Zobrazeno 1 - 2
of 2
pro vyhledávání: '"I. R. Fatkhullina"'
Autor:
E. D. Nikolaeva, D. Yu. Ovsyannikov, V. A. Strel’nikova, D. P. Polyakov, T. V. Tronza, O. A. Karpova, I. R. Fatkhullina, Е. E. Bragina, O. A. Shchagina, M. A. Starinova, S. А. Krasovskiy, T. A. Kyian, E. K. Zhekaite
Publikováno v:
PULMONOLOGIYA. 33:198-209
Primary ciliary dyskinesia (PCD) (Online Mendelian Inheritance in Man - OMIM - #242650) is a rare hereditary disease, which is based on a defect in the ultrastructure of the cilia epithelium of the respiratory tract which leads to the motor function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94ff5f9eac7033db1a4568f7610405d3
https://doi.org/10.18093/0869-0189-2023-33-2-198-209
https://doi.org/10.18093/0869-0189-2023-33-2-198-209
Autor:
E. I. Kondratyeva, N. D. Odinaeva, E. K. Zhekaite, E. V. Pasnova, I. R. Fatkhullina, T. Yu. Maksimycheva, V. D. Sherman, S. I. Kutsev
Publikováno v:
PULMONOLOGIYA. 33:189-197
Pathogenetic therapy for the treatment of cystic fibrosis (CF) has been developed that modulates the CFTR protein and restores its activity as a chloride channel. This treatment is represented by CFTR modulators for various genotypes covering 85 - 90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2140ccfe91d3d04584580c439990461
https://doi.org/10.18093/0869-0189-2023-33-2-189-197
https://doi.org/10.18093/0869-0189-2023-33-2-189-197