Zobrazeno 1 - 10
of 10
pro vyhledávání: '"T V, Shcherbatykh"'
Autor:
T. V. Shcherbatykh, V. E. Golimbet, V. A. Orlova, V. G. Kaleda, I. V. Oleichik, L. M. Abramova, V. Z. Tarantul, E. I. Rogaev
Publikováno v:
Russian Journal of Genetics. 36:1445-1448
Associations of the VNTR-17 and 5-HTTLPR polymorphisms of the serotonin transporter gene with affective disorders, including depression, have been found. These polymorphisms were analyzed in two groups of Russian probands: patients with endogenous ps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3df22086d710729acf65a6a2003824bb
https://doi.org/10.1023/a:1009031626668
https://doi.org/10.1023/a:1009031626668
Publikováno v:
Genetika. 38(5)
Depression disorders are a clinically heterogeneous disease group. Their development is to a substantial extent underlain by dysfunction of the serotonin system, in particular, disturbed serotonin transport. The heterogeneity of depressions is associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::197c9e022a9e43d8c39ba00902078a2d
https://pubmed.ncbi.nlm.nih.gov/12068552
https://pubmed.ncbi.nlm.nih.gov/12068552
Autor:
V E, Golimbet, T V, Shcherbatykh, L I, Abramova, V G, Kaleda, I V, Oleĭchik, V A, Orlova, E I, Rogaev
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 101(10)
Recently association between VNTR-17 (12 copies, allel 12) and schizophrenia has been reported. Relations between allele polymorphism of serotonin transporter gene and schizophrenia in 71 Russian families with schizophrenia (n = 253) were studied. Ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f8e719f1301fd584a63da6c370a2751
https://pubmed.ncbi.nlm.nih.gov/11712269
https://pubmed.ncbi.nlm.nih.gov/11712269
Autor:
V E, Golimbet, N G, Mitiushina, T V, Shcherbatykh, M G, Aksenova, L I, Abramova, V G, Kaleda, V V, Nosikov, Iu B, Iurov, E I, Rogaev
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 101(4)
Molecular-genetic polymorphism of genes-candidates was investigated: the genes of serotonin receptor--type 2a (HTR2A), dopamine receptor gene--type 2, serotonin transporter (5HTTLPR). Thirty one schizophrenic patients whose age was 12.6 +/- 3.6 years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cfdc40fbc9b32bb928a05a5763b106b
https://pubmed.ncbi.nlm.nih.gov/11490436
https://pubmed.ncbi.nlm.nih.gov/11490436
Publikováno v:
Molekuliarnaia biologiia. 35(3)
Some studies associate the insertion/deletion polymorphism of the serotonin transporter (5-HTT) gene with anxiety-related personality traits in mentally healthy people, the short (s) allele being associated with a higher neuroticism score. The 5-HTT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d69f655a9e51ee1efc45feb2064549b
https://pubmed.ncbi.nlm.nih.gov/11443919
https://pubmed.ncbi.nlm.nih.gov/11443919
Autor:
G I, Korovaĭtseva, T V, Shcherbatykh, N V, Selezneva, S I, Gavrilova, V E, Golimbet, N I, Voskresenskaia, E I, Rogaev
Publikováno v:
Genetika. 37(4)
Allele epsilon 4 of the apolipoprotein E (APOE) gene is associated with higher risk of Alzheimer's disease (AD) in many, though not all, ethnic groups. The APOE allele and genotype frequency distributions were studied in 207 AD patients without cereb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ced491f9c74ecd0e6c538ea0b14bfcb3
https://pubmed.ncbi.nlm.nih.gov/11421127
https://pubmed.ncbi.nlm.nih.gov/11421127
Autor:
T V, Shcherbatykh, S A, Kiryanov, G I, Korovaitseva, N D, Selezneva, N I, Voskresenskaya, V E, Golimbet, L, Farrer, S I, Gavrilova, E I, Rogaev
Publikováno v:
Neuroscience and behavioral physiology. 31(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bedc03c34b8d7a4390c65c44a4b96b5b
https://pubmed.ncbi.nlm.nih.gov/11388371
https://pubmed.ncbi.nlm.nih.gov/11388371
Publikováno v:
Genetika. 36(12)
Associations of the VNTR-17 and 5-HTTLPR polymorphisms of the serotonin transporter gene with affective disorders, including depression, have been found. These polymorphisms were analyzed in two groups of Russian probands: patients with endogenous ps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd3cdf2cfb8557938a7a0e8b9a771162
https://pubmed.ncbi.nlm.nih.gov/11190480
https://pubmed.ncbi.nlm.nih.gov/11190480
Autor:
T V, Shcherbatykh, S A, Kir'ianov, G I, Korovaĭtsev, N D, Selezneva, N I, Voskresenskaia, V E, Golimbet, L, Farrr, S I, Gavrilova, E I, Rogaev
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 99(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9dc07393df857c1fe3b3e3bee034d032
https://pubmed.ncbi.nlm.nih.gov/10533256
https://pubmed.ncbi.nlm.nih.gov/10533256
Autor:
Iu K, Moliaka, S V, Petruk, S A, Kir'ianov, A N, Dzhibladze, A O, Chechetkin, T V, Shcherbatykh, E N, Rogaev
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 98(6)
Family and twins study demonstrated that genetic factors may be involved in stroke. Previously, insertion/deletion (I/D) Alu-polymorphism in the angiotensin-converting enzyme (ACE) gene has been suggested as a risk factor for some cardiovascular dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24c96b25413d5f9f02f07595981eb351
https://pubmed.ncbi.nlm.nih.gov/9677696
https://pubmed.ncbi.nlm.nih.gov/9677696