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V Solovyev

Showing results (81-90 of 337) with videos related to

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Nature|February 13, 2004
Community structure and metabolism through reconstruction of microbial genomes from the environmentGene W Tyson, Jarrod Chapman, Philip Hugenholtz, et al.
International Journal of Molecular Sciences|April 30, 2021
The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of SiberiaAlena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova, et al.
Scientific Reports|April 23, 2016
Laser-synthesized oxide-passivated bright Si quantum dots for bioimagingM B Gongalsky, L A Osminkina, A Pereira, et al.
Biochemical and Biophysical Research Communications|November 10, 2015
High-affinity interaction between interleukin-11 and S100P proteinAlexei S Kazakov, Andrei S Sokolov, Victoria A Rastrygina, et al.
International Journal of Environmental Research and Public Health|March 18, 2020
The Role of Leptin Levels in Adaptation to Cold ClimatesAlena A Nikanorova, Nikolay A Barashkov, Sergey S Nakhodkin, et al.
Journal of Human Genetics|September 16, 2025
The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern SiberiaVera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova, et al.
Terapevticheskii Arkhiv|August 3, 2017
[Multiple myeloma: Maintenance therapy after autologous hematopoietic stem cell transplantation, depending on minimal residual disease]M V Solovyev, L P Mendeleeva, O S Pokrovskaya, et al.
Genes|May 27, 2023
The <i>GJB2</i> (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, et al.
BMC Medical Genetics|August 9, 2018
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in SiberiaMarina V Zytsar, Nikolay A Barashkov, Marita S Bady-Khoo, et al.
Bulletin of Experimental Biology and Medicine|July 27, 2019
Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1AA V Solovyev, N A Barashkov, F M Teryutin, et al.
Pageof 34

Showing results (81-90 of 337) with videos related to

Sort By:
Pageof 34
Nature|February 13, 2004
Community structure and metabolism through reconstruction of microbial genomes from the environmentGene W Tyson, Jarrod Chapman, Philip Hugenholtz, et al.
International Journal of Molecular Sciences|April 30, 2021
The Role of Nonshivering Thermogenesis Genes on Leptin Levels Regulation in Residents of the Coldest Region of SiberiaAlena A Nikanorova, Nikolay A Barashkov, Vera G Pshennikova, et al.
Scientific Reports|April 23, 2016
Laser-synthesized oxide-passivated bright Si quantum dots for bioimagingM B Gongalsky, L A Osminkina, A Pereira, et al.
Biochemical and Biophysical Research Communications|November 10, 2015
High-affinity interaction between interleukin-11 and S100P proteinAlexei S Kazakov, Andrei S Sokolov, Victoria A Rastrygina, et al.
International Journal of Environmental Research and Public Health|March 18, 2020
The Role of Leptin Levels in Adaptation to Cold ClimatesAlena A Nikanorova, Nikolay A Barashkov, Sergey S Nakhodkin, et al.
Journal of Human Genetics|September 16, 2025
The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern SiberiaVera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova, et al.
Terapevticheskii Arkhiv|August 3, 2017
[Multiple myeloma: Maintenance therapy after autologous hematopoietic stem cell transplantation, depending on minimal residual disease]M V Solovyev, L P Mendeleeva, O S Pokrovskaya, et al.
Genes|May 27, 2023
The <i>GJB2</i> (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, et al.
BMC Medical Genetics|August 9, 2018
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in SiberiaMarina V Zytsar, Nikolay A Barashkov, Marita S Bady-Khoo, et al.
Bulletin of Experimental Biology and Medicine|July 27, 2019
Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1AA V Solovyev, N A Barashkov, F M Teryutin, et al.
Pageof 34