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Distinct Xp11.2 breakpoint regions in synovial sarcoma revealed by metaphase and interphase FISH: Relationship to histologic subtypes

Autor: M. Balemans, A. Geurts van Kessel, W.M. Molenaar, A.M. Meloni, Avery A. Sandberg, B. de Leeuw, E. van den Berg, Göran Stenman, L.G. Kindblom, D. Olde Weghuis, R.F. Suijkerbuijk

Publikováno v: Cancer Genetics and Cytogenetics. 73:89-94

Fluorescence in situ hybridization (FISH) and molecular analyses of synovial sarcomas with cytogenetically similar (X;18)(p11.2;q11.2) translocations have revealed two alternative breakpoint regions in Xp11.2, one residing in the ornithine aminotrans

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d65b54868964855d25beadadb5d2412
https://doi.org/10.1016/0165-4608(94)90191-0

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Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization

Autor: B. de Jong, Avery A. Sandberg, Richard J. Sinke, R.F. Suijkerbuijk, A. Geurts van Kessel, Jw Oosterhuis, J. van Echten, Jennifer M. Parrington, A.M. Meloni

Publikováno v: Cancer Genetics and Cytogenetics. 70:85-93

Human testicular germ-cell tumors (TGCTs) comprise a heterogeneous group of solid neoplasms. These tumors are characterized by the presence of a highly specific chromosomal abnormality, i.e., an isochromosome of the short arm of chromosome 12. At pre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78f3e8606b3b6ee7a66b18f666db2a32
https://doi.org/10.1016/0165-4608(93)90173-j

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Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case

Autor: C.A. Tirado, A.M. Meloni-Ehrig, T. Edwards, J. Scheerle, K. Burks, C. Repetti, N.C. Christacos, J.C. Kelly, J. Greenberg, C. Murphy, C.D. Croft, D. Heritage, P.N. Mowrey

Publikováno v: Cancer genetics and cytogenetics. 174(2)

We report the chromosomal findings in a 4-year-old female with precursor B-cell acute lymphoblastic leukemia (ALL). The diagnostic karyotype showed an isochromosome 7q, i(7)(q10), as well as questionable rearrangements on 9p and 11q. Fluorescence in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0762822b2aa86261a307172047160986
https://pubmed.ncbi.nlm.nih.gov/17452260

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Allelic loss analysis by capillary electrophoresis: an accurate, automated method for detection of deletions in solid tumors

Autor: Swathi Patel, A.M. Meloni, Susan M. Sell, Darcy Stracner

Publikováno v: Genetic testing. 5(3)

In this report, we describe a fast and accurate capillary electrophoresis, PCR-based method for detecting loss of allelic heterozygosity in solid tumor samples. This automated method requires small sample sizes, and data can be obtained in less than

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb17389a9f6dad7ecc06df05718da816
https://pubmed.ncbi.nlm.nih.gov/11788095

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Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistance

Autor: Alicia A Prowse, A.M. Meloni, Urvashi Surti, Susan M. Sell, Avery A. Sandberg, Oguz Altungoz

Publikováno v: Cancer genetics and cytogenetics. 100(2)

Recent sibling-pair linkage analyses have indicated possible linkage of noninsulin dependent diabetes mellitus (NIDDM) with a number of markers on the long arm of chromosome 7. A coincidental and recent discovery is that specific genetic anomalies id

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77f49fd41ee9ef85ff3feecb5b2adcc6
https://pubmed.ncbi.nlm.nih.gov/9428363

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Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint

Autor: Ed Schuuring, Bauke de Jong, Ad Geurts van Kessel, Bert Janssen, Richard J. Sinke, Gerard Merkx, Eva van den Berg, Trȳnie Dijkhuizen, A.M. Meloni, Daniel Olde Weghuis

Publikováno v: Cancer Genetics and Cytogenetics, 96, pp. 95-101
Cancer Genetics and Cytogenetics, 96, 95-101
Cancer Genetics and Cytogenetics, 96, 2, pp. 95-101
Cancer Genetics and Cytogenetics, 96(2), 95-101. ELSEVIER SCIENCE INC

Recent cytogenetic analysis of a series of human renal oncocytomas revealed the presence of a recurring chromosomal translocation (5;11)(q35;q13) as sole anomaly in a subset of the tumors. The molecular characterization of this translocation was init

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483386d186b5b74f9216e807296082da
https://hdl.handle.net/2066/188228

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Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2

Autor: A.M. Meloni, M.J.M. Wilbrink, M T Geraghty, H.A.P. Janssen, Avery A. Sandberg, B. de Leeuw, R.F. Suijkerbuijk, Richard J. Sinke, Anthony P. Monaco, A. Geurts van Kessel

Publikováno v: Cancer Genetics and Cytogenetics, 71(2), 164-9. ELSEVIER SCIENCE INC

Recently, a specific chromosome abnormality, t(X;1)(p11;q21), was described for a subgroup of human papillary renal cell carcinomas. The translocation breakpoint in Xp11 is located in the same region as that in t(X;18)(p11;q11)-positive synovial sarc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cdc93888f865499ac93a543dbcb46fd
https://pubmed.ncbi.nlm.nih.gov/8281521

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Trisomy 10 in renal cell carcinoma

Autor: J.E. Pontes, A.M. Meloni, Avery A. Sandberg

Publikováno v: Cancer genetics and cytogenetics. 51(1)

We report four renal cell carcinomas, grade II, with trisomy 10 (+10) as the only karyotypic change. We propose that this cytogenetic anomaly may be associated with lowgrade renal carcinoma, although more cases will have to be studied to support the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23bd0c99de502a1983c1be118abea2d
https://pubmed.ncbi.nlm.nih.gov/1984843

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