ŠERÝ, Omar, Radovan PŘIKRYL, Lukáš ČASTULÍK and František ŠŤASTNÝ. A118G polymorphism of OPRM1 gene is associated with schizophrenia. Journal of Molecular Neuroscience. USA: Springer New York, 2010, vol. 40, No 1, p. 1-8. ISSN 0895-8696.
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Basic information
Original name A118G polymorphism of OPRM1 gene is associated with schizophrenia
Name in Czech Polymorfizmus A118G genu pro OPRM1 má vztah ke schizofrenii
Authors ŠERÝ, Omar (203 Czech Republic, guarantor, belonging to the institution), Radovan PŘIKRYL (203 Czech Republic), Lukáš ČASTULÍK (203 Czech Republic) and František ŠŤASTNÝ (203 Czech Republic).
Edition Journal of Molecular Neuroscience, USA, Springer New York, 2010, 0895-8696.
Other information
Original language English
Type of outcome Article in a journal
Field of Study Genetics and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.922
RIV identification code RIV/00216224:14310/10:00040725
Organization unit Faculty of Science
UT WoS 000275905400028
Keywords (in Czech) schizofrenie DNA polymorfizm asociace OPRM1
Keywords in English schizophrenia association study polymorphism OPRM1 DNA
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Omar Šerý, Ph.D., učo 18120. Changed: 23/2/2012 11:36.
Abstract
Schizophrenia is ranked among multifactor diseases in whose pathogenesis, besides environmental factors, an interplay of functional polymorphisms of a larger number of candidate genes is involved. Neurodevelopmental abnormities are among the most accepted hypotheses in the etiology of schizophrenia. Recently, the role of oligodendrocytes in the development of the cortex has been cited repeatedly. During their various phases of differentiation oligodendrocytes present on their surfaces diverse receptors, among others the opioid receptor (OPRM1). The study was focused on the relationship between the functional A118G polymorphism of the OPRM1 gene (rs1799971) and schizophrenia in a groups of 130 male patients and 452 male controls. An association study revealed yet unpublished statistically significant difference of allelic and genotypic frequencies between the control and patient groups.
Abstract (in Czech)
Abnormality v neurovývoji patří mezi nejvíce přijímané hypotézy etiologie schizofrenie. Existují důkazy, že genetické faktory mohou ovlivňovat abnormální neurovývoj u této choroby. Naše studie byla zaměřena na vztah mezi funkčním polymorfizmem A118G genu pro OPMR1 a schizofrenií na skupině 227 mužů. V naší asociační studii jsme objevili doposud nepublikovaný statisticky signifikantní rozdíl alelických a genotypových frekvencí mezi skupinami mužů z kontrolní skupiny a mužů schizofreniků.
Links
MSM0021622413, plan (intention)Name: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministry of Education, Youth and Sports of the CR, Proteins in metabolism and interaction of organisms with the environment
NR9298, research and development projectName: Rizikové faktory u perzistentní formy hyperkinetické poruchy(ADHD).Longitudinální,klinická a molekulárně-genetická studie.
Investor: Ministry of Health of the CR
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