Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour. (Q36115135)

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6 December 2019

title

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour (English)

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6 December 2019

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3

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6 December 2019

author name string

R G Grundy

series ordinal

1

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6 December 2019

J Pritchard

series ordinal

2

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6 December 2019

J K Cowell

series ordinal

4

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6 December 2019

language of work or name

English

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publication date

1 November 1998

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British Journal of Cancer

6 December 2019

published in

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6 December 2019

volume

78

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6 December 2019

issue

9

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6 December 2019

page(s)

1181-1187

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The 1993-94 Généthon human genetic linkage map

6 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

The treatment of Wilms' Tumor: Results of the second national Wilms' Tumor study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Mutation and cancer: a model for Wilms' tumor of the kidney

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Cytogenetics and molecular genetics of Wilms' tumor of childhood

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Allelotype study of primary hepatocellular carcinoma

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Loss of heterozygosity on 6q, 16q, and 17p in human central nervous system primitive neuroectodermal tumors

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Results of the United Kingdom Children's Cancer Study Group first Wilms' Tumor Study.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Cardiac function in Wilms' tumor survivors

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063011

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

23 September 2018

1 reference

12 December 2020

Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour

1 reference

12 December 2020

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

1 reference

12 December 2020

The CEPH consortium linkage map of human chromosome 16

1 reference

12 December 2020

Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers

1 reference

12 December 2020

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

1 reference

12 December 2020

Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)

1 reference

12 December 2020

Cytogenetic changes in Wilms' tumors

1 reference

12 December 2020

Initial congestive heart failure, six to ten years after doxorubicin chemotherapy for childhood cancer

1 reference

12 December 2020

Chromosome analysis of 31 Wilms' tumors

1 reference

12 December 2020

A second nonrandom translocation, der(16)t(1;16)(q21;q13), in Ewing sarcoma and peripheral neuroectodermal tumor

1 reference

12 December 2020

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1038/BJC.1998.651

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9820177%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9820177%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

PubMed publication ID

9820177

1 reference