Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families (Q34178243)

31 July 2017

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

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severe combined immunodeficiency

31 July 2017

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9

Hans D Ochs

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31 July 2017

Norimoto Kobayashi

1

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31 July 2017

Kazunaga Agematsu

2

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31 July 2017

Kanji Sugita

3

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31 July 2017

Masahiro Sako

4

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31 July 2017

Shigeaki Nonoyama

5

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31 July 2017

Akihiro Yachie

6

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31 July 2017

Satoru Kumaki

7

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31 July 2017

Shigeru Tsuchiya

8

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31 July 2017

Katsuo Sugita

10

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31 July 2017

Yoshimitsu Fukushima

11

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31 July 2017

Atsushi Komiyama

12

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31 July 2017

19 February 2003

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31 July 2017

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31 July 2017

112

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31 July 2017

4

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31 July 2017

348-352

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https://scigraph.springernature.com/pub.10.1007/s00439-002-0897-x

31 July 2017

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cites work

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

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12 December 2020

Three-dimensional clustering of human RAG2 gene mutations in severe combined immune deficiency.

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12 December 2020

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency

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12 December 2020

RAG mutations in human B cell-negative SCID.

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12 December 2020

A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p

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12 December 2020

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

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12 December 2020

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

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12 December 2020

10.1007/S00439-002-0897-X

Identifiers

DOI

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