Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Krisztina Hejjas"'
Autor:
Eniko Kubinyi, Judit Vas, Krisztina Hejjas, Zsolt Ronai, Ildikó Brúder, Borbála Turcsán, Maria Sasvari-Szekely, Adám Miklósi
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30271 (2012)
We investigated the association between repeat polymorphism in intron 4 of the tyrosine hydroxylase (TH) gene and two personality traits, activity-impulsivity and inattention, in German Shepherd Dogs. The behaviour of 104 dogs was characterized by tw
Externí odkaz:
https://doaj.org/article/032c4851e6c34812b28b3a4477b4da4b
Autor:
Zsofia Nemoda, Gabriella Balogh, Eszter Dömötör, Anna Szekely, Boglarka Schilling, Zsuzsa Halmai, Maria Sasvari-Szekely, Andrea Sarosi, Krisztina Hejjas, Gabor Faludi
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :295-299
The P2RX7 gene (coding for P2X7 purinergic receptor) has been suggested as a novel candidate gene for major depressive disorder (MDD) and bipolar disorder (BPD). The proposed risk allele (G-allele) of the rs2230912 polymorphism results in an amino ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2547febb6a7873fd07d67d73dbbd5433
https://doi.org/10.1002/ajmg.b.30799
https://doi.org/10.1002/ajmg.b.30799
Autor:
Maria Sasvari-Szekely, Xenia Gonda, Gabor Faludi, Gabriella Balogh, Anna Szekely, Andrea Sarosi, Eszter Dömötör, Krisztina Hejjas
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 32:1667-1672
Background: The aim of our study was to investigate the association of STin2 polymorphism and cognitive dysfunction in major depression. Methods: 71 patients with major depression and 99 controls were genotyped for STin2. All depressive subjects and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea28e4d42f96dbe98b6cb0072c9d5067
https://doi.org/10.1016/j.pnpbp.2008.06.014
https://doi.org/10.1016/j.pnpbp.2008.06.014
Autor:
Zsolt Ronai, Judit Vas, Eszter Szantai, Ádám Miklósi, Maria Sasvari-Szekely, József Topál, Krisztina Hejjas, Zsuzsánna Horváth, Anna Szekely, Enikő Kubinyi
Publikováno v:
Animal Genetics. 38:629-633
Summary A variable number of tandem repeats (VNTR) polymorphism in exon 3 of the human dopamine D4 receptor gene (DRD4) has been associated with attention deficit hyperactivity disorder (ADHD). Rodents possess no analogous repeat sequence, whereas a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4facc416400375d5231d22c40194382d
https://doi.org/10.1111/j.1365-2052.2007.01657.x
https://doi.org/10.1111/j.1365-2052.2007.01657.x
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 18(12)
Genetic polymorphisms of the neurotransmission systems are intensively studied in the human because of a possible influence on personality traits and the risk of psychiatric disorders. The investigation of genetic variations of the dog genome has rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a6aa32a3c207bb436eaeaf627e7e82
https://pubmed.ncbi.nlm.nih.gov/18049838
https://pubmed.ncbi.nlm.nih.gov/18049838
Publikováno v:
Journal of Veterinary Behavior. 4:75
Tyrosine hydroxylase (TH) is the rate-limiting enzyme in the synthesis of dopamine and norepinephrine, which can be converted to norepinephrine and epinephrine. Dopamine plays a role in activity in mice, humans, and in dogs. The polymorphism in the T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b616e32b854955c685b03469c1f5d9a7
https://doi.org/10.1016/j.jveb.2008.10.029
https://doi.org/10.1016/j.jveb.2008.10.029
Autor:
Gabor Faludi, Andrea Sarosi, Xenia Gonda, Maria Sasvari-Szekely, Krisztina Hejjas, Anna Szekely, Gabriella Balogh
Publikováno v:
European Psychiatry. 23:S172
Background:There has been extensive research concerning the role of the serotonin transporter gene (SLC64A) in depression. The STin2 VNTR polymorphism in the second intron has been found to influence the transcriptional activity of the gene, however,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5965122ce006a5ad26aa78ece0e100fa
https://doi.org/10.1016/j.eurpsy.2008.01.977
https://doi.org/10.1016/j.eurpsy.2008.01.977