(Q38317263)

2 September 2017

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders (English)

1 reference

2 September 2017

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1 reference

T Wada

1

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2 September 2017

K Takei

2

1 reference

2 September 2017

M Kudo

3

1 reference

2 September 2017

S Shimura

4

1 reference

2 September 2017

Y Kasahara

5

1 reference

2 September 2017

S Koizumi

6

1 reference

2 September 2017

K Kawa-Ha

7

1 reference

2 September 2017

Y Ishida

8

1 reference

2 September 2017

S Imashuku

9

1 reference

2 September 2017

H Seki

10

1 reference

2 September 2017

A Yachie

11

1 reference

2 September 2017

1 January 2000

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Clinical and Experimental Immunology

2 September 2017

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2 September 2017

119

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2 September 2017

148-155

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2 September 2017

1

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Oxidative stress causes enhanced endothelial cell injury in human heme oxygenase-1 deficiency

2 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

Developmental changes and functional properties of human memory T cell subpopulations defined by CD60 expression.

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

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

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

RAG mutations in human B cell-negative SCID.

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

Omenn's syndrome--pathologic arguments in favor of a graft versus host pathogenesis: a report of nine cases

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

Clinical and immunological findings in four infants with Omenn's syndrome: a form of severe combined immunodeficiency with phenotypically normal T cells, elevated IgE, and eosinophilia

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

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

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

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

16 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905546

Familial Reticuloendotheliosis with Eosinophilia

16 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1046%2FJ.1365-2249.2000.01101.X

Combined immunodeficiency and reticuloendotheliosis with eosinophilia

21 January 2018

1 reference

12 December 2020

Syndrome of erythroderma, failure to thrive, and diarrhea in infancy: a manifestation of immunodeficiency

1 reference

12 December 2020

Novel T-lymphocyte population in combined immunodeficiency with features of graft-versus-host disease

1 reference

12 December 2020

Immune status in two brothers with Omenn's syndrome: no discernible chimerism on FACS analysis using a monoclonal antibody specific for a maternally restricted HLA antigen

1 reference

12 December 2020

Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thrive

1 reference

12 December 2020

A case of Omenn-like immunodeficiency syndrome

1 reference

12 December 2020

T helper type 2-like cells and therapeutic effects of interferon-gamma in combined immunodeficiency with hypereosinophilia (Omenn's syndrome)

1 reference

12 December 2020

Expansion of CD3+CD4-CD8- T cell population expressing high levels of IL-5 in Omenn's syndrome

1 reference

12 December 2020

CD30 cell expression and abnormal soluble CD30 serum accumulation in Omenn's syndrome: evidence for a T helper 2-mediated condition

1 reference

12 December 2020

Oligoclonal expansion of CD45RO+ T lymphocytes in Omenn syndrome

1 reference

12 December 2020

In vitro cell death of activated lymphocytes in Omenn's syndrome

1 reference

12 December 2020

Novel Fas (CD95/APO-1) mutations in infants with a lymphoproliferative disorder

1 reference

12 December 2020

T-cell receptor analysis in Omenn's syndrome: evidence for defects in gene rearrangement and assembly

1 reference

12 December 2020

The Omenn's syndrome: histological, immunohistochemical and ultrastructural evidence for a partial T cell deficiency evolving in an abnormal proliferation of T lymphocytes and S-100 +/T-6 + Langerhans-like cells

1 reference

12 December 2020

10.1046/J.1365-2249.2000.01101.X

Identifiers

DOI

1 reference

2 September 2017

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1 reference