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Literature DB >> 25086867

Familial hypertryptasemia with associated mast cell activation syndrome.

Vito Sabato¹, Els Van De Vijver², Margo Hagendorens³, Inge Vrelust⁴, Edwin Reyniers⁵, Erik Fransen⁵, Chris Bridts¹, Luc De Clerck¹, Geert Mortier⁶, Peter Valent⁷, Didier Ebo⁸.

Abstract

Entities: Disease

Mesh：

Substances：
Tryptases

Year: 2014 PMID： 25086867 DOI： 10.1016/j.jaci.2014.06.007

Source DB: PubMed Journal: J Allergy Clin Immunol ISSN： 0091-6749 Impact factor: 10.793

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Cited

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9 in total

Review 1. Hereditary Alpha-Tryptasemia: a Commonly Inherited Modifier of Anaphylaxis.

Authors: Richard Wu; Jonathan J Lyons
Journal: Curr Allergy Asthma Rep Date: 2021-05-10 Impact factor: 4.806

Review 2. Mast cell proteases as pharmacological targets.

Authors: George H Caughey
Journal: Eur J Pharmacol Date: 2015-05-07 Impact factor: 4.432

3. Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.

Authors: Jonathan J Lyons; Xiaomin Yu; Jason D Hughes; Quang T Le; Ali Jamil; Yun Bai; Nancy Ho; Ming Zhao; Yihui Liu; Michael P O'Connell; Neil N Trivedi; Celeste Nelson; Thomas DiMaggio; Nina Jones; Helen Matthews; Katie L Lewis; Andrew J Oler; Ryan J Carlson; Peter D Arkwright; Celine Hong; Sherene Agama; Todd M Wilson; Sofie Tucker; Yu Zhang; Joshua J McElwee; Maryland Pao; Sarah C Glover; Marc E Rothenberg; Robert J Hohman; Kelly D Stone; George H Caughey; Theo Heller; Dean D Metcalfe; Leslie G Biesecker; Lawrence B Schwartz; Joshua D Milner
Journal: Nat Genet Date: 2016-10-17 Impact factor: 38.330

4. First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease.

Authors: Vito Sabato; Jack Chovanec; Margaretha Faber; Joshua D Milner; Didier Ebo; Jonathan J Lyons
Journal: J Clin Immunol Date: 2018-05-11 Impact factor: 8.317

5. New developments in the field of mastocytosis and mast cell activation syndromes: a summary of the Annual Meeting of the European Competence Network on Mastocytosis (ECNM) 2019.

Authors: Michel Arock; Karl Sotlar; Jason Gotlib; Wolfgang R Sperr; Karin Hartmann; Lawrence B Schwartz; Cem Akin; Hans-Peter Horny; Peter Valent
Journal: Leuk Lymphoma Date: 2019-12-26

Familial hypertryptasemia with associated mast cell activation syndrome.

Review 1. Hereditary Alpha-Tryptasemia: a Commonly Inherited Modifier of Anaphylaxis.

Review 2. Mast cell proteases as pharmacological targets.

3. Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.

4. First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease.

5. New developments in the field of mastocytosis and mast cell activation syndromes: a summary of the Annual Meeting of the European Competence Network on Mastocytosis (ECNM) 2019.

6. Massive release of the histamine-degrading enzyme diamine oxidase during severe anaphylaxis in mastocytosis patients.

7. Lipidomic analysis of urinary exosomes from hereditary α-tryptasemia patients and healthy volunteers.

Review 8. Mediator-Related Symptoms and Anaphylaxis in Children with Mastocytosis.

Review 9. The serum tryptase test: an emerging robust biomarker in clinical hematology.