(Q56901696)

4

object named as

Charlotte Cunningham-Rundles

0 references

author name string

Adina Kay Knight

1

0 references

Davide Serrano

2

0 references

Yaron Tomer

Journal of Clinical Immunology

3

0 references

language of work or name

English

0 references

publication date

January 2007

0 references

published in

0 references

volume

27

0 references

issue

1

0 references

page(s)

95-100

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s10875-006-9049-8

0 references

cites work

CTLA-4 gene polymorphism at position 49 in exon 1 reduces the inhibitory function of CTLA-4 and contributes to the pathogenesis of Graves' disease

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10875-006-9049-8

TLR9 activation is defective in common variable immune deficiency.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10875-006-9049-8

Analysis of the CTLA-4, CD28, and inducible costimulator (ICOS) genes in autoimmune thyroid disease

21 January 2018

1 reference

12 December 2020

Caseating cutaneous granulomas in a child with common variable immunodeficiency.

1 reference

12 December 2020

Pulmonary complications of primary immunodeficiencies

1 reference

12 December 2020

Immune competence and switched memory B cells in common variable immunodeficiency.

1 reference

12 December 2020

Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects.

1 reference

12 December 2020

CTLA-4 and its role in autoimmune thyroid disease

1 reference

12 December 2020

Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID).

1 reference

12 December 2020

Granulomas in common variable immunodeficiency: a diagnostic dilemma

1 reference

12 December 2020

Efficacy of intravenous immunoglobulin in the prevention of pneumonia in patients with common variable immunodeficiency

1 reference

12 December 2020

Mannose Binding Lectin Polymorphisms are Associated With Early Age of Disease Onset and Autoimmunity in Common Variable Immunodeficiency

1 reference

12 December 2020

Autoimmune manifestations in common variable immunodeficiency

1 reference

12 December 2020

Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease

1 reference

12 December 2020

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 reference

12 December 2020

CTLA-4 polymorphisms and systemic lupus erythematosus (SLE): a meta-analysis

1 reference

12 December 2020

Common variable immunodeficiency: clinical and immunological features of 248 patients.

1 reference

12 December 2020

ICOS costimulation requires IL-2 and can be prevented by CTLA-4 engagement

1 reference

12 December 2020

Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease

1 reference

12 December 2020

Clinical and immunologic analyses of 103 patients with common variable immunodeficiency

1 reference

12 December 2020

Inhibition of human T cell proliferation by CTLA-4 utilizes CD80 and requires CD25+ regulatory T cells.

1 reference

12 December 2020

Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

1 reference

12 December 2020

Practice parameter for the diagnosis and management of primary immunodeficiency

1 reference

12 December 2020

Type 1 diabetes is insulin -2221 MspI and CTLA-4 +49 A/G polymorphism dependent

1 reference

12 December 2020

B cell co-receptors regulating T cell-dependent antibody production in common variable immunodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients

1 reference

12 December 2020

Clinical and immunologic studies of common variable immunodeficiency.

1 reference

12 December 2020

Codon 17 polymorphism of the cytotoxic T lymphocyte antigen 4 gene in Hashimoto's thyroiditis and Addison's disease

1 reference

12 December 2020

Primary immunodeficiency disorders: antibody deficiency

1 reference

12 December 2020

Absence of memory B cells in patients with common variable immunodeficiency

1 reference

12 December 2020

Enhanced apoptosis of T cells in common variable immunodeficiency (CVID): role of defective CD28 co-stimulation

1 reference

12 December 2020

Deficient IL-12 and dendritic cell function in common variable immune deficiency

1 reference

12 December 2020

Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma

1 reference

12 December 2020

CTLA-4 blockade in combination with xenogeneic DNA vaccines enhances T-cell responses, tumor immunity and autoimmunity to self antigens in animal and cellular model systems

1 reference

12 December 2020

An association between the CTLA4 exon 1 polymorphism and early rheumatoid arthritis with autoimmune endocrinopathies

1 reference

12 December 2020

A new member of the immunoglobulin superfamily--CTLA-4

1 reference

12 December 2020

Treatment of rheumatoid arthritis by selective inhibition of T-cell activation with fusion protein CTLA4Ig

1 reference

12 December 2020

Costimulatory blockade in patients with rheumatoid arthritis: a pilot, dose-finding, double-blind, placebo-controlled clinical trial evaluating CTLA-4Ig and LEA29Y eighty-five days after the first infusion

1 reference

12 December 2020

Granulomatous disease in common variable immunodeficiency

1 reference

12 December 2020

Study of the B cell memory compartment in common variable immunodeficiency.

1 reference

12 December 2020

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

1 reference

12 December 2020

Autoimmunity correlates with tumor regression in patients with metastatic melanoma treated with anti-cytotoxic T-lymphocyte antigen-4.

1 reference

12 December 2020

CD28 and inducible costimulatory protein Src homology 2 binding domains show distinct regulation of phosphatidylinositol 3-kinase, Bcl-xL, and IL-2 expression in primary human CD4 T lymphocytes

1 reference

12 December 2020

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

1 reference

12 December 2020

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

12 December 2020

Limited genetic susceptibility to severe Graves' ophthalmopathy: no role for CTLA-4 but evidence for an environmental etiology

1 reference

12 December 2020

CTLA-4 and not CD28 is a susceptibility gene for thyroid autoantibody production

1 reference

12 December 2020

Cutaneous granulomas masquerading as tuberculoid leprosy in a patient with congenital combined immunodeficiency

1 reference

12 December 2020