(Q42237835)

English

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity

scientific article published on August 1994

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity (English)

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Caron H

1

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

van Sluis P

2

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

van Roy N

3

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

de Kraker J

4

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Speleman F

5

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Voûte PA

6

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Westerveld A

7

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Slater R

8

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Versteeg R

9

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

language of work or name

0 references

publication date

1 August 1994

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

55

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

2

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

341-347

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Tumour karyotype discriminates between good and bad prognostic outcome in neuroblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Mapping replicational sites in the eucaryotic cell nucleus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

In vitro models of carcinogenesis: expression of recessive genes by chromosomal mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Mitotic recombination is responsible for the loss of heterozygosity in cultured murine cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Neuroblastoma consensus deletion maps to 1p36.1-2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

The CEPH consortium linkage map of human chromosome 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

CEB 15 detects a VNTR locus (Het: 92%) on chromosome 1p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

26 October 2017

Chromosome analysis of human neuroblastoma cell line TR14 showing double minutes and an aberration involving chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

29 May 2018

Cytogenetic features of human neuroblastomas and cell lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

29 May 2018

Definition of a continuous human cell line derived from neuroblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

29 May 2018

Cytogenetic findings and prognosis in neuroblastoma with emphasis on marker chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

29 May 2018

High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

17 August 2018

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918374

17 August 2018

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/8037211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An efficient salt-chloroform extraction of DNA from blood and tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/8037211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A unified model of eukaryotic chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8037211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/8037211

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 October 2017

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