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Immunology and Cell Biology|May 27, 2017
Restimulation-induced T-cell death through NTB-A/SAP signaling pathway is impaired in tuberculosis patients with depressed immune responsesRodrigo E Hernández Del Pino, Joaquín M Pellegrini, Ana I Rovetta, et al.Autophagy|November 27, 2014
IFNG-mediated immune responses enhance autophagy against Mycobacterium tuberculosis antigens in patients with active tuberculosisAna I Rovetta, Delfina Peña, Rodrigo E Hernández Del Pino, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structuresA Teti, S Migliaccio, A Taranta, et al.Journal of Biomedical Materials Research|December 22, 1999
Autologous bone marrow stromal cells loaded onto porous hydroxyapatite ceramic accelerate bone repair in critical-size defects of sheep long bonesE Kon, A Muraglia, A Corsi, et al.Human Molecular Genetics|September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndromeA G Engel, K Ohno, M Milone, et al.European Journal of Immunology|November 30, 2012
Impaired dendritic cell differentiation of CD16-positive monocytes in tuberculosis: role of p38 MAPKLuciana Balboa, María M Romero, Evangelina Laborde, et al.Cell Death and Differentiation|May 21, 2013
Evidence for a common progenitor of epithelial and mesenchymal components of the liverA Conigliaro, L Amicone, V Costa, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 10, 2002
Phenotypic effects of biglycan deficiency are linked to collagen fibril abnormalities, are synergized by decorin deficiency, and mimic Ehlers-Danlos-like changes in bone and other connective tissuesA Corsi, T Xu, X D Chen, et al.Human Molecular Genetics|May 1, 1997
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutationsK Ohno, P A Quiram, M Milone, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1993
Structure and molecular regulation of bone matrix proteinsP G Robey, N S Fedarko, T E Hefferan, et al.Pageof 31