Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gulnaz Faskhutdinova"'
Autor:
Sofia Golenkina, Vadim Stepanov, V. P. Puzyrev, A. Yu. Goltsov, Denis A. Reshetov, I. L. Kuznetsova, Selezneva Nd, Gavrilova Si, Gulnaz Faskhutdinova, A. E. Gareeva, Elza Khusnutdinova, L. M. Samokhodskaya, T. V. Andreeva, A. V. Kolotvin, I. V. Goldenkova-Pavlova, Evgeny I. Rogaev, A. Kazantseva, S. S. Kunizheva, I. Yu. Morozova, A. O. Vyacheslavova, L.I. Shagam, H. Shimshilashvili, Anastasia P. Grigorenko, Aigul Zainullina
Publikováno v:
Molecular Biology. 44:546-551
Mutations in three genes PSEN1, PSEN2, and APP are known to be a cause of familial forms of Alzheimer's disease (AD). APOE gene polymorphism is a strong risk genetic factor for AD. We have evaluated allele and genotype frequency distribution of rs111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d3ac755f818f3c9569d2898fdfa3c1d
https://doi.org/10.1134/s0026893310040072
https://doi.org/10.1134/s0026893310040072
Autor:
Tatyana Noskova, Dorotea Muck Šeler, Elza Khusnutdinova, A. Kazantseva, Gordana Nedić, Darya Gaysina, Zrnka Kovačić, Nela Pivac, Zulfiya Khalilova, Gulnaz Faskhutdinova, Mladen Jokic, Dragica Kozarić Kovačić, A. E. Gareeva
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 32:1735-1739
The serotonin transporter (5-HTT) is a protein that has a major role in divergent psychiatric disorders, personality traits and behaviors, by regulating serotonergic synaptic function. Transcriptional activity of the 5-HTT gene (5-HTT or SLC6A4) is m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f75f810d20efa8b5afc67bc67d57d5
https://doi.org/10.1016/j.pnpbp.2008.07.012
https://doi.org/10.1016/j.pnpbp.2008.07.012
Publikováno v:
Genomics and Health in the Developing World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cf34288f51d0e544fc5ca1c236f0b6c
https://doi.org/10.1093/med/9780195374759.003.0117
https://doi.org/10.1093/med/9780195374759.003.0117
Autor:
Gulnaz Faskhutdinova, Ellen L. W. Kittler, Anastasia P. Grigorenko, Yuri K. Moliaka, Evgeny I. Rogaev
Publikováno v:
Science (New York, N.Y.). 326(5954)
The "royal disease," a blood disorder transmitted from Queen Victoria to European royal families, is a striking example of X-linked recessive inheritance. Although the disease is widely recognized to be a form of the blood clotting disorder hemophili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc62e3f66e9dfee960c5c1ece2e70a9c
https://pubmed.ncbi.nlm.nih.gov/19815722
https://pubmed.ncbi.nlm.nih.gov/19815722
Autor:
Gulnaz Faskhutdinova, Ellen L. W. Kittler, I. Morozova, Anastasia P. Grigorenko, Yuri K. Moliaka, Evgeny I. Rogaev
Publikováno v:
Forensic Science International: Genetics Supplement Series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::240ca8f3de0f81b40b417d4fecb7703c
https://doi.org/10.1016/j.fsigss.2009.09.003
https://doi.org/10.1016/j.fsigss.2009.09.003
Autor:
Gulnaz Faskhutdinova, Irina Morozova, Curtis Hildebrandt, Andrey Goltsov, Evgeny I. Rogaev, Ellen L. W. Kittler, Arlene Lahti, Anastasia P. Grigorenko, Yuri K. Moliaka
Accurate unambiguous identification of ancient or historical specimens can potentially be achieved by DNA analysis. The controversy surrounding the fate of the last Russian Emperor, Nicholas II, and his family has persisted, in part, because the bodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42eafc59dad48bd428f862d900e3a4a
https://europepmc.org/articles/PMC2664067/
https://europepmc.org/articles/PMC2664067/
Autor:
Elza Khusnutdinova, Evgeny I. Rogaev, Nina Kal'ina, Vladimir Anatolyevich Koshechkin, N. K. Yankovsky, Irina Morozova, Vadim Stepanov, S. A. Borinskaya, V. P. Puzyrev, I. A. Kutuev, A. V. Marusin, Gulnaz Faskhutdinova
Publikováno v:
American journal of human genetics. 84(1)
The ADH1B Arg47His polymorphism has been convincingly associated with alcoholism in numerous studies of several populations in Asia and Europe. In a review of literature from the past 30 years, we have identified studies that report allele frequencie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63f67c15a5b9e55d04e145fd4ca6d0c3
https://pubmed.ncbi.nlm.nih.gov/17847010
https://pubmed.ncbi.nlm.nih.gov/17847010