Lista de obras -

Aging and Ambiguous ROS. System Genetics Analysis.

artículo científico publicado en 2016

An enzyme kinetics study of the pH dependence of chloride activation of oxygen evolution in photosystem II.

artículo científico publicado en 2016

Anti-angiogenic treatment of endometriosis via anti-VEGFA siRNA delivery by means of peptide-based carrier in a rat subcutaneous model

scientific article published on 25 September 2018

Arginine-rich cross-linking peptides with different SV40 nuclear localization signal content as vectors for intranuclear DNA delivery.

artículo científico publicado en 2017

Arterial pressure, cardiac output and exercise hyperemia in chemically sympathectomized rats ⬇️

artículo científico publicado el 1 de octubre de 1981

CXCR4-targeted modular peptide carriers for efficient anti-VEGF siRNA delivery

artículo científico publicado en 2016

Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma

artículo científico publicado en 2017

Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations

artículo científico publicado en 2016

Characterization of reducible peptide oligomers as carriers for gene delivery ⬇️

artículo científico publicado el 23 de octubre de 2012

Comparative systems genetics view of endometriosis and uterine leiomyoma: Two sides of the same coin?

artículo científico publicado en 2016

DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy

scientific article published on 24 September 2018

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1 ⬇️

artículo científico publicado el 1 de mayo de 1991

Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations.

artículo científico publicado en 2017

Effect of Peptide AEDG on Telomere Length and Mitotic Index of PHA-Stimulated Human Blood Lymphocytes

scientific article published on 25 November 2019

Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines

artículo científico publicado en 2019

Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III ⬇️

artículo científico publicado el 15 de julio de 2011

Genome-wide 5-hydroxymethylcytosine patterns in human spermatogenesis are associated with semen quality.

artículo científico publicado en 2017

Genomic distribution of 5-formylcytosine and 5-carboxylcytosine in human preimplantation embryos

artículo científico publicado en 2018

Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells

scientific article published on 30 November 2018

Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates

artículo científico publicado en 2018

On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update

artículo científico publicado en 2019

Pathogenomics of Endometriosis Development

artículo científico publicado en 2018

Pathogenomics of Uterine Fibroids Development ⬇️

artículo científico publicado en 2019

Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities

scientific article published on 20 November 2019

Synergistic Anti-Angiogenic Effects Using Peptide-Based Combinatorial Delivery of siRNAs Targeting VEGFA, VEGFR1, and Endoglin Genes

artículo científico publicado en 2019

Systems genetics view of endometriosis: a common complex disorder

artículo científico

Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia.

artículo científico publicado en 2018

The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation

artículo científico publicado en 2019

Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia ⬇️

artículo científico publicado el 1 de marzo de 1993

Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes

scientific article published on 16 October 2019

Lista de obras de

Aging and Ambiguous ROS. System Genetics Analysis.

An enzyme kinetics study of the pH dependence of chloride activation of oxygen evolution in photosystem II.

Anti-angiogenic treatment of endometriosis via anti-VEGFA siRNA delivery by means of peptide-based carrier in a rat subcutaneous model

Arginine-rich cross-linking peptides with different SV40 nuclear localization signal content as vectors for intranuclear DNA delivery.

Arterial pressure, cardiac output and exercise hyperemia in chemically sympathectomized rats ⬇️

CXCR4-targeted modular peptide carriers for efficient anti-VEGF siRNA delivery

Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma

Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations

Characterization of reducible peptide oligomers as carriers for gene delivery ⬇️

Comparative systems genetics view of endometriosis and uterine leiomyoma: Two sides of the same coin?

DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1 ⬇️

Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations.

Effect of Peptide AEDG on Telomere Length and Mitotic Index of PHA-Stimulated Human Blood Lymphocytes

Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines

Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III ⬇️

Genome-wide 5-hydroxymethylcytosine patterns in human spermatogenesis are associated with semen quality.

Genomic distribution of 5-formylcytosine and 5-carboxylcytosine in human preimplantation embryos

Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells

Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates

On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update

Pathogenomics of Endometriosis Development

Pathogenomics of Uterine Fibroids Development ⬇️

Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities

Synergistic Anti-Angiogenic Effects Using Peptide-Based Combinatorial Delivery of siRNAs Targeting VEGFA, VEGFR1, and Endoglin Genes

Systems genetics view of endometriosis: a common complex disorder

Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia.

The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation

Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia ⬇️

Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes