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N. Bulatenko

Observed names: N. V Bulatenko, N. V. Bulatenko, N.V. Bulatenko, N.V. N.V.Bulatenko, Natalia Bulatenko, Nataliya Bulatenko, Natalya V. Bulatenko, Natalya Vadimovna Bulatenko, Н.В. Булатенко
ORCID: 0000-0002-5188-9255
Observed ORCID: 0000-0002-5188-9255
OpenAlex ID: A5036901635
Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy
2022 · Elena Kondratyeva, Anna Efremova, et al. · International Journal of Molecular Sciences · 25
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Airway and Lung Organoids from Human-Induced Pluripotent Stem Cells Can Be Used to Assess CFTR Conductance
2023 · Anna Demchenko, Ekaterina Kondrateva, et al. · International Journal of Molecular Sciences · 24
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Health Characteristics of Patients with Cystic Fibrosis whose Genotype Includes a Variant of the Nucleotide Sequence c.3140-16T>A and Functional Analysis of this Variant
2021 · Elena Kondratyeva, Tatyana Bukharova, et al. · Genes · 17
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Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del]
2022 · Elena Kondratyeva, Nataliya Bulatenko, et al. · Current Issues in Molecular Biology · 14
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Comprehensive Assessment of CFTR Modulators’ Therapeutic Efficiency for N1303K Variant
2024 · Anna Efremova, Nataliya Kashirskaya, et al. · International Journal of Molecular Sciences · 12
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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
2020 · E. Kondratyeva, A. Efremova, et al. · Gene · 12
Estimation of Chloride Channel Residual Function and Assessment of Targeted Drugs Efficiency in the Presence of a Complex Allele [L467F;F508del] in the CFTR Gene
2024 · Anna Efremova, Yuliya Melyanovskaya, et al. · International Journal of Molecular Sciences · 11
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Experience of Evaluating Functionality of Anionic Cftr Channel Methods Application in Patients With Cystic Fibrosis Diagnosed and Supposed
2019 · E.I. Kondratyeva, Yu.L. Melianovskaya, et al. · Siberian medical review · 11
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Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel
2023 · Elena Kondratyeva, Yuliya Melyanovskaya, et al. · Genes · 9
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Description of the clinical picture and assessment of functional activity of the CFTR channel in a patient with a complex allele [S466X; R1070Q]
2023 · M. G. Krasnova, Yu. L. Melianovskaya, et al. · PULMONOLOGIYA · 8
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Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis
2023 · Elena Kondratyeva, Yuliya Melyanovskaya, et al. · International Journal of Molecular Sciences · 7
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Functional tests for assessment of residual CFTR channel activity and personalized selection of efficacious CFTR-modulators for cystic fibrosis patients with ‘mild’ and ‘severe’ genetic variants
2021 · E. L. Amelina, A. S. Efremova, et al. · PULMONOLOGIYA · 6
Description of rare alleles of the CFTR gene in cystic fibrosis using functional tests and forskolin-induced swelling assay in rectal organoids
2021 · A. S. Efremova, Yu. L. Melyanovskaya, et al. · PULMONOLOGIYA · 5
Comparative Analysis of the Paracrine Action of Neuronal and Glial Progenitor Cells Derived from Induced Human Pluripotent Stem Cells
2020 · D. I. Salikhova, G. E. Leonov, et al. · Bulletin of Experimental Biology and Medicine · 5
Comparative impact analysis of neuronal and glial progenitors conditioned medium on cerebellar neurons under glutamate exitotoxicity
2019 · D. I Salikhova, G. E Leonov, et al. · Genes and Cells · 5
Course of the disease with evaluation of the chloride channel function and selection of target therapy in vitro in an adult with cystic fibrosis with 2184insA/L138ins genotype
2020 · Julia Leonidovna Melyanovskaya, Stanislav Aleksandrovich Krasovsky, et al. · Medical news of the North Caucasus · 3
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Clinical and genetic features of cystic fibrosis patients with novel pathogenic variant CFTR c.1083G> A (p.Trp361*) and functional assessment of the activity of the chloride channel
2019 · Е.И. Кондратьева, Ю.Л. Мельяновская, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 3
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Study of a rare variant of the CFTR c.1329_1350del gene in a homozygous state in a child with cystic fibrosis using functional tests
2024 · Е.И. Кондратьева, М.Г. Краснова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2
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Selection of CFTR modulators for children with the W1282R variant
2022 · A.Yu. Voronkova, N.V. N.V.Bulatenko, et al. · Voprosy praktičeskoj pediatrii · 2
Health status of twins with cystic fibrosis and F508del/R334W genotype: opportunities of targeted therapy
2022 · E.I. Kondratyeva, A.Yu. Voronkova, et al. · Voprosy praktičeskoj pediatrii · 2
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Study of CFTR channel functional activity in a patient with cystic fibrosis and E92K/4428insGA genotype
2022 · A.S. Efremova, V.D. Sherman, et al. · Voprosy detskoj dietologii · 2
Therapeutic effect of CFTR modulators in cystic fibrosis patients with the 2789+5G>A splice variant in the genotype
2024 · M. G. Krasnova, A. S. Efremova, et al. · PULMONOLOGIYA · 1
Personalized assessment of the effectiveness of targeted drugs for the treatment of cystic fibrosis in a patient with c.264_268delATATT and c.3139+1G>C rare variants of the CFTR gene
2024 · Anna S. Efremova, Victoria D. Sherman, et al. · Genes and Cells · 1
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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
2021 · E. I. Kondratyeva, N. D. Odinaeva, et al. · Almanac of Clinical Medicine · 1
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P009 Clinical and genetic characteristics of cystic fibrosis patients carrying pathogenic variant c.1083G> A (p.Trp361*)
2020 · E. Kondratyeva, Y. Melyanovskaya, et al. · Journal of Cystic Fibrosis · 1
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Works count: 31
Citation count: 189
H-index: 9
I10-index: 8
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