Detalhe da pesquisa
1.
Comprehensive Assessment of CFTR Modulators' Therapeutic Efficiency for N1303K Variant.
Int J Mol Sci
; 25(5)2024 Feb 27.
Artigo
Inglês
| MEDLINE | ID: mdl-38474016
2.
Combination of 3-O-Levulinoyl and 6-O-Trifluorobenzoyl Groups Ensures α-Selectivity in Glucosylations: Synthesis of the Oligosaccharides Related to Aspergillus fumigatus α-(1 â 3)-d-Glucan.
J Org Chem
; 88(17): 12542-12564, 2023 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37593939
3.
The Effect of Complex Alleles of the CFTR Gene on the Clinical Manifestations of Cystic Fibrosis and the Effectiveness of Targeted Therapy.
Int J Mol Sci
; 25(1)2023 Dec 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38203285
4.
Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome.
Int J Mol Sci
; 24(22)2023 Nov 14.
Artigo
Inglês
| MEDLINE | ID: mdl-38003474
5.
Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis.
Int J Mol Sci
; 24(7)2023 Mar 28.
Artigo
Inglês
| MEDLINE | ID: mdl-37047318
6.
High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients.
BMC Genomics
; 23(1): 252, 2022 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35365085
7.
Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del].
Curr Issues Mol Biol
; 44(10): 5126-5138, 2022 Oct 21.
Artigo
Inglês
| MEDLINE | ID: mdl-36286063
8.
Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy.
Int J Mol Sci
; 23(18)2022 Sep 08.
Artigo
Inglês
| MEDLINE | ID: mdl-36142302
9.
Advances in the Study of Common and Rare CFTR Complex Alleles Using Intestinal Organoids.
J Pers Med
; 14(2)2024 Jan 23.
Artigo
Inglês
| MEDLINE | ID: mdl-38392563
10.
Airway basal cells from human-induced pluripotent stem cells: a new frontier in cystic fibrosis research.
Front Cell Dev Biol
; 12: 1336392, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38737127
11.
Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel.
Genes (Basel)
; 14(9)2023 08 28.
Artigo
Inglês
| MEDLINE | ID: mdl-37761847
12.
Characterization of CFTR mutations in people with cystic fibrosis and severe liver disease who are not eligible for CFTR modulators.
J Cyst Fibros
; 22(2): 263-265, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36739240
13.
Gene Polymorphism of Biotransformation Enzymes and Ciprofloxacin Pharmacokinetics in Pediatric Patients with Cystic Fibrosis.
Biomedicines
; 10(5)2022 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35625789
14.
Ursodeoxycholic acid and liver disease associated with cystic fibrosis: A multicenter cohort study.
J Cyst Fibros
; 21(2): 220-226, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33814323
15.
Vitamin D Status Among Children With Juvenile Idiopathic Arthritis: A Multicenter Prospective, Non-randomized, Comparative Study.
Front Pediatr
; 10: 915943, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35967569
16.
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.
Genes (Basel)
; 12(6)2021 05 28.
Artigo
Inglês
| MEDLINE | ID: mdl-34071719
17.
Factors for severe outcomes following SARS-CoV-2 infection in people with cystic fibrosis in Europe.
ERJ Open Res
; 7(4)2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34984210
18.
Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved Care.
Int J Neonatal Screen
; 6(2): 34, 2020 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-33073029
19.
Purification and characterization of two forms of the homologously expressed lytic polysaccharide monooxygenase (PvLPMO9A) from Penicillium verruculosum.
Biochim Biophys Acta Proteins Proteom
; 1868(1): 140297, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31672609
20.
Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients.
Genes (Basel)
; 11(10)2020 09 27.
Artigo
Inglês
| MEDLINE | ID: mdl-32992607