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606,025 grants found
Showing 35,001 – 35,020 of 606,025 grants
ABSTRACT Impaired ability to respond to the earth’s gravitational field and loss of balance results in high risk of falls with adverse consequences for one’s health, quality of lif...
Phospholipase C b (PLCb) enzymes increase intracellular calcium in response to diverse extracellular signals, regulating numerous processes including cell proliferation and surviva...
Project Summary. Skeletal muscle mass and function are key determinants of an individual’s healthspan and are tightly correlated with both physical and metabolic health. In cancer...
PROJECT SUMMARY Preclinical research relies heavily on appropriate animal models to better understand human biology and to test the safety and efficacy of new therapies. It is impo...
ABSTRACT Tobacco use is the leading cause of preventable death and disease in the United States. The majority of smokers report the desire to quit smoking; however only 3-5% of una...
ABSTRACT Roughly 10% of births in the United States are premature and typically involve a stay in the Neonatal Intensive Care Unit (NICU), where infants endure painful procedures a...
PROJECT SUMMARY Pulmonary fibrosis is a complex disease that limits lung function through development of collagen-rich scar tissue. Although there are currently two FDA-approved th...
ERAD-STING Crosstalk in Microglia: Unraveling the Pathogenesis of Alzheimer's Disease ABSTRACT Alzheimer’s disease (AD) is an age-dependent progressive neurodegenerative disea...
Project Summary Despite public health efforts to reduce prenatal alcohol exposure (PAE), 11.7% of pregnant women in the U.S. consume alcohol and 3.9% binge drink. PAE can lead to g...
Mutations on the LRRK2 gene, which increase the encoded protein's kinase activity, are common genetic causes of familial Parkinson's disease (PD). Noncoding variants at t...
Project Summary/Abstract As the U.S. population ages, the number of individuals living with dementia is rapidly increasing, making the identification of modifiable risk factors mor...
The mission of our Wellstone Center is to perform cutting-edge research that leads to transformative therapies for myotonic dystrophy type 1 (DM1) and 2 (DM2). Our Center is based...
Myotonic dystrophy (dystrophia myotonica, DM) is a dominantly inherited disease that is the most prevalent adult-onset muscular dystrophy. However, congenital DM individuals are th...
Title: Shared Resource Core Summary/abstract Myotonic dystrophy (DM) and facioscapulohumeral muscular dystrophy (FSHD) have multisystem complications that are serious, progressive,...
This Wellstone training core is focused on training the next generation of clinical and bench scientists focused on muscular dystrophies, in particular the myotonic dystrophies, wh...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are dominantly inherited muscular dystrophies caused by short tandem repeat, or microsatellite, expansions in the noncoding regions...
The therapeutic landscape for myotonic dystrophy type 1 (DM1) has advanced dramatically in the past 5-years, but conflicting observations about the metabolism of expanded CUG mRNA...
Myotonic dystrophy type 1 (DM1) is caused by expanded CTG repeats in exon 15 of DMPK, whereas myotonic dystrophy type 2 (DM2) is caused by expanded CCTG repeats in intron 1 of CNPB...
PROJECT SUMMARY Substance use and associated HIV, hepatitis C (HCV), and mental health comorbidities continue to drive morbidity and mortality. Interdisciplinary, interinstitutiona...
Project Summary With age, dividing cells acquire DNA mutations. A small number of these somatic mutations confer a selective advantage leading to clonal outgrowth. In blood, this p...