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Functional and Transcriptional Adaptations of Blood Monocytes Recruited to the Cystic Fibrosis Airway Microenvironment In Vitro

International journal of molecular sciences, 2021-03, Vol.22 (5), p.2530

2021

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Cysteine oxidation impairs systemic glucocorticoid responsiveness in children with difficult-to-treat asthma

Journal of allergy and clinical immunology, 2015-08, Vol.136 (2), p.454-461.e9

2015

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Genetic Polymorphisms Associated with Idiopathic Short Stature and First-Year Response to Growth Hormone Treatment

Hormone research in paediatrics, 2019-01, Vol.91 (3), p.164-174

2019

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Systemic Corticosteroid Responses in Children with Severe Asthma: Phenotypic and Endotypic Features

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2017-03, Vol.5 (2), p.410-419.e4

2017

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Neutrophil‐derived extracellular vesicles promote feed‐forward inflammasome signaling in cystic fibrosis airways

Journal of leukocyte biology, 2022-10, Vol.112 (4), p.707-716

2022

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Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2019-04, Vol.199 (7), p.873-881

2019

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Neutrophil Dysfunction in the Airways of Children with Acute Respiratory Failure Due to Lower Respiratory Tract Viral and Bacterial Coinfections

Scientific reports, 2019-02, Vol.9 (1), p.2874-2874, Article 2874

2019

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Frontline Science: Pathological conditioning of human neutrophils recruited to the airway milieu in cystic fibrosis

Journal of leukocyte biology, 2018-10, Vol.104 (4), p.665-675

2018

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Children with Neutrophil-Predominant Severe Asthma Have Proinflammatory Neutrophils With Enhanced Survival and Impaired Clearance

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-02, Vol.7 (2), p.516-525.e6

2019

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Mature cystic fibrosis airway neutrophils suppress T cell function: evidence for a role of arginase 1 but not programmed death-ligand 1

The Journal of immunology (1950), 2015-06, Vol.194 (11), p.5520-5528

2015

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Faster pharmacokinetics and increased patient acceptance of intradermal insulin delivery using a single hollow microneedle in children and adolescents with type 1 diabetes

Pediatric diabetes, 2013-09, Vol.14 (6), p.459-465

2013

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Distinct compartmentalization of immune cells and mediators characterizes bullous pemphigoid disease

Experimental dermatology, 2020-12, Vol.29 (12), p.1191-1198

2020

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Case-control Association Study of Autoimmunity Associated Variants in PDCD1 and Juvenile Idiopathic Arthritis

Current rheumatology reviews, 2017-12, Vol.13 (3)

2017

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Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA

Pediatric rheumatology online journal, 2013-10, Vol.11 (1), p.40-40, Article 40

2013

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Pilot study of inflammatory biomarkers in matched induced sputum and bronchoalveolar lavage of 2‐year‐olds with cystic fibrosis

Pediatric pulmonology, 2022-09, Vol.57 (9), p.2189-2198

2022

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The effects of hydroxyurea and bone marrow transplant on Anti-Müllerian hormone (AMH) levels in females with sickle cell anemia

Blood cells, molecules, & diseases, 2015-06, Vol.55 (1), p.56-61

2015

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Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function

Journal of cystic fibrosis, 2019-01, Vol.18 (1), p.64-70

2019

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Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Journal of cystic fibrosis, 2022-11, Vol.21 (6), p.967-976

2022

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Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations

European journal of human genetics : EJHG, 2016-03, Vol.24 (3), p.415-420

2016

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Anti-Mullerian hormone levels in American girls by age and race/ethnicity

Journal of Pediatric Endocrinology and Metabolism, 2015-01, Vol.28 (1-2), p.189-193

2015

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Hierarchy of risk of childhood-onset rheumatoid arthritis conferred by HLA-DRB1 alleles encoding the shared epitope

Arthritis & rheumatology (Hoboken, N.J.), 2012-03, Vol.64 (3), p.925-930

2012

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Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci

Arthritis & rheumatology (Hoboken, N.J.), 2013-06, Vol.65 (6), p.1663-1667

2013

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Mutations in PROP1 cause familial combined pituitary hormone deficiency

Nature genetics, 1998-02, Vol.18 (2), p.147-149

1998

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Novel patterns of gene expression in pituitary adenomas identified by complementary deoxyribonucleic acid microarrays and quantitative reverse transcription-polymerase chain reaction

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3097-3107

2001

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Association of glutathione-S-transferase-P1 (GST-P1) polymorphisms with bronchopulmonary dysplasia

Journal of perinatology, 2004-01, Vol.24 (1), p.30-35

2004

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Functional and Transcriptional Adaptations of Blood Monocytes Recruited to the Cystic Fibrosis Airway Microenvironment In Vitro

Cysteine oxidation impairs systemic glucocorticoid responsiveness in children with difficult-to-treat asthma

Genetic Polymorphisms Associated with Idiopathic Short Stature and First-Year Response to Growth Hormone Treatment

Systemic Corticosteroid Responses in Children with Severe Asthma: Phenotypic and Endotypic Features

Neutrophil‐derived extracellular vesicles promote feed‐forward inflammasome signaling in cystic fibrosis airways

Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis

Neutrophil Dysfunction in the Airways of Children with Acute Respiratory Failure Due to Lower Respiratory Tract Viral and Bacterial Coinfections

Frontline Science: Pathological conditioning of human neutrophils recruited to the airway milieu in cystic fibrosis

Children with Neutrophil-Predominant Severe Asthma Have Proinflammatory Neutrophils With Enhanced Survival and Impaired Clearance

Mature cystic fibrosis airway neutrophils suppress T cell function: evidence for a role of arginase 1 but not programmed death-ligand 1

Faster pharmacokinetics and increased patient acceptance of intradermal insulin delivery using a single hollow microneedle in children and adolescents with type 1 diabetes

Distinct compartmentalization of immune cells and mediators characterizes bullous pemphigoid disease

Case-control Association Study of Autoimmunity Associated Variants in PDCD1 and Juvenile Idiopathic Arthritis

Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA

Pilot study of inflammatory biomarkers in matched induced sputum and bronchoalveolar lavage of 2‐year‐olds with cystic fibrosis

The effects of hydroxyurea and bone marrow transplant on Anti-Müllerian hormone (AMH) levels in females with sickle cell anemia

Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function

Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations

Anti-Mullerian hormone levels in American girls by age and race/ethnicity

Hierarchy of risk of childhood-onset rheumatoid arthritis conferred by HLA-DRB1 alleles encoding the shared epitope

Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Novel patterns of gene expression in pituitary adenomas identified by complementary deoxyribonucleic acid microarrays and quantitative reverse transcription-polymerase chain reaction

Association of glutathione-S-transferase-P1 (GST-P1) polymorphisms with bronchopulmonary dysplasia

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