RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours (Q43800251)

26 November 2017

title

RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours (English)

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Astuti D

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Agathanggelou A

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Honorio S

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Dallol A

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Neumann HP

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Voutilainen R

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Dahia P

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Maher ER

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Latif F

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26 November 2017

language of work or name

English

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publication date

1 November 2001

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26 November 2017

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volume

20

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issue

51

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page(s)

7573-7577

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Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.

26 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Germline SDHD mutation in familial phaeochromocytoma

21 January 2018

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Epigenetic inactivation of RASSF1A in lung and breast cancers and malignant phenotype suppression

21 January 2018

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Epigenetic inactivation of a RAS association domain family protein from the lung tumour suppressor locus 3p21.3.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumour-suppressor locus distal to the FHIT gene

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Neurofibromin GTPase-activating protein-related domains restore normal growth in Nf1-/- cells

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Substrate specificities and identification of putative substrates of ATM kinase family members

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1.

21 January 2018

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Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: a strategy for cloning the putative tumor suppressor gene

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Molecular biology of neuroblastoma

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Homozygous deletions at 3p12 in breast and lung cancer

21 January 2018

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Prognostic discrimination among neuroblastomas according to Ha-ras/trk A gene expression: a comparison of the profiles of neuroblastomas detected clinically and those detected through mass screening

21 January 2018

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CpG island methylator phenotype in colorectal cancer

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Ras uses the novel tumor suppressor RASSF1 as an effector to mediate apoptosis

21 January 2018

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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

21 January 2018

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Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours

21 January 2018

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7 January 2021

Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

7 January 2021

Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplification of MYCN

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1204968

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.1204968

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.1204968

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1204968

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Dimensions Publication ID

26 November 2017

1003770571

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