Displaying 421 - 440 of 1020 results

The NIAMS Training Program (T32)

https://www.niams.nih.gov/es/node/14971

Goal of NIAMS Institutional Training Awards NIAMS funds the Ruth L. Kirschstein National Research Service Award (NRSA) Institutional Research Training Grants (T32) (PA-23-048) to enable institutions to support pre-doctoral and postdoctoral research training for individuals in the fields of arthritis and musculoskeletal and skin diseases. The NIAMS T32 program's primary

Community Collaboration Advances NIAMS Resource Development

https://www.niams.nih.gov/es/node/15011

When I joined NIAMS three and a half years ago, I talked about my commitment to collaboration and learning from the NIAMS community in my first director’s letter. Since then, we have done a lot of both collaborating and learning! I highly value the input from the NIAMS community on the development of our resources and in determining the direction of our research so that we are addressing the needs of the various audiences we serve, from researchers and medical providers to patients and caregivers. NIAMS regularly solicits feedback to understand audience needs. Over the past two years, the NIAMS

R03 Information for NIAMS K Award Recipients

https://www.niams.nih.gov/es/node/15121

NIAMS Small Grant Program for New Investigators (R03) Read the NOFO: Limited Competition: Small Grant Program for NIAMS K01, K08, K23, and K25 Recipients (R03) (Clinical Trials Not Allowed) Program Purpose: The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) is seeking small grant (R03) applications to stimulate

Researchers Identify a Disease-Causing Immune Cell Imbalance in Lupus

https://www.niams.nih.gov/es/node/15256

Overview A team of NIAMS-funded researchers discovered an imbalance of T cell subtypes in patients with lupus that contributes to ongoing production of disease-causing autoantibodies. Compared to healthy individuals, patients with lupus have more T cells with specialized B cell helper functions and fewer T cells that are important for wound healing and maintaining the epithelial barrier, which acts to protect the body from pathogens and other invaders. The team identified two molecules that control this imbalance, which could be the targets of lupus treatments in the future. The study was recently published in the journal Nature. Background Systemic lupus

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