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An update on the tools for creating transgenic animal models of human diseases - focus on atherosclerosis

Brazilian journal of medical and biological research, 2019-01, Vol.52 (5), p.e8108-e8108

2019

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Use of Transgenic Animals in Biotechnology: Prospects and Problems

Actanaturae, 2013-01, Vol.5 (1), p.33-46

2013

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Animal models of human atherosclerosis: current progress

Brazilian journal of medical and biological research, 2020-01, Vol.53 (6), p.e9557-e9557

2020

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Production of human lactoferrin in animal milk

Biochemistry and cell biology, 2012-06, Vol.90 (3), p.513

2012

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APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy Associated with Alzheimer's Disease

Molekuliarnaia biologiia, 2023-01, Vol.57 (1), p.85

2023

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APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy Associated with Alzheimer’s Disease

Molecular biology (New York), 2023-02, Vol.57 (1), p.74-82

2023

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Production of Recombinant Proteins in the Milk of Transgenic Animals: Current State and Prospects

Actanaturae, 2018-07, Vol.10 (3), p.40-47

2018

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Development of a Multiplex PCR Test System for the Determination of a Transgene Based on the pBC1 Plasmid and Its Derivatives for the Expression of Recombinant Proteins in Mus musculus Milk

Doklady. Biochemistry and biophysics, 2019-03, Vol.485 (1), p.153-156

2019

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Formation of a Unique Population of CD8+ T Lymphocytes after Adoptive Transfer of Syngeneic Splenocytes to Mice with Lymphopenia

Doklady. Biochemistry and biophysics, 2021-03, Vol.497 (1), p.71-74

2021

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DEVELOPMENT OF MURINE STEM CELLS WITH CONDITIONAL KNOCKOUT OF HUMANIZED SNCA GENE

Farmaciâ i Farmakologiâ (Pâtigorsk), 2022-01, Vol.10 (6), p.525-535

2022

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STUDY OF THE PHARMACOLOGICAL ACTIVITY OF NOVEL EPOR/CD131 HETERORECEPTOR AGONISTS IN MICE WITH ENDOTHELIAL-SPECIFIC EXPRESSION OF MUTANT POLG GENE

Farmaciâ i Farmakologiâ (Pâtigorsk), 2021-01, Vol.9 (4), p.294-305

2021

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Genome Editing As an Approach to the Study of in Vivo Transcription Reprogramming

Doklady. Biochemistry and biophysics, 2020, Vol.490 (1), p.43-46

2020

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Suppression of the Immune Response by Syngeneic Splenocytes Adoptively Transferred to Sublethally Irradiated Mice

Actanaturae, 2021, Vol.13 (1), p.116-126

2021

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NEAT1_1 long non-coding RNA reduces the survival of primary neuronal cells under ER-stress

Bulletin of Russian State Medical University, 2023-12 (2023(6))

2023

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Retinal abnormalities in transgenic mice overexpressing aberrant human FUS[1-359] gene

Bulletin of Russian State Medical University, 2021-08 (2021(4))

2021

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Genetic markers in sheep meat breeding

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2016-12, Vol.20 (5), p.576-583

2016

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Dimebon delays the onset of symptoms of FUS-proteinopathy in transgenic mice

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2017, Vol.117 (4), p.64

2017

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APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy in Alzheimer’s Disease

Молекулярная биология, 2023-01, Vol.57 (1), p.85-94

2023

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Multiplex PCR test-system development for the genotyping of transgenic mice with pBC1 MILK expression vector-based transgene

Доклады Академии наук, 2019-05, Vol.485 (6), p.750-753

2019

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The state of health and the reproductive potential of transgenic mice secreting recombinant human lactoferrin in milk

Doklady. Biochemistry and biophysics, 2009-08, Vol.427 (1), p.195-198

2009

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Retinal Damage in Amyotrophic Lateral Sclerosis: Underlying Mechanisms

Eye and brain, 2021-01, Vol.13, p.131-146

2021

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Modification of the method for analysis of genome editing results using CRISPR/Cas9 system on preimplantation mouse embryos

Bulletin of Russian State Medical University, 2016-05 (3), p.15-20

2016

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Analysis of phenotype expressions of deletions in the dystrophin gene in terms of efficiency of exon skipping as a method for treatment of hereditary dystrophinopathies

Bulletin of Russian State Medical University, 2016-05 (3), p.21-26

2016

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CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene

Disease models & mechanisms, 2019-04, Vol.12 (4)

2019

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Current advances in gene therapy of mitochondrial diseases

Journal of translational medicine, 2022-12, Vol.20 (1), p.562-23, Article 562

2022

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An update on the tools for creating transgenic animal models of human diseases - focus on atherosclerosis

Use of Transgenic Animals in Biotechnology: Prospects and Problems

Animal models of human atherosclerosis: current progress

Production of human lactoferrin in animal milk

APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy Associated with Alzheimer's Disease

APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy Associated with Alzheimer’s Disease

Production of Recombinant Proteins in the Milk of Transgenic Animals: Current State and Prospects

Development of a Multiplex PCR Test System for the Determination of a Transgene Based on the pBC1 Plasmid and Its Derivatives for the Expression of Recombinant Proteins in Mus musculus Milk

Formation of a Unique Population of CD8+ T Lymphocytes after Adoptive Transfer of Syngeneic Splenocytes to Mice with Lymphopenia

DEVELOPMENT OF MURINE STEM CELLS WITH CONDITIONAL KNOCKOUT OF HUMANIZED SNCA GENE

STUDY OF THE PHARMACOLOGICAL ACTIVITY OF NOVEL EPOR/CD131 HETERORECEPTOR AGONISTS IN MICE WITH ENDOTHELIAL-SPECIFIC EXPRESSION OF MUTANT POLG GENE

Genome Editing As an Approach to the Study of in Vivo Transcription Reprogramming

Suppression of the Immune Response by Syngeneic Splenocytes Adoptively Transferred to Sublethally Irradiated Mice

NEAT1_1 long non-coding RNA reduces the survival of primary neuronal cells under ER-stress

Retinal abnormalities in transgenic mice overexpressing aberrant human FUS[1-359] gene

Genetic markers in sheep meat breeding

Dimebon delays the onset of symptoms of FUS-proteinopathy in transgenic mice

APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy in Alzheimer’s Disease

Multiplex PCR test-system development for the genotyping of transgenic mice with pBC1 MILK expression vector-based transgene

The state of health and the reproductive potential of transgenic mice secreting recombinant human lactoferrin in milk

Retinal Damage in Amyotrophic Lateral Sclerosis: Underlying Mechanisms

Modification of the method for analysis of genome editing results using CRISPR/Cas9 system on preimplantation mouse embryos

Analysis of phenotype expressions of deletions in the dystrophin gene in terms of efficiency of exon skipping as a method for treatment of hereditary dystrophinopathies

CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene

Current advances in gene therapy of mitochondrial diseases

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