Tagui A. Adyan

Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 12 publications

Molecular genetic analysis of Rubinstein-Taybi syndrome in Russian patients.

Molecular genetic analysis of Rubinstein-Taybi syndrome in Russian patients.

Journal: Frontiers in genetics

Published: October 24, 2024

Study of the genetic and molecular epidemiology of cystic fibrosis based on the patient registry for planning targeted therapy in Russian Federation.

Study of the genetic and molecular epidemiology of cystic fibrosis based on the patient registry for planning targeted therapy in Russian Federation.

Journal: Frontiers in genetics

Published: February 11, 2024

Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome.

Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome.

Journal: International journal of molecular sciences

Published: October 21, 2023

Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel.

Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel.

Journal: Genes

Published: July 26, 2023

L138ins Variant of the CFTR Gene in Russian Infertile Men.

L138ins Variant of the CFTR Gene in Russian Infertile Men.

Journal: Genes

Published: April 24, 2023

Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis.

Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis.

Journal: International journal of molecular sciences

Published: January 16, 2023

Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del].

Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del].

Journal: Current issues in molecular biology

Published: September 08, 2022

Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy.

Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy.

Journal: International journal of molecular sciences

Published: August 12, 2022

Health Characteristics of Patients with Cystic Fibrosis whose Genotype Includes a Variant of the Nucleotide Sequence c.3140-16T>A and Functional Analysis of this Variant.

Health Characteristics of Patients with Cystic Fibrosis whose Genotype Includes a Variant of the Nucleotide Sequence c.3140-16T>A and Functional Analysis of this Variant.

Journal: Genes

Published: April 22, 2021

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Journal: BMC medical genetics

Published: September 27, 2018

New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

Journal: Gene

Published: May 30, 2016

Clinical/genetic characteristics of patients with congenital muscular dystrophy caused by mutations in the LMNA gene

Clinical/genetic characteristics of patients with congenital muscular dystrophy caused by mutations in the LMNA gene

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Published: March 16, 2016

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Last Updated: 09/26/2026