Detalhe da pesquisa
1.
Can Modern Molecular Modeling Methods Help Find the Area of Potential Vulnerability of Flaviviruses?
Int J Mol Sci;
23(14)2022 Jul 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35887069
2.
Pseudomonas Phage MD8: Genetic Mosaicism and Challenges of Taxonomic Classification of Lambdoid Bacteriophages.
Int J Mol Sci;
22(19)2021 Sep 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34638693
3.
Prompt apoptotic response to high glucose in SGLT-expressing renal cells.
Am J Physiol Renal Physiol;
316(5): F1078-F1089, 2019 05 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30864838
4.
Benign Pleural Mesothelial Cells Have Higher Osmotic Water Permeability than Malignant Pleural Mesothelioma Cells and Differentially Respond to Hyperosmolality.
Cell Physiol Biochem;
52(4): 869-878, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30958661
5.
Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).
ScientificWorldJournal;
2019: 5198931, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31015822
6.
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
BMC Med Genet;
19(1): 138, 2018 08 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30086704
7.
Regulation of Neuronal Na,K-ATPase by Extracellular Scaffolding Proteins.
Int J Mol Sci;
19(8)2018 Jul 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30060621
8.
AT1-receptor response to non-saturating Ang-II concentrations is amplified by calcium channel blockers.
BMC Cardiovasc Disord;
17(1): 126, 2017 05 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28514967
9.
A noncanonical postsynaptic transport route for a GPCR belonging to the serotonin receptor family.
J Neurosci;
32(50): 17998-8008, 2012 Dec 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23238716
10.
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).
Genes (Basel);
14(5)2023 04 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37239361
11.
Biochemical Properties of a Promising Milk-Clotting Enzyme, Moose (Alces alces) Recombinant Chymosin.
Foods;
12(20)2023 Oct 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37893665
12.
Spatial distribution of Na+-K+-ATPase in dendritic spines dissected by nanoscale superresolution STED microscopy.
BMC Neurosci;
12: 16, 2011 Jan 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21272290
13.
Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
Diagnostics (Basel);
11(12)2021 Dec 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34943614
14.
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.
Eur J Hum Genet;
29(6): 965-976, 2021 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33767456
15.
High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect.
Genes (Basel);
11(7)2020 07 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32708339
16.
Unique Mutational Spectrum of the GJB2 Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys).
Genes (Basel);
10(6)2019 06 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31195736
17.
A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia).
Int J Circumpolar Health;
78(1): 1630219, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31213145
18.
A family of silicon transporter structural genes in a pennate diatom Synedra ulna subsp. danica (Kütz.) Skabitsch.
PLoS One;
13(8): e0203161, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30157241
19.
Bioluminescent SNP genotyping technique: Development and application for detection of melanocortin 1 receptor gene polymorphisms.
Talanta;
189: 111-115, 2018 Nov 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30086893
20.
A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2).
Int J Pediatr Otorhinolaryngol;
104: 94-97, 2018 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29287890