NephJC needs your help. Time to open your wallet and help keep the lights on at NephJC HQ. Also score some pretty fly NephJC fleece, hats and tote bags. (Yeah, we know that there has never been a “fly” tote bag. Work with us.
The NephJC Kidneys return for the fourth year. Time for #NephTwitter to nominate their favs.
Some cases of ADTKD are due to mutations of the MUC-1 gene, one mutation is a frame shift mutation that results in a premature stop codon. which results in accumulation of the abnormally short, and toxic protein MUC-1 fs . The researchers found a small protein, BRD4780, that reroute MUC-1fs to lysosomes, preventing proteinopathy and possibly altering the natural history of the disease.
This week is a joint #DermJC and #NephJC. We will discuss two articles - here is the summary of the larger case series, from Vandana Niyyar.
Great to have First Author, Jessica Tangren join us!
Anna Burgner made her debut hosting the American Chat, and Ben did a great job as always with the EU version
New rule for visual abstract. We need to stop adding the logo of the publishing journal. Replace the logo with the authors name. So here is the latest visual abstract in the new style.
