McGill University

Tubulocystic Carcinoma of the Kidney With Poorly Differentiated Foci: A Frequent Morphologic Pattern of Fumarate Hydratase-deficient Renal Cell Carcinoma (2016) Smith SC, Trpkov K, Chen YB, Mehra R, Sirohi D, Ohe C, Cani AK, et al. Journal article Porous Bioactive Nanofibers via Cryogenic Solution Blow Spinning and Their Formation into 3D Macroporous Scaffolds (2016) Medeiros ELG, Braz AL, Porto IJ, Menner A, Bismarck A, Boccaccini AR, Lepry WC, et al. Journal article, Original article A comparative study of the effects of different bioactive fillers in PLGA matrix composites and their suitability as bone substitute materials: A thermo-mechanical and in vitro investigation (2015) Simpson RL, Nazhat SN, Blaker JJ, Bismarck A, Hill R, Boccaccini AR, Hansen UN, Amis AA Journal article, Original article Diagnostic methods and treatment options for focal cortical dysplasia (2015) Guerrini R, Duchowny M, Jayakar P, Krsek P, Kahane P, Tassi L, Melani F, et al. Journal article Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression (2015) Darabi H, Mccue K, Beesley J, Michailidou K, Nord S, Kar S, Humphreys K, et al. Journal article Fabrication and characterization of zein–bioactive glass scaffolds (2015) Naseri S, Hum J, Lepry WC, Miri AK, Nazhat SN, Boccaccini AR Journal article, Original article Effect of ion release from Cu-doped 45S5 Bioglass® on 3D endothelial cell morphogenesis (2015) Staehli C, James-Bhasin M, Hoppe A, Boccaccini AR, Nazhat SN Journal article, Original article A co-design approach for fault-tolerant loop execution on Coarse-Grained Reconfigurable Arrays (2015) Lari V, Tanase AP, Teich J, Witterauf M, Khosravi F, Hannig F, Meyer B Conference contribution, Conference Contribution Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 (2015) Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, et al. Journal article USP18 lack in microglia causes destructive interferonopathy of the mouse brain (2015) Goldmann T, Zeller N, Raasch J, Kierdorf K, Frenzel K, Ketscher L, Basters A, et al. Journal article