(Q64387245)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19953608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events (English)

1 reference

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13 February 2020

9

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13 February 2020

17

Stephan Ehl

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13 February 2020

author name string

Ulrich Pannicke

1

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13 February 2020

Manfred Hönig

2

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13 February 2020

Ilka Schulze

3

1 reference

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13 February 2020

Jan Rohr

4

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13 February 2020

Gitta A Heinz

5

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13 February 2020

Sylvia Braun

6

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13 February 2020

Ingrid Janz

7

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13 February 2020

Eva-Maria Rump

8

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13 February 2020

Susanne Matthes-Martin

10

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13 February 2020

Jan Soerensen

11

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13 February 2020

Johann Greil

12

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13 February 2020

Daniel K Stachel

13

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13 February 2020

Bernd H Belohradsky

14

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13 February 2020

Michael H Albert

15

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13 February 2020

Ansgar Schulz

16

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13 February 2020

Wilhelm Friedrich

18

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13 February 2020

Klaus Schwarz

19

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13 February 2020

language of work or name

English

0 references

publication date

1 February 2010

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13 February 2020

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13 February 2020

volume

31

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13 February 2020

issue

2

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13 February 2020

page(s)

197-207

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Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly

13 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Ataxia-telangiectasia-mutated dependent phosphorylation of Artemis in response to DNA damage.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

A histidine in the beta-CASP domain of Artemis is critical for its full in vitro and in vivo functions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Interplay between Ku, Artemis, and the DNA-dependent protein kinase catalytic subunit at DNA ends

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Omenn syndrome due to ARTEMIS mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Radiation-induced delayed cell death in a hypomorphic Artemis cell line.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

DNA-PK autophosphorylation facilitates Artemis endonuclease activity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Expansion of clonotype-restricted HLA-identical maternal CD4+ T cells in a patient with severe combined immunodeficiency and a homozygous mutation in the Artemis gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Artemis sheds new light on V(D)J recombination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

The DNA-dependent protein kinase catalytic subunit phosphorylation sites in human Artemis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

The Artemis:DNA-PKcs endonuclease cleaves DNA loops, flaps, and gaps

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

The V(D)J recombination/DNA repair factor artemis belongs to the metallo-beta-lactamase family and constitutes a critical developmental checkpoint of the lymphoid system

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Damaging-agent sensitivity of Artemis-deficient cell lines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

DNA-PKcs dependence of Artemis endonucleolytic activity, differences between hairpins and 5' or 3' overhangs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Functional and biochemical dissection of the structure-specific nuclease ARTEMIS

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Phosphorylation of Artemis following irradiation-induced DNA damage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

The metallo-beta-lactamase/beta-CASP domain of Artemis constitutes the catalytic core for V(D)J recombination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

A pathway of double-strand break rejoining dependent upon ATM, Artemis, and proteins locating to gamma-H2AX foci.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

RAG mutations in human B cell-negative SCID.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Artemis phosphorylated by DNA-dependent protein kinase associates preferentially with discrete regions of chromatin.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

MEIG1 localizes to the nucleus and binds to meiotic chromosomes of spermatocytes as they initiate meiosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Defective Artemis nuclease is characterized by coding joints with microhomology in long palindromic-nucleotide stretches

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Artemis deficiency confers a DNA double-strand break repair defect and Artemis phosphorylation status is altered by DNA damage and cell cycle progression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

MEIG1 is essential for spermiogenesis in mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Artemis is a phosphorylation target of ATM and ATR and is involved in the G2/M DNA damage checkpoint response

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21168

7 January 2021

Identifiers

DOI

10.1002/HUMU.21168

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19953608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference