Lista de obras - Matija Rijavec - Dominio Público Uruguay

A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis.

artículo científico publicado en 2017

A very low number of circulating basophils is predictive of a poor response to omalizumab in chronic spontaneous urticarial

scientific article published on 02 September 2020

Association of ORMDL3, STAT6 and TBXA2R gene polymorphisms with asthma

artículo científico publicado en 2011

Asthma MicroRNA Regulome Development Using Validated miRNA-Target Interaction Visualization

artículo científico publicado en 2018

Asthma treatment outcome in adults is associated with rs9910408 in TBX21 gene

scientific article published on 10 October 2013

Asthma treatment outcome in children is associated with vascular endothelial growth factor A (VEGFA) polymorphisms

scientific article published on 01 June 2012

BMI1, ALDH1A1, and CD133 Transcripts Connect Epithelial-Mesenchymal Transition to Cancer Stem Cells in Lung Carcinoma

artículo científico publicado en 2015

Basophils, high-affinity IgE receptors, and CCL2 in human anaphylaxis

artículo científico publicado en 2017

CD3+CD4-CD8- mucosal T cells are associated with uncontrolled chronic rhinosinusitis with nasal polyps

artículo científico publicado en 2018

Deficiency of pulmonary Valpha24 Vbeta11 natural killer T cells in corticosteroid-naïve sarcoidosis patients.

artículo científico publicado en 2009

Disposal of iNKT cell deficiency and an increase in expression of SLAM signaling factors characterizes sarcoidosis remission: a 4-year longitudinal study.

artículo científico publicado en 2014

Down-regulation of FcεRI-mediated CD63 basophil response during short-term VIT determined venom-nonspecific desensitization.

artículo científico publicado en 2014

Escherichia coli bacteriocins: antimicrobial efficacy and prevalence among isolates from patients with bacteraemia

artículo científico publicado en 2011

Expressions of topoisomerase IIα and BCRP in metastatic cells are associated with overall survival in small cell lung cancer patients.

artículo científico publicado en 2011

Filaggrin loss-of-function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood

artículo científico publicado en 2015

Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.

artículo científico publicado en 2016

GLCCI1 polymorphism rs37973 and asthma treatment response to inhaled corticosteroids

artículo científico publicado en 2018

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association

artículo científico publicado en 2015

Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.

artículo científico publicado en 2018

Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 gene

artículo científico publicado en 2013

High BMI1 mRNA expression in peripheral whole blood is associated with favorable prognosis in advanced non-small cell lung cancer patients

artículo científico publicado en 2017

High prevalence of multidrug resistance and random distribution of mobile genetic elements among uropathogenic Escherichia coli (UPEC) of the four major phylogenetic groups.

artículo científico publicado en 2006

Immunological and clinical factors associated with adverse systemic reactions during the build-up phase of honeybee venom immunotherapy.

artículo científico publicado en 2015

Important and specific role for basophils in acute allergic reactions

artículo científico publicado en 2018

Let-7a is differentially expressed in bronchial biopsies of patients with severe asthma.

artículo científico publicado en 2014

Natural killer T cells in pulmonary disorders.

artículo científico publicado en 2011

Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients.

artículo científico publicado en 2016

Prevalence of ColE1-like plasmids and colicin K production among uropathogenic Escherichia coli strains and quantification of inhibitory activity of colicin K.

artículo científico publicado en 2006

Prognostic value of cytokeratin-7 mRNA expression in peripheral whole blood of advanced lung adenocarcinoma patients

scientific article published on 26 August 2015

SPINK5 is associated with early-onset and CHI3L1 with late-onset atopic dermatitis.

artículo científico publicado en 2017

Serum diamine oxidase (DAO) activity as a diagnostic test for histamine intolerance.

artículo científico publicado en 2011

Serum diamine oxidase activity as a diagnostic test for histamine intolerance.

