Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review (Q38123671)

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scientific article published on March 2014

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English	Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review	scientific article published on March 2014

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scholarly article

1 reference

Europe PubMed Central

29 August 2017

Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review (English)

1 reference

Europe PubMed Central

29 August 2017

literature review

1 reference

based on heuristic

inferred from title

DNA mismatch repair

1 reference

based on heuristic

inferred from title

object named as

Amanda B Spurdle

2

0 references

author name string

Alexander M Metcalf

1

1 reference

Europe PubMed Central

29 August 2017

publication date

1 March 2014

1 reference

Europe PubMed Central

29 August 2017

Familial Cancer

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Europe PubMed Central

29 August 2017

13

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Europe PubMed Central

29 August 2017

1-12

1 reference

Europe PubMed Central

29 August 2017

1

1 reference

Europe PubMed Central

29 August 2017

https://scigraph.springernature.com/pub.10.1007/s10689-013-9671-6

0 references

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Surveillance colonoscopy improves survival in a cohort of subjects with a single mismatch repair gene mutation

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Decrease in mortality in Lynch syndrome families because of surveillance.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

The high frequency of de novo promoter methylation in synchronous primary endometrial and ovarian carcinomas.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

BRAF mutation in endometrial carcinoma and hyperplasia: correlation with KRAS and p53 mutations and mismatch repair protein expression.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

RAS/RAF mutation and defective DNA mismatch repair in endometrial cancers.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Epigenetic signatures of familial cancer are characteristic of tumor type and family category.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Hereditary nonpolyposis colorectal cancer in endometrial cancer patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Interobserver variability in the evaluation of mismatch repair protein immunostaining.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Mutations of the BRAF gene in human cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

BRAF V600E mutation in papillary thyroid carcinoma: significant association with node metastases and extra thyroidal invasion

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Association of mammalian target of rapamycin with aggressive type II endometrial carcinomas and poor outcome: a potential target treatment

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Multiplex mutation screening by mass spectrometry evaluation of 820 cases from a personalized cancer medicine registry

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Activation of ERK1/2 occurs independently of KRAS or BRAF status in endometrial cancer and is associated with favorable prognosis

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

BRAF V600E Mutations in Endometrial Adenocarcinoma.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Mucinous adenocarcinoma of the endometrium: case series and review of the literature

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Intra-tumor heterogeneity of MLH1 promoter methylation revealed by deep single molecule bisulfite sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

A cost-effective algorithm for hereditary nonpolyposis colorectal cancer detection.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Integrated genomic characterization of endometrial carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Consistent absence of BRAF mutations in cervical and endometrial cancer despite KRAS mutation status.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

RASSF1A hypermethylation and its inverse correlation with BRAF and/or KRAS mutations in MSI-associated endometrial carcinoma.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

RASSF1A methylation and K-ras and B-raf mutations and recurrent endometrial cancer.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

KRAS mutation and microsatellite instability in endometrial adenocarcinomas showing MELF-type myometrial invasion.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

PIK3CA mutations in patients with advanced cancers treated with PI3K/AKT/mTOR axis inhibitors

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Detection of somatic mutations by high-resolution DNA melting (HRM) analysis in multiple cancers

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Somatic deletions of the polyA tract in the 3' untranslated region of epidermal growth factor receptor are common in microsatellite instability-high endometrial and colorectal carcinomas

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

High-throughput interrogation of PIK3CA, PTEN, KRAS, FBXW7 and TP53 mutations in primary endometrial carcinoma.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

High-resolution methylation analysis of the hMLH1 promoter in sporadic endometrial and colorectal carcinomas.

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Molecular, pathologic, and clinical features of early-onset endometrial cancer: identifying presumptive Lynch syndrome patients

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Large genomic rearrangements and germline epimutations in Lynch syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Low frequency ofBRAFandCDKN2Amutations in endometrial cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Low Frequency of BRAF Mutations in Endometrial and in Cervical Carcinomas

1 reference

https://api.crossref.org/works/10.1007%2FS10689-013-9671-6

21 January 2018

Association of mismatch repair deficiency with PTEN frameshift mutations in endometrial cancers and the precursors in a Japanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of hMLH1 in a population-based series of endometrial carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of extended colectomy and limited resection in patients with Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surveillance on mutation carriers of DNA mismatch repair genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and mismatch repair genes analyses of Chinese suspected hereditary non-polyposis colorectal cancer: a cost-effective screening strategy proposal

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Causes and consequences of microsatellite instability in endometrial carcinoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of prophylactic hysterectomy in patients at high risk for hereditary cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of mutation profiles to refine the classification of endometrial carcinomas.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective mismatch repair and the development of recurrent endometrial carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable MLH1 promoter methylation patterns in endometrial carcinomas of endometrioid subtype lacking DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of CpG in a small region of the hMLH1 promoter invariably correlates with the absence of gene expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathologic features of endometrial carcinoma associated with HNPCC

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of a correlation between the BRAF V600E mutation and abnormal DNA mismatch repair in patients with sporadic endometrial cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of endometrial cancer: a correlative study assessing microsatellite instability, MLH1 hypermethylation, DNA mismatch repair protein expression, and PTEN, PIK3CA, KRAS, and BRAF mutation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23880961

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-013-9671-6

1 reference

Europe PubMed Central

29 August 2017

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0 references

1 reference

Europe PubMed Central

29 August 2017

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