(Q34832611)

English

Relevance of laboratory testing for the diagnosis of primary immunodeficiencies: a review of case-based examples of selected immunodeficiencies

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scholarly article

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Europe PubMed Central

PubMed publication ID

4 August 2017

1 reference

Europe PubMed Central

Relevance of laboratory testing for the diagnosis of primary immunodeficiencies: a review of case-based examples of selected immunodeficiencies (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

author name string

Roshini S Abraham

1

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

publication date

9 April 2011

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Clinical and Molecular Allergy

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

copyright license

Creative Commons Attribution 2.0 Generic

9 April 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

https://scigraph.springernature.com/pub.10.1186/1476-7961-9-6

0 references

A model for harmonizing flow cytometry in clinical trials

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X-linked lymphoproliferative syndromes: brothers or distant cousins?

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8 July 2018

TLR signaling and effector functions are intact in XLA neutrophils

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8 July 2018

Implementing routine testing for severe combined immunodeficiency within Wisconsin's newborn screening program

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8 July 2018

Systematic evidence review of newborn screening and treatment of severe combined immunodeficiency

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8 July 2018

Immune reconstitution after allogeneic transplantation and expanding options for immunomodulation: an update

1 reference

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8 July 2018

WASP: a key immunological multitasker

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8 July 2018

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options

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8 July 2018

Diversity in T cell memory: an embarrassment of riches

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8 July 2018

Laboratory evaluation of primary immunodeficiencies

1 reference

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8 July 2018

Primary immunodeficiencies: 2009 update

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8 July 2018

Thymus microenvironment in human primary immunodeficiency diseases.

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8 July 2018

Mutation analysis in primary immunodeficiency diseases: case studies

1 reference

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8 July 2018

Long-term clinical outcome of patients with severe combined immunodeficiency who received related donor bone marrow transplants without pretransplant chemotherapy or post-transplant GVHD prophylaxis

1 reference

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8 July 2018

Profiling of polychromatic flow cytometry data on B-cells reveals patients' clusters in common variable immunodeficiency.

1 reference

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8 July 2018

Bioinformatics services related to diagnosis of primary immunodeficiencies

1 reference

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8 July 2018

A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity.

1 reference

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8 July 2018

A partial form of recessive STAT1 deficiency in humans

1 reference

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8 July 2018

Primary B cell immunodeficiencies: comparisons and contrasts

1 reference

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8 July 2018

Cortisol and epinephrine control opposing circadian rhythms in T cell subsets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

CD56bright natural killer (NK) cells: an important NK cell subset.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Optimizing outcomes of hematopoietic stem cell transplantation for severe combined immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Human natural killer cell subsets and acute exercise: a brief review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Quantifying the development of the peripheral naive CD4+ T-cell pool in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Is it necessary to identify molecular defects in primary immunodeficiency disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Applications of flow cytometry for the study of primary immune deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

X-linked chronic granulomatous disease secondary to skewed X chromosome inactivation in a female with a novel CYBB mutation and late presentation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

A chemical method for fast and sensitive detection of DNA synthesis in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

T cell subset-specific susceptibility to aging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Hematopoietic stem cell transplantation for primary immunodeficiency disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Population-based newborn screening for severe combined immunodeficiency: steps toward implementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

STAT3 mutations in the hyper-IgE syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Measuring lymphocyte proliferation, survival and differentiation using CFSE time-series data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Monitoring lymphocyte proliferation in vitro and in vivo with the intracellular fluorescent dye carboxyfluorescein diacetate succinimidyl ester

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Delayed immune reconstitution after cord blood transplantation is characterized by impaired thymopoiesis and late memory T-cell skewing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Role of flow cytometry in the diagnosis and monitoring of primary immunodeficiency disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Determining thymic output quantitatively: using models to interpret experimental T-cell receptor excision circle (TREC) data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

The JAK-STAT signaling pathway: input and output integration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Human natural killer cell deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Immunodeficiency mutation databases (IDbases).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Human complete Stat-1 deficiency is associated with defective type I and II IFN responses in vitro but immunity to some low virulence viruses in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

WASP and the phenotypic range associated with deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Immune restoration following hematopoietic stem cell transplantation: an evolving target

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Phagocyte immunodeficiencies and their infections

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

IgA nephropathy associated with X-linked thrombocytopenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Regulation of JAK-STAT signalling in the immune system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Clinical course of patients with WASP gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Immune monitoring: it's prudent to adopt current quality regulations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Reconstitution of thymic function after stem cell transplantation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

X-linked thrombocytopenia in a girl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Molecular characterization of the T cell repertoire using immunoscope analysis and its possible implementation in clinical practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

T cell receptor excision circles as markers for recent thymic emigrants: basic aspects, technical approach, and guidelines for interpretation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

