Zobrazeno 1 - 6
of 6
pro vyhledávání: '"A M, Tazetdinov"'
Autor:
Vera N Tadinova, S. N. Ponidelko, L. U. Dzhemilova, N. R. Maksimova, S. A. Fedorova, S. A. Zhuravskii, T. G. Markova, Nikolay A. Barashkov, Olga L. Posukh, E. K. Khusnutdinova, A. M. Tazetdinov
Publikováno v:
Russian Journal of Genetics. 45:861-869
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=doi_________::318317f67f16b98c779fc8927f7af540
https://doi.org/10.1134/s1022795409070151
https://doi.org/10.1134/s1022795409070151
Publikováno v:
ResearcherID
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=doi_dedup___::ede5597a53e47a8d1f013fc07401afd2
https://doi.org/10.1134/s102279540806001x
https://doi.org/10.1134/s102279540806001x
Autor:
V. V. Musina, Elza Khusnutdinova, A. M. Tazetdinov, Grinberg Er, Lilya U. Dzhemileva, I. S. Zaidullin, Mukharram M. Bikbov
Publikováno v:
Molecular Biology. 42:1-8
The review considers tapetoretinal degeneration (TD), a severe incurable disease occurring at a frequency of 1 per 3500–5000 people. TD is most commonly caused by mutations of the genes for rhodopsin (RHO), peripherin (RDS), and retinol acetyltrans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be63d2250560ff082fc47db6f1e5be3a
https://doi.org/10.1134/s0026893308010019
https://doi.org/10.1134/s0026893308010019
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
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