(Q35745668)

10 August 2017

title

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

1 reference

10 August 2017

1 reference

1 reference

H Dannenberg

1

1 reference

10 August 2017

E J Speel

2

1 reference

10 August 2017

J Zhao

3

1 reference

10 August 2017

P Saremaslani

4

1 reference

10 August 2017

E van Der Harst

5

1 reference

10 August 2017

J Roth

6

1 reference

10 August 2017

P U Heitz

7

1 reference

10 August 2017

H J Bonjer

8

1 reference

10 August 2017

W N Dinjens

9

1 reference

10 August 2017

W J Mooi

10

1 reference

10 August 2017

P Komminoth

11

1 reference

10 August 2017

R R de Krijger

12

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 August 2000

1 reference

10 August 2017

number of pages

7

1 reference

The American Journal of Pathology

inferred from page(s)

published in

1 reference

10 August 2017

volume

157

1 reference

10 August 2017

issue

2

1 reference

10 August 2017

page(s)

353-359

1 reference

Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Analysis of genomic alterations in sporadic adrenocortical lesions. Gain of chromosome 17 is an early event in adrenocortical tumorigenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Germline mutations in the vhl gene in patients presenting with phaeochromocytomas

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Isolation and characterization of a novel human pancreas-specific gene, pancpin, that is down-regulated in pancreatic cancer cells

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Prognostic significance of allelic losses in primary melanoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

The MEN II syndromes and the role of the ret proto-oncogene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Loss of heterozygosity analysis defines a critical region in chromosome 1p22 commonly deleted in human malignant mesothelioma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Von Hippel‐Lindau Syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Neurofibromatosis and cancer.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Human genetics. Neurofibromatosis gene cloned.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Malignant pheochromocytoma: clinical, biological, histologic and therapeutic data in a series of 20 patients with distant metastases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Deletions involving two distinct regions of 6q in B-cell non-Hodgkin lymphoma

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Isolation and mapping of 68 RFLP markers on human chromosome 6

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Cloning of human satellite III DNA: different components are on different chromosomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Molecular genetic analysis of von Hippel-Lindau disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850127

Identification of the von Hippel-Lindau disease tumor suppressor gene

25 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Absence of TP53 alterations in pheochromocytomas and medullary thyroid carcinomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

The relatively high frequency of p53 gene mutations in multiple and malignant phaeochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Expression and prognostic value of c-erbB-2 oncogene product in human phaeochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Expression of c-fos and c-myc proto-oncogenes in human adrenal pheochromocytomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

A hypervariable repeated sequence on human chromosome 1p36

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

MEN1 gene mutation analysis of sporadic adrenocortical lesions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Comparative genomic hybridization analysis of sporadic neuroendocrine tumors of the digestive system

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964547-6

Deletion mapping on the distal third region of chromosome 1p in multiple endocrine neoplasia type IIA

7 January 2021

1 reference

https://pubmed.ncbi.nlm.nih.gov/10934139

12 December 2020

Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10934139

12 December 2020

Marked genetic differences between stage pTa and stage pT1 papillary bladder cancer detected by comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/10934139

12 December 2020

Multiple regions of allelic loss from chromosome arm 6q in malignant mesothelioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/10934139

12 December 2020

10.1016/S0002-9440(10)64547-6

Identifiers

DOI

1 reference

10 August 2017

1 reference

10 August 2017

1 reference