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Frontiers in Cell and Developmental Biology
|
May 28, 2026
HMGB1 regulates mitochondrial structure and reactive oxygen species balance during the transition from naïve to primed pluripotency
Tatiana Y Starkova, Sergey V Ponomartsev, Veniamin S Fishman, et al.
Cell Death Discovery
|
July 8, 2026
FOXM1 inhibition primes terminal differentiation of human iPSC-derived hepatocytes
Kayque Alves Telles-Silva, Lara Pacheco, Sabrina Komatsu, et al.
Journal of Cellular Biochemistry
|
May 21, 2019
Targeted genomic integration of EGFP under tubulin beta 3 class III promoter and mEos2 under tryptophan hydroxylase 2 promoter does not produce sufficient levels of reporter gene expression
Aleksei G Menzorov, Konstantin E Orishchenko, Veniamin S Fishman, et al.
Biochemistry. Biokhimiia
|
June 4, 2024
Modification of the Hi-C Technology for Molecular Genetic Analysis of Formalin-Fixed Paraffin-Embedded Sections of Tumor Tissues
Maria M Gridina, Yana K Stepanchuk, Miroslav A Nurridinov, 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 disability
Anna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Molecular Neurobiology
|
January 13, 2018
Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene
Maria M Gridina, Natalia M Matveeva, Veniamin S Fishman, et al.
Cells
|
August 27, 2025
DNA and Histone Modifications Identify a Putative Controlling Element (CE) on the X Chromosome of <i>Sciara coprophila</i>
Olga V Posukh, Victor V Shloma, Polina A Skrypnik, et al.
Cytogenetic and Genome Research
|
April 13, 2021
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
Stanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, et al.
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Showing results (11-20 of 18) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 18 results.
Frontiers in Cell and Developmental Biology
|
May 28, 2026
HMGB1 regulates mitochondrial structure and reactive oxygen species balance during the transition from naïve to primed pluripotency
Tatiana Y Starkova, Sergey V Ponomartsev, Veniamin S Fishman, et al.
Cell Death Discovery
|
July 8, 2026
FOXM1 inhibition primes terminal differentiation of human iPSC-derived hepatocytes
Kayque Alves Telles-Silva, Lara Pacheco, Sabrina Komatsu, et al.
Journal of Cellular Biochemistry
|
May 21, 2019
Targeted genomic integration of EGFP under tubulin beta 3 class III promoter and mEos2 under tryptophan hydroxylase 2 promoter does not produce sufficient levels of reporter gene expression
Aleksei G Menzorov, Konstantin E Orishchenko, Veniamin S Fishman, et al.
Biochemistry. Biokhimiia
|
June 4, 2024
Modification of the Hi-C Technology for Molecular Genetic Analysis of Formalin-Fixed Paraffin-Embedded Sections of Tumor Tissues
Maria M Gridina, Yana K Stepanchuk, Miroslav A Nurridinov, 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 disability
Anna A Kashevarova, Lyudmila P Nazarenko, Nikolay A Skryabin, et al.
Molecular Neurobiology
|
January 13, 2018
Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene
Maria M Gridina, Natalia M Matveeva, Veniamin S Fishman, et al.
Cells
|
August 27, 2025
DNA and Histone Modifications Identify a Putative Controlling Element (CE) on the X Chromosome of <i>Sciara coprophila</i>
Olga V Posukh, Victor V Shloma, Polina A Skrypnik, et al.
Cytogenetic and Genome Research
|
April 13, 2021
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
Stanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, et al.
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of 2