(Q33395963)

26 July 2017

title

Monozygotic twin pair showing discordant phenotype for X-linked thrombocytopenia and Wiskott-Aldrich syndrome: a role for epigenetics? (English)

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26 July 2017

main subject

Wiskott-Aldrich syndrome

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3

Diane Nugent

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26 July 2017

1

David Buchbinder

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26 July 2017

2

Kari Nadeau

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26 July 2017

publication date

28 June 2011

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Journal of Clinical Immunology

26 July 2017

published in

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26 July 2017

volume

31

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26 July 2017

issue

5

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26 July 2017

page(s)

773-777

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The molecular pathology of primary immunodeficiencies

26 July 2017

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21 January 2018

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Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

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Clinical course of patients with WASP gene mutations

21 January 2018

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Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product

21 January 2018

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21 January 2018

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Regulatory T cell dysfunction in subjects with common variable immunodeficiency complicated by autoimmune disease

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Idiopathic neutropenia of childhood is associated with Fas/FasL expression.

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Selective deregulation in chemokine signaling pathways of CD4+CD25(hi)CD127(lo)/(-) regulatory T cells in human allergic asthma

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Primary immunodeficiencies

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12 December 2020

Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype

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12 December 2020

Epigenetic cancer therapy makes headway

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12 December 2020

The relations between genetics and epigenetics: a historical point of view.

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12 December 2020

Wiskott-Aldrich syndrome in identical twins: abnormality of CD4 and CD8 positive lymphocytes

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12 December 2020

10.1007/S10875-011-9561-3

Identifiers

DOI

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Dimensions Publication ID

26 July 2017

1003551310

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1 reference