(Q33904762)

29 July 2017

0 references

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype (English)

1 reference

29 July 2017

1 reference

1 reference

1 reference

19

1 reference

29 July 2017

Antoinette Hollestelle

6

Antoinette Hollestelle

0 references

Hanne Meijers-Heijboer

1

Hanne Meijers-Heijboer

0 references

Gabriela Möslein

18

Gabriela Möslein

0 references

Riccardo Fodde

Riccardo Fodde

22

0 references

Hans Vasen

Hans Vasen

3

0 references

author name string

Juul Wijnen

2

1 reference

29 July 2017

Marijke Wasielewski

4

1 reference

29 July 2017

Anja Wagner

5

1 reference

29 July 2017

Fons Elstrodt

7

1 reference

29 July 2017

Renate van den Bos

8

1 reference

29 July 2017

Anja de Snoo

9

1 reference

29 July 2017

Grace Tjon A Fat

10

1 reference

29 July 2017

Cecile Brekelmans

11

1 reference

29 July 2017

Shantie Jagmohan

12

1 reference

29 July 2017

Patrick Franken

13

1 reference

29 July 2017

Paul Verkuijlen

14

1 reference

29 July 2017

Ans van den Ouweland

15

1 reference

29 July 2017

Pamela Chapman

16

1 reference

29 July 2017

Carli Tops

17

1 reference

29 July 2017

Gabriela Möslein

18

1 reference

29 July 2017

Henry Lynch

20

1 reference

29 July 2017

Jan Klijn

21

1 reference

29 July 2017

Mieke Schutte

23

1 reference

29 July 2017

language of work or name

English

0 references

publication date

10 April 2003

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

72

1 reference

29 July 2017

1308-1314

1 reference

29 July 2017

5

1 reference

Interfaces between the detection, signaling, and repair of DNA damage

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Suppression of genome instability by redundant S-phase checkpoint pathways in Saccharomyces cerevisiae

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

The DNA damage-dependent intra-S phase checkpoint is regulated by parallel pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

CHK2 kinase--a busy messenger.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

The DNA damage response: putting checkpoints in perspective

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Familial endometrial cancer in female carriers of MSH6 germline mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Tumor Variation in Families With Breast Cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Use of Genetic Testing and Prophylactic Mastectomy and Oophorectomy in Women With Breast or Ovarian Cancer From Families With a BRCA1 or BRCA2 Mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

A robust method for detecting CHK2/RAD53 mutations in genomic DNA.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Suppression of spontaneous chromosomal rearrangements by S phase checkpoint functions in Saccharomyces cerevisiae

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180284

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12690581

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12690581

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/375121

1 reference

29 July 2017

1 reference

29 July 2017

1 reference