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Genomics
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April 1, 1988
The mink proopiomelanocortin gene: characterization of cDNA and chromosomal localization
T M Khlebodarova, G I Karasik, N M Matveeva, et al.
Vavilovskii Zhurnal Genetiki I Selektsii
|
July 1, 2022
Biochemical and technological properties of moose (Alces alces) recombinant chymosin
D V Balabova, A P Rudometov, S V Belenkaya, et al.
Molekuliarnaia Biologiia
|
September 14, 2017
[Dynamics of LINE-1 Retrotransposon Methylation Levels in Circulating DNA from Lung Cancer Patients Undergoing Antitumor Therapy]
A A Ponomaryova, N V Cherdyntseva, A A Bondar, et al.
Genes
|
June 15, 2019
Unique Mutational Spectrum of the <i>GJB2</i> Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys)
Olga L Posukh, Marina V Zytsar, Marita S Bady-Khoo, 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.
International Journal of Molecular Sciences
|
July 27, 2022
Can Modern Molecular Modeling Methods Help Find the Area of Potential Vulnerability of Flaviviruses?
Daniil V Shanshin, Sophia S Borisevich, Alexander A Bondar, 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 Siberia
Vera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova, 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 Siberia
Marina V Zytsar, Nikolay A Barashkov, Marita S Bady-Khoo, 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.
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.
Page
of 45
Search research articles
Search
Showing results (81-90 of 450) with videos related to
Sort By:
Page
of 45
Genomics
|
April 1, 1988
The mink proopiomelanocortin gene: characterization of cDNA and chromosomal localization
T M Khlebodarova, G I Karasik, N M Matveeva, et al.
Vavilovskii Zhurnal Genetiki I Selektsii
|
July 1, 2022
Biochemical and technological properties of moose (Alces alces) recombinant chymosin
D V Balabova, A P Rudometov, S V Belenkaya, et al.
Molekuliarnaia Biologiia
|
September 14, 2017
[Dynamics of LINE-1 Retrotransposon Methylation Levels in Circulating DNA from Lung Cancer Patients Undergoing Antitumor Therapy]
A A Ponomaryova, N V Cherdyntseva, A A Bondar, et al.
Genes
|
June 15, 2019
Unique Mutational Spectrum of the <i>GJB2</i> Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys)
Olga L Posukh, Marina V Zytsar, Marita S Bady-Khoo, 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.
International Journal of Molecular Sciences
|
July 27, 2022
Can Modern Molecular Modeling Methods Help Find the Area of Potential Vulnerability of Flaviviruses?
Daniil V Shanshin, Sophia S Borisevich, Alexander A Bondar, 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 Siberia
Vera G Pshennikova, Fedor M Teryutin, Tuyara V Borisova, 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 Siberia
Marina V Zytsar, Nikolay A Barashkov, Marita S Bady-Khoo, 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.
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.
Page
of 45