5 results match your criteria: "Washington University School of Medicine and Shriners Hospital for Children[Affiliation]"
Arthritis Rheumatol
September 2024
Washington University School of Medicine and Shriners Hospital for Children, St. Louis, Missouri.
Objective: Current therapies targeting individual factors in inflammatory arthritis show variable efficacy, often requiring treatment with combinations of drugs, and are associated with undesirable side effects. NF-ĸB is critical for the production and function of most inflammatory cytokines. However, given its essential role in physiologic processes, targeting NF-ĸB is precarious.
View Article and Find Full Text PDFMethods Mol Biol
January 2022
Department of Orthopedic Surgery, Washington University School of Medicine and Shriners Hospital for Children, Saint Louis, MO, USA.
The skeletal system is constantly undergoing turnover in order to create strong, organized structures, requiring the bone breakdown and building properties by osteoclasts and osteoblasts, respectively. However, in pathological disease states, excessive osteoclast activity can cause bone loss leading to increase in morbidity and mortality. Osteoclasts differentiate from macrophages in the presence of various factors.
View Article and Find Full Text PDFJ Hand Surg Am
March 2020
Department of Orthopaedic Surgery, Washington University School of Medicine and Shriners Hospital for Children, St. Louis, MO. Electronic address:
Purpose: Radial longitudinal deficiency (RLD) presents on a spectrum of severity and associated diagnoses. The literature is limited in describing patient presentation without comparative data between countries. In a study comparing 2 cohorts of patients, 1 in the United States and 1 in Japan, we hypothesized that there would be a similar presentation of forearm deficiency severity, thumb hypoplasia severity, and associated syndromes between the 2 cohorts.
View Article and Find Full Text PDFPLoS Biol
November 2018
Division of Bone and Mineral Diseases, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Mutated NLRP3 assembles a hyperactive inflammasome, which causes excessive secretion of interleukin (IL)-1β and IL-18 and, ultimately, a spectrum of autoinflammatory disorders known as cryopyrinopathies of which neonatal-onset multisystem inflammatory disease (NOMID) is the most severe phenotype. NOMID mice phenocopy several features of the human disease as they develop severe systemic inflammation driven by IL-1β and IL-18 overproduction associated with damage to multiple organs, including spleen, skin, liver, and skeleton. Secretion of IL-1β and IL-18 requires gasdermin D (GSDMD), which-upon activation by the inflammasomes-translocates to the plasma membrane where it forms pores through which these cytokines are released.
View Article and Find Full Text PDFJ Pediatr Orthop
May 2000
Washington University School of Medicine and Shriners Hospital for Children, St. Louis, Missouri, USA.
We prospectively followed 27 consecutive children with tibial circular external fixators applied between July 1, 1995, and June 30, 1997. A simple pin care system with no physical pin cleansing except that provided by daily showers was used. Children with inflamed or infected pin sites were placed on an oral antibiotic (cephalexin) for 10 days.
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