(Q28304011)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Denis Le Paslier

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

S Yu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

D Hewett

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

L Hobson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

E Baker

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

H J Eyre

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

N Lapsys

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

N A Doggett

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

G R Sutherland

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

R I Richards

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

language of work or name

English

0 references

publication date

1 February 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

367-374

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

Basic local alignment search tool

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Characterization of the COL2A1 VNTR polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Identification of mismatch repair genes and their role in the development of cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Fragile chromosome 16(q22) cause a balanced translocation at the same point

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Complex gene conversion events in germline mutation at human minisatellites

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

1H NMR studies on the interaction between distamycin A and a symmetrical DNA dodecamer

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Growing triplet repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Dynamic mutations: a new class of mutations causing human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

The molecular basis of fragile sites in human chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Simple tandem DNA repeats and human genetic disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

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/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

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/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981875-9

7 January 2021

10.1016/S0092-8674(00)81875-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9039263%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference