about
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentEarly-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsDiminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxisERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.GATA3 haploinsufficiency does not block allergic sensitization or atopic disease.FOXP3+ Tregs require WASP to restrain Th2-mediated food allergyMendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities.Atopic dermatitis in children: clinical features, pathophysiology, and treatmentGlycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology.Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseFood allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8-deficient patients.Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.Germline hypomorphic CARD11 mutations in severe atopic disease.Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation.PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients.Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.Primary atopic disorders.First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell DiseaseThe clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolismClinical response to omalizumab in patients with hereditary α-tryptasemiaImpact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia
P50
Q24338530-7E76A3E0-C427-47A8-9788-D00701A5FD2FQ28250725-BA6EF700-E281-41E9-809A-8740DE1302B2Q28383324-3D456039-B0BB-4342-AEBC-6999178C7B5FQ30274910-853F898C-60C4-4E10-8C70-8BDAB5B852D9Q30278844-0EADBC87-DC11-44A3-9508-0FAD3BD538E0Q30354566-A0377CA6-F91F-4B9B-AB90-29CD65C6FF7CQ33594555-A69CFDBF-EFA6-4F26-AB10-55AF78C531FEQ34625597-D0EBD2DE-9DCE-43E6-815A-BFB5475D69F4Q35725275-3F1C77D3-7DE2-4B88-9CD3-6F236C11AD81Q36649404-E26238CA-B450-4D5C-B6FD-76754CCEA520Q36984203-97E44ACD-47AC-4B31-8F73-1537B1AA6090Q38376287-F812AAAF-530A-41E6-88A3-F099C95A677BQ39142799-324D407D-8690-40F6-8027-AE38AEE7AA11Q39623619-B3F97B12-77E4-4A9F-836A-EC65BBC10FCCQ40134025-A5929CC1-411E-421F-9E4A-2F05D4B1C2E5Q41438040-E3251D71-78C8-403B-A575-798B3E0AB159Q52651330-4FFF4973-328B-4CCE-A3E2-EBE179CFBC13Q58616548-ADF28601-A536-4FE8-86D6-77F9D0B39D5BQ90628065-13436A20-5AFC-4A60-88FA-4974A2BA90F5Q90668093-5A374E57-2289-43A4-B8CE-F3AC9761E080Q92133750-5BF0ED67-E75F-4EB0-B4BA-31096A640D02
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jonathan J Lyons
@nl
Jonathan J Lyons
@sl
Jonathan J. Lyons
@en
Jonathan J. Lyons
@es
type
label
Jonathan J Lyons
@nl
Jonathan J Lyons
@sl
Jonathan J. Lyons
@en
Jonathan J. Lyons
@es
prefLabel
Jonathan J Lyons
@nl
Jonathan J Lyons
@sl
Jonathan J. Lyons
@en
Jonathan J. Lyons
@es
P106
P1153
56009824000
P21
P31
P496
0000-0002-2346-8189