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International Journal of Molecular Sciences
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April 30, 2021
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
Andreas 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 Carcinomas
Pavel 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 defect
Andrey 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 methods
Ivan 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 Diseases
Evgeniia 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 Russia
Alexey 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 Profile
Anton 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 Cardiomyopathy
Roman P Myasnikov, Olga V Kulikova, Alexey N Meshkov, et al.
Epigenomes
|
February 20, 2026
Analysis of HERV-K (HML2) Expression in Colorectal Cancer Samples
Valentina S Obrezanenko, Polina M Shulga, Anastasia G Volkova, et al.
Page
of 41
Search research articles
Search
Showing results (321-330 of 408) with videos related to
Sort By:
Page
of 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 Onset
Andreas 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 Carcinomas
Pavel 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 defect
Andrey 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 methods
Ivan 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 Diseases
Evgeniia 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 Russia
Alexey 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 Profile
Anton 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 Cardiomyopathy
Roman P Myasnikov, Olga V Kulikova, Alexey N Meshkov, et al.
Epigenomes
|
February 20, 2026
Analysis of HERV-K (HML2) Expression in Colorectal Cancer Samples
Valentina S Obrezanenko, Polina M Shulga, Anastasia G Volkova, et al.
Page
of 41