Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 2 |
2020 | 3 |
2022 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia.
Genes (Basel). 2022 Nov 23;13(12):2186. doi: 10.3390/genes13122186.
Genes (Basel). 2022.
PMID: 36553453
Free PMC article.
P.F508del editing in cells from cystic fibrosis patients.
Smirnikhina SA, Kondrateva EV, Adilgereeva EP, Anuchina AA, Zaynitdinova MI, Slesarenko YS, Ershova AS, Ustinov KD, Yasinovsky MI, Amelina EL, Voronina ES, Yakushina VD, Tabakov VY, Lavrov AV.
Smirnikhina SA, et al. Among authors: tabakov vy.
PLoS One. 2020 Nov 11;15(11):e0242094. doi: 10.1371/journal.pone.0242094. eCollection 2020.
PLoS One. 2020.
PMID: 33175893
Free PMC article.
Item in Clipboard
Activation of Mitochondrial 2-Oxoglutarate Dehydrogenase by Cocarboxylase in Human Lung Adenocarcinoma Cells A549 Is p53/p21-Dependent and Impairs Cellular Redox State, Mimicking the Cisplatin Action.
Bunik VI, Aleshin VA, Zhou X, Tabakov VY, Karlsson A.
Bunik VI, et al. Among authors: tabakov vy.
Int J Mol Sci. 2020 May 26;21(11):3759. doi: 10.3390/ijms21113759.
Int J Mol Sci. 2020.
PMID: 32466567
Free PMC article.
Item in Clipboard
Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy.
Krylova TD, Sheremet NL, Tabakov VY, Lyamzaev KG, Itkis YS, Tsygankova PG, Andreeva NA, Shmelkova MS, Nevinitsyna TA, Kadyshev VV, Zakharova EY.
Krylova TD, et al. Among authors: tabakov vy.
Mitochondrion. 2020 Jan;50:139-144. doi: 10.1016/j.mito.2019.10.002. Epub 2019 Oct 26.
Mitochondrion. 2020.
PMID: 31669237
Item in Clipboard
A novel variant m.641A>T in the mitochondrial MT-TF gene is associated with epileptic encephalopathy in adolescent.
Itkis Y, Krylova T, Pechatnikova NL, De Grassi A, Tabakov VY, Pierri CL, Aleshin V, Boyko A, Bunik VI, Zakharova EY.
Itkis Y, et al. Among authors: tabakov vy.
Mitochondrion. 2019 Jul;47:10-17. doi: 10.1016/j.mito.2019.04.004. Epub 2019 Apr 19.
Mitochondrion. 2019.
PMID: 31009750
Item in Clipboard
Two novel COL6A3 mutations disrupt extracellular matrix formation and lead to myopathy from Ullrich congenital muscular dystrophy and Bethlem myopathy spectrum.
Marakhonov AV, Tabakov VY, Zernov NV, Dadali EL, Sharkova IV, Skoblov MY.
Marakhonov AV, et al. Among authors: tabakov vy.
Gene. 2018 Sep 25;672:165-171. doi: 10.1016/j.gene.2018.06.026. Epub 2018 Jun 9.
Gene. 2018.
PMID: 29894794
Item in Clipboard
Cite
Cite