FAQ

FRA16C gene

Known as: FRA16C, fragile site, aphidicolin type, common, fra(16)(q22.1) 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2014
01219872014

Related topics

Related topics

1 relation
FRA10A gene

Related mentions per year

Related mentions per year

1987-2014
19801990200020102020
FRA16C gene
FRA10A gene

Papers overview

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2014
2014
Chromosome 16 abnormalities in embryos and in sperm from a male with a fragile site at 16q22.1.
Two fragile sites, FRA16B and FRA16C, are located in the chromosome band 16q22.1. Neither of them is associated with any specific… (More)
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Highly Cited
2011
Highly Cited
2011
Failure of origin activation in response to fork stalling leads to chromosomal instability at fragile sites.
Perturbed DNA replication in early stages of cancer development induces chromosomal instability preferentially at fragile sites… (More)
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2011
2011
Chromosomal instability: A lack of new origins drives fragility
Chromosomal fragile sites initially came to the attention of the cancer research community because they were identified as sites… (More)
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2003
2003
The common fragile site FRA16C does not map within the 16q smallest region of overlap number 2 frequently lost in breast carcinoma.
 
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Highly Cited
2003
Highly Cited
2003
Molecular basis for expression of common and rare fragile sites.
Fragile sites are specific loci that form gaps, constrictions, and breaks on chromosomes exposed to partial replication stress… (More)
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1993
1993
Human zinc finger gene ZNF23 (Kox16) maps to a zinc finger gene cluster on chromosome 16q22, and ZNF32 (Kox30) to chromosome region 10q23-–q24
Two members of the KOX gene family, ZNF23 (KOX16) and ZNF32 (KOX30), have been mapped by in situ hybridization to chromosome… (More)
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1987
1987
Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL.
There is much speculation about fragile sites on human chromosomes predisposing to specific chromosome rearrangements seen in… (More)
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