(Q35745345)

English

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

scientific article published on February 2000

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

phaeochromocytoma

1 reference

based on heuristic

8

object named as

B T Teh

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

author name string

E Edström

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

E Mahlamäki

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

B Nord

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

M Kjellman

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

R Karhu

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

A Höög

6

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

N Goncharov

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

M Bäckdahl

9

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

C Larsson

10

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

language of work or name

0 references

publication date

1 February 2000

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

The American Journal of Pathology

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Europe PubMed Central

PubMed publication ID

10 August 2017

156

1 reference

Europe PubMed Central

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10 August 2017

2

1 reference

Europe PubMed Central

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10 August 2017

651-659

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Positional cloning of the gene for multiple endocrine neoplasia-type 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Loss of neurofibromatosis type I (NF1) gene expression in pheochromocytomas from patients without NF1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

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=1850024

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Loss of heterozygosity on chromosomes 1 and 11 in sporadic pheochromocytomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

12 July 2018

Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

25 September 2018

Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

15 November 2018

Deletion of genes on chromosome 1 in endocrine neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850024

15 November 2018

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

Multiple endocrine neoplasia type 1: clinical and genetic topics

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

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/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

Loss of heterozygosity on chromosomes 1p and 11p in sporadic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

A family with hereditary extra-adrenal paragangliomas without evidence for mutations in the von Hippel-Lindau disease or ret genes

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

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/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locusPGL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964769-4

7 January 2021

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10666394

12 December 2020

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10.1016/S0002-9440(10)64769-4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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