Search Results - "Melyanovskaya, Yu"

Some phytochemicals and sugar contents of black mulberry (Morus nigra L.) genotypes from Simav District, Kütahya Province, Turkey by Okatan, V., Gündeşli, M. A., Melyanovskaya, A. Yu, Panfilova, O. V., Krasova, N. G.

“…The purpose of this research was to determine the biochemical contents in black ( Morus nigra L.) mulberry genotypes grown in Kütahya Province. Total soluble…”
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A clinical case of cystic fibrosis patient with pathogenic N1303K genotype variant with assessment of the CFTR channel function by intestinal current measurement and forskolin-induced swelling in rectal organoids by Kondratyeva, E. I., Odinaeva, N. D., Sherman, V. D., Efremova, A. S., Melyanovskaya, Yu. L., Bulatenko, N. V., Bukharova, T. B., Goldshtein, D. V.

“…Rationale : Cystic fibrosis is a common monogenic disease related to pathogenic nucleotide sequence variants in the Cystic Fibrosis Transmembrane conductance…”
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Assessment of vitamin D supply at different age by Kondratyeva, E. I., Loshkova, E. V., Zakharova, I. N., Shubina, Yu. F., Saprina, T. V., Nikonova, V. S., Melyanovskaya, Yu. L., Zodbinova, A. E., Zhekayte, E. K., Odinaeva, N. D.

“…Introduction . Carrying out studies on the supply of vitamin D in the Russian population is an important task in order to demonstrate the global nature…”
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Assessment of the risk of hearing loss in children with cystic fibrosis by Polyakov, D P, Daikhes, N A, Bazanova, M V, Melyanovskaya, Yu L

“…Cystic fibrosis (CF) is a severe hereditary disease with a multisystem lesion. Manifestations of CF include severe infectious purulent lesions of all parts of…”
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Clinical and genetic characterization of patients with cystic fibrosis and functional assessment of the chloride channel with the pathogenic variant c.831G>A (p.Trp277), described for the first time by Kondratyeva, E., Efremova, A., Melyanovskaya, Yu, Petrova, N., Satsuk, N., Bulatenko, N., Bukharova, T., Zodbinova, A., Sherman, V., Kashirskaya, N., Zinchenko, R., Kutsev, S., Goldshtein, D.

“…•The study results showed c.831G>A in the genotype matches to the severe course of CF.•Using ICM, FIS assay in intestinal organoids confirmed the absence of…”
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