Zobrazeno 1 - 10
of 179
pro vyhledávání: '"T.V. Nikitina"'
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:
D.I. Zhigalina, A.A. Malakhova, O.Yu. Vasilyeva, E.V. Grigor'eva, A.A. Sivtsev, N.A. Kolesnikov, M.E. Lopatkina, R.R. Savchenko, I.Zh. Zhalsanova, A.E. Postrigan', A.A. Zarubin, T.V. Nikitina, A.O. Bueverov, P.O. Bogomolov, S.M. Zakian, N.A. Skryabin
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102556- (2021)
Wilson’s disease is a rare autosomal recessive disorder of copper metabolism. The copper accumulation in the viscera appears due to the functional impairment of copper-transporting ATPase, which is encoded by the ATP7B gene. In this study, PBMCs of
Externí odkaz:
https://doaj.org/article/8d6c5d2f67e44c1bbd16929bb4e7e7d8
Autor:
E.A. Burilova, L.I. Vagapova, Z.A. Nasirova, T.V. Nikitina, A.N. Solodov, J.R. Shaiymova, R.R. Amirov
Publikováno v:
Učënye Zapiski Kazanskogo Universiteta. Seriâ Estestvennye Nauki, Vol 161, Iss 2, Pp 199-210 (2019)
The hydration state of the first coordination sphere of manganese complexes with hydroxyethylidene diphosphonic acid (HEDP, H4L) as well as for Mn(II) systems with salt compositions of aminomethylated calix[4]resorcinol (AMC) of different lipophilici
Externí odkaz:
https://doaj.org/article/598cb799d175402491e7abe560018d03
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:
E.A. Burilova, T.V. Nikitina, L.I. Vagapova, Z.A. Nasirova, A.N. Solodov, J.R. Shaiymova, R.R. Amirov
Publikováno v:
Učënye Zapiski Kazanskogo Universiteta. Seriâ Estestvennye Nauki, Vol 160, Iss 2, Pp 185-199 (2018)
The constants of protolytic equilibria for hydroxyethylidene diphosphonic acid (HEDP), aminomethylated calix[4]resorcinol (AMC), and the composition based on them (AMC-HEDP) in a solution of nonionic surfactant-polyoxyethylated dodecanol Brij-35 have
Externí odkaz:
https://doaj.org/article/e19d06f20225440ba231cb4e8b8288be
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