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Two novel CHN1 variants identified in Duane retraction syndrome pedigrees disrupt development of ocular motor nerves in zebrafish. nature.com/articles/s10038-023

(Dissertation): Developing technologies to produce reproductively sterile finfish and oysters, and characterizing changes of gene expression in the pituitary of sterile fish by single-cell RNA sequencing. mdsoar.org/handle/11603/27320

Synthesis and Biophysical Studies of High-Affinity Oligomers Containing G-Clamp Analogs. pubs.acs.org/doi/10.1021/acs.j

P45 A phase 1/2 study of DYNE-251 in males with DMD mutations amenable to exon 51 skipping: DELIVER study design. nmd-journal.com/article/S0960-

Obinutuzumab-Based Drug-Free Macromolecular Therapeutics Synergizes with Topoisomerase Inhibitors. onlinelibrary.wiley.com/doi/10

Modeling of large-scale hoxbb cluster deletions in zebrafish uncovers a role for segmentation pathways in atrioventricular boundary specification. link.springer.com/article/10.1

An in vivo drug screen reveals that cyclooxygenase 2-derived prostaglandin D2 promotes spinal cord neurogenesis. biorxiv.org/content/10.1101/20

P29 DMD transcript imbalance and nuclear trafficking evaluation in muscle biopsies from baseline and golodirsen treated 4053-101 clinical trial patients. nmd-journal.com/article/S0960-

P23 Evaluation of safety parameters and dystrophin expression by sequential administration of exon-skipping and gene therapy in a DMDmdx mouse model. nmd-journal.com/article/S0960-

Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation. nature.com/articles/s41598-023

(Video): New Exon Skipping Drug in Clinical Development for Duchenne Muscular Dystrophy: Steve Hughes, MD, chief medical officer at AvidityBiosciences youtube.com/watch?v=XV56y_bwBZ PMO are

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