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NIH Pathway to Independence Award in Muscular Dystrophy Research (K99/R00)

Sector: Hospital • Location: United States of America

Source: Grants.gov

Project
Archived

Purpose. The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) are interested in supporting additional career development and mentoring opportunities in muscular dystrophy research. NIAMS and NICHD will provide career development awards to promising clinically trained applic

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The project “NIH Pathway to Independence Award in Muscular Dystrophy Research (K99/R00)” is an infrastructure initiative in the Hospital sector, located in United States of America. Taiyo aggregates data on it from Grants.gov.

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Description

Description

Purpose. The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) are interested in supporting additional career development and mentoring opportunities in muscular dystrophy research. NIAMS and NICHD will provide career development awards to promising clinically trained applicants with the potential to become productive, independent investigators in basic, translational, and clinical research on the muscular dystrophies. This funding opportunity Announcement (FOA) is issued in recognition of the urgent need for highly skilled, interactive investigators who are able to integrate various disciplines and levels of expertise to successfully address the increasing challenges in the current research environment of the muscular dystrophies. This FOA calls for applications for mentored career development awards for clinical scientist engaged in laboratory research. It is expected that this career development program will increase the number of investigators in basic, translational, and clinical research on muscular dystrophy, and will also increase the quality of their research and training. Diseases for this program announcement include, but are not limited to, Duchenne, myotonic, facioscapulohumeral, and congenital muscular dystrophies. Mechanism of Support. This FOA will utilize the K99 grant mechanism and runs in parallel with FOAs of identical scientific scope, PA-11-075 , PA-11-077 and PA-11-076 , that encourage applications under the F32, K08, and K23 mechanisms.

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High

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100%

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