[A new highly-polymorphic marker of the (CA)n type, isolated from a human chromosome 19 library]

The association study of genetic variants with developing musical aptitude in humans.

Vavilovskii zhurnal genetiki i selektsii·2026

[Replicative study of the involvement of long non-coding RNA genes in the manifestation of antisocial behavior].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova·2025

Using polygenic scores to assess liability to antisocial behavior.

Vavilovskii zhurnal genetiki i selektsii·2025

Involvement of transposable elements in Alzheimer's disease pathogenesis.

Vavilovskii zhurnal genetiki i selektsii·2024

[A perspective on the application of CRISPR/CAS9 genome editing system to study of molecular-genetic basis of mental disorders].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova·2024

Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of Bashkortostan.

Journal of ovarian research·2023

[Effect of ESR1 Somatic Mutations on SERM/SERD Binding: Insights from Molecular Docking and Molecular Dynamics Simulations].

Molekuliarnaia biologiia·2026

[Crol Promotes EcR Recruitment to Enhancers of Ecdysone- Dependent Genes in Drosophila melanogaster Salivary Glands].

Molekuliarnaia biologiia·2026

[Optimization of Plant Recombinant Lectin Production Using a Transient Expression System in Nicotiana benthamiana].

Molekuliarnaia biologiia·2026

[Cloning of Mycoplasma gallisepticum Genome in Saccharomyces cerevisiae Cells].

Molekuliarnaia biologiia·2026

[The Search for Associations of Polymorphic Variants of the COMT and MAOA Genes with Suicide Attempts in Patients with Schizophrenia: A Pilot Study].

Molekuliarnaia biologiia·2026

[WRN and Other RecQ Helicases in Life Cycles of Viruses].

Molekuliarnaia biologiia·2026

Integrating transposable elements into blood gene regulatory networks reveals connectivity loss for schizophrenia genes.

The Journal of clinical investigation·2026

T-rex: standardized analysis of germline variants in whole-exome sequencing trios.

Scientific reports·2026

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

EBioMedicine·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

Related Experiment Videos

[A new highly-polymorphic marker of the (CA)n type, isolated from a human chromosome 19 library]

Related Concept Videos

The association study of genetic variants with developing musical aptitude in humans.

[Replicative study of the involvement of long non-coding RNA genes in the manifestation of antisocial behavior].

Using polygenic scores to assess liability to antisocial behavior.

Involvement of transposable elements in Alzheimer's disease pathogenesis.

[A perspective on the application of CRISPR/CAS9 genome editing system to study of molecular-genetic basis of mental disorders].

Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of Bashkortostan.

[Effect of ESR1 Somatic Mutations on SERM/SERD Binding: Insights from Molecular Docking and Molecular Dynamics Simulations].

[Crol Promotes EcR Recruitment to Enhancers of Ecdysone- Dependent Genes in Drosophila melanogaster Salivary Glands].

[Optimization of Plant Recombinant Lectin Production Using a Transient Expression System in Nicotiana benthamiana].

[Cloning of Mycoplasma gallisepticum Genome in Saccharomyces cerevisiae Cells].

[The Search for Associations of Polymorphic Variants of the COMT and MAOA Genes with Suicide Attempts in Patients with Schizophrenia: A Pilot Study].

[WRN and Other RecQ Helicases in Life Cycles of Viruses].

Integrating transposable elements into blood gene regulatory networks reveals connectivity loss for schizophrenia genes.

T-rex: standardized analysis of germline variants in whole-exome sequencing trios.

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Related Experiment Videos

[A new highly-polymorphic marker of the (CA)n type, isolated from a human chromosome 19 library]

Related Concept Videos

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