(Q81352872)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509675%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency (English)

1 reference

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8 January 2020

1 reference

1 reference

8

1 reference

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8 January 2020

5

Barbara H Barendregt

1 reference

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8 January 2020

9

Mirjam van der Burg

1 reference

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8 January 2020

3

Hasibe Artac

1 reference

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8 January 2020

6

Ismail Reisli

1 reference

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8 January 2020

author name string

Tuba Turul

1

1 reference

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8 January 2020

Ilhan Tezcan

2

1 reference

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8 January 2020

Sandra de Bruin-Versteeg

4

1 reference

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8 January 2020

Ozden Sanal

7

1 reference

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8 January 2020

publication date

29 May 2008

1 reference

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European Journal of Pediatrics

8 January 2020

published in

1 reference

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8 January 2020

volume

168

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8 January 2020

issue

1

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8 January 2020

page(s)

87-93

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https://scigraph.springernature.com/pub.10.1007/s00431-008-0718-x

8 January 2020

exact match

0 references

cites work

ZAP-70 and defects of T-cell receptor signaling

1 reference

12 December 2020

Alternative antigen receptor (TCR) signaling in T cells derived from ZAP-70-deficient patients expressing high levels of Syk

1 reference

12 December 2020

Genes, pathways and checkpoints in lymphocyte development and homeostasis.

1 reference

12 December 2020

Molecular defects in T- and B-cell primary immunodeficiency diseases

1 reference

12 December 2020

Defective expression of p56lck in an infant with severe combined immunodeficiency

1 reference

12 December 2020

Primary immunodeficiency diseases: dissectors of the immune system

1 reference

12 December 2020

Specific immunoglobulin E responses in ZAP-70-deficient patients are mediated by Syk-dependent T-cell receptor signalling

1 reference

12 December 2020

Temperature-sensitive ZAP70 mutants degrading through a proteasome-independent pathway. Restoration of a kinase domain mutant by Cdc37.

1 reference

12 December 2020

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

1 reference

12 December 2020

Molecular genetics of the Bare lymphocyte syndrome

1 reference

12 December 2020

Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase

1 reference

12 December 2020

An antibody-deficiency syndrome due to mutations in the CD19 gene

1 reference

12 December 2020

Phenotypic features of selective T cell deficiency characterized by absence of CD8+ T lymphocytes and undetectable mRNA for ZAP-70 kinase

1 reference

12 December 2020

Defective T cell receptor signaling and CD8+ thymic selection in humans lacking zap-70 kinase

1 reference

12 December 2020

Depletion of CD8+ cells in human thymic medulla results in selective immune deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Existence of activated and memory CD4+ T cells in peripheral blood and their skin infiltration in CD8 deficiency.

1 reference

12 December 2020

1 reference

12 December 2020

Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70.

1 reference

12 December 2020

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants

1 reference

12 December 2020

Familial CD8 deficiency due to a mutation in the CD8 alpha gene.

1 reference

12 December 2020