Cargando…

Integrative transcriptomic analysis in human and mouse model of anaphylaxis identifies gene signatures associated with cell movement, migration and neuroinflammatory signalling

BACKGROUND: Anaphylaxis is an acute life-threatening allergic reaction and a concern at a global level; therefore, further progress in understanding the underlying mechanisms and more effective strategies for diagnosis, prevention and management are needed. OBJECTIVE: We sought to identify the globa...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rijavec, Matija, Maver, Aleš, Turner, Paul J., Hočevar, Keli, Košnik, Mitja, Yamani, Amnah, Hogan, Simon P., Custovic, Adnan, Peterlin, Borut, Korošec, Peter
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Immunology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772259/ https://www.ncbi.nlm.nih.gov/pubmed/36569939 http://dx.doi.org/10.3389/fimmu.2022.1016165

Ejemplares similares

Basophils, high-affinity IgE receptors, and CCL2 in human anaphylaxis
por: Korosec, Peter, et al.
Publicado: (2017)

Actionable Pharmacogenetic Variation in the Slovenian Genomic Database
por: Hočevar, Keli, et al.
Publicado: (2019)

Fatal Hymenoptera Venom–Triggered Anaphylaxis in Patients with Unrecognized Clonal Mast Cell Disorder—Is Mastocytosis to Blame?
por: Rijavec, Matija, et al.
Publicado: (2023)

Vaginal Microbiome Signature Is Associated With Spontaneous Preterm Delivery
por: Hočevar, Keli, et al.
Publicado: (2019)

Serum diamine oxidase (DAO) activity as a diagnostic test for histamine intolerance
por: Music, Ema, et al.
Publicado: (2011)

Hymenoptera Venom Immunotherapy: Immune Mechanisms of Induced Protection and Tolerance
por: Demšar Luzar, Ajda, et al.
Publicado: (2021)

Hereditary Angioedema Nationwide Study in Slovenia Reveals Four Novel Mutations in SERPING1 Gene
por: Rijavec, Matija, et al.
Publicado: (2013)

Combination of Experimental and Bioinformatic Approaches for Identification of Immunologically Relevant Protein–Peptide Interactions
por: Debeljak, Jerneja, et al.
Publicado: (2023)

Down-Regulation of FcεRI-Mediated CD63 Basophil Response during Short-Term VIT Determined Venom-Nonspecific Desensitization
por: Čelesnik Smodiš, Nina, et al.
Publicado: (2014)

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association
por: Andrejević, Slađana, et al.
Publicado: (2015)

Oral microbiome and preterm birth
por: Vidmar Šimic, Marijana, et al.
Publicado: (2023)

let-7b and miR-126 Are Down-Regulated in Tumor Tissue and Correlate with Microvessel Density and Survival Outcomes in Non–Small–Cell Lung Cancer
por: Jusufović, Edin, et al.
Publicado: (2012)

Evaluation of Serum Diamine Oxidase as a Diagnostic Test for Histamine Intolerance
por: Arih, Kristina, et al.
Publicado: (2023)

Local and genetic determinants of vascular endothelial growth factor expression in advanced proliferative diabetic retinopathy
por: Petrovič, Mojca Globočnik, et al.
Publicado: (2008)

Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21
por: Volk, Marija, et al.
Publicado: (2013)

Transcriptomic signatures for human male infertility
por: Hodžić, Alenka, et al.
Publicado: (2023)

Pharmacogenomics of Multiple Sclerosis: A Systematic Review
por: Hočevar, Keli, et al.
Publicado: (2019)

Chemokines during anaphylaxis: the importance of CCL2 and CCL2-dependent chemotactic activity for basophils
por: Vantur, Romana, et al.
Publicado: (2020)

Whole-Genome Sequencing in Diagnostics of Selected Slovenian Undiagnosed Patients with Rare Disorders
por: Bergant, Gaber, et al.
Publicado: (2021)

Importance of basophil activation testing in insect venom allergy
por: Kosnik, Mitja, et al.
Publicado: (2009)

Transcriptomic Differentiation of Phenotypes in Chronic Rhinosinusitis and Its Implications for Understanding the Underlying Mechanisms
por: Urbančič, Jure, et al.
Publicado: (2023)

DNA Methylation Profiles in Whole Blood of Huntington's Disease Patients
por: Zadel, Maja, et al.
Publicado: (2018)

Improving diagnostics of rare genetic diseases with NGS approaches
por: Vinkšel, Mateja, et al.
Publicado: (2021)

Assessment of pathogenic variation in gynecologic cancer genes in a national cohort
por: Kotnik, Urška, et al.
Publicado: (2023)

Transcription Factors Gene Expression in Chronic Rhinosinusitis with And Without Nasal Polyps
por: Soklic, Tanja Kosak, et al.
Publicado: (2019)

Important and specific role for basophils in acute allergic reactions
por: Korošec, P., et al.
Publicado: (2018)

Integration of Data from Omic Studies with the Literature-Based Discovery towards Identification of Novel Treatments for Neovascularization in Diabetic Retinopathy
por: Maver, Ales, et al.
Publicado: (2013)

Disposal of iNKT cell deficiency and an increase in expression of SLAM signaling factors characterizes sarcoidosis remission: a 4-year longitudinal study
por: Osolnik, Katarina, et al.
Publicado: (2014)

Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21
por: Volk, Marija, et al.
Publicado: (2017)

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder
por: Writzl, Karin, et al.
Publicado: (2023)

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss
por: Likar, Tina, et al.
Publicado: (2018)

Mast cell activation test in the diagnosis of allergic disease and anaphylaxis
por: Bahri, Rajia, et al.
Publicado: (2018)

Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre
por: Babić Božović, Ivana, et al.
Publicado: (2021)

Asthma treatment outcome in adults is associated with rs9910408 in TBX21 gene
por: Lopert, Anton, et al.
Publicado: (2013)

T2-high Asthma, Classified by Sputum mRNA Expression of IL4, IL5, and IL13, is Characterized by Eosinophilia and Severe Phenotype
por: Rijavec, Matija, et al.
Publicado: (2021)

Utility of Telomerase Gene Mutation Testing in Patients with Idiopathic Pulmonary Fibrosis in Routine Practice
por: Šelb, Julij, et al.
Publicado: (2022)

Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility
por: Hodžić, Alenka, et al.
Publicado: (2013)

Angiogenin and vascular endothelial growth factor expression in lungs of lung cancer patients
por: Rozman, Ales, et al.
Publicado: (2012)

A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis
por: Planinsek Rucigaj, Tanja, et al.
Publicado: (2017)

Let-7a is differentially expressed in bronchial biopsies of patients with severe asthma
por: Rijavec, Matija, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_m03bpo9qn39g5u6mdpc4f6alla