Mitochondrial markers (<i>cytochrome c oxidase subunit I</i> and <i>16S ribosomal RNA</i>) as supporting biomarkers for wild bird identification. [PDF]
Marín-Villa J+5 more
europepmc +1 more source
Alteration of 5S RNA conformation by ribosomal proteins L18 and L25 [PDF]
David G. Bear+3 more
openalex +1 more source
Dynamic eIF3‐S6 Phase Separation Switch Instructed by m6A Modification Drives the Molting of Locusts
This research reveals that reduced m6A modifications during insect molting trigger liquid–liquid phase separation (LLPS) of the m6A reader eIF3‐S6, which binds and stabilizes key molting mRNAs, including EcR and Cht10. Disrupting m6A or LLPS causes cuticle remodeling defects and molting failure, highlighting the synergistic control of gene expression ...
Zhihao Hu+8 more
wiley +1 more source
Identification of leader-trailer helices of precursor ribosomal RNA in all phyla of bacteria and archaea. [PDF]
Gemler BT+3 more
europepmc +1 more source
Nucleotide sequence relationships between vertebrate 5.8 S ribosomal RNAs [PDF]
M.S.N. Khan, B.E.H. Maden
openalex +1 more source
OxSpred, an eXtreme‐Gradient‐Boosting‐‐based supervised learning model, accurately annotates oxidative stress in innate immune cells at the single‐cell level, providing interpretable embeddings with significant biological relevance. This innovative tool revolutionizes the understanding of innate immune cell functions during inflammation and enhances ...
Po‐Yuan Chen, Tai‐Ming Ko
wiley +1 more source
Characterization of the regions from E. coli 16 S RNA covalently linked to ribosomal proteins S4 and S20 after ultraviolet irradiation [PDF]
Bernard Ehresmann+3 more
openalex +1 more source
RNA helicase DDX21 coordinates transcription and ribosomal RNA processing
Eliezer Calo+5 more
semanticscholar +1 more source
A Splice‐Region Variant Causes an Atypical Presentation of GNAS Inactivation Disorder
ABSTRACT Pathogenic variants in GNAS can cause a wide range of diseases including pseudohypoparathyroidism, pseudopseudohypoparathyroidism, McCune‐Albright syndrome, among others. The specific phenotypic features that may be seen are influenced by the variant type and location in the gene, whether it causes loss or gain of function, and whether it is ...
Brandon S. Stone+11 more
wiley +1 more source