroectodermal tumor.

Douglass EC, Rowe ST, Valentine M, Parham D, Meyer WH, Thompson EI. Douglass EC, et al. Among authors: rowe st. Cytogenet Cell Genet. 1990;53(2-3):87-90. doi: 10.1159/000132901. Cytogenet Cell Genet. 1990. PMID: 2164462

4

Alveolar rhabdomyosarcoma with the t(2;13): cytogenetic findings and clinicopathologic correlations.

Douglass EC, Shapiro DN, Valentine M, Rowe ST, Carroll AJ, Raney RB, Ragab AH, Abella SM, Parham DM. Douglass EC, et al. Among authors: rowe st. Med Pediatr Oncol. 1993;21(2):83-7. doi: 10.1002/mpo.2950210202. Med Pediatr Oncol. 1993. PMID: 8433683

5

Tumor-cell DNA content predicts outcome in children and adolescents with clinical group III embryonal rhabdomyosarcoma. The Intergroup Rhabdomyosarcoma Study Committee of the Children's Cancer Group and the Pediatric Oncology Group.

Pappo AS, Crist WM, Kuttesch J, Rowe S, Ashmun RA, Maurer HM, Newton WA, Asmar L, Luo X, Shapiro DN. Pappo AS, et al. Among authors: rowe s. J Clin Oncol. 1993 Oct;11(10):1901-5. doi: 10.1200/JCO.1993.11.10.1901. J Clin Oncol. 1993. PMID: 8410116

6

Variant translocations of chromosome 13 in alveolar rhabdomyosarcoma.

Douglass EC, Rowe ST, Valentine M, Parham DM, Berkow R, Bowman WP, Maurer HM. Douglass EC, et al. Among authors: rowe st. Genes Chromosomes Cancer. 1991 Nov;3(6):480-2. doi: 10.1002/gcc.2870030611. Genes Chromosomes Cancer. 1991. PMID: 1777415

7

Detection of N-myc gene amplification by fluorescence in situ hybridization. Diagnostic utility for neuroblastoma.

Shapiro DN, Valentine MB, Rowe ST, Sinclair AE, Sublett JE, Roberts WM, Look AT. Shapiro DN, et al. Among authors: rowe st. Am J Pathol. 1993 May;142(5):1339-46. Am J Pathol. 1993. PMID: 7684192 Free PMC article.

8

Fluorescence in situ hybridization analysis of chromosome 1p36 deletions in human MYCN amplified neuroblastoma.

Komuro H, Valentine MB, Rowe ST, Kidd VJ, Makino S, Brodeur GM, Cohn SL, Look AT. Komuro H, et al. Among authors: rowe st. J Pediatr Surg. 1998 Nov;33(11):1695-8. doi: 10.1016/s0022-3468(98)90612-1. J Pediatr Surg. 1998. PMID: 9856898

9

Lack of homozygously inactivated p73 in single-copy MYCN primary neuroblastomas and neuroblastoma cell lines.

Kong XT, Valentine VA, Rowe ST, Valentine MB, Ragsdale ST, Jones BG, Wilkinson DA, Brodeur GM, Cohn SL, Look AT. Kong XT, et al. Among authors: rowe st. Neoplasia. 1999 Apr;1(1):80-9. doi: 10.1038/sj.neo.7900010. Neoplasia. 1999. PMID: 10935473 Free PMC article.

10

Detection of MYCN gene amplification in neuroblastoma by fluorescence in situ hybridization: a pediatric oncology group study.

Mathew P, Valentine MB, Bowman LC, Rowe ST, Nash MB, Valentine VA, Cohn SL, Castleberry RP, Brodeur GM, Look AT. Mathew P, et al. Among authors: rowe st. Neoplasia. 2001 Mar-Apr;3(2):105-9. doi: 10.1038/sj.neo.7900146. Neoplasia. 2001. PMID: 11420745 Free PMC article.

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