Detection of chromosomal aberrations in tumor cells and tumor infiltrating lymphocytes by molecular cytogenetics in patients with gynecological cancer (Q77495465)

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scientific article published on 01 October 1998

Language	Label	Description	Also known as
English	Detection of chromosomal aberrations in tumor cells and tumor infiltrating lymphocytes by molecular cytogenetics in patients with gynecological cancer	scientific article published on 01 October 1998

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scholarly article

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6 December 2019

Detection of chromosomal aberrations in tumor cells and tumor infiltrating lymphocytes by molecular cytogenetics in patients with gynecological cancer (English)

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6 December 2019

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H Engel

1

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6 December 2019

J Friedrich

2

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6 December 2019

C Kleespies

3

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6 December 2019

C M Kurbacher

4

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6 December 2019

T Schöndorf

5

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6 December 2019

O Grecu

6

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6 December 2019

H Kolhagen

7

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6 December 2019

P Mallmann

8

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6 December 2019

publication date

1 October 1998

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6 December 2019

Cancer Genetics and Cytogenetics

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6 December 2019

106

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6 December 2019

2

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6 December 2019

159-165

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6 December 2019

Characterization of chromosomal anomalies in human breast cancer. A comparison of 30 paradiploid cases with few chromosome changes

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Establishment and characterization of 7 ovarian carcinoma cell lines and one granulosa tumor cell line: growth features and cytogenetics.

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Detection of chromosome aneuploidy in breast lesions with fluorescence in situ hybridization: comparison of whole nuclei to thin tissue sections and correlation with flow cytometric DNA analysis

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Identification of chromosomal structural alterations in human ovarian carcinoma cells using combined GTG-banding and repetitive fluorescence in situ hybridization (FISH).

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Cytogenetics of breast cancer.

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Interphase cytogenetics reveals a high incidence of aneuploidy and intra-tumour heterogeneity in breast cancer.

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Comparative study of interphase cytogenetics, flow cytometric analysis, and nuclear grade of fine-needle aspirates of breast carcinoma

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Analysis of numerical aberrations of specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer

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Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue

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Fluorescence in situ hybridization analysis of trisomy 12 in ovarian tumors

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Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes

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Detection of genetic alterations in micrometastatic cells in bone marrow of cancer patients by fluorescence in situ hybridization

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Aneuploidy in human lymphocytes: an extensive study of eight individuals of various ages

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Interphase fluorescence in situ hybridization improves the detection of malignant cells in effusions from breast cancer patients

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The application of flow cytometric DNA analysis in detecting the presence of malignant cells in ovarian carcinoma peritoneal fluids

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

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Clonal chromosome abnormalities in human breast carcinomas. II. Thirty-four cases with metastatic disease

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Identifiers

10.1016/S0165-4608(98)00070-3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9797783%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9797783%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

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