(Q73048152)

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31 October 2019

title

Molecular analysis of region t(5;6)(q21;q21) in Wilms tumor (English)

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31 October 2019

author name string

C K Bruce

1

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31 October 2019

P Howard

2

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31 October 2019

N J Nowak

3

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31 October 2019

P R Hoban

4

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31 October 2019

publication date

1 March 2003

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Cancer Genetics and Cytogenetics

31 October 2019

published in

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31 October 2019

volume

141

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31 October 2019

issue

2

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31 October 2019

page(s)

106-113

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Wilms' tumour: reconciling genetics and biology

31 October 2019

cites work

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7 January 2021

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

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7 January 2021

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

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7 January 2021

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

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7 January 2021

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

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7 January 2021

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

1 reference

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7 January 2021

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

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7 January 2021

A clinical overview of WT1 gene mutations

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7 January 2021

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

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7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

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7 January 2021

High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor

1 reference

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7 January 2021

Loss of heterozygosity at 7p in Wilms' tumour development

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7 January 2021

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

1 reference

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7 January 2021

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

1 reference

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7 January 2021

Physical localisation of the breakpoints of a constitutional translocation t(5;6)(q21;q21) in a child with bilateral Wilms' tumour.

1 reference

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7 January 2021

Genetic and physical mapping around the properdin P gene

1 reference

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7 January 2021

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

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7 January 2021

Chapter 1 DNA Sequence Localization in Metaphase and Interphase Cells by Fluorescence in Situ Hybridization

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7 January 2021

The neural cell adhesion molecule (NCAM) as a regulator of cell-cell interactions

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7 January 2021

Reexpression of poly(sialic acid) units of the neural cell adhesion molecule in Wilms tumor

1 reference

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7 January 2021

Polysialylated neural cell adhesion molecule as a marker for differential diagnosis in pediatric tumors

1 reference

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7 January 2021

A splice variant of Skp2 is retained in the cytoplasm and fails to direct cyclin D1 ubiquitination in the uterine cancer cell line SK-UT.

1 reference

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7 January 2021

The purification, characterization and analysis of primary and secondary-structure of prolyl oligopeptidase from human lymphocytes. Evidence that the enzyme belongs to the alpha/beta hydrolase fold family.

1 reference

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7 January 2021

Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree

1 reference

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7 January 2021

Identification of a new WT1 mutation in a sporadic Wilms' tumour

1 reference

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7 January 2021

Identification of a tumor-specific methylation site in the Wilms tumor suppressor gene

1 reference

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7 January 2021

Chromosome 5 allele loss in human colorectal carcinomas.

1 reference

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7 January 2021

Loss of heterozygosity on chromosome 5 in sporadic ovarian carcinoma is a late event and is not associated with mutations in APC at 5q21-22

1 reference

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7 January 2021

Microsatellite instability and/or loss of heterozygosity in young gastric cancer patients in Italy

1 reference

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7 January 2021

Genetic instability and mutation of the TGF-beta-receptor-II gene in ampullary carcinomas

1 reference

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7 January 2021

Analysis of chromosome 6 deletions in lymphoid malignancies provides evidence for a region of minimal deletion within a 2-megabase segment of 6q21

1 reference

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7 January 2021

Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms' tumour from a BWS patient

1 reference

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7 January 2021

10.1016/S0165-4608(02)00669-6

Identifiers

DOI

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31 October 2019

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