306 related articles for article (PubMed ID: 11242790)
1. Congenital-infantile fibrosarcoma. A clinicopathologic study of 10 cases and molecular detection of the ETV6-NTRK3 fusion transcripts using paraffin-embedded tissues.
Sheng WQ; Hisaoka M; Okamoto S; Tanaka A; Meis-Kindblom JM; Kindblom LG; Ishida T; Nojima T; Hashimoto H
Am J Clin Pathol; 2001 Mar; 115(3):348-55. PubMed ID: 11242790
[TBL] [Abstract][Full Text] [Related]
2. A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma.
Knezevich SR; McFadden DE; Tao W; Lim JF; Sorensen PH
Nat Genet; 1998 Feb; 18(2):184-7. PubMed ID: 9462753
[TBL] [Abstract][Full Text] [Related]
3. Detection of the ETV6-NTRK3 chimeric RNA of infantile fibrosarcoma/cellular congenital mesoblastic nephroma in paraffin-embedded tissue: application to challenging pediatric renal stromal tumors.
Argani P; Fritsch M; Kadkol SS; Schuster A; Beckwith JB; Perlman EJ
Mod Pathol; 2000 Jan; 13(1):29-36. PubMed ID: 10658907
[TBL] [Abstract][Full Text] [Related]
4. Molecular detection of the ETV6-NTRK3 gene fusion differentiates congenital fibrosarcoma from other childhood spindle cell tumors.
Bourgeois JM; Knezevich SR; Mathers JA; Sorensen PH
Am J Surg Pathol; 2000 Jul; 24(7):937-46. PubMed ID: 10895816
[TBL] [Abstract][Full Text] [Related]
5. Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma.
Rubin BP; Chen CJ; Morgan TW; Xiao S; Grier HE; Kozakewich HP; Perez-Atayde AR; Fletcher JA
Am J Pathol; 1998 Nov; 153(5):1451-8. PubMed ID: 9811336
[TBL] [Abstract][Full Text] [Related]
6. The ETV6-NTRK3 gene fusion encodes a chimeric protein tyrosine kinase that transforms NIH3T3 cells.
Wai DH; Knezevich SR; Lucas T; Jansen B; Kay RJ; Sorensen PH
Oncogene; 2000 Feb; 19(7):906-15. PubMed ID: 10702799
[TBL] [Abstract][Full Text] [Related]
7. ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma.
Knezevich SR; Garnett MJ; Pysher TJ; Beckwith JB; Grundy PE; Sorensen PH
Cancer Res; 1998 Nov; 58(22):5046-8. PubMed ID: 9823307
[TBL] [Abstract][Full Text] [Related]
8. Non-resectable congenital tumors with the ETV6-NTRK3 gene fusion are highly responsive to chemotherapy.
McCahon E; Sorensen PH; Davis JH; Rogers PC; Schultz KR
Med Pediatr Oncol; 2003 May; 40(5):288-92. PubMed ID: 12652616
[TBL] [Abstract][Full Text] [Related]
9. Identification of various exon combinations of the ews/fli1 translocation: an optimized RT-PCR method for paraffin embedded tissue -- a report by the CWS-study group.
Stegmaier S; Leuschner I; Aakcha-Rudel E; Münch P; Kazanowska B; Bekassy A; Treuner J; Koscielniak E
Klin Padiatr; 2004; 216(6):315-22. PubMed ID: 15565546
[TBL] [Abstract][Full Text] [Related]
10. A fluorescence in situ hybridization study of ETV6-NTRK3 fusion gene in secretory breast carcinoma.
Makretsov N; He M; Hayes M; Chia S; Horsman DE; Sorensen PH; Huntsman DG
Genes Chromosomes Cancer; 2004 Jun; 40(2):152-7. PubMed ID: 15101049
[TBL] [Abstract][Full Text] [Related]
11. Reduced sensitivity of paraffin-based RT-PCR assays for ETV6-NTRK3 fusion transcripts in morphologically defined infantile fibrosarcoma.
