List of works - Uroš Potočnik

22q11 deletion syndrome in childhood onset schizophrenia: an update

scientific article published on 01 March 2004

A novel in frame deletion of codons 188-190 in the hMSH2 gene of a slovenian patient with hereditary non-polyposis colorectal cancer.

scientific article

Association among ORMDL3 gene expression, 17q21 polymorphism and response to treatment with inhaled corticosteroids in children with asthma

article

Association of CCR5-delta32 mutation with reduced risk of nonatopic asthma in Slovenian children.

scientific article published on November 2008

CD14 gene polymorphism is not associated with asthma but rather with bronchial obstruction and hyperreactivity in Slovenian children with non-atopic asthma

article

CTLA4 CT60 single-nucleotide polymorphism is associated with Slovenian inflammatory bowel disease patients and regulates expression of CTLA4 isoforms

scientific article published on 01 October 2010

Causes of microsatellite instability in colorectal tumors

scientific article published on 01 April 2001

Common germline MDR1/ABCB1 functional polymorphisms and haplotypes modify susceptibility to colorectal cancers with high microsatellite instability

Correlation of MFOLD-predicted DNA secondary structures with separation patterns obtained by capillary electrophoresis single-strand conformation polymorphism (CE-SSCP) analysis.

scientific article published in April 2002

Determining the Molecular Background of Endometrial Receptivity in Adenomyosis

scientific article published on 11 September 2020

Functional polymorphism in CTLA4 gene influences the response to therapy with inhaled corticosteroids in Slovenian children with atopic asthma.

scientific article published in March 2010

Gene Expression Profiles of Methyltransferases and Demethylases Associated with Metastasis, Tumor Invasion, CpG73 Methylation, and HPV Status in Head and Neck Squamous Cell Carcinoma

scientific article published in 2023

Genetic polymorphism inATG16L1gene influences the response to adalimumab in Crohn's disease patients

article

Haplotype in the IBD5 region is associated with refractory Crohn’s disease in Slovenian patients and modulates expression of the SLC22A5 gene

article

High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients.

scientific article published on January 2011

Limited evidence for parent-of-origin effects in inflammatory bowel disease associated loci

scientific article

Low microsatellite instability and high loss of heterozygosity rates indicate dominant role of the suppressor pathway in squamous cell carcinoma of head and neck and loss of heterozygosity of 11q14.3 correlates with tumor grade

scientific article published on 01 October 2003

Molecular Dynamics Simulations Predict That rSNP Located in the <i>HNF‑1α</i> Gene Promotor Region Linked with MODY3 and Hepatocellular Carcinoma Promotes Stronger Binding of the HNF‑4α Transcription Factor

scientific article published on 21 December 2020

Molecular Genetic Architecture of Monogenic Pediatric IBD Differs from Complex Pediatric and Adult IBD

scientific article published on 26 November 2020

Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis

article

Polymorphisms in recent GWA identified asthma genes CA10, SGK493, and CTNNA3 are associated with disease severity and treatment response in childhood asthma.

scientific article

Rapid differentiation of bacterial species by high resolution melting curve analysis

article

Reference genes for real-time qPCR in leukocytes from asthmatic patients before and after anti-asthma treatment

scientific article published on 4 June 2015

Relationship between genome and epigenome--challenges and requirements for future research

scientific article published on 18 June 2014

Solitary and multiple uterine leiomyomas among Caucasian women: two different disorders?

scientific article published on 19 February 2010

List of works by Uroš Potočnik

22q11 deletion syndrome in childhood onset schizophrenia: an update

A novel in frame deletion of codons 188-190 in the hMSH2 gene of a slovenian patient with hereditary non-polyposis colorectal cancer.

Association among ORMDL3 gene expression, 17q21 polymorphism and response to treatment with inhaled corticosteroids in children with asthma

Association of CCR5-delta32 mutation with reduced risk of nonatopic asthma in Slovenian children.

CD14 gene polymorphism is not associated with asthma but rather with bronchial obstruction and hyperreactivity in Slovenian children with non-atopic asthma

CTLA4 CT60 single-nucleotide polymorphism is associated with Slovenian inflammatory bowel disease patients and regulates expression of CTLA4 isoforms

Causes of microsatellite instability in colorectal tumors

Common germline MDR1/ABCB1 functional polymorphisms and haplotypes modify susceptibility to colorectal cancers with high microsatellite instability

Correlation of MFOLD-predicted DNA secondary structures with separation patterns obtained by capillary electrophoresis single-strand conformation polymorphism (CE-SSCP) analysis.

Determining the Molecular Background of Endometrial Receptivity in Adenomyosis

Functional polymorphism in CTLA4 gene influences the response to therapy with inhaled corticosteroids in Slovenian children with atopic asthma.

Gene Expression Profiles of Methyltransferases and Demethylases Associated with Metastasis, Tumor Invasion, CpG73 Methylation, and HPV Status in Head and Neck Squamous Cell Carcinoma

Genetic polymorphism inATG16L1gene influences the response to adalimumab in Crohn's disease patients

Haplotype in the IBD5 region is associated with refractory Crohn’s disease in Slovenian patients and modulates expression of the SLC22A5 gene

High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients.

Limited evidence for parent-of-origin effects in inflammatory bowel disease associated loci

Low microsatellite instability and high loss of heterozygosity rates indicate dominant role of the suppressor pathway in squamous cell carcinoma of head and neck and loss of heterozygosity of 11q14.3 correlates with tumor grade

Molecular Dynamics Simulations Predict That rSNP Located in the <i>HNF‑1α</i> Gene Promotor Region Linked with MODY3 and Hepatocellular Carcinoma Promotes Stronger Binding of the HNF‑4α Transcription Factor

Molecular Genetic Architecture of Monogenic Pediatric IBD Differs from Complex Pediatric and Adult IBD

Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis

Polymorphisms in recent GWA identified asthma genes CA10, SGK493, and CTNNA3 are associated with disease severity and treatment response in childhood asthma.

Rapid differentiation of bacterial species by high resolution melting curve analysis

Reference genes for real-time qPCR in leukocytes from asthmatic patients before and after anti-asthma treatment

Relationship between genome and epigenome--challenges and requirements for future research

Solitary and multiple uterine leiomyomas among Caucasian women: two different disorders?