(Q77580366)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

title

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference

6

George P Chrousos

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

author name string

Christian A Koch

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Steve C Huang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Zhengping Zhuang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Catherine Stolle

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Norio Azumi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Alexander O Vortmeyer

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

Karel Pacak

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

language of work or name

English

0 references

publication date

1 January 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

page(s)

479-482

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11821960%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.onc.1205133

6 December 2019

exact match

0 references

cites work

The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas

1 reference

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7 January 2021

Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

von Hippel-Lindau disease: genetic, clinical, and imaging features

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Activation of HIF1alpha ubiquitination by a reconstituted von Hippel-Lindau (VHL) tumor suppressor complex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Genetics of human cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

The von Hippel-Lindau tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Genetic instabilities in human cancers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Mutations in the RET protooncogene in sporadic pheochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

von Hippel-Lindau disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Expression of the ret proto-oncogene product in human normal and neoplastic tissues of neural crest origin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Neurofibromatosis: past, present, and future

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021

Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205133

7 January 2021