EyeDNA Therapeutics’ HORA-PDE6b gets US FDA rare pediatric disease designation for patients with retinal dystrophy due to PDE6b gene mutations: Paris, France Friday, December 20 ...

The company is advancing its Phase I/II trial and exploring accelerated approval pathways in the US and Europe.

Briola and co-authors determined the structure of the human CTF18 clamp loader bound to PCNA to high resolution, analyzed the structure, and tested a new mechanism involving a human-specific Ctf18 ...

According to a recent study, the virus, linked to several human infections in the United States in 2024, primarily targets avian receptors but can switch to human receptors with a critical mutation.

So, it is essential to address the communication-architecture synthesis problem through mapping of cores ... The paper is organized as follows. We review the related work in Section 2. Section 3 and ...

Researchers at the Indian Institute of Technology (IIT), Madras have developed a machine learning-based predictor for protein mutations which has surpassed existing methods that are time-consuming and ...

The researchers discovered that the RNAP transcribing the mRNA deploys two different anchors to rope in the ribosome and ensure a solid footing and start of protein synthesis. This is similar to a ...

The researchers discovered that the RNAP transcribing the mRNA deploys two different anchors to rope in the ribosome and ensure a solid footing and start of protein synthesis. This is similar to a ...

They’re called mutations. Inside each of your cells ... Give directly to The Spokesman-Review's Northwest Passages community forums series -- which helps to offset the costs of several reporter ...