Showing 1 - 13 results of 13 for search 'A. A. Kashevarova', query time: 0.05s
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Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene by M.M. Gridina, T.V. Nikitina, I.E. Pristyazhnyuk, A.A. Kashevarova, M.E. Lopatkina, S.A. Vasilyev, L.P. Nazarenko, I.N. Lebedev, O.L. Serov
Published 2019-10-01
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Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13 by T.V. Nikitina, A.G. Menzorov, A.A. Kashevarova, M.M. Gridina, A.A. Khabarova, Yu.S. Yakovleva, M.E. Lopatkina, I.E. Pristyazhnyuk, S.A. Vasilyev, O.L. Serov, I.N. Lebedev
Published 2018-12-01
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Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22 by T.V. Nikitina, A.G. Menzorov, A.A. Kashevarova, M.M. Gridina, A.A. Khabarova, Yu.S. Yakovleva, M.E. Lopatkina, E.A. Kizilova, S.A. Vasilyev, O.L. Serov, I.N. Lebedev
Published 2018-08-01
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Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18 by A.A. Khabarova, I.E. Pristyazhnyuk, P.A. Orlova, T.V. Nikitina, A.A. Kashevarova, M.E. Lopatkina, E.O. Belyaeva, N.N. Sukhanova, L.P. Nazarenko, I.N. Lebedev, O.L. Serov
Published 2020-12-01
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Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability by T.A. Shnaider, I.E. Pristyazhnyuk, A.G. Menzorov, N.M. Matveeva, T.V. Nikitina, A.A. Khabarova, N.A. Skryabin, A.A. Kashevarova, M.E. Lopatkina, L.P. Nazarenko, I.N. Lebedev, O.L. Serov
Published 2019-12-01
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Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism by M.M. Gridina, T.V. Nikitina, P.A. Orlova, J.M. Minina, A.A. Kashevarova, Yu.S. Yakovleva, M.E. Lopatkina, S.A. Vasilyev, D.A. Fedotov, L.I. Mikhailik, L.P. Nazarenko, I.N. Lebedev, O.L. Serov
Published 2020-12-01
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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies by E. A. Fonova, A. A. Kashevarova, M. E. Lopatkina, A. A. Sivtsev, A. A. Zarubin, V. V. Demeneva, G. N. Seitova, L. I. Minaycheva, O. A. Salyukova, S. V. Fadyushina, V. V. Petrova, E. O. Belyaeva, L. P. Nazarenko, I. N. Lebedev
Published 2023-03-01
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Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4 by M.M. Gridina, A.R. Nurislamov, J.M. Minina, M.E. Lopatkina, G.V. Drozdov, S.A. Vasilyev, L.I. Minaycheva, E.O. Belyaeva, T.V. Nikitina, A.A. Kashevarova, I.N. Lebedev, T.V. Karamysheva, N.B. Rubtsov, O.L. Serov
Published 2022-05-01
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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability by A. A. Kashevarova, E. O. Belyaeva, E. A. Fonova, M. E. Lopatkina, O. Y. Vasilyeva, D. A. Fedotov, A. A. Zarubin, A. A. Sivtsev, V. V. Demeneva, O. A. Salyukova, V. V. Petrova, S. V. Fadiushina, L. I. Minaycheva, G. N. Seitova, L. P. Nazarenko, I. N. Lebedev
Published 2023-03-01
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Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1... by A. A. Kashevarova, M. E. Lopatkina, O. Yu. Vasilyeva, D. A. Fedotov, A. D. Lobanov, E. A. Fonova, I. Z. Zhalsanova, A. A. Zarubin, O. A. Salyukova, E. O. Belyaeva, V. V. Petrova, E. G. Ravzhaeva, A. A. Agafonova, A. D. Cheremnykh, N. B. Torkhova, S. L. Vovk, I. N. Lebedev
Published 2025-01-01
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A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication by T. V. Karamysheva, T. V. Karamysheva, I. N. Lebedev, I. N. Lebedev, L. I. Minaycheva, L. P. Nazarenko, L. P. Nazarenko, A. A. Kashevarova, D. A. Fedotov, N. A. Skryabin, M. E. Lopatkina, A. D. Cheremnykh, E. A. Fonova, E. A. Fonova, T. V. Nikitina, E. A. Sazhenova, M. M. Skleimova, N. A. Kolesnikov, G. V. Drozdov, Y. S. Yakovleva, Y. S. Yakovleva, G. N. Seitova, K. E. Orishchenko, K. E. Orishchenko, N. B. Rubtsov, N. B. Rubtsov
Published 2024-03-01
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