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Anna Kiseleva

Showing results (11-20 of 19) with videos related to

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Biorxiv : the Preprint Server for Biology|September 26, 2025
Disruption of theta-timescale spiking impairs learning but spares hippocampal replayAbhilasha Joshi, Alison E Comrie, Samuel Bray, et al.
International Journal of Molecular Sciences|November 27, 2024
The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome PatientsAnna Bukaeva, Alexandra Ershova, Maria Kharlap, et al.
International Journal of Molecular Sciences|July 2, 2021
The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case ReportRoman Myasnikov, Andreas Brodehl, Alexey Meshkov, et al.
Plos One|June 21, 2013
Uniparental genetic heritage of belarusians: encounter of rare middle eastern matrilineages with a central European mitochondrial DNA poolAlena Kushniarevich, Larysa Sivitskaya, Nina Danilenko, et al.
Genes|February 25, 2022
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the <i>FHOD3</i> GeneRoman Myasnikov, Anna Bukaeva, Olga Kulikova, et al.
International Journal of Molecular Sciences|July 27, 2024
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac AbnormalitiesAnna Bukaeva, Roman Myasnikov, Olga Kulikova, et al.
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.
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.
Nature Communications|June 30, 2016
The genetic regulatory signature of type 2 diabetes in human skeletal muscleLaura J Scott, Michael R Erdos, Jeroen R Huyghe, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Disruption of theta-timescale spiking impairs learning but spares hippocampal replayAbhilasha Joshi, Alison E Comrie, Samuel Bray, et al.
International Journal of Molecular Sciences|November 27, 2024
The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome PatientsAnna Bukaeva, Alexandra Ershova, Maria Kharlap, et al.
International Journal of Molecular Sciences|July 2, 2021
The Double Mutation <i>DSG2</i>-p.S363X and <i>TBX20</i>-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case ReportRoman Myasnikov, Andreas Brodehl, Alexey Meshkov, et al.
Plos One|June 21, 2013
Uniparental genetic heritage of belarusians: encounter of rare middle eastern matrilineages with a central European mitochondrial DNA poolAlena Kushniarevich, Larysa Sivitskaya, Nina Danilenko, et al.
Genes|February 25, 2022
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the <i>FHOD3</i> GeneRoman Myasnikov, Anna Bukaeva, Olga Kulikova, et al.
International Journal of Molecular Sciences|July 27, 2024
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac AbnormalitiesAnna Bukaeva, Roman Myasnikov, Olga Kulikova, et al.
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.
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.
Nature Communications|June 30, 2016
The genetic regulatory signature of type 2 diabetes in human skeletal muscleLaura J Scott, Michael R Erdos, Jeroen R Huyghe, et al.
Pageof 2