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

Mast cell activation in the context of elevated basal serum tryptase: genetics and presentations.

Current allergy and asthma reports - 27 Nov 2019

Khoury Paneez, Lyons Jonathan J

Abstract excerpt

PURPOSE OF REVIEW: To describe inherited and acquired genetic variants and clinical entities associated with increased basal serum tryptase (BST), distinguish these levels from those which acutely rise due to mast cell activation, and finally to characterize the association between chronically elevated basal serum tryptase and episodic mast cell activation. RECENT FINDINGS: Hereditary alpha-tryptasemia is a...

Read the complete abstract on PubMed

Topics

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

Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
Share to Eosinophilic Disorders and Syndromes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to Genetic Variation

Share to Mast Cells

Share to Mast cells and histamine

Share to Tryptases

Source

Identifiers

PMID: 31776770
DOI: 10.1007/s11882-019-0887-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mast cell activation in the context of elevated basal serum tryptase: genetics and presentations.PMID 31776770Read ↗

Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn.Semantic proximity Read ↗

Resolving the genetics of human tryptases: implications for health, disease, and clinical use as a biomarkerSemantic proximity Read ↗

Mastocytosis and Mast Cell Activation Disorders: Clearing the AirSemantic proximity Read ↗

Hereditary alpha-tryptasemiaSemantic proximity Read ↗

Incorporating Tryptase Genotyping Into the Workup and Diagnosis of Mast Cell Diseases and Reactions.Semantic proximity Read ↗

Diagnosis, Classification and Management of Mast Cell Activation Syndromes (MCAS) in the Era of Personalized Medicine.Semantic proximity Read ↗

Hereditary Alpha-Tryptasemia: a Commonly Inherited Modifier of Anaphylaxis.Semantic proximity Read ↗

Hereditary alpha-tryptasemia in 101 patients with mast cell activation–related symptomatology including anaphylaxisSemantic proximity Read ↗

Clinical impact of the TPSAB1 genotype in mast cell diseases: A REMA study in a cohort of 959 individuals.Semantic proximity Read ↗

Mast cell tryptases in allergic inflammation and immediate hypersensitivity.Semantic proximity Read ↗

Genetically determining individualized clinical reference ranges for the biomarker tryptase can limit unnecessary procedures and unmask myeloid neoplasmsSemantic proximity Read ↗

The Clinical Features of Hereditary Alpha-Tryptasemia—Implications for Interdisciplinary Practice.Semantic proximity Read ↗

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