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Veniamin Fishman

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

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Scientific Reports|October 4, 2019
Time origin and structural analysis of the induced CRISPR/cas9 megabase-sized deletions and duplications involving the Cntn6 gene in miceInna E Pristyazhnyuk, Julia Minina, Alexey Korablev, et al.
Research Square|January 3, 2024
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generationsSilvia Souza Costa, Veniamin Fishman, Mara Pinheiro, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 20, 2024
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generationsSilvia Souza da Costa, Veniamin Fishman, Mara Pinheiro, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2014
A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassiumManiselvan Kuppusamy, Brasilina Caroccia, Julia Stindl, et al.
Nucleic Acids Research|January 18, 2023
Annotation of uORFs in the OMIM genes allows to reveal pathogenic variants in 5'UTRsAlexandra Filatova, Ivan Reveguk, Maria Piatkova, et al.
Epigenetics & Chromatin|March 21, 2021
A cookbook for DNase Hi-CMaria Gridina, Evgeniy Mozheiko, Emil Valeev, et al.
Nature Communications|April 13, 2022
Anopheles mosquitoes reveal new principles of 3D genome organization in insectsVarvara Lukyanchikova, Miroslav Nuriddinov, Polina Belokopytova, et al.
Molecular Omics|February 9, 2026
Zooming into rearranged genome: applying pipeline of cytological, genomic, and transcriptomic methods for structural variant interpretationMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Molecular Neurobiology|December 15, 2024
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental SyndromeLaura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Genome Medicine|May 7, 2025
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variantsMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
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Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Scientific Reports|October 4, 2019
Time origin and structural analysis of the induced CRISPR/cas9 megabase-sized deletions and duplications involving the Cntn6 gene in miceInna E Pristyazhnyuk, Julia Minina, Alexey Korablev, et al.
Research Square|January 3, 2024
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generationsSilvia Souza Costa, Veniamin Fishman, Mara Pinheiro, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 20, 2024
A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generationsSilvia Souza da Costa, Veniamin Fishman, Mara Pinheiro, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2014
A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassiumManiselvan Kuppusamy, Brasilina Caroccia, Julia Stindl, et al.
Nucleic Acids Research|January 18, 2023
Annotation of uORFs in the OMIM genes allows to reveal pathogenic variants in 5'UTRsAlexandra Filatova, Ivan Reveguk, Maria Piatkova, et al.
Epigenetics & Chromatin|March 21, 2021
A cookbook for DNase Hi-CMaria Gridina, Evgeniy Mozheiko, Emil Valeev, et al.
Nature Communications|April 13, 2022
Anopheles mosquitoes reveal new principles of 3D genome organization in insectsVarvara Lukyanchikova, Miroslav Nuriddinov, Polina Belokopytova, et al.
Molecular Omics|February 9, 2026
Zooming into rearranged genome: applying pipeline of cytological, genomic, and transcriptomic methods for structural variant interpretationMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Molecular Neurobiology|December 15, 2024
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental SyndromeLaura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Genome Medicine|May 7, 2025
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variantsMaria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Pageof 3