Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study (Q80960675)

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scientific article published on 01 August 2005

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English	Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study	scientific article published on 01 August 2005

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scholarly article

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4 January 2020

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study (English)

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4 January 2020

colorectal cancer

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colorectal carcinoma

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inferred from title

prostate cancer

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Christoph Engel

3

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Magnus von Knebel Doeberitz

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Magnus von Knebel Doeberitz

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Elke Holinski-Feder

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Elke Holinski-Feder

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Wolfgang Dietmaier

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Wolfgang Dietmaier

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Hans Konrad Schackert

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Hans K Schackert

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Gabriela Moeslein

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Gabriela Moeslein

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Heike Görgens

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Josef Rüschoff

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Josef Rüschoff

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4 January 2020

Elisabeth Mangold

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Elisabeth Mangold

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4 January 2020

Constanze Pagenstecher

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Constanze Pagenstecher

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Ann-Sophie Silber

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Ann-Sophie Silber

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Waltraut Friedl

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Waltraut Friedl

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4 January 2020

author name string

Stefan Krüger

1

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4 January 2020

Susanne Stemmler

11

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4 January 2020

German Hereditary Non-Polyposis Colorectal Cancer Consortium

15

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publication date

1 August 2005

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4 January 2020

Lancet Oncology Commission

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6

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8

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4 January 2020

566-572

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4 January 2020

Expression cloning of 2-5A-dependent RNAase: a uniquely regulated mediator of interferon action

1 reference

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7 January 2021

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Implications for RNase L in prostate cancer biology

1 reference

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7 January 2021

based on heuristic

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A study of the interferon antiviral mechanism: apoptosis activation by the 2-5A system

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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Activation of the IFN-inducible enzyme RNase L causes apoptosis of animal cells.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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Interferon action and apoptosis are defective in mice devoid of 2',5'-oligoadenylate-dependent RNase L

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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The role of 2'-5' oligoadenylate-activated ribonuclease L in apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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Caspase-dependent apoptosis by 2',5'-oligoadenylate activation of RNase L is enhanced by IFN-beta

1 reference

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7 January 2021

based on heuristic

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An apoptotic signaling pathway in the interferon antiviral response mediated by RNase L and c-Jun NH2-terminal kinase

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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HPC1/RNASEL mediates apoptosis of prostate cancer cells treated with 2',5'-oligoadenylates, topoisomerase I inhibitors, and tumor necrosis factor-related apoptosis-inducing ligand.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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Tumor-suppressor genes: news about the interferon connection

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

RNASEL mutations in hereditary prostate cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of the RNASEL gene in familial and sporadic prostate cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of the RNASEL gene in hereditary, familial, and sporadic prostate cancer

1 reference

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7 January 2021

based on heuristic

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Mutation screening and association study of RNASEL as a prostate cancer susceptibility gene

1 reference

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7 January 2021

based on heuristic

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Predicting deleterious amino acid substitutions

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Association of susceptibility alleles in ELAC2/HPC2, RNASEL/HPC1, and MSR1 with prostate cancer severity in European American and African American men.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

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A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

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7 January 2021

based on heuristic

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Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The codon 72 polymorphic variants of p53 have markedly different apoptotic potential

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970253-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

LightCycler assay in the analysis of haplotypes of the type 2 diabetes susceptibility gene CAPN10.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for an age-related influence of microsatellite instability on colorectal cancer survival

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The synergistic cytocidal effect produced by immune interferon and tumor necrosis factor in HT-29 cells is associated with inhibition of rRNA processing and (2',5') oligo (A) activation of RNase L.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Skin allograft rejection is suppressed in mice lacking the antiviral enzyme, 2',5'-oligoadenylate-dependent RNase L.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Role of genetic polymorphisms of the RNASEL gene on familial prostate cancer risk in a Japanese population

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1470-2045(05)70253-9

1 reference

Europe PubMed Central

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4 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16054567%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

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