Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells (Q77361278)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746990%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells (English)

1 reference

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5 December 2019

author name string

Martin F Arlt

1

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5 December 2019

Diane E Miller

2

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5 December 2019

David G Beer

3

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5 December 2019

Thomas W Glover

4

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5 December 2019

publication date

1 January 2002

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Genes, Chromosomes and Cancer

5 December 2019

published in

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5 December 2019

volume

33

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5 December 2019

issue

1

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5 December 2019

page(s)

82-92

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Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis

5 December 2019

cites work

1 reference

Fhit, a putative tumor suppressor in humans, is a dinucleoside 5',5"'-P1,P3-triphosphate hydrolase

21 January 2018

1 reference

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

21 January 2018

1 reference

The canine copper toxicosis locus is not syntenic with ATP7B or ATX1 and maps to a region showing homology to human 2p21

21 January 2018

1 reference

FHIT gene therapy prevents tumor development in Fhit-deficient mice.

21 January 2018

1 reference

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

21 January 2018

1 reference

Muir-Torre-like syndrome in Fhit-deficient mice

21 January 2018

1 reference

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

21 January 2018

1 reference

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer

21 January 2018

1 reference

An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome

21 January 2018

1 reference

A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins

21 January 2018

1 reference

A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.

21 January 2018

1 reference

Isolation of a new gene GS2 (DXS1283E) from a CpG island between STS and KAL1 on Xp22.3.

21 January 2018

1 reference

Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas

21 January 2018

1 reference

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

21 January 2018

1 reference

Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation

21 January 2018

1 reference

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

21 January 2018

1 reference

Protein expression and functional analysis of the FHIT gene in human tumor cells

21 January 2018

1 reference

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

21 January 2018

1 reference

Replacement of Fhit in cancer cells suppresses tumorigenicity

21 January 2018

1 reference

The origin of interspersed repeats in the human genome

21 January 2018

1 reference

The FHIT gene 3p14.2 is abnormal in lung cancer.

21 January 2018

1 reference

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

21 January 2018

1 reference

Restored expression of fragile histidine triad protein and tumorigenicity of cervical carcinoma cells

21 January 2018

1 reference

Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange

21 January 2018

1 reference

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution

21 January 2018

1 reference

Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

21 January 2018

1 reference

Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation

21 January 2018

1 reference

Instability at chromosomal fragile sites

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GCC.10000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11746990%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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