Zobrazeno 1 - 10
of 121
pro vyhledávání: '"L U, Dzhemileva"'
Publikováno v:
Russian Chemical Bulletin. 72:404-414
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa58b2ce99f4f9bd0262cde14e6f34ad
https://doi.org/10.1007/s11172-023-3808-8
https://doi.org/10.1007/s11172-023-3808-8
Publikováno v:
Doklady Chemistry. 504:106-117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f40f169700f7e5ba1fe422483973503e
https://doi.org/10.1134/s0012500822600080
https://doi.org/10.1134/s0012500822600080
Autor:
N. N. Makhmudiyarova, L. U. Dzhemileva, A. G. Ibragimov, V. A. Dyakonov, I. R. Ishmukhametova
Publikováno v:
Вестник Башкирского университета. :717
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3915c6050b9a9d83381fee1147c22975
https://doi.org/10.33184/bulletin-bsu-2021.3.32
https://doi.org/10.33184/bulletin-bsu-2021.3.32
Autor:
Makarova, E. Kh., Makarov, A. A.
Publikováno v:
Russian Chemical Bulletin; Jul2024, Vol. 73 Issue 7, p1916-1922, 7p
Publikováno v:
Russian Chemical Bulletin; Jun2024, Vol. 73 Issue 6, p1623-1630, 8p
Autor:
L U, Dzhemileva, O L, Posukh, A M, Tazetdinov, N A, Barashkov, S G, Zhuravskiĭ, S N, Ponidelko, T G, Markova, V N, Tadinova, S A, Fedorova, N R, Maksimova, E K, Khusnutdinova
Publikováno v:
Genetika. 45(7)
Mitochondrial DNA (mtDNA) mutations play an important role in etiology of hereditary hearing loss. In various regions of the world, patients suffer from nonsyndromic sensorineural hearing loss initiated by aminoglycoside antibiotics. Mutations that h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80d980d3641fb2192963de89c6bfd63f
https://pubmed.ncbi.nlm.nih.gov/19705751
https://pubmed.ncbi.nlm.nih.gov/19705751
Autor:
F M, Teriutin, N A, Barashkov, L U, Dzhemileva, O L, Posukh, E E, Fedotova, E E, Gurinova, S A, Fedorova, G A, Tavartkiladze, E K, Khusnutdinova
Publikováno v:
Vestnik otorinolaringologii. (2)
This paper reports the first case of cochlear implantation performed in this country in a child with congenital non-syndromic sensorineural loss of hearing having hereditary etiology and attributable to autosomal-recessive 35 delG mutation in locus D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3c9cf7f6da60c011e00f60332f9bb06
https://pubmed.ncbi.nlm.nih.gov/19491791
https://pubmed.ncbi.nlm.nih.gov/19491791
Publikováno v:
Vestnik otorinolaringologii. (5)
The aim of the study was to elucidate the causes of hereditary non-syndromic loss of hearing, a frequent monogene pathology in the Republic of Sakha (Yakutia). A search for mutations in the coding sequence of the connexin 26 gene gap-junction B2 (GJB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66d8adce74c1d2ec45e95ecf820da52a
https://pubmed.ncbi.nlm.nih.gov/19008837
https://pubmed.ncbi.nlm.nih.gov/19008837
Publikováno v:
Genetika. 44(6)
Usher syndrome (USH) is inherited in an autosomal recessive mode. The disease is characterized by hearing loss, progressing vision loss, and vestibular dysfunction. In most cases, it is the reason for deafness and blindness in school-age children. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d30bf72b9277914e4bfad644a5cd379d
https://pubmed.ncbi.nlm.nih.gov/18727382
https://pubmed.ncbi.nlm.nih.gov/18727382
Autor:
L U, Dzhemileva, E R, Grinberg, A M, Tazetdinov, I S, Zaĭĭdullin, M M, Bibkov, V V, Musina, E K, Khusnutdinova
Publikováno v:
Molekuliarnaia biologiia. 42(1)
The review on problem tapetoretinal degeneration (TD) which represents serious enough and incurable disease revealed with frequency 1 : 3500-5000 in general population is presented. The most often reason of occurrence TD are mutations in RHO, RDS and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f14aafa830d73dc02272ab529309d3c6
https://pubmed.ncbi.nlm.nih.gov/18389614
https://pubmed.ncbi.nlm.nih.gov/18389614