artículo científico publicado en 2013

Short-term venom immunotherapy induces desensitization of FcεRI-mediated basophil response.

artículo científico publicado en 2012

The Variants in the 3' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with Asthma

artículo científico publicado en 2018

The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE

scientific article published on 23 July 2019

The prognostic value of whole blood SOX2, NANOG and OCT4 mRNA expression in advanced small-cell lung cancer

artículo científico publicado en 2016

Virulence factors and biofilm production among Escherichia coli strains causing bacteraemia of urinary tract origin.

artículo científico publicado en 2008

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.

artículo científico publicado en 2012

Lista de obras de Matija Rijavec

A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis.

A very low number of circulating basophils is predictive of a poor response to omalizumab in chronic spontaneous urticarial

Association of ORMDL3, STAT6 and TBXA2R gene polymorphisms with asthma

Asthma MicroRNA Regulome Development Using Validated miRNA-Target Interaction Visualization

Asthma treatment outcome in adults is associated with rs9910408 in TBX21 gene

Asthma treatment outcome in children is associated with vascular endothelial growth factor A (VEGFA) polymorphisms

BMI1, ALDH1A1, and CD133 Transcripts Connect Epithelial-Mesenchymal Transition to Cancer Stem Cells in Lung Carcinoma

Basophils, high-affinity IgE receptors, and CCL2 in human anaphylaxis

CD3+CD4-CD8- mucosal T cells are associated with uncontrolled chronic rhinosinusitis with nasal polyps

Deficiency of pulmonary Valpha24 Vbeta11 natural killer T cells in corticosteroid-naïve sarcoidosis patients.

Disposal of iNKT cell deficiency and an increase in expression of SLAM signaling factors characterizes sarcoidosis remission: a 4-year longitudinal study.

Down-regulation of FcεRI-mediated CD63 basophil response during short-term VIT determined venom-nonspecific desensitization.

Escherichia coli bacteriocins: antimicrobial efficacy and prevalence among isolates from patients with bacteraemia

Expressions of topoisomerase IIα and BCRP in metastatic cells are associated with overall survival in small cell lung cancer patients.

Filaggrin loss-of-function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood

Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.

GLCCI1 polymorphism rs37973 and asthma treatment response to inhaled corticosteroids

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association

Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.

Hereditary angioedema nationwide study in Slovenia reveals four novel mutations in SERPING1 gene

High BMI1 mRNA expression in peripheral whole blood is associated with favorable prognosis in advanced non-small cell lung cancer patients

High prevalence of multidrug resistance and random distribution of mobile genetic elements among uropathogenic Escherichia coli (UPEC) of the four major phylogenetic groups.

Immunological and clinical factors associated with adverse systemic reactions during the build-up phase of honeybee venom immunotherapy.

Important and specific role for basophils in acute allergic reactions

Let-7a is differentially expressed in bronchial biopsies of patients with severe asthma.

Natural killer T cells in pulmonary disorders.

Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients.

Prevalence of ColE1-like plasmids and colicin K production among uropathogenic Escherichia coli strains and quantification of inhibitory activity of colicin K.

Prognostic value of cytokeratin-7 mRNA expression in peripheral whole blood of advanced lung adenocarcinoma patients

SPINK5 is associated with early-onset and CHI3L1 with late-onset atopic dermatitis.

Serum diamine oxidase (DAO) activity as a diagnostic test for histamine intolerance.

Serum diamine oxidase activity as a diagnostic test for histamine intolerance.

Short-term venom immunotherapy induces desensitization of FcεRI-mediated basophil response.

The Variants in the 3' Untranslated Region of the Matrix Metalloproteinase 9 Gene as Modulators of Treatment Outcome in Children with Asthma

The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE

The prognostic value of whole blood SOX2, NANOG and OCT4 mRNA expression in advanced small-cell lung cancer

Virulence factors and biofilm production among Escherichia coli strains causing bacteraemia of urinary tract origin.

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.