(Q40807218)

English

Aberrations of chromosome 8 in 16 breast cancer cell lines by comparative genomic hybridization, fluorescence in situ hybridization, and spectral karyotyping

scientific article published on April 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Aberrations of chromosome 8 in 16 breast cancer cell lines by comparative genomic hybridization, fluorescence in situ hybridization, and spectral karyotyping (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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author name string

Rummukainen J

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Kytölä S

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Karhu R

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Farnebo F

4

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Larsson C

5

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Isola JJ

6

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Europe PubMed Central

PubMed publication ID

23 September 2017

publication date

1 April 2001

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Europe PubMed Central

PubMed publication ID

23 September 2017

Cancer Genetics and Cytogenetics

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Europe PubMed Central

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23 September 2017

126

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23 September 2017

1

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23 September 2017

1-7

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Europe PubMed Central

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23 September 2017

Genome screening by comparative genomic hybridization

1 reference

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Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

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Genetic alterations in lobular breast cancer by comparative genomic hybridization

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Molecular cytogenetics of primary breast cancer by CGH

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Different genetic pathways in the evolution of invasive breast cancer are associated with distinct morphological subtypes

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Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection

1 reference

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Multicolor Spectral Karyotyping of Human Chromosomes

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Karyotyping human chromosomes by combinatorial multi-fluor FISH.

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Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping

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Genetic alterations in breast cancer.

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Genetic alterations in primary breast cancers and their metastases: direct comparison using modified comparative genomic hybridization

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Genetic alteration of the c-myc protooncogene (MYC) in human primary breast carcinomas

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MYC oncogenes and human neoplastic disease

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Four-color CGH: a new method for quality control of comparative genomic hybridization

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Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups

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Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique

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Amplification and overexpression of p40 subunit of eukaryotic translation initiation factor 3 in breast and prostate cancer.

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Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.

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Assignment of the gene encoding human Krüppel-related zinc finger protein 4 (GLI4) to 8q24.3 by fluorescent in situ hybridization

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Characterization of Human FAST-1, a TGFβ and Activin Signal Transducer

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Molecular cytogenetic analysis of consistent abnormalities at 8q12-q22 in breast cancer.

1 reference

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7 January 2021

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Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions

1 reference

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CCND1 and FGFR1 coamplification results in the colocalization of 11q13 and 8p12 sequences in breast tumor nuclei.

1 reference

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FGFRI andPLAT genes and DNA amplification at 8p 12 in breast and ovarian cancers

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Human E2F5 gene is oncogenic in primary rodent cells and is amplified in human breast tumors

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Identifiers

10.1016/S0165-4608(00)00387-3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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