(Q50950766)

English

Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.

scientific article published on 15 June 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

4

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

author name string

Necil Kutukculer

1

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Nesrin Gulez

2

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Neslihan E Karaca

3

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Afig Berdeli

5

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

publication date

15 June 2012

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Journal of Clinical Immunology

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

32

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

6

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

1165-1179

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Common variable immunodeficiency: a new look at an old disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Antibody deficiency diseases.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Common variable immunodeficiency: The power of co-stimulation.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

The European internet-based patient and research database for primary immunodeficiencies: update 2011.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Genetic defects in common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

CD20 deficiency in humans results in impaired T cell-independent antibody responses

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Memory B cells in common variable immunodeficiency: clinical associations and sex differences

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

The EUROclass trial: defining subgroups in common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Current perspectives on common variable immunodeficiency (CVID).

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

The French national registry of primary immunodeficiency diseases.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Common variable immunodeficiency: 20-yr experience at a single centre

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

[Common variable immunodeficiency. Prognostic factors for lung damage].

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Common variable immune deficiency and autoimmunity

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Memory switched B cell percentage and not serum immunoglobulin concentration is associated with clinical complications in children and adults with specific antibody deficiency and common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Utility of peripheral blood B cell subsets analysis in common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Age-matched reference values for B-lymphocyte subpopulations and CVID classifications in children

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Differential surrogate light chain expression governs B-cell differentiation

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

TACItly changing tunes: farewell to a yin and yang of BAFF receptor and TACI in humoral immunity? New genetic defects in common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Lymphocyte characteristics in children with common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

HLA class I supertypes: a revised and updated classification

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

The role of costimulation in antibody deficiencies: ICOS and common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

ICOS deficiency in patients with common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9717-9

21 January 2018

Common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary immunodeficiencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and Clinical Manifestations of Patients with Primary Immunodeficiency Disorders in Iran: Update from the Iranian Primary Immunodeficiency Registry

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum immunoglobulin (IgG, IgM, IgA) and IgG subclass concentrations in healthy children: a study using nephelometric technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peripheral blood lymphocyte subsets in healthy Turkish children

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of functional and positional candidate genes in families with common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Granulomatous disease in common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pre-B cell receptor and its function during B cell development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased susceptibility to Mycoplasma infection in patients with hypogammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22699762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10875-012-9717-9

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 March 2018

http://europepmc.org/abstract/MED/22699762

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