about
Metagenomic analyses reveal antibiotic-induced temporal and spatial changes in intestinal microbiota with associated alterations in immune cell homeostasis.Community-wide response of the gut microbiota to enteropathogenic Citrobacter rodentium infection revealed by deep sequencing.Malaria parasite mutants with altered erythrocyte permeability: a new drug resistance mechanism and important molecular tool.A tool kit for quantifying eukaryotic rRNA gene sequences from human microbiome samples.A blasticidin S-resistant Plasmodium falciparum mutant with a defective plasmodial surface anion channelLymph node hypertrophy following Leishmania major infection is dependent on TLR9.Commensal bacteria-derived signals regulate basophil hematopoiesis and allergic inflammation.The epidemiologic characteristics of healthcare provider-diagnosed eczema, asthma, allergic rhinitis, and food allergy in children: a retrospective cohort study.The influence of commensal bacteria-derived signals on basophil-associated allergic inflammation.Electrophysiological studies of malaria parasite-infected erythrocytes: current status.The Immunologic Mechanisms of Eosinophilic Esophagitis.Thymic stromal lymphopoietin-elicited basophil responses promote eosinophilic esophagitis.Intestinal bacteria and the regulation of immune cell homeostasis.The Prevalence of Eosinophilic Esophagitis in Pediatric Patients with IgE-Mediated Food Allergy.Maintaining diplomatic relations between mammals and beneficial microbial communities.The development of IgE-mediated immediate hypersensitivity after the diagnosis of eosinophilic esophagitis to the same food.Babesia and plasmodia increase host erythrocyte permeability through distinct mechanisms.Reply to: Medication contaminants as a potential cause of anaphylaxis to vincristine: What about drug specific antigens?Medication contaminants as a potential cause of anaphylaxis to vincristine.Physiological Suppression of Lipotoxic Liver Damage by Complementary Actions of HDAC3 and SCAP/SREBP.The atopic march: Critical evidence and clinical relevance.Is eosinophilic esophagitis a member of the atopic march?Epithelial acid imbalance in eosinophilic esophagitisResolution of acute IgE-mediated allergy with development of eosinophilic esophagitis triggered by the same foodSevere immunodeficiency associated with acute lymphoblastic leukemia and its treatmentDistinct macrophage populations direct inflammatory versus physiological changes in adipose tissueEosinophilic Esophagitis Is a Late Manifestation of the Allergic MarchA march by any other namePPARγ is a nexus controlling alternative activation of macrophages via glutamine metabolismScreening children for eosinophilic esophagitis: allergic and other risk factorsEosinophilic esophagitis during sublingual and oral allergen immunotherapyAllergic Comorbidity in Eosinophilic Esophagitis: Mechanistic Relevance and Clinical ImplicationsHeterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early ThymopoiesisLipid-Associated Macrophages Control Metabolic Homeostasis in a Trem2-Dependent Manner
P50
Q30920058-54442CB7-8485-489B-A68E-6A9AC638E028Q33487584-9F52E5D3-CB08-4A59-AE17-2F96E864173AQ33641507-90754100-9140-43A9-B55A-C4943C906791Q33741719-C4E5B199-A10D-4D58-A95A-8A73AF2ADE9DQ35612124-B37A9B6F-38C8-4EF2-ABD2-EE938BD634C8Q35685422-534DA0D4-111D-4E3B-BBB9-02E2CA8ECA34Q35874723-00638363-814B-4A18-B72B-B15D2C8DAD56Q36108088-74D32410-4FD9-4804-BFF3-B4F5364AA83BQ36564726-612675C6-CE50-46FA-A727-ED0C14CB5D84Q36733096-50470165-FA1E-458A-9FFE-2F4E68CED281Q37019844-738EF4FE-30E7-4E4E-ABF4-585045B2F8C0Q37632813-B0EB7751-A256-4AEE-BC54-89FB6B9B26BCQ37700728-E176AB30-5D37-4C90-B391-179443629C0EQ39044967-F3E85499-21DB-45F4-B179-66BB1E4B4E9FQ39443081-36CC5802-2A87-4607-93A9-FDEE52B94E96Q41080416-F6A5CB45-1A97-424A-A4AD-14B8A26DAFA6Q44989495-34776285-2D48-499A-B9EF-F760D44EB4D2Q48160261-269C4B56-3C08-4DDB-BE71-395A275796B2Q48189072-056FDCFF-541F-471C-B003-C20BE42960D6Q49706850-B3E87528-9B2E-4049-83F4-D25CA1FEA0CDQ50138867-D1AF37D9-D6EE-4916-BC43-41E0D0B2560AQ50138888-E46DB36A-B83E-4292-BB99-8C70FAAC9144Q57478340-7F6630C8-B354-463E-9908-A4D7286CE477Q87455687-9BAE4C40-95B1-463D-9F49-BA595D464C5EQ88123147-7ED9F2DD-E521-49A5-9A9A-5E9E6EA03C8BQ88669893-848A4FC1-9C48-43E3-8B04-67720B7443A9Q89320219-75187F20-EFB2-4E5F-A289-76A3F305AA7FQ89364202-D4BC48FA-996B-4C7A-97CB-04C1A8D2C45FQ90102090-B3EB9AC1-B42C-4B4E-8D8B-C55DBC605F22Q91358833-D2AD15DF-C5C5-492C-837D-8CF48AF728D7Q91782655-2C5EAD28-0004-4609-9D2F-AD3AD397A4BEQ92567008-9766F9B4-8B66-478D-9F34-457E2815F1B1Q92853580-29317AB6-576F-473D-B451-E335EC6B4306Q93137723-7058A82F-9AFA-491E-8A2F-85CC139B768D
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
David A Hill
@nl
David A Hill
@sl
David A. Hill
@en
David A. Hill
@es
دايفيد أ. هيل
@ar
type
label
David A Hill
@nl
David A Hill
@sl
David A. Hill
@en
David A. Hill
@es
دايفيد أ. هيل
@ar
prefLabel
David A Hill
@nl
David A Hill
@sl
David A. Hill
@en
David A. Hill
@es
دايفيد أ. هيل
@ar
P106
P1153
57056849200
P21
P31
P496
0000-0001-9286-4268