http://www.cnr.it/ontology/cnr/individuo/prodotto/ID213128
Involvement of the HMGI(Y) Gene in a Microfollicular Adenoma of the Thyroid (Articolo in rivista)
- Type
- Label
- Involvement of the HMGI(Y) Gene in a Microfollicular Adenoma of the Thyroid (Articolo in rivista) (literal)
- Anno
- 1999-01-01T00:00:00+01:00 (literal)
- Alternative label
Paola Dal Cin,1 Alfredo Fusco,2 Gazanfer Belge,3 Gennaro Chiappetta,4 Monica Fedele,5 Patrick Pauwels,6
Jo¨ rn Bullerdiek,3 and Herman Van den Berghe1 (1999)
Involvement of the HMGI(Y) Gene in a Microfollicular Adenoma of the Thyroid
in Genes chromosomes & cancer (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Paola Dal Cin,1 Alfredo Fusco,2 Gazanfer Belge,3 Gennaro Chiappetta,4 Monica Fedele,5 Patrick Pauwels,6
Jo¨ rn Bullerdiek,3 and Herman Van den Berghe1 (literal)
- Pagina inizio
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- Rivista
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- 1Center for Human Genetics, University of Leuven, Leuven, Belgium
2Dipartimento di Medicina Sperimentale e Clinica, Facolta` di Medicina e Chirurgia di Catanzaro, Universita` di Catanzaro, Catanzaro, Italy
3Center for Human Genetics and Genetic Counseling, University of Bremen, Bremen, Germany
4Istituto Nazionale die Tumori di Napoli, Fondazione Senatore Pascale, Naples, Italy
5Centro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Ricerche, Dipartimento di Biologia e Patologia
Cellulare e Molecolare and Facolta` di Medicina e Chirurgia, Universita` di Napoli ''Federico II'', Naples, Italy
6Department of Pathology, Stichting PAMM, Catharina Ziekenhuis, Eindhoven, the Netherlands (literal)
- Titolo
- Involvement of the HMGI(Y) Gene in a Microfollicular Adenoma of the Thyroid (literal)
- Abstract
- Follicular thyroid adenomas are epithelial tumors characterized by subgroups with specific chromosomal aberrations. Here we
present a case with translocation t(1;6)(p35;p21). In 1p35 and 6p21, two genes of the high-mobility group of proteins are
located. With P1-derived Artificial Chromosome (PACs) derived from the HMG17 gene located at 1p35 and HMGI(Y) located at
6p21, fluorescence in situ hybridization was performed. The breakpoints were located distal to HMG17 and proximal to
HMGI(Y), but no rearrangement of the genes was shown by FISH. However, an overexpression of the HMGI(Y) gene was
detected by RT-PCR as well as by immunohistochemistry techniques. This suggests a breakpoint in the proximity of the
HMGI(Y) deregulating HMGI(Y) gene expression, a situation found in a variety of human benign mesenchymal tumors with
involvement of chromosome band 6p21. (literal)
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