A rapid flow cytometric screening test for X‐linked lymphoproliferative disease due to XIAP deficiency

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Cytometry. Part B, Clinical cytometry

• Publication date

  2009-09-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/cyto.b.20473PMID 19288545PMCID PMC2728163
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Natural killer T cells and X-linked lymphoproliferative syndrome

  2007cited by this paper
• XIAP: cell death regulation meets copper homeostasis.

  2007cited by this paper
• XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

  2006influential reference
• Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members.

  2005cited by this paper
• Diagnosis and carrier detection of chronic granulomatous disease in five families by flow cytometry.

  1997cited by this paper
• A conserved family of cellular genes related to the baculovirus iap gene and encoding apoptosis inhibitors.

  1996cited by this paper
• Flow cytometric analysis of the granulocyte respiratory burst: a comparison study of fluorescent probes.

  1995cited by this paper
• Generation of Epstein‐Barr Virus (EBV)–Immortalized B Cell Lines

  1991cited by this paper

• Comprehensive flow cytometry-based diagnosis of XIAP deficiency.

  2025cites this paper
• Epstein–Barr virus infection plays a crucial role in triggering hemophagocytic lymphohistiocytosis in patients with X-linked inhibitor of apoptosis protein deficiency

  2025cites this paper
• Issue highlights—September 2024

  2024cites this paper
• Approaching hemophagocytic lymphohistiocytosis

  2023cites this paper
• Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.

  2023cites this paper
• Genes vs environment in inflammatory bowel disease: an update

  2022cites this paper
• X‐linked inhibitor of apoptosis protein represents a promising therapeutic target for relapsed/refractory ALL

  2022cites this paper
• Mechanisms underlying genetic susceptibility to multisystem inflammatory syndrome in children (MIS-C)

  2021cites this paper
• The Growing Need to Understand Very Early Onset Inflammatory Bowel Disease

  2021cites this paper
• Evolution of Our Understanding of XIAP Deficiency

  2021cites this paper
• Application of Cytometry in Primary Immunodeficiencies

  2020cites this paper
• EBV susceptibility

  2020cites this paper
• Laboratory evaluation of primary immunodeficiency disorders

  2020cites this paper
• The role of allogeneic hematopoietic stem cell transplantation and Epstein‐Barr virus infection on the treatment for child primary hemophagocytic lymphohistiocytosis patients with X‐linked lymphoproliferative disease: A rare case report and family survey study

  2020cites this paper
• SLAMF6 in health and disease: Implications for therapeutic targeting.

  2019cites this paper
• Current Flow Cytometric Assays for the Screening and Diagnosis of Primary HLH

  2019cites this paper
• Flow cytometry: Surface markers and beyond

  2019cites this paper
• Early Onset Granulomatous Colitis Associated with a Mutation in NCF4 Resolved with Hematopoietic Stem Cell Transplantation.

  2019cites this paper
• Flow cytometry-based diagnosis of primary immunodeficiency diseases.

  2018cites this paper
• Quantitative Flow Cytometry: Concerns and Recommendations in Clinic and Research

  2018cites this paper
• Diagnostic Tools for Inborn Errors of Human Immunity (Primary Immunodeficiencies and Immune Dysregulatory Diseases)

  2018cites this paper
• 208 – Epstein-Barr Virus (Mononucleosis and Lymphoproliferative Disorders)

  2018cites this paper
• Primer İmmün Yetmezliklerde Akan Hücre Ölçer ile Hücre İçi Protein İfadesinin Tanısal Kullanımı; Marmara Deneyimi

  2018influential citation
• BIRC3 single nucleotide polymorphism associate with asthma susceptibility and the abundance of eosinophils and neutrophils

  2017cites this paper
• Flow cytometry-based diagnosis of primary immunode fi ciency diseases

  2017cites this paper
• Diagnostic dilemmas in HLH: Can T‐cell phenotyping help?

  2017cites this paper
• Nucleotide-binding oligomerization domain (NOD) signaling defects and cell death susceptibility cannot be uncoupled in X-linked inhibitor of apoptosis (XIAP)-driven inflammatory disease

  2017cites this paper
• Primary Hemophagocytic Lymphohistiocytosis

  2017cites this paper
• Evaluation of Natural Killer (NK) Cell Defects

  2016cites this paper
• A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele

  2015cites this paper
• Hemophagocytic lymphohistiocytosis in a female patient due to a heterozygous XIAP mutation and skewed X chromosome inactivation

  2015cites this paper
• Hemophagocytic lymphohistiocytosis: review of etiologies and management

  2014cites this paper
• Issue highlights—July 2014

  2014cites this paper
• Immunodefi ciency Diseases

  2014cites this paper
• XIAP variants in male Crohn's disease

  2014cites this paper
• The X-Linked Lymphoproliferative Syndromes

  2014cites this paper
• Important supplementary tests

  2014cites this paper
• Clinical flow cytometric screening of SAP and XIAP expression accurately identifies patients with SH2D1A and XIAP/BIRC4 mutations

  2014cites this paper
• Hemophagocytic lymphohistiocytosis: advances in pathophysiology, diagnosis, and treatment.

  2013cites this paper
• Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.

  2013cites this paper
• Flow cytometric measurement of SLAM-associated protein and X-linked inhibitor of apoptosis.

  2013cites this paper
• Clinical Cases in Primary Immunodeficiency Diseases

  2012cites this paper
• Modulation of immune signalling by inhibitors of apoptosis.

  2012cites this paper
• Primary immunodeficiency associated with defects in CD1 and CD1‐restricted T cells

  2012cites this paper
• Immune Dysregulation Diseases

  2012cites this paper
• Genetic, cellular and clinical studies of hemophagocytic lymphohistiocytosis

  2012cites this paper
• Clinical features and outcome of X‐linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis

  2012cites this paper
• A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.

  2012cites this paper
• Clinical and Genetic Characteristics of XIAP Deficiency in Japan

  2012influential citation
• Familial hemophagocytic lymphohistiocytosis and X‐linked lymphoproliferative disease

  2011cites this paper
• Treatment of Epstein-Barr Virus-related Hemophagocytic Lymphohistiocytosis (EBV-HLH); Update 2010

  2011cites this paper
• X‐linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma

  2011influential citation
• Early and rapid detection of X‐linked lymphoproliferative syndrome with SH2D1A mutations by flow cytometry

  2011cites this paper
• Secondary hemophagocytic syndrome in adults: a case series of 18 patients in a single institution and a review of literature

  2011cites this paper
• Contemporary diagnostic methods for hemophagocytic lymphohistiocytic disorders.

  2011cites this paper
• Using flow cytometry to screen patients for X-linked lymphoproliferative disease due to SAP deficiency and XIAP deficiency.

  2010cites this paper
• XIAP as a ubiquitin ligase in cellular signaling

  2010cites this paper
• A novel XIAP mutation in a Japanese boy with recurrent pancytopenia and splenomegaly

  2010cites this paper
• Laboratory evaluation of primary immunodeficiencies.

  2010cites this paper
• X-linked lymphoproliferative syndromes: brothers or distant cousins?

  2010cites this paper
• XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease.

  2010cites this paper
• Angeborene Störungen der Immunregulation

  2009cites this paper
• Phenotypic differences between mice deficient in XIAP and SAP, two factors targeted in X-linked lymphoproliferative syndrome (XLP).

  2009cites this paper
• Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome

  2008cites this paper