Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yu V Maksimova"'
Autor:
O. M. Lesnyak, E. N. Gladkova, O. B. Ershova, I. A. Skripnikova, O. N. Anoshenkova, Yu. R. Akhverdyan, K. Yu. Belova, I. B. Belousova, E. V. Bolshakova, A. V. Dreval, B. V. Zavodovsky, M. V. Ilyin, O. V. Kosmatova, L. V. Kryukova, A. A. Latfullin, E. A. Leikauskene, N. V. Leonova, Yu. V. Maksimova, M. A. Myagkova, V. E. Novikov, A. R. Nuriev, E. Yu. Polyakova, Yu. V. Polyakova, L. E. Sivordova, V. A. Tavluev, L. R. Shavalieva
Publikováno v:
Научно-практическая ревматология, Vol 57, Iss 6, Pp 626-635 (2019)
Objective: to analyze the clinical and organizational feasibility of using different intervention thresholds for the Russian population.Subjects and methods. The probability of fractures using the Russian FRAX model was calculated on a sample of 3,86
Externí odkaz:
https://doaj.org/article/9687aecbe1de425f96c5ed3306860f1b
Autor:
O. N. Anoshenkova, A. N. Kalyagin, Yu. V. Maksimova, N. G. Sindykheeva, A. V. Sinkov, G. M. Sinkova
Publikováno v:
Современная ревматология, Vol 12, Iss 4, Pp 112-117 (2018)
Management of patients with knee osteoarthritis (OA) in the presence of comorbidity causes significant difficulties associated with the limitations of pharmacotherapy.Objective: to evaluate the clinical efficacy of ultraphonophoresis with a hyaluroni
Externí odkaz:
https://doaj.org/article/9462e8563fb84b0882c06d0084cef786
Publikováno v:
Атеросклероз, Vol 14, Iss 3, Pp 64-69 (2018)
The review provides information on studies that have studied the relationship between the number of copies of mitochondrial DNA (mtDNA) in peripheral blood leukocytes with coronary heart disease and sudden cardiac death (SCD). Mitochondrial dysfuncti
Externí odkaz:
https://doaj.org/article/b16a6b71fc5743eb90ee9d7c62113946
Autor:
I. S. Kolesnikova, A. A. Tulupov, A. A. Dolskiy, M. A. Lemskaya, A. A. Savelov, E. D. Petrovsky, A. A. Antonov, Yu. V. Maksimova, A. R. Shorina, I. G. Sergeeva, A. S. Telepova, A. S. Graphodatsky, D. V. Yudkin
Publikováno v:
Бюллетень сибирской медицины, Vol 17, Iss 1, Pp 243-253 (2018)
A study of a child with intellectual disability revealed an enlarged p-arm in chromosome 13 and amplified rDNA. qRT-PCR showed an approximately 6-fold increased level of rRNA in the patient’s blood samples. fMRI study revealed changes in uncinate f
Externí odkaz:
https://doaj.org/article/f9f58ee6363c40e193145f147a66f87d
Autor:
N.O. Artemyeva Artemyeva, Yu. V. Maksimova, E.V. Svechnikova Svechnikova, V.N. Maksimov Maksimov
Publikováno v:
Pharmateca. :99-103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c6c0181c279340afeadc74993cfe992
https://doi.org/10.18565/pharmateca.2021.8.99-103
https://doi.org/10.18565/pharmateca.2021.8.99-103
Autor:
Yu. V. Maksimova, Asia R. Shorina, Dmitry V. Yudkin, Irina V. Grishchenko, Natalya A. Lemskaya, M.M. Gridina, E.M. Shitik, J.M. Minina, Alexander A. Dolskiy
Publikováno v:
Stem Cell Research, Vol 57, Iss, Pp 102615-(2021)
Trinucleotide repeat expansion diseases such as fragile X syndrome are of great interest to study since the mechanism of its development is still unknown. IPS cell lines are some of the most convenient models for studying. The ICGi032-A iPS cell line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50c0d382ceafbeba45ddd856f46d7461
https://pubmed.ncbi.nlm.nih.gov/34864218
https://pubmed.ncbi.nlm.nih.gov/34864218
Autor:
A. S. Telepova, Natalya A. Lemskaya, Yu. V. Maksimova, Asia R. Shorina, Svetlana A. Romanenko, Dmitry V. Yudkin
Publikováno v:
Molecular Genetics, Microbiology and Virology. 33:241-244
Marker chromosomes are structurally abnormal chromosomes that may be supernumerary in karyotype or replace one of the chromosomes. Marker chromosomes very frequently can be a cause of different pathologies, including a intellectual disability. This s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a72e627978d348a3a79613b970df414
https://doi.org/10.3103/s0891416818040080
https://doi.org/10.3103/s0891416818040080
Autor:
Yu. V. Maksimova, E.M. Shitik, P.A. Orlova, Natalya A. Lemskaya, Oleg L. Serov, J.M. Minina, Asia R. Shorina, Dmitry V. Yudkin, M.M. Gridina, Alexander A. Dolskiy, Irina V. Grishchenko
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102070-(2020)
Expansion over 200 CGG repeats in FMR1 gene causes inherited intellectual disability or autism spectrum disorder named as fragile X syndrome. Despite the known cause fragile X syndrome pathogenesis has not been specified yet. The ICGi026-A iPSCs line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::193eac7765baaa62a435627da25ca98e
https://doi.org/10.1016/j.scr.2020.102070
https://doi.org/10.1016/j.scr.2020.102070
Autor:
A. S. Telepova, Natalya A. Lemskaya, Dmitry V. Yudkin, Svetlana A. Romanenko, Asia R. Shorina, Yu. V. Maksimova
Publikováno v:
Molecular Genetics Microbiology and Virology (Russian version). 36:199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbd53d66e81f9814d1823f0e3395194c
https://doi.org/10.17116/molgen201836041199
https://doi.org/10.17116/molgen201836041199
Publikováno v:
Arkhiv patologii. 80:54
To summarize an update on epidermolysis bullosa as a polymorphic group of inherited diseases with a failure of epidermal-dermal integrity. Emphasis is placed on the role of transmission electron microscopy in diagnosis and search directions for new t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::241f6f1bcad612aec2571a5faa68d224
https://doi.org/10.17116/patol201880454
https://doi.org/10.17116/patol201880454