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Lista de obras de Daniel P Potaczek

A comparative search for human FcεRIα gene (FCER1A) 3'-UTR polymorphisms in Japanese and Polish populations

artículo científico publicado en 2011

A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction

artículo científico publicado en 2013

A polymorphism in the TH 2 locus control region is associated with changes in DNA methylation and gene expression

scientific article published on 14 July 2014

A role of FCER1A and FCER2 polymorphisms in IgE regulation.

artículo científico publicado en 2013

Additive association between FCER1A and FCER1B genetic polymorphisms and total serum IgE levels

artículo científico publicado en 2007

Allergic burden and the risk of venous thromboembolism

artículo científico publicado en 2013

An association between functional FceRIalpha polymorphisms and total serum IgE levels in patients with inflammatory bowel disease

artículo científico publicado en 2010

An association of TLR2–16934A >T polymorphism and severity/phenotype of atopic dermatitis

artículo científico publicado en 2011

Antibodies to N-homocysteinylated albumin and haemoglobin in patients with rheumatoid arthritis: a potential new marker of disease severity.

artículo científico publicado en 2013

Antisense molecules: A new class of drugs.

artículo científico publicado en 2016

Assessment of Brain Derived Neurotrophic Factor in hair to study stress responses: A pilot investigation.

artículo científico publicado en 2017

Association between atopic diseases and venous thromboembolism: a case-control study in patients aged 45 years or less

scientific article published on 01 April 2011

Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis

artículo científico publicado en 2015

Atorvastatin favorably modulates proinflammatory cytokine profile in patients following deep vein thrombosis

artículo científico publicado en 2013

Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact.

artículo científico publicado en 2015

Coding region for the high affinity receptor of immunoglobulin E is highly conservative in allergic patients

artículo científico publicado en 2007

Current concepts of IgE regulation and impact of genetic determinants.

artículo científico

Decreased Histone Acetylation Levels at Th1 and Regulatory Loci after Induction of Food Allergy

scientific article published on 19 October 2020

Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation

artículo científico publicado en 2017

Development and characterization of DNAzyme candidates demonstrating significant efficiency against human rhinoviruses

scientific article published on 14 August 2018

Different FCER1A polymorphisms influence IgE levels in asthmatics and non-asthmatics

artículo científico publicado en 2013

Editorial of Special Issue “Molecular Mechanisms of Allergy and Asthma 2.0”

artículo científico publicado en 2023

Effects of obesity on asthma: immunometabolic links

scientific article published on 27 July 2018

Elements of Immunoglobulin E Network Associate with Aortic valve Area in Patients with Acquired Aortic Stenosis

artículo científico publicado en 2020

Epigenetic Modifications in Placenta are Associated with the Child's Sensitization to Allergens

artículo científico publicado en 2019

Epigenetic Regulation in Early Childhood: A Miniaturized and Validated Method to Assess Histone Acetylation.

artículo científico publicado en 2016

Epigenetic Regulation of Airway Epithelium Immune Functions in Asthma

scientific article published on 18 August 2020

Epigenetics and allergy: from basic mechanisms to clinical applications.

artículo científico publicado en 2017

Ezetimibe combined with simvastatin compared with simvastatin alone results in a greater suppression of oxidative stress and enhanced fibrinolysis in patients after acute coronary events

artículo científico publicado en 2011

FCER1A genetic variability and serum IgE levels

artículo científico publicado en 2009

FCERIA gene promoter polymorphisms: lack of association with aspirin hypersensitivity in whites

artículo científico publicado en 2007

FcepsilonRIalpha gene (FCER1A) promoter polymorphisms and total serum IgE levels in Japanese atopic dermatitis patients

scientific article published on 05 February 2010

FcepsilonRIalpha gene -18483A>C polymorphism affects transcriptional activity through YY1 binding

artículo científico publicado en 2009

Fine-mapping of IgE-associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data

artículo científico publicado en 2014

First report of the genetic background of Marfan syndrome in Polish patients.

artículo científico publicado en 2013

Genetic associations of variants of the high affinity receptor for immunoglobulin E in Wegener's granulomatosis

artículo científico publicado en 2009

Genetic causes of resistance to vitamin K antagonists in Polish patients: a novel p.Ile123Met mutation in VKORC1 gene

artículo científico publicado en 2018

Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.

artículo científico publicado en 2017

Genetic polymorphisms of the novel FCERIA gene region: relation to total serum IgE levels

artículo científico publicado en 2007

Genetic variability of the high-affinity IgE receptor alpha subunit (Fc epsilon RI alpha) is related to total serum IgE levels in allergic subjects

artículo científico publicado en 2007

Genetic variability of the high-affinity IgE receptor alpha-subunit (FcepsilonRIalpha).

artículo científico publicado en 2009

Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosis

artículo científico publicado en 2014

Hepatic gene expression in mouse models of non-alcoholic fatty liver disease after acute exercise

artículo científico publicado en 2019

Histone Acetylation of Immune Regulatory Genes in Human Placenta in Association with Maternal Intake of Olive Oil and Fish Consumption

article

Histone modifications and their role in epigenetics of atopy and allergic diseases.

artículo científico publicado en 2018

IgE Levels to Ascaris and House Dust Mite Allergens Are Associated With Increased Histone Acetylation at Key Type-2 Immune Genes

scientific article published on 28 April 2020

Increased activity of lipoprotein-associated phospholipase A2 in non-severe asthma.

