Results 101 to 110 of about 57,483 (236)
Large language models for bioinformatics
Abstract With the rapid advancements in large language model technology and the emergence of bioinformatics‐specific language models (BioLMs), there is a growing need for a comprehensive analysis of the current landscape, computational characteristics, and diverse applications.
Wei Ruan +54 more
wiley +1 more source
Secreted ferritin in the mosquito, Aedes aegypti, has several subunits that are the products of at least two genes, one encoding a homologue of the vertebrate heavy chain (HCH) and the other the light chain homologue (LCH).
Boris C. Dunkov +4 more
doaj
Cleavage and polyadenylation factor 1 subunit 1 (CLP1) [PDF]
Josef Penninger
openalex +1 more source
APAview: A web-based platform for alternative polyadenylation analyses in hematological cancers
Xi Hu +9 more
openalex +1 more source
Interplay between RNA‐protein interactions and RNA structures in gene regulation
Methodological advances in mapping transcriptome‐wide RNA‐protein interactions and RNA structures have started to uncover the potential of RNP conformations in gene regulation. Competing RNA–RNA, RNA‐protein and protein–protein interactions shape the compaction and function of RNPs throughout their lifetime and may provide novel therapeutic targets in ...
Jenni Rapakko +2 more
wiley +1 more source
Regulation of polyadenylation site choice in plant nuclear mRNA
The polyadenylation machinery plays a critical role in the processing of pre-mRNA into mature mRNA. This process involves a large multiprotein complex that recognizes polyadenylation signals and determines the polyadenylation sites (PASs).
Wei Zeng +3 more
doaj +1 more source
The use of alternative polyadenylation sites renders integrin β1 (Itgb1) mRNA isoforms with differential stability during mammary gland development [PDF]
Julián Naipauer +9 more
openalex +1 more source
Advances in the Bioinformatics Knowledge of mRNA Polyadenylation in Baculovirus Genes [PDF]
Iván Gabriel Peros +5 more
openalex +1 more source
Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular Dystrophy
ABSTRACT A five‐year‐old boy with clinical features of Duchenne muscular dystrophy was found to have a rare de novo DMD exon 2–9 duplication. Reporting such atypical duplications improves genotype–phenotype interpretation and highlights the need for multidisciplinary care, particularly in resource‐limited settings.
Nada Assaf +4 more
wiley +1 more source

