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- FUNDACIO INSTITUT D'INVESTIGACIO EN CIENCIES DE LA SALUT GERMANS TRIAS I PUJOL
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mechanisms by which the circadian clock regulates skeletal muscle physiology, regeneration, metabolism, and muscular dystrophy. Our laboratory integrates molecular biology, genomics, pharmacology, mouse
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of neurodegenerative and neuromuscular disorders, including amyotrophic lateral sclerosis (ALS) and myotonic dystrophy (DM). Despite their importance in disease, the mechanisms through which repeat
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FUNDACIO INSTITUT D'INVESTIGACIO EN CIENCIES DE LA SALUT GERMANS TRIAS I PUJOL | Spain | 28 days ago
at Germans Trias i Pujol University Hospital. The line of research in which the candidate would work focuses on Duchenne muscular dystrophy (DMD), the most prevalent muscular dystrophy in childhood. We
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ongoing Duchenne Muscular Dystrophy (DMD) research project. The successful candidate will work closely with senior lab members and researchers to bridge our initial metabolic model study—investigating
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regulates skeletal muscle physiology, regeneration, metabolism, and muscular dystrophy. Our laboratory integrates molecular biology, genomics, pharmacology, mouse genetics, and physiology to identify
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. Postdoctoral Associate – Regenerative CAR T Therapy for Duchenne Muscular Dystrophy This Postdoctoral Associate will serve on a project focused on developing regenerative CAR T-based therapeutic strategies
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and inflammatory eye diseases, pediatric ophthalmic conditions, and corneal dystrophies. The Genetic Counselor will collaborate with faculty and clinical teams to assess genetic risk, obtain and
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research programs focused on a variety of diseases/disorders, including osteoporosis, muscular dystrophy, diabetes, chronic kidney disease, etc. The department has a long history of synthesizing different
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research programs focused on a variety of diseases/disorders, including osteoporosis, muscular dystrophy, diabetes, chronic kidney disease, etc. The department has a long history of synthesizing different
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assist/work on Stem Cell Regenerative Medicine to treat inherited dystrophies leading to blindness. diseases include retinitis pigmentosa, age-related macular degeneration, and Stargardt disease