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 (Q28291193)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	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	scientific article

Statements

scholarly article

0 references

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 (English)

0 references

author name string

C M Wilke

1

0 references

B K Hall

2

0 references

A Hoge

3

0 references

W Paradee

4

0 references

D I Smith

5

0 references

T W Glover

6

0 references

language of work or name

0 references

publication date

February 1996

0 references

Human Molecular Genetics

0 references

5

0 references

2

0 references

187-95

0 references

The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

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/10.1093%2FHMG%2F5.2.187

21 January 2018

Constitutive fragile sites and cancer.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Protein traffic on the heat shock promoter: parking, stalling, and trucking along

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Preferential sites for viral integration on mammalian genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Prevalence of human papillomavirus in cervical cancer: a worldwide perspective. International biological study on cervical cancer (IBSCC) Study Group

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

The human minisatellite consensus at breakpoints of oncogene translocations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Fragile sites, cancer chromosome breakpoints, and oncogenes all cluster in light G bands.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Chromosomal organization of viral integration sites in human papillomavirus-immortalized human keratinocyte cell lines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Viral integration and fragile sites in human papillomavirus-immortalized human keratinocyte cell lines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Genetic alterations by human papillomaviruses in oncogenesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Integration site of human papillomavirus type-18 DNA in chromosome band 8q22.1 of C4-I cervical carcinoma: DNase I hypersensitivity and methylation of cellular flanking sequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

A tumor suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Isolation of a partial candidate gene for Menkes disease by positional cloning

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Genomic sequencing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Cancer biology: Heritable fragile sites in cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.2.187

21 January 2018

Identifiers

10.1093/HMG/5.2.187

0 references

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28291193&oldid=1642484794"