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Meshkov

Showing results (321-330 of 408) with videos related to

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International Journal of Molecular Sciences|April 30, 2021
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early OnsetAndreas Brodehl, Alexey Meshkov, Roman Myasnikov, et al.
Cancers|October 16, 2024
Benchmarking of Approaches for Gene Copy-Number Variation Analysis and Its Utility for Genetic Aberration Detection in High-Grade Serous Ovarian CarcinomasPavel Alekseevich Grebnev, Ivan Olegovich Meshkov, Pavel Viktorovich Ershov, et al.
Terapevticheskii Arkhiv|July 4, 2013
[Severe adverse events from treatment with genetically engineered biological agents in patients with rheumatic diseases]S V Moiseev, P I Novikov, E N Semenkova, et al.
Human Mutation|March 26, 2019
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defectAndrey V Marakhonov, Andreas Brodehl, Roman P Myasnikov, et al.
Frontiers in Medicine|February 13, 2025
Diagnostics of lung cancer by fragmentated blood circulating cell-free DNA based on machine learning methodsIvan O Meshkov, Alexander P Koturgin, Pavel V Ershov, et al.
Journal of Personalized Medicine|July 27, 2022
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive DiseasesEvgeniia A Sotnikova, Anna V Kiseleva, Vladimir A Kutsenko, et al.
Genes|January 9, 2021
The <i>LDLR</i>, <i>APOB</i>, and <i>PCSK9</i> Variants of Index Patients with Familial Hypercholesterolemia in RussiaAlexey Meshkov, Alexandra Ershova, Anna Kiseleva, et al.
Sensors (Basel, Switzerland)|May 20, 2022
Twisted Few-Mode Optical Fiber with Improved Height of Quasi-Step Refractive Index ProfileAnton V Bourdine, Vladimir V Demidov, Artem A Kuznetsov, et al.
Genes|October 27, 2022
A Splice Variant of the <i>MYH7</i> Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction CardiomyopathyRoman P Myasnikov, Olga V Kulikova, Alexey N Meshkov, et al.
Epigenomes|February 20, 2026
Analysis of HERV-K (HML2) Expression in Colorectal Cancer SamplesValentina S Obrezanenko, Polina M Shulga, Anastasia G Volkova, et al.
Pageof 41

Showing results (321-330 of 408) with videos related to

Sort By:
Pageof 41
International Journal of Molecular Sciences|April 30, 2021
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early OnsetAndreas Brodehl, Alexey Meshkov, Roman Myasnikov, et al.
Cancers|October 16, 2024
Benchmarking of Approaches for Gene Copy-Number Variation Analysis and Its Utility for Genetic Aberration Detection in High-Grade Serous Ovarian CarcinomasPavel Alekseevich Grebnev, Ivan Olegovich Meshkov, Pavel Viktorovich Ershov, et al.
Terapevticheskii Arkhiv|July 4, 2013
[Severe adverse events from treatment with genetically engineered biological agents in patients with rheumatic diseases]S V Moiseev, P I Novikov, E N Semenkova, et al.
Human Mutation|March 26, 2019
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defectAndrey V Marakhonov, Andreas Brodehl, Roman P Myasnikov, et al.
Frontiers in Medicine|February 13, 2025
Diagnostics of lung cancer by fragmentated blood circulating cell-free DNA based on machine learning methodsIvan O Meshkov, Alexander P Koturgin, Pavel V Ershov, et al.
Journal of Personalized Medicine|July 27, 2022
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive DiseasesEvgeniia A Sotnikova, Anna V Kiseleva, Vladimir A Kutsenko, et al.
Genes|January 9, 2021
The <i>LDLR</i>, <i>APOB</i>, and <i>PCSK9</i> Variants of Index Patients with Familial Hypercholesterolemia in RussiaAlexey Meshkov, Alexandra Ershova, Anna Kiseleva, et al.
Sensors (Basel, Switzerland)|May 20, 2022
Twisted Few-Mode Optical Fiber with Improved Height of Quasi-Step Refractive Index ProfileAnton V Bourdine, Vladimir V Demidov, Artem A Kuznetsov, et al.
Genes|October 27, 2022
A Splice Variant of the <i>MYH7</i> Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction CardiomyopathyRoman P Myasnikov, Olga V Kulikova, Alexey N Meshkov, et al.
Epigenomes|February 20, 2026
Analysis of HERV-K (HML2) Expression in Colorectal Cancer SamplesValentina S Obrezanenko, Polina M Shulga, Anastasia G Volkova, et al.
Pageof 41