Daria I. Zhigalina

Ushaika Street 10
Tomsk, TOM 634050, Russian Federation

Last Updated: 09/26/2026

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Found 20 publications

Embryoid bodies as a model system for exploring early human embryonic development.

Embryoid bodies as a model system for exploring early human embryonic development.

Journal: Journal of assisted reproduction and genetics

Published: March 26, 2025

Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X.

Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X.

Journal: Journal of assisted reproduction and genetics

Published: October 25, 2024

Cystic fibrosis therapy: from symptoms to the cause of the disease.

Cystic fibrosis therapy: from symptoms to the cause of the disease.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: August 16, 2024

PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical cases.

PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical cases.

Journal: Journal of assisted reproduction and genetics

Published: January 31, 2024

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.

Journal: Nature medicine

Published: May 26, 2023

Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.

Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.

Journal: International journal of molecular sciences

Published: February 22, 2023

Case Report: Compound Heterozygous Variants of the MAN1B1 Gene in a Russian Patient with Rafiq Syndrome.

Case Report: Compound Heterozygous Variants of the MAN1B1 Gene in a Russian Patient with Rafiq Syndrome.

Journal: International journal of molecular sciences

Published: August 09, 2022

Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene.

Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene.

Journal: Stem cell research

Published: September 09, 2021

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.

Journal: Biomedicines

Published: June 04, 2021

Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter.

Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter.

Journal: MethodsX

Published: May 07, 2021

Identification of differentially methylated genes in first-trimester placentas with trisomy 16.

Identification of differentially methylated genes in first-trimester placentas with trisomy 16.

Journal: Scientific reports

Published: April 30, 2021

From contemplation to classification of chromosomal mosaicism in human preimplantation embryos.

From contemplation to classification of chromosomal mosaicism in human preimplantation embryos.

Journal: Journal of assisted reproduction and genetics

Published: April 06, 2021

Showing 1-12 of 20

Last Updated: 09/26/2026