Baydakova GV - Search Results

1

Oxidized DNA induces an adaptive response in human fibroblasts.

Kostyuk SV, Tabakov VJ, Chestkov VV, Konkova MS, Glebova KV, Baydakova GV, Ershova ES, Izhevskaya VL, Baranova A, Veiko NN. Kostyuk SV, et al. Among authors: baydakova gv. Mutat Res. 2013 Jul-Aug;747-748:6-18. doi: 10.1016/j.mrfmmm.2013.04.007. Epub 2013 May 1. Mutat Res. 2013. PMID: 23644378

2

Functional Analysis of the PCCA and PCCB Gene Variants Predicted to Affect Splicing.

Bychkov I, Galushkin A, Filatova A, Nekrasov A, Kurkina M, Baydakova G, Ilyushkina A, Skoblov M, Zakharova E. Bychkov I, et al. Int J Mol Sci. 2021 Apr 16;22(8):4154. doi: 10.3390/ijms22084154. Int J Mol Sci. 2021. PMID: 33923806 Free PMC article.

3

Additive effect of frequent polymorphism and rare synonymous variant alters splicing in twin patients with Niemann-Pick disease type C.

Bychkov I, Filatova A, Perelman G, Proshlyakova T, Korotkova D, Klyushnikov S, Karpova M, Tabakov V, Baydakova G, Ilyushkina A, Skoblov M, Zakharova E. Bychkov I, et al. Eur J Hum Genet. 2022 Jan;30(1):133-136. doi: 10.1038/s41431-021-00898-7. Epub 2021 May 6. Eur J Hum Genet. 2022. PMID: 33958742 Free PMC article.

4

Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease.

Grigor'eva EV, Kopytova AE, Yarkova ES, Pavlova SV, Sorogina DA, Malakhova AA, Malankhanova TB, Baydakova GV, Zakharova EY, Medvedev SP, Pchelina SN, Zakian SM. Grigor'eva EV, et al. Among authors: baydakova gv. Int J Mol Sci. 2023 Feb 23;24(5):4437. doi: 10.3390/ijms24054437. Int J Mol Sci. 2023. PMID: 36901867 Free PMC article.

5

Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson's Disease.

Kopytova AE, Rychkov GN, Cheblokov AA, Grigor'eva EV, Nikolaev MA, Yarkova ES, Sorogina DA, Ibatullin FM, Baydakova GV, Izyumchenko AD, Bogdanova DA, Boitsov VM, Rybakov AV, Miliukhina IV, Bezrukikh VA, Salogub GN, Zakharova EY, Pchelina SN, Emelyanov AK. Kopytova AE, et al. Among authors: baydakova gv. Int J Mol Sci. 2023 May 22;24(10):9105. doi: 10.3390/ijms24109105. Int J Mol Sci. 2023. PMID: 37240451 Free PMC article.

6

Gene symbol: ACADVL. Disease: Very long chain acyl-CoA dehydrogenase deficiency.

Tsygankova P, Zakharova EY, Baydakova GV. Tsygankova P, et al. Among authors: baydakova gv. Hum Genet. 2008 Oct;124(3):299. Hum Genet. 2008. PMID: 18846621 No abstract available.

7

Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease.

Pchelina S, Emelyanov A, Baydakova G, Andoskin P, Senkevich K, Nikolaev M, Miliukhina I, Yakimovskii A, Timofeeva A, Fedotova E, Abramycheva N, Usenko T, Kulabukhova D, Lavrinova A, Kopytova A, Garaeva L, Nuzhnyi E, Illarioshkin S, Zakharova E. Pchelina S, et al. Neurosci Lett. 2017 Jan 1;636:70-76. doi: 10.1016/j.neulet.2016.10.039. Epub 2016 Oct 22. Neurosci Lett. 2017. PMID: 27780739

8

Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations.

Pchelina S, Baydakova G, Nikolaev M, Senkevich K, Emelyanov A, Kopytova A, Miliukhina I, Yakimovskii A, Timofeeva A, Berkovich O, Fedotova E, Illarioshkin S, Zakharova E. Pchelina S, et al. Mov Disord. 2018 Aug;33(8):1325-1330. doi: 10.1002/mds.27393. Epub 2018 Sep 7. Mov Disord. 2018. PMID: 30192031

9

The Unique Spectrum of Mutations in Patients with Hereditary Tyrosinemia Type 1 in Different Regions of the Russian Federation.

Baydakova GV, Ivanova TA, Mikhaylova SV, Saydaeva DK, Dzhudinova LL, Akhlakova AI, Gamzatova AI, Bychkov IO, Zakharova EY. Baydakova GV, et al. JIMD Rep. 2019;45:89-93. doi: 10.1007/8904_2018_144. Epub 2018 Nov 11. JIMD Rep. 2019. PMID: 30414057 Free PMC article.

10

Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up.

Lipiński P, Kuchar L, Zakharova EY, Baydakova GV, Ługowska A, Tylki-Szymańska A. Lipiński P, et al. Among authors: baydakova gv. Orphanet J Rare Dis. 2019 Feb 22;14(1):55. doi: 10.1186/s13023-019-1029-1. Orphanet J Rare Dis. 2019. PMID: 30795770 Free PMC article.

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