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N Lebedev

Showing results (211-220 of 239) with videos related to

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Scientific Reports|January 22, 2022
Identification of differentially methylated genes in first-trimester placentas with trisomy 16Ekaterina N Tolmacheva, Stanislav A Vasilyev, Tatiana V Nikitina, et al.
Stem Cell Research|November 4, 2019
Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disabilityT A Shnaider, I E Pristyazhnyuk, A G Menzorov, et al.
Journal of Assisted Reproduction and Genetics|April 5, 2024
PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical casesElena V Soloveva, Maria M Skleimova, Larisa I Minaycheva, et al.
Journal of Assisted Reproduction and Genetics|November 10, 2020
LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidyStanislav A Vasilyev, Ekaterina N Tolmacheva, Oksana Yu Vasilyeva, et al.
Vavilovskii Zhurnal Genetiki I Selektsii|September 26, 2025
A family case of a rare Xq28 duplicationA E Kopytova, E N Tolmacheva, D A Emelina, et al.
American Journal of Medical Genetics. Part A|February 25, 2026
Novel Biallelic Variants in IQSEC1 in a Patient With Intellectual Developmental Disorder With Short Stature and Behavioral Abnormalities (IDDSSBA) and Corpus Callosum DysgenesisA A Kashevarova, L I Minaycheva, E A Fonova, et al.
Cytotechnology|June 11, 2020
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cellsElena V Grigor'eva, Tuyana B Malankhanova, Aizhan Surumbayeva, et al.
Molecular Cytogenetics|January 22, 2015
Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Soren Schultz-Pedersen, et al.
Cytogenetic and Genome Research|June 3, 2020
Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy LossEkaterina N Tolmacheva, Anna A Kashevarova, Lyudmila P Nazarenko, et al.
Genes|December 15, 2020
46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case StudyAnna A Kashevarova, Tatyana V Nikitina, Larisa I Mikhailik, et al.
Pageof 24

Showing results (211-220 of 239) with videos related to

Sort By:
Pageof 24
Scientific Reports|January 22, 2022
Identification of differentially methylated genes in first-trimester placentas with trisomy 16Ekaterina N Tolmacheva, Stanislav A Vasilyev, Tatiana V Nikitina, et al.
Stem Cell Research|November 4, 2019
Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disabilityT A Shnaider, I E Pristyazhnyuk, A G Menzorov, et al.
Journal of Assisted Reproduction and Genetics|April 5, 2024
PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical casesElena V Soloveva, Maria M Skleimova, Larisa I Minaycheva, et al.
Journal of Assisted Reproduction and Genetics|November 10, 2020
LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidyStanislav A Vasilyev, Ekaterina N Tolmacheva, Oksana Yu Vasilyeva, et al.
Vavilovskii Zhurnal Genetiki I Selektsii|September 26, 2025
A family case of a rare Xq28 duplicationA E Kopytova, E N Tolmacheva, D A Emelina, et al.
American Journal of Medical Genetics. Part A|February 25, 2026
Novel Biallelic Variants in IQSEC1 in a Patient With Intellectual Developmental Disorder With Short Stature and Behavioral Abnormalities (IDDSSBA) and Corpus Callosum DysgenesisA A Kashevarova, L I Minaycheva, E A Fonova, et al.
Cytotechnology|June 11, 2020
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cellsElena V Grigor'eva, Tuyana B Malankhanova, Aizhan Surumbayeva, et al.
Molecular Cytogenetics|January 22, 2015
Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disabilityAnna A Kashevarova, Lyudmila P Nazarenko, Soren Schultz-Pedersen, et al.
Cytogenetic and Genome Research|June 3, 2020
Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy LossEkaterina N Tolmacheva, Anna A Kashevarova, Lyudmila P Nazarenko, et al.
Genes|December 15, 2020
46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case StudyAnna A Kashevarova, Tatyana V Nikitina, Larisa I Mikhailik, et al.
Pageof 24