[Vegetovascular dysfunction as an integral parameter of high risk for cardiovascular diseases development in young subjects]

Autor: Ea, Oteva, Aa, Nikolaeva, Nikolaev KIu, Ab, Maslennikov, Nb, Pikovskaia, Gi, Lifshits

Publikováno v: Konstantin Nikolaev
Europe PubMed Central

To study manifestations of vegetative dystonia in children of probands from families with hereditary IHD load regarding the main risk factors.44 individuals aged 21 +/- 0.7 years were selected out of 111 children from 103 examined families the father

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a359006b656f9f588a405bc44494ae84
http://europepmc.org/abstract/med/10833795

Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay.

Autor: Vasilyev SA; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Skryabin NA; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Kashevarova AA; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Tolmacheva EN; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Savchenko RR; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Vasilyeva OY; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Lopatkina ME; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Zarubin AA; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Fishman VS; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russian Federation., Belyaeva EO; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Filippova MO; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Shorina AR; Novosibirsk City Clinical Hospital, Novosibirsk, Russian Federation., Maslennikov AB; Novosibirsk City Clinical Hospital, Novosibirsk, Russian Federation., Shestovskikh OL; City Perinatal Clinical Center, Omsk, Russian Federation., Gayner TA; Group of Companies 'Center of New Medical Technologies,', Novosibirsk, Russian Federation.; Institute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russian Federation., Čulić V; Gynecology and Obstetrics Private Outpatient Clinic, Split, Croatia., Vulić R; Gynecology and Obstetrics Private Outpatient Clinic, Split, Croatia., Nazarenko LP; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation., Lebedev IN; Research Institute of Medical Genetics, Tomsk National Research Medical Center, Tomsk, Russian Federation.

Publikováno v: Cytogenetic and genome research [Cytogenet Genome Res] 2021; Vol. 161 (3-4), pp. 105-119. Date of Electronic Publication: 2021 Apr 13.

[Risk factors of gastropathy development in workers exposed to dust].

Autor: Dorn OIu, Peskov SA, Poteriaeva EL, Tsikalenko EA, Maslennikov AB, Smirnova EL, Poliakov AIa, Gerasimova EV

Publikováno v: Meditsina truda i promyshlennaia ekologiia [Med Tr Prom Ekol] 2011 (2), pp. 23-7.

[Mutation in the structure of exon 7 of the phenylalanine hydroxylase in phenylketonuria patients from the Novosibirsk area].

Autor: Smagulova FO; Novosibirsk Institute of Bioorganic Chemistry, Russian Academy of Sciences, Novosibirsk, Russia. fatimas@niboch.nsc.ru, Maslennikov AB, Morozov IV, Kitaĭnik GP

Publikováno v: Genetika [Genetika] 2000 Jun; Vol. 36 (6), pp. 849-52.

[Analysis of the distribution of alleles of a tetranucleotide repeat in intron 6 of the lipoprotein lipase gene among residents of Novosibirsk].

Autor: Timofeeva OA; Novosibirsk Institute of Bioorganic Chemistry, Siberian Division, Russian Academy of Sciences, Russia., Filipenko ML, Aul'chenko IuS, Voronina EA, Maslennikov AB, Mertvetsov NP

Publikováno v: Genetika [Genetika] 1999 Jun; Vol. 35 (6), pp. 862-4.