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International Journal of Cancer
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May 17, 2021
BiasCorrector: Fast and accurate correction of all types of experimental biases in quantitative DNA methylation data derived by different technologies
Lorenz A Kapsner, Mikhail G Zavgorodnij, Svetlana P Majorova, et al.
Oncotarget
|
October 6, 2017
Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44<sup>+</sup>CD24<sup>-</sup> stemness
Evgeny V Denisov, Nikolay A Skryabin, Tatiana S Gerashchenko, et al.
Journal of Assisted Reproduction and Genetics
|
September 23, 2021
NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss
Elena A Sazhenova, Tatyana V Nikitina, Stanislav A Vasilyev, et al.
Scientific Reports
|
January 22, 2022
Identification of differentially methylated genes in first-trimester placentas with trisomy 16
Ekaterina N Tolmacheva, Stanislav A Vasilyev, Tatiana V Nikitina, 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 cases
Elena 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 aneuploidy
Stanislav A Vasilyev, Ekaterina N Tolmacheva, Oksana Yu Vasilyeva, et al.
Cytotechnology
|
June 11, 2020
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
Elena 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 disability
Anna 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 Loss
Ekaterina 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 Study
Anna A Kashevarova, Tatyana V Nikitina, Larisa I Mikhailik, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 40) with videos related to
Sort By:
Page
of 4
International Journal of Cancer
|
May 17, 2021
BiasCorrector: Fast and accurate correction of all types of experimental biases in quantitative DNA methylation data derived by different technologies
Lorenz A Kapsner, Mikhail G Zavgorodnij, Svetlana P Majorova, et al.
Oncotarget
|
October 6, 2017
Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44<sup>+</sup>CD24<sup>-</sup> stemness
Evgeny V Denisov, Nikolay A Skryabin, Tatiana S Gerashchenko, et al.
Journal of Assisted Reproduction and Genetics
|
September 23, 2021
NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss
Elena A Sazhenova, Tatyana V Nikitina, Stanislav A Vasilyev, et al.
Scientific Reports
|
January 22, 2022
Identification of differentially methylated genes in first-trimester placentas with trisomy 16
Ekaterina N Tolmacheva, Stanislav A Vasilyev, Tatiana V Nikitina, 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 cases
Elena 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 aneuploidy
Stanislav A Vasilyev, Ekaterina N Tolmacheva, Oksana Yu Vasilyeva, et al.
Cytotechnology
|
June 11, 2020
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
Elena 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 disability
Anna 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 Loss
Ekaterina 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 Study
Anna A Kashevarova, Tatyana V Nikitina, Larisa I Mikhailik, et al.
Page
of 4