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Igor Bychkov

Showing results (21-30 of 37) with videos related to

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Cellular and Molecular Life Sciences : CMLS|May 9, 2022
The role of NSD1, NSD2, and NSD3 histone methyltransferases in solid tumorsIuliia Topchu, Rajendra P Pangeni, Igor Bychkov, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Musashi-2 (MSI2) regulation of DNA damage response in lung cancerIgor Bychkov, Alexander Deneka, Iuliia Topchu, et al.
NPJ Genomic Medicine|November 14, 2022
Publisher Correction: Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscapeIgor Bychkov, Antonina Kuznetsova, Galina Baydakova, et al.
Human Mutation|July 18, 2025
Functional Analysis of Complex Structural and Splice-Altering Variants in the <i>ARSB</i> Gene Towards the Personalized Antisense-Based Therapy for Mucopolysaccharidosis Type VI PatientsIgor Bychkov, Alexandra Filatova, Galina Baydakova, et al.
Epilepsia|June 21, 2025
Splicing variants in DEPDC5-related epilepsies: From functional characterization to correctionEvgeniya Osipova, Igor Bychkov, Alexandra Filatova, et al.
International Journal of Molecular Sciences|May 4, 2026
Identification and Targeted Correction of a Pathogenic <i>PMP22</i> Deep Intronic VariantPolina Chausova, Aysylu Murtazina, Igor Bychkov, et al.
Clinical Neurology and Neurosurgery|January 12, 2021
POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adultsEvgenii Nuzhnyi, Yury Seliverstov, Sergey Klyushnikov, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Additive effect of frequent polymorphism and rare synonymous variant alters splicing in twin patients with Niemann-Pick disease type CIgor Bychkov, Alexandra Filatova, Grigory Perelman, et al.
International Journal of Molecular Sciences|October 13, 2021
Complex Transposon Insertion as a Novel Cause of Pompe DiseaseIgor Bychkov, Galina Baydakova, Alexandra Filatova, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
Expanding the genetic spectrum of the pyruvate carboxylase deficiency with novel missense, deep intronic and structural variantsPolina Tsygankova, Igor Bychkov, Marina Minzhenkova, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Cellular and Molecular Life Sciences : CMLS|May 9, 2022
The role of NSD1, NSD2, and NSD3 histone methyltransferases in solid tumorsIuliia Topchu, Rajendra P Pangeni, Igor Bychkov, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Musashi-2 (MSI2) regulation of DNA damage response in lung cancerIgor Bychkov, Alexander Deneka, Iuliia Topchu, et al.
NPJ Genomic Medicine|November 14, 2022
Publisher Correction: Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscapeIgor Bychkov, Antonina Kuznetsova, Galina Baydakova, et al.
Human Mutation|July 18, 2025
Functional Analysis of Complex Structural and Splice-Altering Variants in the <i>ARSB</i> Gene Towards the Personalized Antisense-Based Therapy for Mucopolysaccharidosis Type VI PatientsIgor Bychkov, Alexandra Filatova, Galina Baydakova, et al.
Epilepsia|June 21, 2025
Splicing variants in DEPDC5-related epilepsies: From functional characterization to correctionEvgeniya Osipova, Igor Bychkov, Alexandra Filatova, et al.
International Journal of Molecular Sciences|May 4, 2026
Identification and Targeted Correction of a Pathogenic <i>PMP22</i> Deep Intronic VariantPolina Chausova, Aysylu Murtazina, Igor Bychkov, et al.
Clinical Neurology and Neurosurgery|January 12, 2021
POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adultsEvgenii Nuzhnyi, Yury Seliverstov, Sergey Klyushnikov, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Additive effect of frequent polymorphism and rare synonymous variant alters splicing in twin patients with Niemann-Pick disease type CIgor Bychkov, Alexandra Filatova, Grigory Perelman, et al.
International Journal of Molecular Sciences|October 13, 2021
Complex Transposon Insertion as a Novel Cause of Pompe DiseaseIgor Bychkov, Galina Baydakova, Alexandra Filatova, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
Expanding the genetic spectrum of the pyruvate carboxylase deficiency with novel missense, deep intronic and structural variantsPolina Tsygankova, Igor Bychkov, Marina Minzhenkova, et al.
Pageof 4