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Vestnik Otorinolaringologii
|
September 5, 2020
[Presentation of a rare case of hereditary hearing loss with X-linked recessive inheritance associated with the POU3F4 gene]
N E Petrina, A V Marakhonov, R A Zinchenko
Molekuliarnaia Biologiia
|
October 17, 2008
[Antisense regulation of human gene MAP3K13: true phenomenon or artifact]
A V Marakhonov, A V Baranova, M Iu Skoblov
Molekuliarnaia Biologiia
|
August 15, 2012
[Therapeutic siRNAs and non-viral systems for their delivery]
K V Glebova, A V Marakhonov, A V Baranova, et al.
Molekuliarnaia Biologiia
|
August 15, 2012
[Types of non-viral delivery systems of small interfering RNA]
K V Glebova, A V Marakhonov, A V Baranova, et al.
Molekuliarnaia Biologiia
|
April 7, 2015
[RANDTRAN: random transcriptome sequence generator that accounts for partition specific features in eukaryotic mRNA datasets]
E A Borzov, A V Marakhonov, M V Ivanov, et al.
Vestnik Oftalmologii
|
March 16, 2023
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]
T A Vasilyeva, V V Kadyshev, A V Marakhonov, et al.
Clinical Genetics
|
March 22, 2017
Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations
T A Vasilyeva, A A Voskresenskaya, B Käsmann-Kellner, et al.
Arkhiv Patologii
|
December 30, 2014
[Follicular cell (papillary and follicular) thyroid carcinoma, genetic inheritance, and molecular diagnostic markers]
T P Kazubskaia, V M Kozlova, T T Kondrat'eva, et al.
Vestnik Oftalmologii
|
February 21, 2021
[Fundus albipunctatus with mutations in the RDH5 gene (clinical case)]
I V Zolnikova, V V Kadyshev, A V Marakhonov, et al.
BMC Medical Genetics
|
March 23, 2019
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus
N V Petrova, N Y Kashirskaya, D K Saydaeva, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Vestnik Otorinolaringologii
|
September 5, 2020
[Presentation of a rare case of hereditary hearing loss with X-linked recessive inheritance associated with the POU3F4 gene]
N E Petrina, A V Marakhonov, R A Zinchenko
Molekuliarnaia Biologiia
|
October 17, 2008
[Antisense regulation of human gene MAP3K13: true phenomenon or artifact]
A V Marakhonov, A V Baranova, M Iu Skoblov
Molekuliarnaia Biologiia
|
August 15, 2012
[Therapeutic siRNAs and non-viral systems for their delivery]
K V Glebova, A V Marakhonov, A V Baranova, et al.
Molekuliarnaia Biologiia
|
August 15, 2012
[Types of non-viral delivery systems of small interfering RNA]
K V Glebova, A V Marakhonov, A V Baranova, et al.
Molekuliarnaia Biologiia
|
April 7, 2015
[RANDTRAN: random transcriptome sequence generator that accounts for partition specific features in eukaryotic mRNA datasets]
E A Borzov, A V Marakhonov, M V Ivanov, et al.
Vestnik Oftalmologii
|
March 16, 2023
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]
T A Vasilyeva, V V Kadyshev, A V Marakhonov, et al.
Clinical Genetics
|
March 22, 2017
Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations
T A Vasilyeva, A A Voskresenskaya, B Käsmann-Kellner, et al.
Arkhiv Patologii
|
December 30, 2014
[Follicular cell (papillary and follicular) thyroid carcinoma, genetic inheritance, and molecular diagnostic markers]
T P Kazubskaia, V M Kozlova, T T Kondrat'eva, et al.
Vestnik Oftalmologii
|
February 21, 2021
[Fundus albipunctatus with mutations in the RDH5 gene (clinical case)]
I V Zolnikova, V V Kadyshev, A V Marakhonov, et al.
BMC Medical Genetics
|
March 23, 2019
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus
N V Petrova, N Y Kashirskaya, D K Saydaeva, et al.
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of 2