Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Maria Sasvari-Szekely"'
Autor:
Maria Sasvari-Szekely, Zsolt Ronai, Eniko Kubinyi, Giulia Cimarelli, Zsófia Virányi, Zsófia Bánlaki
Publikováno v:
Molecular Genetics and Genomics. 292:685-697
A growing body of evidence highlights the relationship between epigenetics, especially DNA methylation, and population divergence as well as speciation. However, little is known about how general the phenomenon of epigenetics-wise separation of diffe
Autor:
Zsofia Nemoda, Nora Angyal, Zsanett Tarnok, Emma Birkas, Emese Bognar, Maria Sasvari-Szekely, Judit Gervai, Krisztina Lakatos
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 12 (2019)
Frontiers in Neuroscience, Vol 12 (2019)
Among the monoaminergic modulatory neurotransmitters, norepinephrine is involved in task orienting, hence noradrenergic genetic variants have been studied in connection to attentional processes. The role of this catecholamine system is also highlight
Publikováno v:
Orvosi Hetilap. 152:498-504
Diabetes mellitus and depression are public health concerns of the present and, as predicted, also the future. The observation that depression is seen more frequently in diabetic patients compared to the non-diabetic population has been proven by sev
Autor:
Sigurdur Boðvarsson, Maria Sasvari-Szekely, Zsolt Ronai, G.J. Arason, George Füst, Perla Thorbjornsdottir, Ragnhildur Kolka, Zoltán Prohászka, Sigurður Thór Sigurðarson, G. Thorgeirsson, Margit Kovács, Garðar Sigurðsson, Bernadett Blaskó
Publikováno v:
International Immunology. 20:31-37
Background and Objectives: Some recent data indicate that risk of death after acute coronary syndrome is under genetic control. Previously, we found that the C4B*Q0 genotype (low copy number of the C4B gene that encodes the fourth component of comple
Publikováno v:
Clinical Chemistry. 52:1756-1762
Background: Investigation of the genetic background of complex traits is the focus of recent interest, as several common diseases or the individual response to treatments of various illnesses have not yet been explored. These studies require the deve
Autor:
Zsolt Ronai, Maria Sasvari-Szekely, Krisztina Ney, Ildikó Tóth, Zsofia Nemoda, Judit Gervai, Krisztina Lakatos
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :126-130
Following up the results of a previous population association study (Lakatos et al. [2000: Mol Psychiatry 5:633-637; Lakatos et al. [2002: Mol Psychiatry 7:27-31]) by analyses based on parental genetic data confirmed the link between infant attachmen
Autor:
Judit Gervai, Eszter Szantai, Zsolt Ronai, Maria Sasvari-Szekely, Zsofia Nemoda, András Guttman, Anna Szekely, R. Szmola
Publikováno v:
American Journal of Medical Genetics. :74-78
The polymorphic 5′ upstream region of the dopamine D4 receptor (DRD4) gene containing several single nucleotide polymorphisms (SNPs) has recently become a focus of association studies in psychiatric genetics. Most SNP genotyping methods are based o
Publikováno v:
International journal of immunogenetics. 41(6)
Summary Several lines of evidence suggest that certain subtypes of obsessive-compulsive and tic disorders might be paediatric manifestations of post-streptococcal autoimmunity caused by cross-reactive autoantibodies. As tumor necrosis factor (TNF) is
Autor:
Zsolt Ronai, Maria Sasvari-Szekely, András Guttman, Judit Gervai, Maria Staub, Csaba Barta, Krisztina Lakatos
Publikováno v:
ELECTROPHORESIS. 22:1102-1105
The -521C/Tsingle nucleotide polymorphism (SNP) in the promoter region of the dopamine D4 receptor gene (DRD4) has recently been detected in oriental (Japanese) individuals and related to novelty seeking and schizophrenia. Here, we report the analysi
Publikováno v:
Neuropharmacology. 57:731-733
Methylphenidate (MPH) is the most frequently prescribed drug in the treatment of attention deficit hyperactivity disorder (ADHD). Several pharmacogenetic studies suggested that catecholamine candidate genes influence individual MPH-responses, but the