(Q81333176)

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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

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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)

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7 January 2020

phaeochromocytoma

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7 January 2020

Francien H van Nederveen

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Francien H van Nederveen

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7 January 2020

Ronald de Krijger

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Ronald R de Krijger

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7 January 2020

Winand N M Dinjens

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Winand N M Dinjens

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7 January 2020

Hilde Dannenberg

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7 January 2020

Albert A Verhofstad

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Albert A Verhofstad

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7 January 2020

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Ronald J deLeeuw

3

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7 January 2020

J W Lenders

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7 January 2020

Ernst Jan M Speel

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7 January 2020

Wan L Lam

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7 January 2020

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1 January 2006

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7 January 2020

Genes, Chromosomes and Cancer

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7 January 2020

45

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7 January 2020

1

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7 January 2020

83-93

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7 January 2020

Genomic microarrays in human genetic disease and cancer

1 reference

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Germline SDHD mutation in familial phaeochromocytoma

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

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

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

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Phenotypic dichotomy in mitochondrial complex II genetic disorders.

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

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

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

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

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

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

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7 January 2021

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

1 reference

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7 January 2021

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Ever since Knudson.

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

1 reference

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

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

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Genome screening by comparative genomic hybridization

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

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

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

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

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

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7 January 2021

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

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7 January 2021

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

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

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7 January 2021

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Identification of the von Hippel-Lindau disease tumor suppressor gene

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

1 reference

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7 January 2021

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The pressure rises: update on the genetics of phaeochromocytoma

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7 January 2021

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Deregulated human Cdc14A phosphatase disrupts centrosome separation and chromosome segregation

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

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

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

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Germ-line mutations in nonsyndromic pheochromocytoma

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

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

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

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

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

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

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Detailed molecular analysis of 1p36 in neuroblastoma

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Identifiers

10.1002/GCC.20268

1 reference

Europe PubMed Central

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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

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