Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
All age groups are affected by one of the most prevalent chronic medical disorders globally: chronic rhinosinusitis (CRS). Its estimated incidence is 10.9% in Europe, 13% in China, and 12.3% in the United States. For many years, the 16S rRNA gene has been the backbone of sequence-based bacterial study. Still, it is only recently that the possibility of high-throughput sequencing the entire gene has been feasible. A unique gene regulation mechanism known as "RNA silencing" limits the transcript level by either starting specific RNA degradation or blocking translation. RNA interference (RNAi) is commonly induced by viruses or exogenously produced small interfering RNAs. Small RNAs like these have been utilized in biomedical research to specifically silence genes. The purpose of a short hairpin RNA is to create interference by inserting an artificial RNA molecule with a hairpin or loop-like structure into a specially designed siRNA. Every stage of life, including cell development, metabolism, the cell cycle, and signal transmission, depends on gene regulatory networks. Total fifteen mRNAs of 16SrRNA gene examined, siRNA regions is unique and isolated through 3′ to 5′ position nucleotide. Networking of both genes lies varieties of path in human being, so early to utilized siRNA technique to silence the effect of 16SrRNA gene in CRS illness. The gene encoding 16S rRNA has around ten target sites that siRNAs can attach to. The siRNAs are made to be complementary sequences to each of the target sites. Verify the 16S rRNA gene expression in CRS illness and other types across the body. Since a cystic fibrosis transmembrane conductance regulator (CFTR) mutation causes CRS illness, we isolated a mutant form of CFTR with an accession ID of 1XMJ and 16S rRNA protein quotes in 8SR6. Examine the two proteins interaction (1xmj, 8sr6) describe the inhibition of CRS illness through new way. Utilizing in-vitro exploratory approaches, both this computational study of siRNA and protein-protein interaction may be employed further to verify efficacy and appropriateness.
All age groups are affected by one of the most prevalent chronic medical disorders globally: chronic rhinosinusitis (CRS). Its estimated incidence is 10.9% in Europe, 13% in China, and 12.3% in the United States. For many years, the 16S rRNA gene has been the backbone of sequence-based bacterial study. Still, it is only recently that the possibility of high-throughput sequencing the entire gene has been feasible. A unique gene regulation mechanism known as "RNA silencing" limits the transcript level by either starting specific RNA degradation or blocking translation. RNA interference (RNAi) is commonly induced by viruses or exogenously produced small interfering RNAs. Small RNAs like these have been utilized in biomedical research to specifically silence genes. The purpose of a short hairpin RNA is to create interference by inserting an artificial RNA molecule with a hairpin or loop-like structure into a specially designed siRNA. Every stage of life, including cell development, metabolism, the cell cycle, and signal transmission, depends on gene regulatory networks. Total fifteen mRNAs of 16SrRNA gene examined, siRNA regions is unique and isolated through 3′ to 5′ position nucleotide. Networking of both genes lies varieties of path in human being, so early to utilized siRNA technique to silence the effect of 16SrRNA gene in CRS illness. The gene encoding 16S rRNA has around ten target sites that siRNAs can attach to. The siRNAs are made to be complementary sequences to each of the target sites. Verify the 16S rRNA gene expression in CRS illness and other types across the body. Since a cystic fibrosis transmembrane conductance regulator (CFTR) mutation causes CRS illness, we isolated a mutant form of CFTR with an accession ID of 1XMJ and 16S rRNA protein quotes in 8SR6. Examine the two proteins interaction (1xmj, 8sr6) describe the inhibition of CRS illness through new way. Utilizing in-vitro exploratory approaches, both this computational study of siRNA and protein-protein interaction may be employed further to verify efficacy and appropriateness.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.