(Q35946132)

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Expansion of somatically reverted memory CD8+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Expansion of somatically reverted memory CD8+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Epstein–Barr virus

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3

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28 January 2020

4

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28 January 2020

5

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28 January 2020

6

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28 January 2020

7

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28 January 2020

15

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28 January 2020

19

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28 January 2020

Bodo Grimbacher

13

object named as

Bodo Grimbacher

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Europe PubMed Central

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28 January 2020

author name string

Umaimainthan Palendira

1

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28 January 2020

Carol Low

2

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28 January 2020

Sharon Choo

8

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28 January 2020

Joanne M Smart

9

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28 January 2020

Vassilios Lougaris

10

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28 January 2020

Silvia Giliani

11

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28 January 2020

Rebecca H Buckley

12

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28 January 2020

Frank Alvaro

14

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Europe PubMed Central

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28 January 2020

Kim E Nichols

16

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Stephen Adelstein

17

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Alan B Rickinson

18

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28 January 2020

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9 April 2012

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28 January 2020

Journal of Experimental Medicine

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28 January 2020

209

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28 January 2020

5

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

913-924

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

SLAM family receptors and SAP adaptors in immunity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Revertant T lymphocytes in a patient with Wiskott-Aldrich syndrome: analysis of function and distribution in lymphoid organs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Restimulation-induced apoptosis of T cells is impaired in patients with X-linked lymphoproliferative disease caused by SAP deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

SLAM receptors and SAP influence lymphocyte interactions, development and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Somatic mosaicism in primary immune deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Reversion mutations in patients with leukocyte adhesion deficiency type-1 (LAD-1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Cellular responses to viral infection in humans: lessons from Epstein-Barr virus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Regulation of cellular and humoral immune responses by the SLAM and SAP families of molecules.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Signaling lymphocyte activation molecule-associated protein is a negative regulator of the CD8 T cell response in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

The impact of telomere erosion on memory CD8+ T cells in patients with X-linked lymphoproliferative syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Impaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

In vivo reversion to normal of inherited mutations in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Absence of Epstein-Barr virus DNA in the tumor cells of European hepatocellular carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Expression of CD57 defines replicative senescence and antigen-induced apoptotic death of CD8+ T cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

X-linked recessive progressive combined variable immunodeficiency (Duncan's disease)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

2 October 2017

Impaired Epstein-Barr virus-specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Revertant mosaicism--patchwork in the skin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Rapid identification and sorting of viable virus-reactive CD4(+) and CD8(+) T cells based on antigen-triggered CD137 expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Epstein-Barr virus persistence in the absence of conventional memory B cells: IgM+IgD+CD27+ B cells harbor the virus in X-linked lymphoproliferative disease patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

SAP controls the cytolytic activity of CD8+ T cells against EBV-infected cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348103

24 September 2018

Sensitive and viable identification of antigen-specific CD8+ T cells by a flow cytometric assay for degranulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infectious mononucleosis in a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of NKT cell development by SAP, the protein defective in XLP

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense mutations in SH2D1A identified in patients with X-linked lymphoproliferative disease differentially affect the expression and function of SAP

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic revertant mosaicism in a patient with leukocyte adhesion deficiency type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased proliferation of CD8+ T cells in SAP-deficient mice is associated with impaired activation-induced cell death

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and immunologic consequences of a somatic reversion in a patient with X-linked severe combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenomenon of spontaneous genetic reversions in the Wiskott-Aldrich syndrome: a report of the workshop of the ESID Genetics Working Party at the XIIth Meeting of the European Society for Immunodeficiencies (ESID). Budapest, Hungary October 4-7,

1 reference

https://pubmed.ncbi.nlm.nih.gov/22493517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1084/JEM.20112391

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22493517%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

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