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Biology
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February 25, 2022
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population
Georgii P Romanov, Anna A Smirnova, Vladimir I Zamyatin, et al.
Plos One
|
November 30, 2020
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Georgii P Romanov, Vera G Pshennikova, Sergey A Lashin, et al.
Scientific Reports
|
July 3, 2024
High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect
Tuyara V Borisova, Aleksandra M Cherdonova, Vera G Pshennikova, et al.
Molecules (Basel, Switzerland)
|
December 6, 2016
Expression, Purification, and Characterization of Interleukin-11 Orthologues
Andrei S Sokolov, Alexei S Kazakov, Valery V Solovyev, et al.
Terapevticheskii Arkhiv
|
August 3, 2017
[Prognostic value of 1q21 amplification in multiple myeloma]
T V Abramova, T N Obukhova, L P Mendeleeva, et al.
International Journal of Circumpolar Health
|
June 20, 2019
A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the <i>MITF</i> gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia)
Nikolay A Barashkov, Georgii P Romanov, Uigulaana P Borisova, et al.
Journal of Community Genetics
|
March 22, 2017
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
Aisen V Solovyev, Lilya U Dzhemileva, Olga L Posukh, et al.
Human Genetics
|
November 28, 2021
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia
Aisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, et al.
International Journal of Pediatric Otorhinolaryngology
|
December 31, 2017
A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2)
Nikolay A Barashkov, Leonid A Klarov, Fedor M Teryutin, et al.
Scientific Reports
|
November 26, 2025
Hydrothermal upgrading and adsorption of a water-soluble nickel-based catalyst precursor in a porous media of carbonate oil-saturated rock
Ilgiz F Minkhanov, Vladislav V Chalin, Aidar R Tazeev, et al.
Page
of 34
Search research articles
Search
Showing results (91-100 of 337) with videos related to
Sort By:
Page
of 34
Biology
|
February 25, 2022
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population
Georgii P Romanov, Anna A Smirnova, Vladimir I Zamyatin, et al.
Plos One
|
November 30, 2020
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Georgii P Romanov, Vera G Pshennikova, Sergey A Lashin, et al.
Scientific Reports
|
July 3, 2024
High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect
Tuyara V Borisova, Aleksandra M Cherdonova, Vera G Pshennikova, et al.
Molecules (Basel, Switzerland)
|
December 6, 2016
Expression, Purification, and Characterization of Interleukin-11 Orthologues
Andrei S Sokolov, Alexei S Kazakov, Valery V Solovyev, et al.
Terapevticheskii Arkhiv
|
August 3, 2017
[Prognostic value of 1q21 amplification in multiple myeloma]
T V Abramova, T N Obukhova, L P Mendeleeva, et al.
International Journal of Circumpolar Health
|
June 20, 2019
A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the <i>MITF</i> gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia)
Nikolay A Barashkov, Georgii P Romanov, Uigulaana P Borisova, et al.
Journal of Community Genetics
|
March 22, 2017
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
Aisen V Solovyev, Lilya U Dzhemileva, Olga L Posukh, et al.
Human Genetics
|
November 28, 2021
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia
Aisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, et al.
International Journal of Pediatric Otorhinolaryngology
|
December 31, 2017
A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2)
Nikolay A Barashkov, Leonid A Klarov, Fedor M Teryutin, et al.
Scientific Reports
|
November 26, 2025
Hydrothermal upgrading and adsorption of a water-soluble nickel-based catalyst precursor in a porous media of carbonate oil-saturated rock
Ilgiz F Minkhanov, Vladislav V Chalin, Aidar R Tazeev, et al.
Page
of 34