Natalia A. Semenova

1 Moskvorechye Street
Moscow, MOW 115522, Russian Federation

Last Updated: 09/26/2026

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Found 49 publications

Application of Nanoparticles in Plant In Vitro Culture for Micropropagation and Secondary Metabolite Production: A Review.

Application of Nanoparticles in Plant In Vitro Culture for Micropropagation and Secondary Metabolite Production: A Review.

Journal: Plants (Basel, Switzerland)

Published: May 20, 2026

Evaluation of MgO Nanoparticle Foliar Treatment on the Early Stages of Sweet Basil (Ocimum basilicum L.) Vegetation.

Evaluation of MgO Nanoparticle Foliar Treatment on the Early Stages of Sweet Basil (Ocimum basilicum L.) Vegetation.

Journal: Plants (Basel, Switzerland)

Published: May 04, 2026

First Symptomatic Pediatric Case of Hb Rothschild (HBB: c.112T>C, p.Trp38Arg): Low-Oxygen-Affinity Hemoglobin Presenting with Persistent Pseudohypoxemia.

First Symptomatic Pediatric Case of Hb Rothschild (HBB: c.112T>C, p.Trp38Arg): Low-Oxygen-Affinity Hemoglobin Presenting with Persistent Pseudohypoxemia.

Journal: Diagnostics (Basel, Switzerland)

Published: November 18, 2025

Prenatal-Onset Autosomal Dominant Polycystic Kidney Disease: Clinical Spectrum and Genetic Complexity of a Pseudo-Recessive Phenotype.

Prenatal-Onset Autosomal Dominant Polycystic Kidney Disease: Clinical Spectrum and Genetic Complexity of a Pseudo-Recessive Phenotype.

Journal: Prenatal diagnosis

Published: August 11, 2025

A novel homozygous splice-site variant in the FOCAD gene causing infantile liver cirrhosis and neutropenia: expanding disease phenotype and successful surgical treatment.

A novel homozygous splice-site variant in the FOCAD gene causing infantile liver cirrhosis and neutropenia: expanding disease phenotype and successful surgical treatment.

Journal: Frontiers in medicine

Published: August 06, 2025

Case Report: Mild BRIC-like cholestasis despite a gross USP53 deletion-novel findings and literature review.

Case Report: Mild BRIC-like cholestasis despite a gross USP53 deletion-novel findings and literature review.

Journal: Frontiers in genetics

Published: July 21, 2025

Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings.

Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings.

Journal: Human genomics

Published: June 30, 2025

Clinical and genetic characteristics of a large cohort of children with Alagille syndrome: identification of 57 new variants in the JAG1 gene.

Clinical and genetic characteristics of a large cohort of children with Alagille syndrome: identification of 57 new variants in the JAG1 gene.

Journal: Journal of human genetics

Published: May 20, 2025

RNA Analysis Uncovers Pathogenic PARN Variant in Dyskeratosis Congenita.

RNA Analysis Uncovers Pathogenic PARN Variant in Dyskeratosis Congenita.

Journal: Clinical genetics

Published: May 07, 2025

Exploring the Phenotypic Heterogeneity and Bioenergetic Profile of the m.13513G>A mtDNA Substitution: A Heteroplasmy Perspective.

Exploring the Phenotypic Heterogeneity and Bioenergetic Profile of the m.13513G>A mtDNA Substitution: A Heteroplasmy Perspective.

Journal: International journal of molecular sciences

Published: March 31, 2025

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Journal: Journal of medical genetics

Published: March 19, 2025

uAUG-creating variant in the LDLR gene causes mild Familial hypercholesterolemia.

uAUG-creating variant in the LDLR gene causes mild Familial hypercholesterolemia.

Journal: Human genetics

Published: March 15, 2025

Showing 1-12 of 49

Last Updated: 09/26/2026