(Q80119055)

English

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen

scientific article published on 09 April 2007

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17417663%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen (English)

1 reference

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28 December 2019

13

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28 December 2019

author name string

Tono C

1

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28 December 2019

Takahashi Y

2

1 reference

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28 December 2019

Terui K

3

1 reference

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28 December 2019

Sasaki S

4

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28 December 2019

Kamio T

5

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28 December 2019

Tandai S

6

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28 December 2019

Sato T

7

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28 December 2019

Kudo K

8

1 reference

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28 December 2019

Toki T

9

1 reference

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28 December 2019

Tachibana N

10

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28 December 2019

Yoshioka T

11

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28 December 2019

Nakahata T

12

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28 December 2019

Nishikomori R

14

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28 December 2019

Ito E

15

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28 December 2019

publication date

9 April 2007

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28 December 2019

Bone Marrow Transplantation

1 reference

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28 December 2019

39

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28 December 2019

801-804

1 reference

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28 December 2019

12

1 reference

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28 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.bmt.1705658

0 references

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

Transient hemophagocytosis with deficient cellular cytotoxicity, monoclonal immunoglobulin M gammopathy, increased T-cell numbers, and hypomorphic NEMO mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

Single centre experience of umbilical cord stem cell transplantation for primary immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimen

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1705658

7 January 2021

based on heuristic

inferred from DOI database lookup

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