(Q81333176)

English

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

scientific article published on 01 January 2006

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

phaeochromocytoma

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Francien H van Nederveen

4

object named as

Francien H van Nederveen

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Ronald de Krijger

10

object named as

Ronald R de Krijger

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Winand N M Dinjens

7

object named as

Winand N M Dinjens

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

Hilde Dannenberg

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Ronald J deLeeuw

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Albert A Verhofstad

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

J W Lenders

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Ernst Jan M Speel

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Wan L Lam

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

1 January 2006

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

45

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

83-93

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Genomic microarrays in human genetic disease and cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline SDHD mutation in familial phaeochromocytoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Smallest region of overlapping deletion in 1p36 in human neuroblastoma: a 1 Mbp cosmid and PAC contig

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic dichotomy in mitochondrial complex II genetic disorders.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel, evolutionarily conserved gene family with putative sequence-specific single-stranded DNA-binding activity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Ever since Knudson.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of Heterozygosity on the Short Arm of Chromosome 1 in Pheochromocytoma and Abdominal Paraganglioma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome screening by comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional collaboration between different cyclin-dependent kinase inhibitors suppresses tumor growth with distinct tissue specificity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Involvement of multiple developmental genes on chromosome 1p in lung tumorigenesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel regions of amplification on 8q distinct from the MYC locus and frequently altered in oral dysplasia and cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small-cell lung carcinoma cells.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of BMP2, Smad8, and Smad4 expression in prostate cancer progression.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Generation of neuroendocrine chromaffin cells from sympathoadrenal progenitors: beyond the glucocorticoid hypothesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of p73 localized at chromosome 1p36.3 in primary neuroblastomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the von Hippel-Lindau disease tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

The pressure rises: update on the genetics of phaeochromocytoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Deregulated human Cdc14A phosphatase disrupts centrosome separation and chromosome segregation

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide copy number imbalances identified in familial and sporadic medullary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Suppression of tumorigenesis and activation of Wnt signaling by bone morphogenetic protein 4 in human cancer cells

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential effects of leukocyte common antigen-related protein on biochemical and biological activities of RET-MEN2A and RET-MEN2B mutant proteins

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion mapping suggests that the 1p22 melanoma susceptibility gene is a tumor suppressor localized to a 9-mb interval

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Detailed molecular analysis of 1p36 in neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic structure, chromosomal location, and mutation analysis of the human CDC14A gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of Pten and Ink4a/Arf interactions in the suppression of tumorigenesis in mice

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20268

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20268

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16215979%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q81333176&oldid=2119254290"