Detalhe da pesquisa
1.
Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant ß-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson's Disease.
Int J Mol Sci
; 24(10)2023 May 22.
Artigo
Inglês
| MEDLINE | ID: mdl-37240451
2.
ABCA1 and ABCG1 DNA methylation in epicardial adipose tissue of patients with coronary artery disease.
BMC Cardiovasc Disord
; 21(1): 566, 2021 11 27.
Artigo
Inglês
| MEDLINE | ID: mdl-34837967
3.
FABP4 and omentin-1 gene expression in epicardial adipose tissue from coronary artery disease patients.
Genet Mol Biol
; 44(4): e20200441, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34609443
4.
Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?
Mov Disord
; 37(8): 1779-1781, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35792565
5.
Downregulation of Exosomal hsa-miR-551b-3p in Obesity and Its Link to Type 2 Diabetes Mellitus.
Noncoding RNA
; 9(6)2023 Nov 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37987363
6.
Cryo-electron microscopy of adipose tissue extracellular vesicles in obesity and type 2 diabetes mellitus.
PLoS One
; 18(2): e0279652, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36827314
7.
Pediatric Patients with Sitosterolemia: Next-Generation Sequencing and Biochemical Examination in Clinical Practice.
J Pers Med
; 13(10)2023 Oct 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37888103
8.
Identification of novel variants in the LDLR gene in Russian patients with familial hypercholesterolemia using targeted sequencing.
Biomed Rep
; 14(1): 15, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-33269076
9.
Mutation analysis of Parkinson's disease genes in a Russian data set.
Neurobiol Aging
; 71: 267.e7-267.e10, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30146349
10.
Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson's Disease.
Front Aging Neurosci
; 10: 136, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29867446
11.
The frequency of cytochrome P450 2C9 genetic variants in the Russian population and their associations with individual sensitivity to warfarin therapy.
Thromb Res
; 115(3): 199-203, 2005.
Artigo
Inglês
| MEDLINE | ID: mdl-15617742
12.
G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia.
Mov Disord
; 21(12): 2234-6, 2006 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-17044089