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English
Fragile sites still breaking
scientific article published on 01 December 1998
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Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
review article
1 reference
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Europe PubMed Central
title
Fragile sites still breaking
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author
Grant R Sutherland
series ordinal
1
object named as
G R Sutherland
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
E Baker
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
R I Richards
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 December 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
501-506
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
The molecular basis of fragile sites in human chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of three rare fragile sites: chromosomal truncation, amplification of distal segment and telomeric renewal
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common fragile sites on human chromosomes represent transcriptionally active regions: evidence from camptothecin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fish mapping of YAC clones at human chromosomal band 7q31.2: Identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Metaphase fragility of the human RNU1 and RNU2 loci is induced by actinomycin D through a p53-dependent pathway
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the full fragile X syndrome mutation in fetal gametes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the gene FMR2, associated with FRAXE mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FRAXA and FRAXE: Evidence against segregation distortion and for an effect of intermediate alleles on learning disability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The intermediate alleles of the fragile X CGG repeat in patients with mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion and Length-Dependent Fragility of CTG Repeats in Yeast
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Simple repeat DNA is not replicated simply
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Repeat expansion--all in a flap?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive fragile sites and cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
AnFHIT tumor suppressor gene?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Replacement of Fhit in cancer cells suppresses tumorigenicity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901628-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(98)01628-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
9865156
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9865156
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9865156%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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