Nonrandom breakpoints of unbalanced chromosome translocations in human hepatocellular carcinoma cell lines (Q40954645)

25 September 2017

title

Nonrandom breakpoints of unbalanced chromosome translocations in human hepatocellular carcinoma cell lines (English)

1 reference

25 September 2017

Keck CL

1

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25 September 2017

Zimonjic DB

2

1 reference

25 September 2017

Yuan BZ

3

1 reference

25 September 2017

Thorgeirsson SS

4

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25 September 2017

Popescu NC

5

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25 September 2017

publication date

1 May 1999

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Cancer Genetics and Cytogenetics

25 September 2017

published in

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25 September 2017

volume

111

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25 September 2017

issue

1

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25 September 2017

page(s)

37-44

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The molecular genetics of cancer

25 September 2017

cites work

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Chromosomal translocations in human cancer.

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A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

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Molecular cytogenetic characterization of cancer cell alterations

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An improved procedure for chromosome preparations from solid tumors

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7 January 2021

Molecular cytogenetics of human papillomavirus-negative cervical carcinoma cell lines

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7 January 2021

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

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7 January 2021

Chromosomal rearrangements in a primary hepatocellular carcinoma.

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7 January 2021

Cytogenetic findings in three primary hepatocellular carcinomas

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7 January 2021

Chromosome 1 abnormalities in hepatocellular carcinoma

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7 January 2021

Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma

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7 January 2021

Interphase cytogenetic studies of human hepatocellular carcinomas by fluorescent in situ hybridization

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7 January 2021

Cytogenetic analyses of hepatocellular carcinoma by in situ hybridization with a chromosome-specific DNA probe

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7 January 2021

Report of a complex karyotype in recurrent metastatic fibrolamellar hepatocellular carcinoma and a review of hepatocellular carcinoma cytogenetics

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7 January 2021

Chromosomal aberrations in hepatocellular carcinomas: Relationship with pathological features

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7 January 2021

Comprehensive allelotyping of human hepatocellular carcinoma

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7 January 2021

Multiple recurrent genomic rearrangements and fragile sites in human cancer

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7 January 2021

Chromosome fragility and instability in human cancer

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Site-specific integration by adeno-associated virus

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Rearrangement of chromosome 1p in breast cancer correlates with poor prognostic features

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Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma

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Chromosomal aberrations in human neuroblastomas

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7 January 2021

Neuroblastoma consensus deletion maps to 1p36.1-2.

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7 January 2021

Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma

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7 January 2021

Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization

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7 January 2021

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

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7 January 2021

Replacement of Fhit in cancer cells suppresses tumorigenicity

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7 January 2021

Hepatitis B virus integration site in hepatocellular carcinoma at chromosome 17;18 translocation

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7 January 2021

10.1016/S0165-4608(98)00210-6

Identifiers

DOI

1 reference

release_32rby7pp5vedhowoqxerijln6i

25 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/32rby7pp5vedhowoqxerijln6i

24 November 2022

mapped directly with Wikidata item

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