(Q39219607)

10 September 2017

title

From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family (English)

1 reference

severe combined immunodeficiency

10 September 2017

main subject

1 reference

1 reference

Oscar de la Calle-Martin

object named as

Oscar de la Calle-Martin

9

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Andrea Martín-Nalda

object named as

Andrea Martin-Nalda

4

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Laia Alsina

object named as

Laia Alsina

8

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author name string

Laura Martinez-Martinez

1

1 reference

10 September 2017

Marta Vazquez-Ortiz

2

1 reference

10 September 2017

Cecilia Gonzalez-Santesteban

3

1 reference

10 September 2017

Asunción Vicente

5

1 reference

10 September 2017

Ana M Plaza

6

1 reference

10 September 2017

Isabel Badell

7

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10 September 2017

publication date

13 August 2012

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Pediatric Allergy & Immunology

10 September 2017

published in

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10 September 2017

volume

23

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10 September 2017

issue

7

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10 September 2017

page(s)

660-666

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RAG mutations in human B cell-negative SCID.

10 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

RAG-1 and RAG-2, adjacent genes that synergistically activate V(D)J recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Partial V(D)J recombination activity leads to Omenn syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Impaired thymic output and restricted T-cell repertoire in two infants with immunodeficiency and early-onset generalized dermatitis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Omenn syndrome does not live by V(D)J recombination alone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Sequence and chromosome assignment to 11p13-p12 of human RAG genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Stem cell transplantation for congenital immunodeficiencies using reduced-intensity conditioning

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Making sense of inflammation, epigenetics, and memory CD8+ T-cell differentiation in the context of infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

Gene-Specific Epigenetic Regulation in Serious Infections with Systemic Inflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-3038.2012.01339.X

10.1111/J.1399-3038.2012.01339.X

21 January 2018

Identifiers

DOI

1 reference

10 September 2017

1 reference