Detalhe da pesquisa
1.
Refinement of Rf1-gene localization and development of the new molecular markers for fertility restoration in sunflower.
Mol Biol Rep
; 50(9): 7919-7926, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37453962
2.
Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study.
Int J Mol Sci
; 24(17)2023 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37685967
3.
The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.
Int J Mol Sci
; 22(13)2021 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34202524
4.
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
Int J Mol Sci
; 22(7)2021 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33917638
5.
Comparative Study of Plastomes in Solanum tuberosum with Different Cytoplasm Types.
Plants (Basel)
; 12(23)2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38068632
6.
Genetic landscape in Russian patients with familial left ventricular noncompaction.
Front Cardiovasc Med
; 10: 1205787, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37342443
7.
Personalized approach in arrhythmology by genetic-based data: a case report.
Per Med
; 19(2): 83-91, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35060774
8.
Phenotypic vs. genetic cascade screening for familial hypercholesterolemia: A case report.
Front Cardiovasc Med
; 9: 982607, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36093134
9.
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.
J Pers Med
; 12(7)2022 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35887629
10.
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.
Genes (Basel)
; 13(2)2022 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35205353
11.
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.
Genes (Basel)
; 13(10)2022 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36292635
12.
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
Genes (Basel)
; 12(1)2021 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33478057
13.
Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region.
Front Genet
; 12: 709419, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34691145
14.
The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Genes (Basel)
; 12(1)2021 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33418990
15.
Cystic Fibrosis Polymorphic Variants in a Russian Population.
Pharmgenomics Pers Med
; 13: 679-686, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33623413
16.
A Data-Driven Approach to Carrier Screening for Common Recessive Diseases.
J Pers Med
; 10(3)2020 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32971794