(Q44250300)

1 December 2017

Evidence that instability within the FRA3B region extends four megabases (English)

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1 December 2017

Nicole A Becker

1

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1 December 2017

Erik C Thorland

2

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1 December 2017

Stacy R Denison

3

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1 December 2017

Leslie A Phillips

4

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1 December 2017

David I Smith

5

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1 December 2017

language of work or name

English

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publication date

1 December 2002

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1 December 2017

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1 December 2017

21

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1 December 2017

8713-8722

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1 December 2017

57

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1205950

1 December 2017

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cites work

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Protein tyrosine phosphatases in cell transformation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Complex genomic rearrangement within the 12q15 multiple aberration region induced by integrated human papillomavirus 18 in a cervical carcinoma cell line.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

First admissions of native-born and immigrant patients to psychiatric hospitals.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Chromosome 3p loss of heterozygosity and mutation analysis of the FHIT and beta-cat genes in squamous cell carcinoma of the head and neck

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Cervical cancer in older women: a molecular analysis of human papillomavirus types, HLA types, and p53 mutations.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Chromosome 3p tumor-suppressor gene alterations in cervical carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

FRA7G extends over a broad region: coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

The role of the FHIT/FRA3B locus in cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Structure of the human receptor tyrosine phosphatase gamma gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

The Characterization of the Common Fragile Site FRA16D and Its Involvement in Multiple Myeloma Translocations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Nucleotide excision repair affects the stability of long transcribed (CTG*CAG) tracts in an orientation-dependent manner in Escherichia coli

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Viral integration, fragile sites, and proto-oncogenes in human neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Cell density and culture factors regulate keratinocyte commitment to differentiation and expression of suprabasal K1/K10 keratins.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Chromosomal translocations in human cancer.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Restriction-site PCR: a direct method of unknown sequence retrieval adjacent to a known locus by using universal primers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

The most common fragile site in man is 3p14

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Chromosome aberrations and cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Characterization of the human TESTIN gene localized in the FRA7G region at 7q31.2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Human papillomavirus is a necessary cause of invasive cervical cancer worldwide

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205950

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1205950

1 reference

Dimensions Publication ID

1 December 2017

0 references

1 reference