(Q30502393)

19 September 2017

Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung (English)

1 reference

adenocarcinoma of the lung

19 September 2017

1 reference

1 reference

Yokota J

1

1 reference

19 September 2017

Wada M

2

1 reference

19 September 2017

Shimosato Y

3

1 reference

19 September 2017

Terada M

4

1 reference

19 September 2017

Sugimura T

5

1 reference

19 September 2017

language of work or name

English

0 references

publication date

1 December 1987

1 reference

Proceedings of the National Academy of Sciences of the United States of America

19 September 2017

1 reference

19 September 2017

84

1 reference

19 September 2017

9252-9256

1 reference

19 September 2017

24

1 reference

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

19 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Polymorphic human somatostatin gene is located on chromosome 3.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Genetic origin of mutations predisposing to retinoblastoma.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Transforming gene from human stomach cancers and a noncancerous portion of stomach mucosa

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Heterogeneous cytogenetic abnormalities in small cell lung cancer cell lines.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Structural evidence for the authenticity of the human retinoblastoma gene.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC).

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299731

Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23)

26 November 2018

1 reference

12 December 2020

Amplification and expression of the c-myc oncogene in human lung cancer cell lines

1 reference

12 December 2020

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1 reference

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

L-myc, a new myc-related gene amplified and expressed in human small cell lung cancer

1 reference

12 December 2020

Loss of genes on the short arm of chromosome 11 in bladder cancer

1 reference

12 December 2020

Alterations of myc, myb, and rasHa proto-oncogenes in cancers are frequent and show clinical correlation

1 reference

12 December 2020

Loss of alleles at polymorphic loci on chromosome 2 in uveal melanoma

1 reference

12 December 2020

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.84.24.9252

1 reference

19 September 2017

0 references

1 reference

19 September 2017

1 reference