Zobrazeno 1 - 10
of 60
pro vyhledávání: '"A.A. Kashevarova"'
Autor:
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
Publikováno v:
Stem Cell Research, Vol 61, Iss , Pp 102740- (2022)
Human induced pluripotent stem cell (iPSC) line, ICGi040-A, was obtained from skin fibroblasts derived from a male patient with mosaic ring small supernumerary marker chromosome 4 (sSMS(4)) and infertility. ICGi040-A cells have karyotype 47,XY,+r(4)
Externí odkaz:
https://doaj.org/article/d7f5a9e8c14e463f96b52dab8a7e1f5d
Autor:
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
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 260-264 (2018)
Skin fibroblasts from a patient with neurodevelopmental and speech delay, anxiety disorder, macrocephaly, microorchidism, multiple anomalies of internal organs and ring chromosome 13 were reprogrammed into induced pluripotent stem cells (iPSCs) to ge
Externí odkaz:
https://doaj.org/article/1c1ecdbddc4147e38877fa949de094e4
Autor:
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
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102024- (2020)
Ring chromosomes are structural aberrations commonly associated with disease phenotype. We consider necessary to create the iPSCs with a ring chromosome 8, which can be used for disease modeling and related research. The ICGi025-A iPSCs line was obta
Externí odkaz:
https://doaj.org/article/78ecab7e9a1c48df933c645bcd48b054
Autor:
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
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102076- (2020)
Ring chromosome 18 is a rare chromosomal disorders that usually originate de novo and correlate with clinical manifestation: developmental delay as well as microcephaly, brain and ocular malformations, hypotonia and skeletal abnormalities. We generat
Externí odkaz:
https://doaj.org/article/59a35783c80f4d2cb8ead57dc53f533d
Autor:
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
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
The human induced pluripotent stem cell (iPSC) lines, ICGi009-A, ICGi009-B, ICGi013-A and ICGi013-B, were generated from skin fibroblasts of two siblings with intellectual disability. Both patients were carriers of CNTN6 gene microdeletion (Kashevaro
Externí odkaz:
https://doaj.org/article/729db15e2ea6400985dcec4c9b9e49cc
Autor:
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
Publikováno v:
Stem Cell Research, Vol 31, Iss , Pp 244-248 (2018)
Skin fibroblasts from a patient with intellectual disability and ring chromosome 22 were reprogrammed into induced pluripotent stem cells (iPSCs) to establish a clonal stem cell lines, IMGTi001-A (iTAF5-29) and IMGTi001-B (iTAF5-32). Because of ring
Externí odkaz:
https://doaj.org/article/9344b4359702432ca779b7e21ed80c73
Autor:
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
Publikováno v:
Stem Cell Research, Vol 40, Iss , Pp - (2019)
The 3p26.3 microduplication involving the CNTN6 gene cause developmental delay and the intellectual disability. However, the incomplete penetrance is described for this copy number variation (CNV). Here we describe ICAGi002-A line, which is supposed
Externí odkaz:
https://doaj.org/article/d8934db88da6445ba9404553b6a10a7d
Autor:
A.A. Khabarova, I.E. Pristyazhnyuk, T.V. Nikitina, T.A. Gayner, N.B. Torkhova, N.A. Skryabin, A.A. Kashevarova, N.P. Babushkina, Zh.G. Markova, M.E. Minzhenkova, L.P. Nazarenko, N.V. Shilova, A.R. Shorina, I.N. Lebedev, O.L. Serov
Publikováno v:
Stem Cell Research, Vol 34, Iss , Pp - (2019)
Skin fibroblasts from a patient with developmental delay and chromosome 2p25.3 deletion syndrome were reprogrammed into induced pluripotent stem cells (iPSCs) and the clonal stem cell line ICAGi001-A (iTAF9-11) was established. ICAGi001-A pluripotenc
Externí odkaz:
https://doaj.org/article/4b43b86ada254fb2a11ebe43842241dc
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Akademický článek
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