(Q28280022)

18

0 references

Peter Lichtner

8

0 references

Christian Kubisch

13

Christian Kubisch

0 references

Christoph Engel

Christoph Engel

17

0 references

Christopher G. Mathew

Christopher G Mathew

21

0 references

Barbara Wappenschmidt

5

Barbara Wappenschmidt

0 references

Alfons Meindl

1

Alfons Meindl

0 references

Rita Schmutzler

23

Rita K Schmutzler

0 references

Detlev Schindler

22

Detlev Schindler

0 references

Juliane Ramser

11

Juliane Ramser

0 references

author name string

Heide Hellebrand

2

0 references

Constanze Wiek

3

0 references

Verena Erven

4

0 references

Dieter Niederacher

6

0 references

Marcel Freund

7

0 references

Linda Hartmann

9

0 references

Heiner Schaal

10

0 references

Ellen Honisch

12

0 references

Hans E Wichmann

14

0 references

Karin Kast

15

0 references

Helmut Deissler

16

0 references

Kornelia Neveling

19

0 references

Marion Kiechle

20

0 references

Helmut Hanenberg

RAD51C facilitates checkpoint signaling by promoting CHK2 phosphorylation

24

0 references

language of work or name

English

0 references

publication date

May 2010

0 references

published in

Nature Genetics

0 references

volume

42

0 references

issue

5

0 references

page(s)

410-4

0 references

cites work

1 reference

RAD51C is required for Holliday junction processing in mammalian cells

21 April 2017

1 reference

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

21 April 2017

1 reference

Isolation and characterization of RAD51C, a new human member of the RAD51 family of related genes

21 April 2017

1 reference

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

21 April 2017

1 reference

Extended base pair complementarity between U1 snRNA and the 5' splice site does not inhibit splicing in higher eukaryotes, but rather increases 5' splice site recognition

21 April 2017

1 reference

Biallelic inactivation of BRCA2 in Fanconi anemia

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.569

Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.569

Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells

21 April 2017

1 reference

12 December 2020

The ATR-Chk1 pathway plays a role in the generation of centrosome aberrations induced by Rad51C dysfunction

1 reference

12 December 2020

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

1 reference

12 December 2020

Ten genes for inherited breast cancer.

1 reference

12 December 2020

Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.

1 reference

12 December 2020

MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases

1 reference

12 December 2020

Loss of Rad51c leads to embryonic lethality and modulation of Trp53-dependent tumorigenesis in mice

1 reference

12 December 2020

Pathology of ovarian cancers in BRCA1 and BRCA2 carriers

1 reference

12 December 2020

Structural and functional relationships of the XPF/MUS81 family of proteins

1 reference

12 December 2020

Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population

1 reference

12 December 2020

KORA--a research platform for population based health research

1 reference

12 December 2020

Optimization of fibronectin-assisted retroviral gene transfer into human CD34+ hematopoietic cells

1 reference

12 December 2020

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

1 reference

12 December 2020

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

1 reference

12 December 2020

A novel approach to describe a U1 snRNA binding site.

1 reference

12 December 2020

The RAD51 gene family, genetic instability and cancer

1 reference

12 December 2020

Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.

1 reference

12 December 2020

Genetic predisposition to breast cancer: past, present, and future

1 reference

12 December 2020

Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins

1 reference

12 December 2020

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

1 reference

12 December 2020

Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype

1 reference

12 December 2020

Chip-based genotyping by mass spectrometry

1 reference

12 December 2020

Genotype-phenotype correlations in Fanconi anemia

1 reference

12 December 2020

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations

1 reference

12 December 2020

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

1 reference

12 December 2020

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG.569

7 January 2021