240481 RESULTS
COMMENT These two papers on CSF1R deficiency in humans are obviously rather interesting in the context of our own work. CSF1R mutations have been associated with the autosomal-dominant disease, hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS, ...
Mater Research-University of QueenslandBrisbane, Australia
COMMENT How about we just close the book on naproxen? NSAIDs is a broad class of drugs, and it hardly seems appropriate to castigate the whole lot of them based on INTREPAD and ADAPT. If one were to simply follow the strongest epidemiological signal, then testing ...
JOB 2019-04-22 Employer Washington University School of Medicine Contact Send CV, a statement of interest (no more than one page), and names and contact information for three references familiar with the applicant's work directly to Anil Cashikar by e-mail ...
JOB 2019-04-22 Employer University of Alberta Contact daude@ualberta.ca Description The University of Alberta seeksa talented and passionate scientist to join the Westaway lab. Dr. Westaway’s group is interested in understanding the molecular mechanisms of initiation ...
University of AlbertaEdmonton, Canada
Neuron23
PAPER Pridans C, Raper A, Davis GM, Alves J, Sauter KA, Lefevre L, Regan T, Meek S, Sutherland L, Thomson AJ, Clohisey S, Bush SJ, Rojo R, Lisowski ZM, Wallace R, Grabert K, Upton KR, Tsai YT, Brown D, Smith LB, Summers KM, Mabbott NA, Piccardo P, Cheeseman MT, Burdon T, Hume DA
University of EdinburghEdinburgh, United Kingdom
vTv TherapeuticsHigh Point, United States
vTv TheapeuticsHigh Point, United States
Queensland University of Technology, AustraliaBrisbane , Australia
PAPER Leung YY, Valladares O, Chou YF, Lin HJ, Kuzma AB, Cantwell L, Qu L, Gangadharan P, Salerno WJ, Schellenberg GD, Wang LS
No filters selected
