Sudbury police constable nominated for mental health advocacy award - CTV News

IndictmentWednesday, October 21, 2026 3:29AMA Fort Bend County constable's deputy is out of a job after being indicted on felony theft and tampering charges, according to authorities. SUGAR LAND, Texas (KTRK) -- A now-former Fort Bend County deputy constable is out of a job after being indicted on felony theft and tampering charges, according to authorities. Eric Lister, who served as a lieutenant in the Precinct 3 Constable's Office until last month, was arrested Sept. 29. Texas Commission of Law Enforcement records show his employment ended on Sept. 30. According to the indictments, Lister is accused of stealing more than $2,500 from the constable's office and writing warnings for traffic stops he never made. The date of both offenses is listed in court records as of March 15, just days after he placed fourth in the Democratic primary for Fort Bend County treasurer. According to his campaign website, Lister ran on a platform of fiscal integrity. Top StoriesThe Precinct 3 Constable's Office released the following statement:"Lt. Lister was immediately placed on administrative leave when concerns about his conduct were identified.

We’re sharing this article early to provide faster access to peer-reviewed, accepted research. It is citable and carries a permanent DOI. This version is subject to further edits and will be replaced automatically by the final Version of Record. All legal disclaimers apply. AbstractBunyamwera virus (BUNV) is the prototypical member of the Peribunyaviridae family of arthropod-borne viruses and possesses a genome comprising three segments of negative-sense RNA, named small, medium and large. The medium segment encodes a polyprotein that is processed to form Gn and Gc spikes and a non-structural protein, NSm. The role of NSm during replication in mammalian cells is poorly characterized, although it associates with a Golgi-derived structure called the virus factory (VF), the site of BUNV genome replication and virion assembly. To further define NSm function, we generated an epitope-tagged BUNV and used co-immunoprecipitation and quantitative proteomics to identify host interacting partners.

Scientists co-led by St. Jude Children's Research Hospital have identified a potential therapeutic vulnerability in some forms of osteosarcoma. Published today in the Journal of Experimental Medicine, a combination approach slowed tumor growth and prolonged survival in preclinical models of this pediatric bone cancer. The therapies degraded EP300 (a protein that is co-opted to express oncogenes in many cancers) and inhibited AKT (a well-known cancer drug target), highlighting the combination's clinical potential. Osteosarcoma has lower survival compared to many other cancers, with relapsed and metastatic disease showing especially poor outcomes. As no new treatments have been approved for the disease in the last 40 years, the findings provide a much-needed new therapeutic avenue to explore.