Effects of common functional MMP12 gene polymorphisms on PD in a Polish population

2017 ◽  
Vol 51 (5) ◽  
pp. 347-353 ◽  
Author(s):  
Monika Białecka ◽  
Mateusz Kurzawski ◽  
Tatyana Vlaykova ◽  
Tanya Tacheva ◽  
Violetta Dziedziejko ◽  
...  
Keyword(s):  
Gene Polymorphisms ◽  
Polish Population

scholarly journals Relationship between CETP gene polymorphisms with coronary artery disease in Polish population

2018 ◽  
Vol 45 (6) ◽  
pp. 1929-1935 ◽  
Author(s):  
Joanna Iwanicka ◽  
Tomasz Iwanicki ◽  
Paweł Niemiec ◽  
Anna Balcerzyk ◽  
Jolanta Krauze ◽  
...  
Keyword(s):  
Coronary Artery Disease ◽  
Coronary Artery ◽  
Gene Polymorphisms ◽  
Polish Population ◽  
Artery Disease

scholarly journals Interleukin-6 gene –174 C/G and apolipoprotein E gene polymorphisms and the risk of Alzheimer disease in a Polish population

2010 ◽  
Vol 44 (6) ◽  
pp. 537-541 ◽  
Author(s):  
Aleksandra Klimkowicz-Mrowiec ◽  
Paweł Wotkow ◽  
Karolina Spisak ◽  
Aleksandra Maruszak ◽  
Maria Styczyńska ◽  
...  
Keyword(s):  
Alzheimer Disease ◽  
Apolipoprotein E ◽  
Interleukin 6 ◽  
Gene Polymorphisms ◽  
Polish Population ◽  
E Gene ◽  
Apolipoprotein E Gene

Association of IL1β and IL4 gene polymorphisms with nasal polyps in a Polish population

2014 ◽  
Vol 41 (7) ◽  
pp. 4653-4658 ◽  
Author(s):  
Malgorzata Mrowicka ◽  
Hanna Zielinska-Blizniewska ◽  
Jaroslaw Milonski ◽  
Ireneusz Majsterek ◽  
Jurek Olszewski
Keyword(s):  
Gene Polymorphisms ◽  
Nasal Polyps ◽  
Polish Population

scholarly journals Vitamin D receptor gene polymorphisms in relation to the risk of colorectal cancer in the Polish population

Tumor Biology ◽  
2014 ◽  
Vol 35 (12) ◽  
pp. 12397-12401 ◽  
Author(s):  
Izabela Laczmanska ◽  
Lukasz Laczmanski ◽  
Marek Bebenek ◽  
Pawel Karpinski ◽  
Halina Czemarmazowicz ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Vitamin D ◽  
Vitamin D Receptor ◽  
Gene Polymorphisms ◽  
Receptor Gene ◽  
Vitamin D Receptor Gene ◽  
Polish Population ◽  
Receptor Gene Polymorphisms

scholarly journals ICOS gene polymorphisms in B-cell chronic lymphocytic leukemia in the Polish population

2011 ◽  
Vol 49 (1) ◽  
pp. 49-54 ◽  
Author(s):  
Lidia Karabon ◽  
Anna Jedynak ◽  
Anna Tomkiewicz ◽  
Dariusz Wolowiec ◽  
Marek Kielbinski ◽  
...  
Keyword(s):  
Chronic Lymphocytic Leukemia ◽  
B Cell ◽  
Gene Polymorphisms ◽  
Lymphocytic Leukemia ◽  
Polish Population ◽  
I Gene ◽  
Cell Chronic Lymphocytic Leukemia

scholarly journals Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population

2021 ◽  
Vol Volume 14 ◽  
pp. 417-425
Author(s):  
Beata Kaleta ◽  
Mieszko Lachota ◽  
Jacek Łukaszkiewicz ◽  
Anna Woźniacka ◽  
Jarosław Bogaczewicz
Keyword(s):  
Atopic Dermatitis ◽  
Gene Polymorphisms ◽  
Polish Population

scholarly journals Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population

2021 ◽  
Author(s):  
Tomasz Iwanicki ◽  
Anna Balcerzyk ◽  
Beata Kazek ◽  
Ewa Emich-Widera ◽  
Wirginia Likus ◽  
...  
Keyword(s):  
Association Study ◽  
Association Analysis ◽  
Transmission Disequilibrium Test ◽  
Gene Polymorphisms ◽  
Autistic Spectrum Disorder ◽  
Carrier State ◽  
Spectrum Disorder ◽  
Polish Population ◽  
Biological Parents ◽  
Family Based

AbstractThe aim of the study was to perform family-based association analysis of PRKCB1, CBLN1 and KCNMB4 gene polymorphisms and autism disorder. We comprised 206 Caucasian children with autistic spectrum disorder (ASD) and their biological parents. In transmission/disequilibrium test we observed that T-allele of the rs198198 polymorphism of the PRKCB1 gene was more often transmitted to affected children in the male subgroup (p = 0.010). Additionally, the T carrier state was significantly associated with hypotonia (p = 0.048). In the female subgroup, the T-allele carriers more often showed more mobile/vital behavior (p = 0.046). In conclusion, our study showed that the rs198198 of the PRKCB1 gene may be associated with ASD in men and with some features characteristic for the disorder.

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