Liam Aspit
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View article: The Landscape and Regulatory Determinants of A-to-I RNA Editing in <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i> Isolated From Patients With Urinary Tract and Ear Infections
The Landscape and Regulatory Determinants of A-to-I RNA Editing in <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i> Isolated From Patients With Urinary Tract and Ear Infections Open
Background Adenosine-to-inosine (A-to-I) mRNA editing can alter protein sequence and function, enabling bacteria to express two RNA and protein versions encoded by the same gene. However, its prevalence and significance in clinical bacteri…
A-to-I mRNA editing recodes hundreds of genes in dozens of species and produces endogenous protein isoforms in bacteria Open
Adenosine-to-inosine (A-to-I) messenger RNA (mRNA) editing can affect the sequence and function of translated proteins and has been extensively investigated in eukaryotes. However, the prevalence of A-to-I mRNA editing in bacteria, its gov…
View article: A-to-I mRNA editing in bacteria can affect protein sequence, disulfide bond formation, and function
A-to-I mRNA editing in bacteria can affect protein sequence, disulfide bond formation, and function Open
Adenosine-to-inosine (A-to-I) mRNA editing can alter genetic information at the RNA level and is known to affect protein sequence and function in eukaryotes. However, the ability of A-to-I mRNA editing to recode protein sequences in bacter…
A Novel Mutation in the ADAMTS10 Associated with Weil–Marchesani Syndrome with a Unique Presentation of Developed Membranes Causing Severe Stenosis of the Supra Pulmonic, Supramitral, and Subaortic Areas in the Heart Open
Weill–Marchesani syndrome (WMS) is a rare genetic inherited disorder with autosomal recessive and dominant modes of inheritance. WMS is characterized by the association of short stature, brachydactyly, joint stiffness, eye anomalies, inclu…
Duchenne Muscular Dystrophy and Early Onset Hypertrophic Cardiomyopathy associated with Mutations in Dystrophin and Hypertrophic Cardiomyopathy-Associated Genes Open
Duchenne muscular dystrophy (DMD) is a progressive muscular damage disorder caused by mutations in dystrophin gene. Cardiomyopathy may first be evident after 10 years of age and increases in incidence with age. We present a boy diagnosed a…