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Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach

Diabetologia, 2007-05, Vol.50 (5), p.990-999

2007

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CARIOGENIC MICROFLORA IN CHILDREN WITH EARLY CHILDHOOD CARIES AND THEIR MOTHERS

Česká Stomatologie a Praktické Zubní Lékařství, 2021-03, Vol.121 (1), p.19-27

2021

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Genetic variations in the matrix metalloproteinase-1 promoter and risk of susceptibility and/or severity of chronic periodontitis in the Czech population

Journal of clinical periodontology, 2004-08, Vol.31 (8), p.685-690

2004

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Relationship between Breastfeeding and Severe Early Childhood Caries

Česká Stomatologie a Praktické Zubní Lékařství, 2018-09, Vol.118 (3), p.59-67

2018

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Two CD14 promoter polymorphisms and atopic phenotypes in Czech patients with IgE‐mediated allergy

Allergy (Copenhagen), 2003-10, Vol.58 (10), p.1023-1026

2003

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Pharmacotherapy of recurrent aphthous stomatitis in patients with genetically impaired ability to metabolize folic acid - pilot study

Česká Stomatologie a Praktické Zubní Lékařství, 2019-03, Vol.119 (1), p.4-11

2019

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Effect of mutations in the PCSK9 gene on the cell surface LDL receptors

Human molecular genetics, 2006-05, Vol.15 (9), p.1551-1558

2006

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QT prolongation predicts short-term mortality independent of comorbidity

Europace (London, England), 2019-08, Vol.21 (8), p.1254-1260

2019

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Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis

Journal of medical genetics, 2023-01, Vol.60 (1), p.57-64

2023

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Genetic Predisposition to Recurrent Aphthous Stomatitis

Česká Stomatologie a Praktické Zubní Lékařství, 2017-06, Vol.117 (2), p.27-34

2017

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TGF-β1 gene polymorphisms

Allergy (Copenhagen), 2001-12, Vol.56 (12), p.1236-1237

2001

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Plasminogen-activator-inhibitor-1 promoter polymorphism as a risk factor for adult periodontitis in non-smokers

Genes and immunity, 2002-08, Vol.3 (5), p.292-294

2002

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Influence of Diabetes Mellitus on Dental Condition and Periodontal Status

Česká Stomatologie a Praktické Zubní Lékařství, 2018-03, Vol.118 (1), p.3-12

2018

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Obstructive sleep apnea in relation to orthodontic treatment in children

Česká Stomatologie a Praktické Zubní Lékařství, 2020-03, Vol.120 (1), p.13-25

2020

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Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acidification

Human molecular genetics, 2012-03, Vol.21 (6), p.1402-1409

2012

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An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP

American journal of human genetics, 2023-11, Vol.110 (11), p.1959-1975

2023

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De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

American journal of human genetics, 2019-07, Vol.105 (1), p.213-220

2019

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Prevalence of endothelial nitric oxide synthase gene polymorphisms in patients with atopic asthma

Clinical and experimental allergy, 2002-08, Vol.32 (8), p.1193-1198

2002

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Next-generation sequencing of the monogenic obesity genes LEP, LEPR, MC4R, PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls

Molecular genetics and metabolism, 2017-05, Vol.121 (1), p.51-56

2017

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Micro-RNAs miR125b and miR137 are frequently upregulated in response to capecitabine chemoradiotherapy of rectal cancer

International journal of oncology, 2008-09, Vol.33 (3), p.541-547

2008

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Prevalence of Dental Anomalies in Orthodontic Patients

Česká Stomatologie a Praktické Zubní Lékařství, 2013-12, Vol.113 (4), p.95-103

2013

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A Nationwide Study of GATA2 Deficiency in Norway—the Majority of Patients Have Undergone Allo-HSCT

Journal of clinical immunology, 2022-02, Vol.42 (2), p.404-420

2022

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Characterization of novel mutations in the catalytic domain of the PCSK9 gene

Journal of internal medicine, 2008-04, Vol.263 (4), p.420-431

2008

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Platelet-rich plasma, platelet-rich fibrin, and enamel matrix derivative for oral mucosal wound healing

Polish journal of veterinary sciences, 2020-06, Vol.23 (2), p.169-176

2020

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Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors

Journal of lipid research, 2011-10, Vol.52 (10), p.1787-1794

2011

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Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach

CARIOGENIC MICROFLORA IN CHILDREN WITH EARLY CHILDHOOD CARIES AND THEIR MOTHERS

Genetic variations in the matrix metalloproteinase-1 promoter and risk of susceptibility and/or severity of chronic periodontitis in the Czech population

Relationship between Breastfeeding and Severe Early Childhood Caries

Two CD14 promoter polymorphisms and atopic phenotypes in Czech patients with IgE‐mediated allergy

Pharmacotherapy of recurrent aphthous stomatitis in patients with genetically impaired ability to metabolize folic acid - pilot study

Effect of mutations in the PCSK9 gene on the cell surface LDL receptors

QT prolongation predicts short-term mortality independent of comorbidity

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis

Genetic Predisposition to Recurrent Aphthous Stomatitis

TGF-β1 gene polymorphisms

Plasminogen-activator-inhibitor-1 promoter polymorphism as a risk factor for adult periodontitis in non-smokers

Influence of Diabetes Mellitus on Dental Condition and Periodontal Status

Obstructive sleep apnea in relation to orthodontic treatment in children

Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acidification

An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

Prevalence of endothelial nitric oxide synthase gene polymorphisms in patients with atopic asthma

Next-generation sequencing of the monogenic obesity genes LEP, LEPR, MC4R, PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls

Micro-RNAs miR125b and miR137 are frequently upregulated in response to capecitabine chemoradiotherapy of rectal cancer

Prevalence of Dental Anomalies in Orthodontic Patients

A Nationwide Study of GATA2 Deficiency in Norway—the Majority of Patients Have Undergone Allo-HSCT

Characterization of novel mutations in the catalytic domain of the PCSK9 gene

Platelet-rich plasma, platelet-rich fibrin, and enamel matrix derivative for oral mucosal wound healing

Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors

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