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Vavilovskii Zhurnal Genetiki I Selektsii
|
December 26, 2024
Transcription factor TCF4: structure, function, and associated diseases
R R Savchenko, N A Skryabin
Vavilovskii Zhurnal Genetiki I Selektsii
|
April 29, 2025
Cystic fibrosis therapy: from symptoms to the cause of the disease
T N Kireeva, D I Zhigalina, N A Skryabin
Genetika
|
May 18, 2016
[Preimplantation Genetic Diagnosis by Blastocentesis: Problems and Perspectives]
D I Zhigalina, N A Skryabin, V G Artyukhova, et al.
Tsitologiia
|
September 8, 2018
MOLECULAR KARYOTYPING BY USING CELL-FREE DNA FROM HUMAN BLASTOCOELE FLUID, EMBRYOBLAST AND TROPHOBLAST CELLS
D I Zhigalina, N A Skryabin, V G Artyukhova, et al.
Genetika
|
February 6, 2016
[Molecular Karyotyping of Cell-Free DNA from Blastocoele Fluid as a Basis for Noninvasive Preimplantation Genetic Screening of Aneuploidy]
N A Skryabin, I N Lebedev, V G Artukhova, et al.
Stem Cell Research
|
August 2, 2020
Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease
A A Malakhova, E V Grigor'eva, O Yu Vasilyeva, 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 disability
T A Shnaider, I E Pristyazhnyuk, A G Menzorov, et al.
Klinicheskaia Laboratornaia Diagnostika
|
May 16, 2022
Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing
A A Sivtsev, I Zh Zhalsanova, A E Postrigan, 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 duplication
A 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.
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
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Vavilovskii Zhurnal Genetiki I Selektsii
|
December 26, 2024
Transcription factor TCF4: structure, function, and associated diseases
R R Savchenko, N A Skryabin
Vavilovskii Zhurnal Genetiki I Selektsii
|
April 29, 2025
Cystic fibrosis therapy: from symptoms to the cause of the disease
T N Kireeva, D I Zhigalina, N A Skryabin
Genetika
|
May 18, 2016
[Preimplantation Genetic Diagnosis by Blastocentesis: Problems and Perspectives]
D I Zhigalina, N A Skryabin, V G Artyukhova, et al.
Tsitologiia
|
September 8, 2018
MOLECULAR KARYOTYPING BY USING CELL-FREE DNA FROM HUMAN BLASTOCOELE FLUID, EMBRYOBLAST AND TROPHOBLAST CELLS
D I Zhigalina, N A Skryabin, V G Artyukhova, et al.
Genetika
|
February 6, 2016
[Molecular Karyotyping of Cell-Free DNA from Blastocoele Fluid as a Basis for Noninvasive Preimplantation Genetic Screening of Aneuploidy]
N A Skryabin, I N Lebedev, V G Artukhova, et al.
Stem Cell Research
|
August 2, 2020
Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease
A A Malakhova, E V Grigor'eva, O Yu Vasilyeva, 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 disability
T A Shnaider, I E Pristyazhnyuk, A G Menzorov, et al.
Klinicheskaia Laboratornaia Diagnostika
|
May 16, 2022
Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing
A A Sivtsev, I Zh Zhalsanova, A E Postrigan, 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 duplication
A 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.
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of 2