☰

Roscoe O. Brady

Affiliations: 
National Institutes of Health, Bethesda, MD 
Area:
hereditary metabolic disorders
Website:
http://www.ninds.nih.gov/news_and_events/news_articles/pressrelease_20081006_Brady.htm
Google:
"Roscoe O. Brady"
Bio:

http://www.nasonline.org/member-directory/members/57455.html

Mean distance: 14.79 (cluster 11)
 		SNBCP
Cross-listing: Chemistry Tree

Tree Publications Grants Similar researchers PubMed Report error

Parents

Sign in to add mentor
Samuel Gurin post-doc 1952 University of Pennsylvania School of Medicine (Chemistry Tree)
Seymour S. Kety research scientist 1954- NIH

Children

Sign in to add trainee
Bernard Agranoff grad student 1952-1958 National Institute of Neurological Disorders and Stroke, NIH
John Tallman post-doc NIH
Joseph J Higgins post-doc 1990-1993 National Institutes of Health-NINDS
Norman W Barton research scientist 1982-1996 National Institutes of Health-NINDS

Collaborators

Sign in to add collaborator
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Long Y, Xu M, Li R, et al. (2016) Induced Pluripotent Stem Cells for Disease Modeling and Evaluation of Therapeutics for Niemann-Pick Disease Type A. Stem Cells Translational Medicine
Kaneski CR, Brady RO, Hanover JA, et al. (2016) Development of a model system for neuronal dysfunction in Fabry disease. Molecular Genetics and Metabolism
Yang C, Wang H, Zhu D, et al. (2015) Mutant glucocerebrosidase in Gaucher disease recruits Hsp27 to the Hsp90 chaperone complex for proteasomal degradation. Proceedings of the National Academy of Sciences of the United States of America. 112: 1137-42
Schiffmann R, Swift C, Wang X, et al. (2015) A prospective 10year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease Molecular Genetics and Metabolism. 114: S103
El-Amouri SS, Dai M, Han JF, et al. (2014) Normalization and improvement of CNS deficits in mice with hurler syndrome after long-term peripheral delivery of BBB-targeted iduronidase. Molecular Therapy : the Journal of the American Society of Gene Therapy. 22: 2028-37
Mistry PK, Liu J, Sun L, et al. (2014) Glucocerebrosidase 2 gene deletion rescues type 1 Gaucher disease. Proceedings of the National Academy of Sciences of the United States of America. 111: 4934-9
Dai M, Han J, El-Amouri SS, et al. (2014) Platelets are efficient and protective depots for storage, distribution, and delivery of lysosomal enzyme in mice with Hurler syndrome. Proceedings of the National Academy of Sciences of the United States of America. 111: 2680-5
Barranger JA, Brady RO, Grabowski GA, et al. (2014) Position statement: National Gaucher Foundation Medical Advisory Board, January 7, 2014. American Journal of Hematology. 89: 457-8
Meng X, Shen J, Kong M, et al. (2014) Abnormal intracellular calcium handling: a key pathogenic and therapeutic target of the cardiac manifestations in Fabry disease Molecular Genetics and Metabolism. 111: S77
Erba PA, Minichilli F, Giona F, et al. (2013) 99mTc-sestamibi scintigraphy to monitor the long-term efficacy of enzyme replacement therapy on bone marrow infiltration in patients with Gaucher disease. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. 54: 1717-24
See more...