Sunday, March 16, 2025

New members of the CDKL family of genes linked to neurodevelopmental disorders

Researchers have deepened our understanding of two of the five members of the CDKL family of genes, CDKL2 and CDKL1. They show that variants in these genes can lead to neurodevelopmental conditions, including epilepsy, and propose a mechanism by which the defective variants may cause the neurological symptoms in affected individuals.

from Top Health News -- ScienceDaily https://ift.tt/SB71YLe
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FDA clears IND for clinical trial testing switchable CAR-T therapy in patients with autoimmune diseases, without chemotherapy

FDA has cleared an investigational new drug (IND) application to study switchable chimeric antigen receptor T cell (sCAR-T) therapy (CLBR001...