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Elena Repnikova

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The Journal of Biological Chemistry|February 18, 2026
Sialylation in the Nervous System: Functions and MechanismsKate Koles, Elena Repnikova, Boris Novikov, et al.
Clinical Genetics|September 4, 2021
Diagnostic yield of genetic testing in 324 infants with hypotoniaSonal Sharma, Elena Repnikova, Janelle R Noel-MacDonnell, et al.
Glycoconjugate Journal|June 24, 2008
Sialylation in protostomes: a perspective from Drosophila genetics and biochemistryKate Koles, Elena Repnikova, Galina Pavlova, et al.
Genetics|October 13, 2005
The twisted gene encodes Drosophila protein O-mannosyltransferase 2 and genetically interacts with the rotated abdomen gene encoding Drosophila protein O-mannosyltransferase 1Dmitry Lyalin, Kate Koles, Sigrid D Roosendaal, et al.
Ear, Nose, & Throat Journal|September 26, 2019
Next-Generation Sequencing in the Diagnosis of Rare Pediatric Sinonasal TumorsAtif A Ahmed, Divya Vundamati, Midhat Farooqi, et al.
Cancer Genetics|June 26, 2026
An atypical RUNX1::ETV6::RUNX1 fusion in a pediatric patient with precursor B-cell acute lymphoblastic leukemiaAravindh Nagarajan, John Herriges, Lisa A Lansdon, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformationsJennifer Roberts, Dmitry Lyalin, Norwood Tosatto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 7, 2010
Sialyltransferase regulates nervous system function in DrosophilaElena Repnikova, Kate Koles, Michiko Nakamura, et al.
Human Mutation|July 2, 2019
Structural variation at the CYP2C locus: Characterization of deletion and duplication allelesMariana R Botton, Xingwu Lu, Geping Zhao, et al.
Pathology, Research and Practice|August 28, 2019
Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two casesElena Repnikova, Jennifer Roberts, Sarah Mc Dermott, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
The Journal of Biological Chemistry|February 18, 2026
Sialylation in the Nervous System: Functions and MechanismsKate Koles, Elena Repnikova, Boris Novikov, et al.
Clinical Genetics|September 4, 2021
Diagnostic yield of genetic testing in 324 infants with hypotoniaSonal Sharma, Elena Repnikova, Janelle R Noel-MacDonnell, et al.
Glycoconjugate Journal|June 24, 2008
Sialylation in protostomes: a perspective from Drosophila genetics and biochemistryKate Koles, Elena Repnikova, Galina Pavlova, et al.
Genetics|October 13, 2005
The twisted gene encodes Drosophila protein O-mannosyltransferase 2 and genetically interacts with the rotated abdomen gene encoding Drosophila protein O-mannosyltransferase 1Dmitry Lyalin, Kate Koles, Sigrid D Roosendaal, et al.
Ear, Nose, & Throat Journal|September 26, 2019
Next-Generation Sequencing in the Diagnosis of Rare Pediatric Sinonasal TumorsAtif A Ahmed, Divya Vundamati, Midhat Farooqi, et al.
Cancer Genetics|June 26, 2026
An atypical RUNX1::ETV6::RUNX1 fusion in a pediatric patient with precursor B-cell acute lymphoblastic leukemiaAravindh Nagarajan, John Herriges, Lisa A Lansdon, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformationsJennifer Roberts, Dmitry Lyalin, Norwood Tosatto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 7, 2010
Sialyltransferase regulates nervous system function in DrosophilaElena Repnikova, Kate Koles, Michiko Nakamura, et al.
Human Mutation|July 2, 2019
Structural variation at the CYP2C locus: Characterization of deletion and duplication allelesMariana R Botton, Xingwu Lu, Geping Zhao, et al.
Pathology, Research and Practice|August 28, 2019
Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two casesElena Repnikova, Jennifer Roberts, Sarah Mc Dermott, et al.
Pageof 2