Zobrazeno 1 - 10
of 31
pro vyhledávání: '"E V, Vasilyev"'
Autor:
Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 25, Iss 1, Pp 81-88 (2022)
Mutations in the GLIS3 gene encoding the GLIS3 transcription factor are cause of a rare syndromic form of neonatal diabetes mellitus (NDM) with congenital hypothyroidism. Additional features include congenital glaucoma, hepatic fibrosis, polycystic k
Externí odkaz:
https://doaj.org/article/15276206fcaa42249961e40a5ce1fb10
Autor:
M. Yu. Yukina, V. R. Mustafina, E. V. Vasilyev, E. A. Troshina, N. M. Platonova, D. G. Beltsevich
Publikováno v:
Медицинский совет, Vol 0, Iss 7, Pp 150-154 (2021)
Pheochromocytoma/paraganglioma is a neuroendocrine tumor of chromaffin and nonchromaffin cells of the autonomic nervous system, in most cases localized in the medullary layer of the adrenal gland. Its development is often associated with genetic pred
Externí odkaz:
https://doaj.org/article/64d9aa005006432183cb570b2bee2f6c
Autor:
E O Mamedova, N G Mokrysheva, E A Pigarova, E G Przhiyalkovskaya, I A Voronkova, E V Vasilyev, V M Petrov, V A Gorbunova, L Ya Rozhinskaya, Zh E Belaya, A N Tyulpakov
Publikováno v:
Терапевтический архив, Vol 88, Iss 10, Pp 57-62 (2016)
The article describes two clinical cases of severe primary hyperparathyroidism (PHPT) caused by parathyroid carcinoma in young female patients who underwent molecular genetic testing to rule out the hereditary forms of PHPT. In both patients, heteroz
Externí odkaz:
https://doaj.org/article/38ae1e1d8f9441e8beb204f3d5ea36c7
Publikováno v:
Journal of Experimental and Theoretical Physics. 132:334-340
Features of the spectral broadening of femtosecond optical vortices at self-action in a medium with the anomalous group velocity dispersion have been studied experimentally and numerically. It has been found that the broadening of the frequency–ang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e37ba89401da9d69bbabc3673bb7695e
https://doi.org/10.1134/s1063776121030183
https://doi.org/10.1134/s1063776121030183
Autor:
Anna Eremkina, Natalia Mokrysheva, E V Vasilyev, Ekaterina Bibik, Ju. A. Krupinova, A A Almaskhanova
Publikováno v:
Problems of Endocrinology. 66:61-69
Familial hypocalciuric hypercalcemia (FHH) - rare disease with predominantly autosomal dominant inheritance. FHH typically develops due to a heterozygous inactivating mutation in the calcium-sensitive receptor gene (CASR), less commonly due to hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da772e439d32bf76298b59c83879979
https://doi.org/10.14341/probl12537
https://doi.org/10.14341/probl12537
Publikováno v:
Polymer Journal. 52:1279-1287
Single- and two-photon holographic recordings were performed in a photopolymer material consisting of two types of monomers: an acrylamide (1,4-bis(acryloyl)piperazine) and an epoxide ((bis(4-oxiran-2-ylmethoxy)phenyl) sulfide). Thus, cationic ring-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8ae2bb9e9bee62996ad03eb752059ae
https://doi.org/10.1038/s41428-020-0381-2
https://doi.org/10.1038/s41428-020-0381-2
Autor:
D. A. Trukhina, E. O. Mamedova, A. M. Lapshina, E. V. Vasilyev, A. N. Tiulpakov, Zh. E. Belaya
Publikováno v:
Problemy endokrinologii. 67(6)
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN 1) is a rare autosomal dominant disorder caused by mutations in the MEN1 gene, which encodes the menin protein. If a patient has the MEN 1 phenotype in the absence of mutations in the MEN1 gene, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0ccd56094ad16d3b97e8337d607cff
https://pubmed.ncbi.nlm.nih.gov/35018761
https://pubmed.ncbi.nlm.nih.gov/35018761
Autor:
A. S. Gorbenko, M. A. Stolyar, Yu. Yu. Komarovsky, M. A. Mikhalev, V. V. Potylitsyna, E. V. Vasilyev, I. A. Olkhovsky
Publikováno v:
Medical alphabet. 3:11-14
A large-scale study of DNA sequencing databases (Jorgenson E., et al., 2018) to search for hereditary susceptibility to early erectile dysfunction revealed an association with the rs17185536-T polymorphism regulating the expression of topologically a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f646f64c7e24bf7d77024288add31b4b
https://doi.org/10.33667/2078-5631-2019-3-22(397)-11-14
https://doi.org/10.33667/2078-5631-2019-3-22(397)-11-14
Publikováno v:
Optics and Spectroscopy. 126:16-24
We analyze numerically the femtosecond filamentation of a vortex beam with the topological charge m = 1 at wavelength λ0 = 1800 nm in fused silica under anomalous group velocity dispersion conditions. We show that, as a pulse with a fivefold excess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf9ae2877b2aa32e9786353eb9943067
https://doi.org/10.1134/s0030400x19010181
https://doi.org/10.1134/s0030400x19010181
Autor:
N A, Makretskaya, M V, Gerasimova, E V, Vasilyev, N A, Zubkova, N Y, Kalinchenko, A A, Kolodkina, V M, Petrov, T V, Pogoda, A V, Panova, E B, Frolova, A V, Poliakov, A N, Tiulpakov
Publikováno v:
Problemy endokrinologii. 67(3)
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterised by lack of pubertal development and infertility, due to deficient production, secretion or action of gonadotropin-releasing hormone (GnRH). Clinically, there are variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9e687ac918143a100a7bbb44018d50e
https://pubmed.ncbi.nlm.nih.gov/34297503
https://pubmed.ncbi.nlm.nih.gov/34297503