(Q44111571)

29 November 2017

title

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

1 reference

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

deletion mutation

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

restriction fragment length polymorphism

9 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

tumor suppressor gene

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

1 reference

https://api.crossref.org/works/10.1002/GCC.2870050416

22 November 2023

1 reference

https://api.crossref.org/works/10.1002/GCC.2870050416

22 November 2023

1 reference

Rouleau GA

1 reference

29 November 2017

N. Tanaka

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

I. Nishisho

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

M. Yamamoto

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

A. Miya

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

E. Shin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

K. Karakawa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

S. Fujita

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

T. Kobayashi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

T. Mori

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1283329

9 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1283329

9 September 2022

publication date

1 November 1992

1 reference

full work available at URL

29 November 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fgcc.2870050416

1 reference

DOI

https://api.crossref.org/works/10.1002/GCC.2870050416

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.2870050416

22 November 2023

1 reference

DOI

https://api.crossref.org/works/10.1002/GCC.2870050416

Genes, Chromosomes and Cancer

22 November 2023

published in

1 reference

29 November 2017

1 reference

29 November 2017

1 reference

29 November 2017

page(s)

399-403

1 reference

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

29 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Identification of a chromosome 18q gene that is altered in colorectal cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

The p53 proto-oncogene can act as a suppressor of transformation

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Report of the committee on the genetic constitution of chromosome 22.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Deletion of genes on chromosome 1 in endocrine neoplasia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Isolation of DNA clones revealing restriction fragment length polymorphisms in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

A genetic linkage map of the long arm of human chromosome 22.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Genetic alterations during colorectal-tumor development

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Close linkage of MEN2A with RBP3 locus in Japanese kindreds

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870050416

7 January 2021

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma

1 reference

https://api.crossref.org/works/10.1002/GCC.2870050416

Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma

22 November 2023

1 reference

https://api.crossref.org/works/10.1002/GCC.2870050416

Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma

22 November 2023

1 reference

https://api.crossref.org/works/10.1002/GCC.2870050416

22 November 2023

Identifiers

DOI

1 reference

29 November 2017

1 reference