Denis A. Reshetov
Moscow, MOW 119333, Russian Federation
Last Updated: 09/26/2026
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Found 10 publications
An Extremely Rare ZP4 Missense Variant in a Patient with Abnormal Zona Pellucida Morphology and Female Infertility: A Case Report.
Journal: Reports (MDPI)
Published: July 02, 2026
RNA Interference Effectors Selectively Silence the Pathogenic Variant GNAO1 c.607 G > A In Vitro.
Journal: Nucleic acid therapeutics
Published: January 12, 2024
Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.
Journal: Cells
Published: December 07, 2021
Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression.
Journal: Scientific reports
Published: September 20, 2021
Chromatin profiling of cortical neurons identifies individual epigenetic signatures in schizophrenia.
Journal: Translational psychiatry
Published: June 15, 2019
CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene.
Journal: Disease models & mechanisms
Published: October 25, 2018
Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.
Journal: Scientific reports
Published: November 04, 2015
Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.
Journal: European journal of human genetics : EJHG
Published: January 13, 2015
The ctenophore genome and the evolutionary origins of neural systems.
Journal: Nature
Published: September 15, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026