Overview of distinct 8-oxoguanine profiles of messenger RNA in normal and senescent cancer cells. [PDF]
Huang J, Lin Y, Zhao Y, Wei L.
europepmc +1 more source
Lack of poly(A) sequence in half of the messenger RNA coding for ewe αscasein
L. M. Houdebine, P. Gaye, A. Favre
openalex +2 more sources
Synthesis of lens protein in vitro V. Isolation of messenger‐like RNA from lens by high resolution zonal centrifugation [PDF]
Anton Berns+4 more
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The contribution of extracellular RNA and its derived biomaterials in disease management
The implications of exRNA's biological function and the structural uniqueness of RNA help establish a close connection between RNA, material, and modern medicine. Abstract The RNA found in the circular system is known as extracellular RNA (exRNA). This kind of RNA has been found to play a biological role similar to that of a messenger. They can be used
Yu Wei+8 more
wiley +1 more source
Enhanced mitochondrial activity reshapes a gut microbiota profile that delays NASH progression
Improved mitochondrial activity, due to the lack of methylation‐controlled J protein (MCJ), creates a specific microbiota signature that when transferred through cecal microbiota transplantation delays NASH progression by restoring the gut‐liver axis and enhancing hepatic fatty acid oxidation.
María Juárez‐Fernández+18 more
wiley +1 more source
Sequencing of messenger RNA in the healing process of diabetes foot ulcer. [PDF]
Wang G+6 more
europepmc +1 more source
Isolation of Messenger RNA Coding for Eggshell Protein of the DNA‐Eliminating Nematode Ascaris lumbricoides [PDF]
Erich Zulauf, Charlotte GUT
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This review highlights the complex roles of cellular senescence in cancer progression and suppression, discusses the mechanisms and regulatory pathways involved, and evaluates the efficacy of the “One‐Two punch” sequential treatment approach while addressing emerging challenges in this novel therapeutic strategy.
Qiuming Pan+12 more
wiley +1 more source
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan+19 more
wiley +1 more source
Altered Protein Structures and Neoepitopes in Lupus Neutrophils From Dysregulated Splicing of Messenger RNA. [PDF]
Najjar R+7 more
europepmc +1 more source