(Q55671559)

4

object named as

Yvonne Hilhorst-Hofstee

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author name string

Chantal Stoepker

1

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Karolina Hain

2

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Beatrice Schuster

3

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Martin A Rooimans

5

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Jurgen Steltenpool

6

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Anneke B Oostra

7

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Katharina Eirich

8

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Elisabeth T Korthof

9

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Aggie W M Nieuwint

10

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Nicolaas G J Jaspers

11

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Thomas Bettecken

12

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Hans Joenje

13

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John Rouse

15

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Johan P de Winter

https://scigraph.springernature.com/pub.10.1038/ng.751

16

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language of work or name

English

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publication date

February 2011

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published in

Nature Genetics

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volume

43

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page(s)

138-41

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issue

2

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exact match

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cites work

The genetic and molecular basis of Fanconi anemia

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel diagnostic screen for defects in the Fanconi anemia pathway

21 January 2018

1 reference

Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases

21 January 2018

1 reference

Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair

21 January 2018

1 reference

Drosophila MUS312 and the vertebrate ortholog BTBD12 interact with DNA structure-specific endonucleases in DNA repair and recombination

21 January 2018

1 reference

Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair

21 January 2018

1 reference

First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure

21 January 2018

1 reference

Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients

21 January 2018

1 reference

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

21 January 2018

1 reference

12 December 2020

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype

1 reference

12 December 2020

Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia

1 reference

12 December 2020

Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.

1 reference

12 December 2020

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

1 reference

7 January 2021