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N Lebedev

Showing results (221-230 of 239) with videos related to

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Vavilovskii Zhurnal Genetiki I Selektsii|March 16, 2023
Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancyV V Demeneva, E N Tolmacheva, T V Nikitina, et al.
Stem Cell Research|October 18, 2020
Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,-8 mosaicismM M Gridina, T V Nikitina, P A Orlova, et al.
Cytogenetic and Genome Research|May 31, 2022
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy LossElizaveta A Fonova, Ekaterina N Tolmacheva, Anna A Kashevarova, et al.
Scientific Reports|February 23, 2021
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogrammingT V Nikitina, A A Kashevarova, M M Gridina, et al.
Biomedicines|August 27, 2021
Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome SequencingIgor N Lebedev, Tatyana V Karamysheva, Eugeny A Elisaphenko, et al.
Molecular Cytogenetics|May 9, 2018
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22Anna A Kashevarova, Elena O Belyaeva, Aleksandr M Nikonov, et al.
Stem Cell Research|March 18, 2022
Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4M M Gridina, A R Nurislamov, J M Minina, et al.
Stem Cell Research|January 8, 2019
Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplicationA A Khabarova, I E Pristyazhnyuk, T V Nikitina, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 11, 2013
[Clinical and genetic analysis of idiopathic intellectual disability based on array comparative genomic hybridization]A A Kashevarova, N A Skryabin, A D Cheremnykh, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Pageof 24

Showing results (221-230 of 239) with videos related to

Sort By:
Pageof 24
Vavilovskii Zhurnal Genetiki I Selektsii|March 16, 2023
Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancyV V Demeneva, E N Tolmacheva, T V Nikitina, et al.
Stem Cell Research|October 18, 2020
Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,-8 mosaicismM M Gridina, T V Nikitina, P A Orlova, et al.
Cytogenetic and Genome Research|May 31, 2022
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy LossElizaveta A Fonova, Ekaterina N Tolmacheva, Anna A Kashevarova, et al.
Scientific Reports|February 23, 2021
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogrammingT V Nikitina, A A Kashevarova, M M Gridina, et al.
Biomedicines|August 27, 2021
Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome SequencingIgor N Lebedev, Tatyana V Karamysheva, Eugeny A Elisaphenko, et al.
Molecular Cytogenetics|May 9, 2018
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22Anna A Kashevarova, Elena O Belyaeva, Aleksandr M Nikonov, et al.
Stem Cell Research|March 18, 2022
Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4M M Gridina, A R Nurislamov, J M Minina, et al.
Stem Cell Research|January 8, 2019
Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplicationA A Khabarova, I E Pristyazhnyuk, T V Nikitina, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 11, 2013
[Clinical and genetic analysis of idiopathic intellectual disability based on array comparative genomic hybridization]A A Kashevarova, N A Skryabin, A D Cheremnykh, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Pageof 24