artículo científico publicado en 2019

Increased blood levels of cellular fibronectin in asthma: Relation to the asthma severity, inflammation, and prothrombotic blood alterations

artículo científico publicado en 2018

Influenza-derived peptides cross-react with allergens and provide asthma protection.

artículo científico publicado en 2017

Interaction between functional polymorphisms in FCER1A and TLR2 and the severity of atopic dermatitis

artículo científico publicado en 2020

Interaction of functional FCER2 promoter polymorphism and phenotype-associated haplotypes

scientific article published on 21 October 2009

Interleukin-6 (IL-6)-174 G/C polymorphism--lack of association with inflammatory and haemostatic variables in patients with coronary heart disease treated with atorvastatin and quinapril

artículo científico publicado en 2005

Interleukin-6 -174 G/C promoter polymorphism and effects of fenofibrate and simvastatin on inflammatory markers in hypercholesterolemic patients

artículo científico publicado en 2006

Interleukin-6 receptor Asp358Ala gene polymorphism is associated with plasma C-reactive protein levels and severity of aortic valve stenosis

artículo científico publicado en 2014

Internal medicine and biomedicine in Poland: views from the inside and outside

scientific article published on 28 October 2016

Iron deficiency: a novel risk factor of recurrence in patients after unprovoked venous thromboembolism

scientific article published on 04 March 2016

Links between allergy and cardiovascular or hemostatic system.

artículo científico publicado en 2013

Local and Systemic Production of Pro-Inflammatory Eicosanoids Is Inversely Related to Sensitization to Aeroallergens in Patients with Aspirin-Exacerbated Respiratory Disease

artículo científico publicado en 2022

Naturally occurring FCER1A N222K mutation - its ethnicity-dependent distribution and a role in atopic dermatitis

artículo científico publicado en 2011

Non-severe allergic asthma is associated with elevated plasma protein C and protein S

artículo científico publicado en 2012

Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7

scientific article published on 22 September 2020

Novel exon 2A of the high-affinity receptor for the IgE alpha-chain gene (FCER1A) and autoimmunity in patients with asthma or urticaria

artículo científico publicado en 2006

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

artículo científico publicado en 2014

PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy

artículo científico publicado en 2014

Plasma Fibrin Clot Properties as Determinants of Bleeding Time in Human Subjects: Association with Histidine-Rich Glycoprotein

artículo científico publicado en 2020

Plasma platelet activation markers in patients with atopic dermatitis and concomitant allergic diseases

artículo científico publicado en 2011

Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.

artículo científico publicado en 2013

Raw Cow's Milk Reduces Allergic Symptoms in a Murine Model for Food Allergy-A Potential Role For Epigenetic Modifications

artículo científico publicado en 2019

Recent developments in epigenetics of pediatric asthma.

artículo científico publicado en 2016

Role of airway epithelial cells in the development of different asthma phenotypes

artículo científico publicado en 2020

Single-stranded conformation polymorphism (SSCP)-driven indirect sequencing in detection of short deletion

artículo científico publicado en 2008

The I allele of the angiotensin-converting enzyme gene polymorphism may determine an increase in homocysteine levels in fibrate-treated subjects

scientific article published on 01 June 2006

The Impact of Milk and Its Components on Epigenetic Programming of Immune Function in Early Life and Beyond: Implications for Allergy and Asthma

artículo científico publicado en 2020

The Relationship between Total Serum IgE Levels and Atopic Sensitization in Subjects with or without Atopic Dermatitis

artículo científico publicado en 2014

The angiotensin-converting enzyme gene insertion/deletion polymorphism and effects of quinapril and atorvastatin on haemostatic parameters in patients with coronary artery disease

artículo científico publicado en 2005

The role of PKCζ in cord blood T-cell maturation towards Th1 cytokine profile and its epigenetic regulation by fish oil.

artículo científico publicado en 2017

The role of epigenetics in allergy and asthma development

scientific article published on 01 February 2020

Tissue factor +5466A>G and -1208D>I genetic polymorphisms and severity of rheumatoid arthritis

artículo científico publicado en 2010

Tissue factor +5466A>G polymorphism determines thrombin formation following vascular injury and thrombin-lowering effects of simvastatin in patients with ischemic heart disease

artículo científico publicado en 2008

Tissue factor +5466A>G polymorphism predicts plasma TF levels in subjects with cryptogenic ischaemic stroke

scientific article published on 01 July 2009

Tissue factor -1208D>I polymorphism is associated with D-dimer levels in patients with inflammatory bowel disease

artículo científico publicado en 2010

Tissue factor genetic polymorphisms and haplotypes in Japanese population

artículo científico publicado en 2009

Two different transcription factors discriminate the -315C>T polymorphism of the Fc epsilon RI alpha gene: binding of Sp1 to -315C and of a high mobility group-related molecule to -315T.

artículo científico publicado en 2008

Very rare minor homozygous GG genotype of tissue factor +5466A>G mutation in a patient with two cryptogenic cerebrovascular ischemic events

artículo científico publicado en 2009

[Interleukin-1beta C+3953T gene polymorphism and peripheral arterial occlusive disease in Polish population]

scientific article published on 01 January 2005