(Q43094703)

13 November 2017

title

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

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13 November 2017

11

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15

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13 November 2017

18

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13 November 2017

Christopher G. Mathew

20

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13 November 2017

19

Detlev Schindler

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13 November 2017

Fiona Vaz

1

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13 November 2017

Helmut Hanenberg

2

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13 November 2017

Beatrice Schuster

3

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13 November 2017

Karen Barker

4

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13 November 2017

Constanze Wiek

5

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13 November 2017

Verena Erven

6

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13 November 2017

Kornelia Neveling

7

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13 November 2017

Daniela Endt

8

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13 November 2017

Ian Kesterton

9

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13 November 2017

Flavia Autore

10

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13 November 2017

Marcel Freund

12

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13 November 2017

Linda Hartmann

13

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13 November 2017

David Grimwade

14

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13 November 2017

Heiner Schaal

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13 November 2017

Shehla Mohammed

17

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13 November 2017

language of work or name

English

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publication date

18 April 2010

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13 November 2017

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13 November 2017

volume

42

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13 November 2017

issue

5

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13 November 2017

page(s)

406-409

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How the fanconi anemia pathway guards the genome

13 November 2017

cites work

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Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry

21 January 2018

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Eme1 is involved in DNA damage processing and maintenance of genomic stability in mammalian cells

21 January 2018

1 reference

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability

21 January 2018

1 reference

Role of mammalian RAD51L2 (RAD51C) in recombination and genetic stability

21 January 2018

1 reference

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

21 January 2018

1 reference

Full-length archaeal Rad51 structure and mutants: mechanisms for RAD51 assembly and control by BRCA2

21 January 2018

1 reference

Cancer. Complicated supercomplexes

21 January 2018

1 reference

Selective accumulation of virus-specific CD8+ T cells within the peripheral blood stem cell compartment.

21 January 2018

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

21 January 2018

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RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females

21 January 2018

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RAD51C is required for Holliday junction processing in mammalian cells

21 January 2018

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Role of RAD51C and XRCC3 in genetic recombination and DNA repair.

21 January 2018

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RAD51C facilitates checkpoint signaling by promoting CHK2 phosphorylation

21 January 2018

1 reference

Characterization of ATM gene mutations in 66 ataxia telangiectasia families.

21 January 2018

1 reference

A severe form of human combined immunodeficiency due to mutations in DNA ligase IV.

21 January 2018

1 reference

Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder

21 January 2018

1 reference

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

21 January 2018

1 reference

A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network

21 January 2018

1 reference

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

21 January 2018

1 reference

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

21 January 2018

1 reference

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

21 January 2018

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Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

21 January 2018

1 reference

Homology-extended sequence alignment

21 January 2018

1 reference

Comparative protein structure modeling of genes and genomes

21 January 2018

1 reference

GROMACS: A message-passing parallel molecular dynamics implementation

21 January 2018

1 reference

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

21 January 2018

1 reference

12 December 2020

International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity

1 reference

12 December 2020

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.

1 reference

12 December 2020

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

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12 December 2020

Parametrization of aliphatic CHn united atoms of GROMOS96 force field

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7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.570

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Dimensions Publication ID

13 November 2017

1041080199

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