(Q39927458)

English

MethyQESD, a robust and fast method for quantitative methylation analyses in HNPCC diagnostics using formalin-fixed and paraffin-embedded tissue samples

scientific article published on 20 October 2008

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scholarly article

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Europe PubMed Central

PubMed publication ID

15 September 2017

MethyQESD, a robust and fast method for quantitative methylation analyses in HNPCC diagnostics using formalin-fixed and paraffin-embedded tissue samples (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

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inferred from title

Elke Holinski-Feder

8

object named as

Elke Holinski-Feder

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Europe PubMed Central

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15 September 2017

author name string

Marcus Bettstetter

1

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Europe PubMed Central

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15 September 2017

Stefan Dechant

2

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Europe PubMed Central

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15 September 2017

Petra Ruemmele

3

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Europe PubMed Central

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15 September 2017

Corinna Vogel

4

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Europe PubMed Central

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15 September 2017

Katrin Kurz

5

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Europe PubMed Central

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15 September 2017

Monika Morak

6

1 reference

Europe PubMed Central

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15 September 2017

Gisela Keller

7

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Europe PubMed Central

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15 September 2017

Ferdinand Hofstaedter

9

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15 September 2017

Wolfgang Dietmaier

10

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15 September 2017

publication date

20 October 2008

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15 September 2017

Laboratory Investigation

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15 September 2017

88

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15 September 2017

12

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15 September 2017

1367-1375

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Europe PubMed Central

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15 September 2017

https://scigraph.springernature.com/pub.10.1038/labinvest.2008.100

0 references

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Cancer epigenomics

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The usefulness of the detection of GSTP1 methylation in urine as a biomarker in the diagnosis of prostate cancer.

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Diagnostic application of hMLH1 methylation in hereditary non-polyposis colorectal cancer

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Bethesda guidelines: relation to microsatellite instability and MLH1 promoter methylation in patients with colorectal cancer.

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

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Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

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Nuclear Maspin expression is associated with response to adjuvant 5-fluorouracil based chemotherapy in patients with stage III colon cancer

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Conversion-specific detection of DNA methylation using real-time polymerase chain reaction (ConLight-MSP) to avoid false positives

1 reference

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21 January 2018

Preoperative serum DNA GSTP1 CpG island hypermethylation and the risk of early prostate-specific antigen recurrence following radical prostatectomy

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MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

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BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes

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BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing

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

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Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

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Distinction of hereditary nonpolyposis colorectal cancer and sporadic microsatellite-unstable colorectal cancer through quantification of MLH1 methylation by real-time PCR

1 reference

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7 January 2021

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Mutations predisposing to hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2008.100

7 January 2021

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Morphology of sporadic colorectal cancer with DNA replication errors

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2008.100

7 January 2021

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Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2008.100

7 January 2021

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Poor Survival Associated with theBRAFV600E Mutation in Microsatellite-Stable Colon Cancers

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2008.100

7 January 2021

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Sensitive and quantitative universal Pyrosequencing methylation analysis of CpG sites

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2008.100

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/LABINVEST.2008.100

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

ResearchGate publication ID

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