File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/ng1094-155
- Scopus: eid_2-s2.0-0028001095
- PMID: 7842014
- WOS: WOS:A1994PL12300017
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection
Title | Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection |
---|---|
Authors | |
Issue Date | 1994 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com |
Citation | Nature Genetics, 1994, v. 8 n. 2, p. 155-161 How to Cite? |
Abstract | We have performed microdissection of 16 putative homogeneously staining regions (hsrs) from nine different breast cancer cell lines in order to determine their chromosomal origin and composition. As expected, the most commonly amplified chromosomal band-region was 17q12 (containing ERBB2). However, regions not containing known oncogenes were also identified, including 13q31 (5/9 cases) and 20q12-13.2 (4/9 cases). The chromosomal composition of the integrated amplified DNA within each hsr was determined and in 13/16 cases (81%), hsrs were shown to be composed of two or more chromosomal regions. These studies shed light on the mechanism of formation of hsrs, and identify chromosomal regions likely to harbour genes amplified in breast cancer. |
Persistent Identifier | http://hdl.handle.net/10722/150705 |
ISSN | 2023 Impact Factor: 31.7 2023 SCImago Journal Rankings: 17.300 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Guan, XY | en_US |
dc.contributor.author | Meltzer, PS | en_US |
dc.contributor.author | Dalton, WS | en_US |
dc.contributor.author | Trent, JM | en_US |
dc.date.accessioned | 2012-06-26T06:09:01Z | - |
dc.date.available | 2012-06-26T06:09:01Z | - |
dc.date.issued | 1994 | en_US |
dc.identifier.citation | Nature Genetics, 1994, v. 8 n. 2, p. 155-161 | en_US |
dc.identifier.issn | 1061-4036 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/150705 | - |
dc.description.abstract | We have performed microdissection of 16 putative homogeneously staining regions (hsrs) from nine different breast cancer cell lines in order to determine their chromosomal origin and composition. As expected, the most commonly amplified chromosomal band-region was 17q12 (containing ERBB2). However, regions not containing known oncogenes were also identified, including 13q31 (5/9 cases) and 20q12-13.2 (4/9 cases). The chromosomal composition of the integrated amplified DNA within each hsr was determined and in 13/16 cases (81%), hsrs were shown to be composed of two or more chromosomal regions. These studies shed light on the mechanism of formation of hsrs, and identify chromosomal regions likely to harbour genes amplified in breast cancer. | en_US |
dc.language | eng | en_US |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com | en_US |
dc.relation.ispartof | Nature Genetics | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Breast Neoplasms - Genetics | en_US |
dc.subject.mesh | Chromosome Banding | en_US |
dc.subject.mesh | Chromosomes, Human - Ultrastructure | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 13 - Ultrastructure | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 17 - Ultrastructure | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 20 - Ultrastructure | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Gene Amplification | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | In Situ Hybridization, Fluorescence - Methods | en_US |
dc.subject.mesh | Micromanipulation | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Oncogenes | en_US |
dc.subject.mesh | Tumor Cells, Cultured | en_US |
dc.title | Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection | en_US |
dc.type | Article | en_US |
dc.identifier.email | Guan, XY:xyguan@hkucc.hku.hk | en_US |
dc.identifier.authority | Guan, XY=rp00454 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1038/ng1094-155 | en_US |
dc.identifier.pmid | 7842014 | - |
dc.identifier.scopus | eid_2-s2.0-0028001095 | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 155 | en_US |
dc.identifier.epage | 161 | en_US |
dc.identifier.isi | WOS:A1994PL12300017 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Guan, XY=7201463221 | en_US |
dc.identifier.scopusauthorid | Meltzer, PS=7102464641 | en_US |
dc.identifier.scopusauthorid | Dalton, WS=35379799400 | en_US |
dc.identifier.scopusauthorid | Trent, JM=7201692482 | en_US |
dc.identifier.issnl | 1061-4036 | - |