(Q74164781)

English

Detection of hyperdiploidy and chromosome breakage affecting the 1 (1cen-q12) region in lentigo malignant melanoma (LMM), superficial spreading melanoma (SSM) and congenital nevus (CN) cells in vitro by the multicolor FISH technique

scientific article published on 01 December 1997

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Detection of hyperdiploidy and chromosome breakage affecting the 1 (1cen-q12) region in lentigo malignant melanoma (LMM), superficial spreading melanoma (SSM) and congenital nevus (CN) cells in vitro by the multicolor FISH technique (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

E Dopp

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

T Papp

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

D Schiffmann

3

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Europe PubMed Central

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9 November 2019

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1 December 1997

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

120

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

157-163

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Chromosome aberrations and cancer

1 reference

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Cytogenetic findings in 21 malignant melanomas

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Cytogenetic homogeneity in eight independent sites in a case of malignant melanoma

1 reference

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Detection of hyperdiploidy and chromosome breakage in interphase human lymphocytes following exposure to the benzene metabolite hydroquinone using multicolor fluorescence in situ hybridization with DNA probes

1 reference

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7 January 2021

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Detection of aneuploidy and aneuploidy-inducing agents in human lymphocytes using fluorescence in situ hybridization with chromosome-specific DNA probes

1 reference

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Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat

1 reference

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Induction of micronuclei, hyperdiploidy and chromosomal breakage affecting the centric/pericentric regions of chromosomes 1 and 9 in human amniotic fluid cells after treatment with asbestos and ceramic fibers

1 reference

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Nonrandom distribution of chromosomal aberrations induced by three chemicals.

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The molecular mechanism underlying formation of deletions in Fanconi anemia cells may involve a site-specific recombination

1 reference

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Effects of topoisomerase II inhibition in lymphoblasts from patients with progeroid and "chromosome instability" syndromes

1 reference

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7 January 2021

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Is polyploidy an important genotoxic lesion?

1 reference

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7 January 2021

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Cytogenetic analysis of melanocytes from premalignant nevi and melanomas

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic heterogeneity in bladder cancer as detected by fluorescence in situ hybridization

1 reference

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7 January 2021

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Analysis of ras mutations in human melanocytic lesions: activation of the ras gene seems to be associated with the nodular type of human malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3835%2897%2900305-4

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based on heuristic

inferred from DOI database lookup

Lack of p53 mutations and loss of heterozygosity in non-cultured human melanocytic lesions

1 reference

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7 January 2021

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inferred from DOI database lookup

Identifiers

10.1016/S0304-3835(97)00305-4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9461032%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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