Natalia Y. Shved
Saint Petersburg, SPE 199034, Russian Federation
Last Updated: 09/26/2026
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Found 13 publications
Establishment of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in Saint Petersburg.
Journal: International journal of neonatal screening
Published: December 14, 2023
Serum-Resistant Ternary DNA Polyplexes for Suicide Gene Therapy of Uterine Leiomyoma.
Journal: International journal of molecular sciences
Published: November 24, 2023
Polycondensed Peptide Carriers Modified with Cyclic RGD Ligand for Targeted Suicide Gene Delivery to Uterine Fibroid Cells.
Journal: International journal of molecular sciences
Published: December 31, 2021
Development of Primary Monolayer Cell Model and Organotypic Model of Uterine Leiomyoma.
Journal: Methods and protocols
Published: November 03, 2021
Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison.
Journal: Biomedicines
Published: October 22, 2021
Development of iRGD-Modified Peptide Carriers for Suicide Gene Therapy of Uterine Leiomyoma.
Journal: Pharmaceutics
Published: October 31, 2020
Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro.
Journal: Cytogenetic and genome research
Published: April 15, 2020
Cys-Flanked Cationic Peptides For Cell Delivery of the Herpes Simplex Virus Thymidine Kinase Gene for Suicide Gene Therapy of Uterine Leiomyoma
Journal: Molekuliarnaia biologiia
Published: November 14, 2019
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.
Journal: Molecular medicine reports
Published: March 16, 2019
Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma.
Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: September 04, 2017
Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations.
Journal: Bulletin of experimental biology and medicine
Published: September 29, 2016
Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations.
Journal: Journal of clinical pathology
Published: June 25, 2016
Last Updated: 09/26/2026