The biology of human natural killer-cell subsets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

11-color, 13-parameter flow cytometry: identification of human naive T cells by phenotype, function, and T-cell receptor diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Primary immunodeficiency mutation databases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Dynamics of T lymphocyte responses: intermediates, effectors, and memory cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Identification of a human recent thymic emigrant phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

A direct estimate of the human alphabeta T cell receptor diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Effects of sleep and circadian rhythm on human circulating immune cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Flow cytometric analysis of the granulocyte respiratory burst: a comparison study of fluorescent probes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Rapid whole-blood flow cytometry assay for diagnosis of chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

X-linked inheritance in females with chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as 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=3080807

8 July 2018

Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

8 July 2018

Functional flow cytometry testing: an emerging approach for the evaluation of genetic disease.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Genotype/phenotype correlations in X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Identification of a Btk mutation in a dysgammaglobulinemic patient with reduced B cells: XLA diagnosis or not?

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Possible application of flow cytometry for evaluation of the structure and functional status of WASP in peripheral blood mononuclear cells.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

The Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivation.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Carriers of X-linked chronic granulomatous disease at risk

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Measurement of peripheral B cell subpopulations in common variable immunodeficiency (CVID) using a whole blood method.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

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/10.1186%2F1476-7961-9-6

21 January 2018

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

The EUROclass trial: defining subgroups in common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Two subsets of naive T helper cells with distinct T cell receptor excision circle content in human adult peripheral blood

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

The descent of memory T-cell subsets.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Primary defect in CD8+ lymphocytes in the antibody deficiency disease (common variable immunodeficiency): abnormalities in intracellular production of interferon-gamma (IFN-gamma) in CD28+ ('cytotoxic') and CD28- ('suppressor') CD8+ subsets.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Phenotypically and functionally distinct subsets of natural killer cells in human PBMCs.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

T-cell repertoires in healthy and diseased human tissues analysed by T-cell receptor beta-chain CDR3 size determination: evidence for oligoclonal expansions in tumours and inflammatory diseases

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Analysis of in vitro lymphocyte proliferation as a screening tool for cellular immunodeficiency

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

CFSE flow cytometric quantification of lymphocytic proliferation in extracorporeal photopheresis: use for quality control

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

EdU incorporation is an alternative non-radioactive assay to [(3)H]thymidine uptake for in vitro measurement of mice T-cell proliferations

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Intracellular phospho-protein staining techniques for flow cytometry: monitoring single cell signaling events

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutation.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Development of a routine newborn screening protocol for severe combined immunodeficiency

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

High-throughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cards.

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Assessment of lymphocyte proliferation: CFSE kills dividing cells and modulates expression of activation markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Unravelling the complexity of T cell abnormalities in common variable immunodeficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Determination of carrier status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wiskott-Aldrich syndrome protein expression in peripheral blood mononuclear cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Renal transplantation in Wiskott-Aldrich syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3080807

26 October 2018

Genotype-dependent variability in flow cytometric evaluation of reduced nicotinamide adenine dinucleotide phosphate oxidase function in patients with chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

Defect of regulatory T cells in patients with Omenn syndrome

1 reference

https://api.crossref.org/works/10.1186%2F1476-7961-9-6

21 January 2018

T cell repertoire development in humans with SCID after nonablative allogeneic marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked thrombocytopenia identified by flow cytometric demonstration of defective Wiskott-Aldrich syndrome protein in lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activated human T cells accomplish MHC class II expression through T cell-specific occupation of class II transactivator promoter III

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

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/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early determinants of long-term T-cell reconstitution after hematopoietic stem cell transplantation for severe combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired Toll-like receptor 8-mediated IL-6 and TNF-alpha production in antigen-presenting cells from patients with X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wiskott-Aldrich syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunologic defects in 22q11.2 deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thymectomy in early childhood: significant alterations of the CD4(+)CD45RA(+)CD62L(+) T cell compartment in later life

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statewide newborn screening for severe T-cell lymphopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluctuation of peripheral blood T, B, and NK cells during a menstrual cycle of normal healthy women

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of peripheral blood B cells in patients with X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of lymphomas in a subgroup of wiskott–aldrich syndrome patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studying X inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked agammaglobulinemia: report on a United States registry of 201 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of immunodeficiency in a patient with growth hormone insensitivity secondary to a novel STAT5b gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interferon gamma, IL-12, IL-12R and STAT-1 immunodeficiency diseases: disorders of the interface of innate and adaptive immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency: a heterogeneous group needs further subclassification

1 reference

https://pubmed.ncbi.nlm.nih.gov/21477322

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1476-7961-9-6

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 August 2017

ResearchGate publication ID

0 references

Sitelinks

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