Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis (Q34106298)

31 July 2017

Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis (English)

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31 July 2017

M Gentile

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31 July 2017

M Ahnström

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2

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31 July 2017

F Schön

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3

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31 July 2017

S Wingren

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4

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31 July 2017

language of work or name

English

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publication date

1 November 2001

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31 July 2017

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31 July 2017

20

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31 July 2017

53

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31 July 2017

7753-7760

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1204993

31 July 2017

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ATM-heterozygous germline mutations contribute to breast cancer-susceptibility

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Cancer risks in A-T heterozygotes

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Allelic deletion at 11q23.3-q25 is an early event in cervical neoplasia.

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Heterozygous ATM mutations do not contribute to early onset of breast cancer

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Frequent allelic losses at 11q24.1-q25 in young women with breast cancer: association with poor survival

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ei24, a p53 response gene involved in growth suppression and apoptosis

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The p53-inducible gene EI24/PIG8 localizes to human chromosome 11q23 and the proximal region of mouse chromosome 9.

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How sensitive is PCR-SSCP?

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Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

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Allelic deletions at chromosome 11q22-q23.1 and 11q25-qterm are frequent in sporadic breast but not colorectal cancers.

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Screening breast cancer patients for Norwegian ATM mutations

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Molecular cloning and characterization of LOH11CR2A, a new gene within a refined minimal region of LOH at 11q23.

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Localization of tumor suppressor activity important in nonsmall cell lung carcinoma on chromosome 11q

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Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries

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A model for p53-induced apoptosis

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Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25

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A single ataxia telangiectasia gene with a product similar to PI-3 kinase

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The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species

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Microsatellite instability markers in breast cancer: a review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancer

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Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers

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Alterations of the PPP2R1B gene in human lung and colon cancer

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Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer

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7 January 2021

CHK1 frameshift mutations in genetically unstable colorectal and endometrial cancers

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7 January 2021

Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms

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7 January 2021

p53 and survival in early onset breast cancer: analysis of gene mutations, loss of heterozygosity and protein accumulation

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Deletion mapping of chromosome segment 11q24-q25, exhibiting extensive allelic loss in early onset breast cancer

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Identification of two distinct deletion targets at 11q23 in cutaneous malignant melanoma

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Identification of germline missense mutations and rare allelic variants in theATM gene in early-onset breast cancer

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Rapid and efficient ATM mutation detection by fluorescent chemical cleavage of mismatch: identification of four novel mutations

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7 January 2021

Antioxidant status of liver, erythrocytes, and blood serum of rats in acute methanol intoxication

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Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome

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7 January 2021

Protein truncation test (PTT) for rapid detection of translation-terminating mutations

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7 January 2021

Incidence of cancer in 161 families affected by ataxia-telangiectasia

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7 January 2021

The association of nonsense codons with exon skipping

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7 January 2021

Protein serine/threonine phosphatases and cell transformation

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7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1204993

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Dimensions Publication ID

31 July 2017

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