Argani P; Fritsch MK; Shuster AE; Perlman EJ; Coffin CM
Am J Surg Pathol; 2001 Nov; 25(11):1461-4. PubMed ID: 11684968
[No Abstract] [Full Text] [Related]
12. Morphologic Overlap between Infantile Myofibromatosis and Infantile Fibrosarcoma: A Pitfall in Diagnosis.
Alaggio R; Barisani D; Ninfo V; Rosolen A; Coffin CM
Pediatr Dev Pathol; 2008; 11(5):355-62. PubMed ID: 19006426
[TBL] [Abstract][Full Text] [Related]
13. The detection of Tel-TrkC chimeric transcripts is more specific than TrkC immunoreactivity for the diagnosis of congenital fibrosarcoma.
Dubus P; Coindre JM; Groppi A; Jouan H; Ferrer J; Cohen C; Rivel J; Copin MC; Leroy JP; de Muret A; Merlio JP
J Pathol; 2001 Jan; 193(1):88-94. PubMed ID: 11169520
[TBL] [Abstract][Full Text] [Related]
14. Molecular detection of FUS-CREB3L2 fusion transcripts in low-grade fibromyxoid sarcoma using formalin-fixed, paraffin-embedded tissue specimens.
Matsuyama A; Hisaoka M; Shimajiri S; Hayashi T; Imamura T; Ishida T; Fukunaga M; Fukuhara T; Minato H; Nakajima T; Yonezawa S; Kuroda M; Yamasaki F; Toyoshima S; Hashimoto H
Am J Surg Pathol; 2006 Sep; 30(9):1077-84. PubMed ID: 16931951
[TBL] [Abstract][Full Text] [Related]
15. ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization.
Adem C; Gisselsson D; Dal Cin P; Nascimento AG
Mod Pathol; 2001 Dec; 14(12):1246-51. PubMed ID: 11743047
[TBL] [Abstract][Full Text] [Related]
16. Cellular mesoblastic nephroma: morphologic, cytogenetic and molecular links with congenital fibrosarcoma.
Henno S; Loeuillet L; Henry C; D'Hervé D; Azzis O; Ferrer J; Poulain P; Babut JM; Merlio JP; Jouan H; Dubus P
Pathol Res Pract; 2003; 199(1):35-40. PubMed ID: 12650516
[TBL] [Abstract][Full Text] [Related]
17. Mixed epithelial and stromal tumor of the kidney lacks the genetic alterations of cellular congenital mesoblastic nephroma.
Pierson CR; Schober MS; Wallis T; Sarkar FH; Sorensen PH; Eble JN; Srigley JR; Jones EC; Grignon DJ; Adsay V
Hum Pathol; 2001 May; 32(5):513-20. PubMed ID: 11381370
[TBL] [Abstract][Full Text] [Related]
18. Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11: fluorescence in situ hybridization and IGF2 allelic expression analysis.
Watanabe N; Kobayashi H; Hirama T; Kikuta A; Koizumi S; Tsuru T; Kaneko Y
Cancer Genet Cytogenet; 2002 Jul; 136(1):10-6. PubMed ID: 12165445
[TBL] [Abstract][Full Text] [Related]
19. Translocation-positive low-grade fibromyxoid sarcoma: clinicopathologic and molecular analysis of a series expanding the morphologic spectrum and suggesting potential relationship to sclerosing epithelioid fibrosarcoma: a study from the French Sarcoma Group.
Guillou L; Benhattar J; Gengler C; Gallagher G; Ranchère-Vince D; Collin F; Terrier P; Terrier-Lacombe MJ; Leroux A; Marquès B; Aubain Somerhausen Nde S; Keslair F; Pedeutour F; Coindre JM
Am J Surg Pathol; 2007 Sep; 31(9):1387-402. PubMed ID: 17721195
[TBL] [Abstract][Full Text] [Related]
20. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.
Odero MD; Vizmanos JL; Román JP; Lahortiga I; Panizo C; Calasanz MJ; Zeleznik-Le NJ; Rowley JD; Novo FJ
Genes Chromosomes Cancer; 2002 Sep; 35(1):11-9. PubMed ID: 12203785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
