Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation

30 Jan 2020

Abstract excerpt

International audience

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autoimmune and Inflammatory Disorders Research
Share to Immune Cell Function and Interaction
Share to Immunodeficiency and Autoimmune Disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33054089
DOI: 10.3324/haematol.2019.231399

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulationPMID 33054089Read ↗

PI3K pathway defects leading to immunodeficiency and immune dysregulationSemantic proximity Read ↗

Immunodeficiency due to a novel variant in PIK3CD: a case report.Semantic proximity Read ↗

The double-edged sword of PI3Kδ pathway-related immune dysregulation: insights from two case reports.Semantic proximity Read ↗

Genomic crossroads between non-Hodgkin’s lymphoma and common variable immunodeficiencySemantic proximity Read ↗

Somatic mutations and T-cell clonality in patients with immunodeficiency.Semantic proximity Read ↗

Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency.Semantic proximity Read ↗

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.Semantic proximity Read ↗

The Iceberg Map of germline mutations in childhood cancer: focus on primary immunodeficiencies.Semantic proximity Read ↗

An overview of germline variations in genes of primary immunodeficiences through integrative analysis of ClinVar, HGMD® and dbSNP databases.Semantic proximity Read ↗

Complicated Common Variable Immunodeficiency is Driven by Aberrant IL-10/IL-21 Signaling and Predisposed Polygenic RiskSemantic proximity Read ↗

Hyperactivation of the PI3K pathway in inborn errors of immunity: current understanding and therapeutic perspectivesSemantic proximity Read ↗

A human immunodeficiency caused by mutations in the PIK3R1 gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.