Lista de obras - Jonathan J. Lyons - Dominio Público Uruguay

Atopic dermatitis in children: clinical features, pathophysiology, and treatment

artículo científico publicado en 2014

Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

artículo científico publicado en 2014

Clinical relevance of inherited genetic differences in human tryptases

artículo científico publicado en 2021

Clinical response to omalizumab in patients with hereditary α-tryptasemia

artículo científico publicado en 2019

Defining baseline variability of serum tryptase levels improves accuracy in identifying anaphylaxis

artículo científico publicado en 2022

Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis

artículo científico publicado en 2016

Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.

artículo científico publicado en 2015

ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

artículo científico publicado en 2017

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

artículo científico publicado en 2015

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

artículo científico

FOXP3+ Tregs require WASP to restrain Th2-mediated food allergy

artículo científico publicado en 2016

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

scientific article published on 11 May 2018

Food allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8-deficient patients.

artículo científico publicado en 2016

GATA3 haploinsufficiency does not block allergic sensitization or atopic disease

artículo científico publicado en 2015

Germline hypomorphic CARD11 mutations in severe atopic disease

artículo científico publicado en 2017

Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology

artículo científico publicado en 2015

Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia

artículo científico publicado en 2019

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

artículo científico publicado en 2015

Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities

artículo científico publicado en 2014

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

artículo científico publicado en 2017

Primary atopic disorders.

artículo científico publicado en 2018

Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation

artículo científico publicado en 2016

The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism

artículo científico publicado en 2019

Lista de obras de Jonathan J. Lyons

Atopic dermatitis in children: clinical features, pathophysiology, and treatment

Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

Clinical relevance of inherited genetic differences in human tryptases

Clinical response to omalizumab in patients with hereditary α-tryptasemia

Defining baseline variability of serum tryptase levels improves accuracy in identifying anaphylaxis

Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis

Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.

ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

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

FOXP3+ Tregs require WASP to restrain Th2-mediated food allergy

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

Food allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8-deficient patients.

GATA3 haploinsufficiency does not block allergic sensitization or atopic disease

Germline hypomorphic CARD11 mutations in severe atopic disease

Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology

Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

Primary atopic disorders.

Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation

The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism