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Page 1
Asymmetric scapuloperoneal phenotype of MATR3-related distal myopathy: case series.
Murtazina A, Subbotin D, Kuchina A, Gilvanova O, Degterev D, Shchagina O, Cherevatova T, Bulakh M, Sherstyukova D, Ryzhkova O, Kurushina O, Skoblov M, Borovikov A, Kutsev S. Murtazina A, et al. Among authors: kuchina a. Front Genet. 2024 Aug 13;15:1414928. doi: 10.3389/fgene.2024.1414928. eCollection 2024. Front Genet. 2024. PMID: 39192891 Free PMC article.
Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3.
Murtazina A, Borovikov A, Kuchina A, Ovsova O, Bulakh M, Chukhrova A, Braslavskaya S, Ryzhkova O, Skryabin N, Kutsev S, Dadali E. Murtazina A, et al. Among authors: kuchina a. Int J Mol Sci. 2023 Dec 21;25(1):129. doi: 10.3390/ijms25010129. Int J Mol Sci. 2023. PMID: 38203298 Free PMC article.
Pediatric Patients with Sitosterolemia: Next-Generation Sequencing and Biochemical Examination in Clinical Practice.
Miroshnikova VV, Vasiluev PA, Linkova SV, Soloviov VM, Ivanova ON, Tolmacheva ER, Udalova VY, Baranova PV, Aleksandrova DY, Strokova TV, Miklashevich IM, Izumchenko AD, Dracheva KV, Grunina MN, Smirnova NN, Kuchina AS, Zakharova EY, Pchelina SN. Miroshnikova VV, et al. Among authors: kuchina as. J Pers Med. 2023 Oct 14;13(10):1492. doi: 10.3390/jpm13101492. J Pers Med. 2023. PMID: 37888103 Free PMC article.
[A case of spastic paraplegia with SPG4 and SPG3 associated mutations].
Rudenskaya GE, Kuchina AS, Kadnikova VA, Ryzhkova OP. Rudenskaya GE, et al. Among authors: kuchina as. Zh Nevrol Psikhiatr Im S S Korsakova. 2023;123(5):171-176. doi: 10.17116/jnevro2023123051171. Zh Nevrol Psikhiatr Im S S Korsakova. 2023. PMID: 37315258 Russian.
Microbial single-cell RNA sequencing by split-pool barcoding.
Kuchina A, Brettner LM, Paleologu L, Roco CM, Rosenberg AB, Carignano A, Kibler R, Hirano M, DePaolo RW, Seelig G. Kuchina A, et al. Science. 2021 Feb 19;371(6531):eaba5257. doi: 10.1126/science.aba5257. Epub 2020 Dec 17. Science. 2021. PMID: 33335020 Free PMC article.
17 results