(Q28292549)

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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes (English)

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5

object named as

L Manuelidis

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author name string

T Cremer

1

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P Lichter

2

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J Borden

3

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D C Ward

4

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language of work or name

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publication date

November 1988

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80

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235-46

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3

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describes a project that uses

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in situ hybridization

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based on heuristic

inferred from title

Structure and localization of genes encoding aberrant and normal epidermal growth factor receptor RNAs from A431 human carcinoma cells

1 reference

https://api.crossref.org/works/10.1007%2FBF01790091

21 January 2018

Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome

1 reference

https://api.crossref.org/works/10.1007%2FBF01790091

21 January 2018

Amplification of the structurally and functionally altered epidermal growth factor receptor gene (c-erbB) in human brain tumors

1 reference

https://api.crossref.org/works/10.1007%2FBF01790091

21 January 2018

Specific staining of human chromosomes in Chinese hamster x man hybrid cell lines demonstrates interphase chromosome territories

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification, enhanced expression and possible rearrangement of EGF receptor gene in primary human brain tumours of glial origin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reproducible compartmentalization of individual chromosome domains in human CNS cells revealed by in situ hybridization and three-dimensional reconstruction

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between gene amplification and chromosomal deviations in malignant human gliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic cell fusion as a source of genetic rearrangement leading to metastatic variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of cancer predisposition.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic features of human neuroblastomas and cell lines.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumor cells by in situ hybridization with chemically modified DNA probes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of human cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene Amplification in Malignant Human Gliomas: Clinical and Histopathologic Aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biology of gliomas: heterogeneity, oncogenes, growth factors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On trisomy of chromosome 7 in human gliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitive system for visualising biotinylated DNA probes hybridised in situ: rapid sex determination of intact cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of chromosomal translocations in B- and T-cell neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies of human brain tumors and their clinical significance. II. Meningioma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Individual interphase chromosome domains revealed by in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 1 aberrations in cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal evolution in malignant human gliomas starts with specific and usually numerical deviations

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic analysis of malignancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3192213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01790091

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Springer Nature article ID

10.1007/bf01790091

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