(Q80075929)

English

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)]

scientific article published on 01 May 2004

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scholarly article

1 reference

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28 December 2019

1 reference

Europe PubMed Central

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)] (English)

1 reference

Europe PubMed Central

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28 December 2019

colorectal cancer

1 reference

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inferred from title

colorectal carcinoma

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author name string

J Rüschoff

1

1 reference

Europe PubMed Central

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28 December 2019

B Roggendorf

2

1 reference

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28 December 2019

F Brasch

3

1 reference

Europe PubMed Central

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28 December 2019

M Mathiak

4

1 reference

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28 December 2019

D E Aust

5

1 reference

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28 December 2019

J Plaschke

6

1 reference

Europe PubMed Central

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28 December 2019

W Mueller

7

1 reference

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28 December 2019

C Poremba

8

1 reference

Europe PubMed Central

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28 December 2019

M Kloor

9

1 reference

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28 December 2019

G Keller

10

1 reference

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28 December 2019

M Muders

11

1 reference

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28 December 2019

S Blasenbreu-Vogt

12

1 reference

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28 December 2019

P Rümmele

13

1 reference

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28 December 2019

A Müller

14

1 reference

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28 December 2019

R Büttner

15

1 reference

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28 December 2019

Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)]

16

1 reference

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28 December 2019

publication date

1 May 2004

1 reference

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28 December 2019

1 reference

Europe PubMed Central

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28 December 2019

25

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28 December 2019

3

1 reference

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28 December 2019

178-192

1 reference

Europe PubMed Central

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28 December 2019

https://scigraph.springernature.com/pub.10.1007/s00292-003-0641-x

0 references

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of hereditary nonpolyposis colorectal cancer in the general population. The 6-year experience of a population-based registry

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Piffalls in diagnostic molecular pathology--significance of sampling error

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication error phenotype in colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathological identification of colon cancer with microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Poorly differentiated colonic adenocarcinoma, medullary type: clinical, phenotypic, and molecular characteristics.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability in cancer of the proximal colon

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemical Pattern of MLH1/MSH2 Expression Is Related to Clinical and Pathological Features in Colorectal Adenocarcinomas with Microsatellite Instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overview of natural history, pathology, molecular genetics and management of HNPCC (Lynch Syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent microsatellite instability in sporadic tumors of the upper urinary tract

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor-infiltrating lymphocytes are a marker for microsatellite instability in colorectal carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non-polyposis colorectal cancer in young patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular epidemiology of hereditary nonpolyposis colorectal cancer in Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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