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Sergey Nikolaev

Showing results (21-30 of 51) with videos related to

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BMC Genomics|November 22, 2015
The effect of heterogeneous Transcription Start Sites (TSS) on the translatome: implications for the mammalian cellular phenotypeFrancois-Xavier Dieudonné, Patrick B F O'Connor, Pascale Gubler-Jaquier, et al.
Biology|October 27, 2022
Application of Multigene Panels Testing for Hereditary Cancer SyndromesAirat Bilyalov, Sergey Nikolaev, Leila Shigapova, et al.
IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 29, 2021
COMBING: Clustering in Oncology for Mathematical and Biological Identification of Novel Gene SignaturesEnzo Battistella, Maria Vakalopoulou, Roger Sun, et al.
International Journal of Molecular Sciences|May 11, 2024
Extreme Tolerance of Extraocular Muscles to Diseases and Aging: Why and How?Angelina Titova, Sergey Nikolaev, Airat Bilyalov, et al.
The Journal of Investigative Dermatology|April 18, 2021
Subtype-Specific Analyses Reveal Infiltrative Basal Cell Carcinomas Are Highly Interactive with their EnvironmentRehan Villani, Valentine Murigneux, Josue Alexis, et al.
Current Issues in Molecular Biology|August 25, 2023
The Spectrum of Germline Nucleotide Variants in Gastric Cancer Patients in the Kyrgyz RepublicAirat Bilyalov, Sergey Nikolaev, Anastasiia Danishevich, et al.
Genetics and Molecular Biology|October 1, 2020
First description of ultramutated endometrial cancer caused by germline loss-of-function and somatic exonuclease domain mutations in POLE geneReginaldo Cruz Alves Rosa, Andrey A Yurchenko, Fernando Chahud, et al.
Inorganic Chemistry|June 23, 2022
Two Distinct Cu(II)-V(IV) Superexchange Interactions with Similar Bond Angles in a Triangular "CuV<sub>2</sub>" FragmentYiran Wang, Masayuki Fukuda, Sergey Nikolaev, et al.
BMC Medical Genomics|August 12, 2023
Brazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case reportAna Rafaela de Souza Timoteo, Isabel Cristina Pinheiro de Almeida, Andrey A Yurchenko, et al.
Genome Research|December 15, 2017
Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selectionKonstantin Popadin, Stephan Peischl, Marco Garieri, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
BMC Genomics|November 22, 2015
The effect of heterogeneous Transcription Start Sites (TSS) on the translatome: implications for the mammalian cellular phenotypeFrancois-Xavier Dieudonné, Patrick B F O'Connor, Pascale Gubler-Jaquier, et al.
Biology|October 27, 2022
Application of Multigene Panels Testing for Hereditary Cancer SyndromesAirat Bilyalov, Sergey Nikolaev, Leila Shigapova, et al.
IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 29, 2021
COMBING: Clustering in Oncology for Mathematical and Biological Identification of Novel Gene SignaturesEnzo Battistella, Maria Vakalopoulou, Roger Sun, et al.
International Journal of Molecular Sciences|May 11, 2024
Extreme Tolerance of Extraocular Muscles to Diseases and Aging: Why and How?Angelina Titova, Sergey Nikolaev, Airat Bilyalov, et al.
The Journal of Investigative Dermatology|April 18, 2021
Subtype-Specific Analyses Reveal Infiltrative Basal Cell Carcinomas Are Highly Interactive with their EnvironmentRehan Villani, Valentine Murigneux, Josue Alexis, et al.
Current Issues in Molecular Biology|August 25, 2023
The Spectrum of Germline Nucleotide Variants in Gastric Cancer Patients in the Kyrgyz RepublicAirat Bilyalov, Sergey Nikolaev, Anastasiia Danishevich, et al.
Genetics and Molecular Biology|October 1, 2020
First description of ultramutated endometrial cancer caused by germline loss-of-function and somatic exonuclease domain mutations in POLE geneReginaldo Cruz Alves Rosa, Andrey A Yurchenko, Fernando Chahud, et al.
Inorganic Chemistry|June 23, 2022
Two Distinct Cu(II)-V(IV) Superexchange Interactions with Similar Bond Angles in a Triangular "CuV<sub>2</sub>" FragmentYiran Wang, Masayuki Fukuda, Sergey Nikolaev, et al.
BMC Medical Genomics|August 12, 2023
Brazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case reportAna Rafaela de Souza Timoteo, Isabel Cristina Pinheiro de Almeida, Andrey A Yurchenko, et al.
Genome Research|December 15, 2017
Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selectionKonstantin Popadin, Stephan Peischl, Marco Garieri, et al.
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