(Q79872546)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

title

Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

Beckwith-Wiedemann syndrome

26 December 2019

main subject

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

author name string

Wendy N Cooper

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Rebecca Curley

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Fiona Macdonald

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

publication date

6 March 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

volume

89

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

page(s)

613-617

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

Variation in human meiotic recombination

26 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Termini of human chromosomes display elevated rates of mitotic recombination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Uniparental paternal disomy in Angelman's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

The Bloom's syndrome helicase suppresses crossing over during homologous recombination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Human recombination hot spots hidden in regions of strong marker association

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Mosaic and polymorphic imprinting of the WT1 gene in humans.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Paternal expression of WT1 in human fibroblasts and lymphocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Antisense WT1 transcription parallels sense mRNA and protein expression in fetal kidney and can elevate protein levels in vitro.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

Comprehensive human genetic maps: individual and sex-specific variation in recombination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2007.01.005

10.1016/J.YGENO.2007.01.005

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17337339%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference