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1992 1
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2017 1
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Page 1
The role of cytogenetics in the classification of soft tissue tumours.
Dei Tos AP, Dal Cin P. Dei Tos AP, et al. Virchows Arch. 1997 Aug;431(2):83-94. doi: 10.1007/s004280050073. Virchows Arch. 1997. PMID: 9293889 Review.
Among the group of fibrous lesions, superficial fibromatosis exhibits trisomy 8. This genomic change is also observed in desmoid fibromatosis in association with trisomy 20. Trisomy 11 is the most frequently observed chromosomal aberration in congenital fi
Among the group of fibrous lesions, superficial fibromatosis exhibits trisomy 8. This genomic change is also observed in desmoid fibr …
Pan-Trk Immunohistochemistry Is an Efficient and Reliable Screen for the Detection of NTRK Fusions.
Hechtman JF, Benayed R, Hyman DM, Drilon A, Zehir A, Frosina D, Arcila ME, Dogan S, Klimstra DS, Ladanyi M, Jungbluth AA. Hechtman JF, et al. Am J Surg Pathol. 2017 Nov;41(11):1547-1551. doi: 10.1097/PAS.0000000000000911. Am J Surg Pathol. 2017. PMID: 28719467 Free PMC article.
Pan-Trk IHC is a time-efficient and tissue-efficient screen for NTRK fusions, particularly in driver-negative advanced malignancies and potential cases of secretory carcinoma and congenital fibrosarcoma. Pan-Trk IHC can help determine whether translation occurs for …
Pan-Trk IHC is a time-efficient and tissue-efficient screen for NTRK fusions, particularly in driver-negative advanced malignancies and pote …
Ultrastructural, immunocytochemical, and cytogenetic characterization of a large congenital fibrosarcoma.
Argyle JC, Tomlinson GE, Stewart D, Schneider NR. Argyle JC, et al. Arch Pathol Lab Med. 1992 Sep;116(9):972-5. Arch Pathol Lab Med. 1992. PMID: 1524466 Review.
Cytogenetic, immunocytochemical, and ultrastructural studies were performed on a large congenital fibrosarcoma. To our knowledge, this is the first report of a congenital fibrosarcoma characterized by all of these techniques. ...The karyotype of the tu …
Cytogenetic, immunocytochemical, and ultrastructural studies were performed on a large congenital fibrosarcoma. To our knowled …
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. Henno S, et al. Pathol Res Pract. 2003;199(1):35-40. doi: 10.1078/0344-0338-00350. Pathol Res Pract. 2003. PMID: 12650516
Cytogenetic study evidenced a trisomy 11, and real time RT-PCR, but not conventional karyotype, allowed for the detection of the Tel-ETV6/TrkC-NTRK3 fusion transcript as a consequence of a cryptic t(12-15)(p13;q25). As in congenital fibrosarcoma (CFS), two Tel-ETV6/ …
Cytogenetic study evidenced a trisomy 11, and real time RT-PCR, but not conventional karyotype, allowed for the detection of the Tel-ETV6/Tr …
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. Dubus P, et al. J Pathol. 2001 Jan;193(1):88-94. doi: 10.1002/1096-9896(2000)9999:9999<::AID-PATH724>3.0.CO;2-S. J Pathol. 2001. PMID: 11169520
The t(12;15)(p13;q25) translocation, a recurrent chromosomal abnormality of congenital fibrosarcoma, leads to the expression of a Tel-TrkC fusion transcript. ...Furthermore, several Tel-TrkC transcripts encoding for kinase isoforms of the Tel-TrkC protein were detec …
The t(12;15)(p13;q25) translocation, a recurrent chromosomal abnormality of congenital fibrosarcoma, leads to the expression o …
Posttranslational modification of TEL and TEL/AML1 by SUMO-1 and cell-cycle-dependent assembly into nuclear bodies.
Chakrabarti SR, Sood R, Nandi S, Nucifora G. Chakrabarti SR, et al. Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13281-5. doi: 10.1073/pnas.240315897. Proc Natl Acad Sci U S A. 2000. PMID: 11078523 Free PMC article.
The E-26 transforming specific (ETS)-related gene, TEL, also known as ETV6, encodes a strong transcription repressor that is rearranged in several recurring chromosomal rearrangements associated with leukemia and congenital fibrosarcoma. TEL is a nuclear phosphoprot …
The E-26 transforming specific (ETS)-related gene, TEL, also known as ETV6, encodes a strong transcription repressor that is rearranged in s …
A case of congenital infantile fibrosarcoma of the right hand.
Kimura C, Kitamura T, Sugihara T. Kimura C, et al. J Dermatol. 1998 Nov;25(11):735-41. doi: 10.1111/j.1346-8138.1998.tb02493.x. J Dermatol. 1998. PMID: 9863287
Congenital infantile fibrosarcoma is a rare soft-tissue malignant tumor that usually presents as a mass involving the arm or leg. We report a case of congenital fibrosarcoma on the right hand of a newborn infant. The patient was a 12-day-old male. ...One year and 7 …
Congenital infantile fibrosarcoma is a rare soft-tissue malignant tumor that usually presents as a mass involving the arm or leg. We report …
A multiplex real-time pcr assay for the detection of gene fusions observed in solid tumors.
Peter M, Gilbert E, Delattre O. Peter M, et al. Lab Invest. 2001 Jun;81(6):905-12. doi: 10.1038/labinvest.3780299. Lab Invest. 2001. PMID: 11406651 Free article.
Specific gene fusions observed in solid tumors are extremely useful diagnostic markers. We report the development of a method based on real-time PCR which enables the detection upon identical PCR conditions of the different fusions specifically observed in Ewing tum …
Specific gene fusions observed in solid tumors are extremely useful diagnostic markers. We report the development of a method based o …
In utero ultrasound detection of a large fetal sarcoma of the back.
Meizner I, Potlog-Nahari C, Mashiach R, Shalev J, Vardimon D, Ben-Sira L. Meizner I, et al. Ultrasound Obstet Gynecol. 2001 Nov;18(5):540-2. doi: 10.1046/j.0960-7692.2001.00514.x. Ultrasound Obstet Gynecol. 2001. PMID: 11844181 Free article.
A congenital fibrosarcoma, a very rare soft-tissue tumor of infancy, was suspected on prenatal ultrasound at 23 weeks' gestation. On sonography, a large soft tissue growth on the left side of the fetal back, measuring 53 x 65 x 22 mm, was observed. The diagno …
A congenital fibrosarcoma, a very rare soft-tissue tumor of infancy, was suspected on prenatal ultrasound at 23 weeks' gestati …
Hydrops fetalis and fibrosarcoma: case report of an uncommon association.
Navajas A, Astigarraga I, Fernández-Teijeiro A, Lopez-Heredia J, Biritxinaga B, Camarero C. Navajas A, et al. Eur J Pediatr. 1997 Jan;156(1):62-4. doi: 10.1007/s004310050554. Eur J Pediatr. 1997. PMID: 9007494
The child could not be operated upon because of rapid clinical deterioration. The autopsy findings confirmed the diagnosis of congenital fibrosarcoma. This is, to our knowledge, the first case of hydrops fetalis associated with fibrosarcoma. CONCLUSION: The associat …
The child could not be operated upon because of rapid clinical deterioration. The autopsy findings confirmed the diagnosis of congenital
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