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Documents dont l'auteur est "Tran-Khanh, Nicolas"

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Nombre de documents: 20

A

Alameh, M., Lavertu, M., Tran-Khanh, N., Chang, C.-Y., Lesage, F., Bail, M., Darras, V., Chevrier, A., & Buschmann, M. D. (2018). siRNA delivery with chitosan: influence of chitosan molecular weight, degree of deacetylation, and amine to phosphate ratio on in vitro silencing efficiency, hemocompatibility, biodistribution, and in vivo efficacy. Biomacromolecules, 19(1), 112-131. Lien externe

B

Buschmann, M. D., Lavertu, M., Nelea, M., Darras, V., Alameh, M. G., Chevrier, A., Tran-Khanh, N., Naeini Tavakoli, A., & Veilleux, D. (2018). Coated chitosan-based polyplex for delivery of nucleic acids. (Demande de brevet no US20180028458). Lien externe

Bizet, A. A., Tran-Khanh, N., Saksena, A., Liu, K. A. I., Buschmann, M. D., & Philip, A. (2012). CD109-mediated degradation of TGF-ß receptors and inhibition of TGF-ß responses involve regulation of SMAD7 and SMURF2 localization and function. Journal of Cellular Biochemistry, 113(1), 238-246. Lien externe

Bizet, A. A., Liu, K., Tran-Khanh, N., Saksena, A., Vorstenbosch, J., Finnson, K. W., Buschmann, M. D., & Philip, A. (2011). The TGF-ß co-receptor, CD109, promotes internalization and degradation of TGF-ß receptors. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1813(2), 742-753. Lien externe

Blanc, A., Tran-Khanh, N., Filion, D., & Buschmann, M. D. (2005). Optimal Processing Method to Obtain Four-Color Confocal Fluorescent Images of the Cytoskeleton and Nucleus in Three-Dimensional Chondrocyte Cultures. Journal of Histochemistry & Cytochemistry, 53(9), 1171-1175. Lien externe

D

Deprés-Tremblay, G., Chevrier, A., Tran-Khanh, N., Nelea, M., & Buschmann, M. D. (2018). Chitosan inhibits platelet-mediated clot retraction, increases platelet-derived growth factor release, and increases residence time and bioactivity of platelet-rich plasma in vivo. Biomedical Materials, 13(1), 11 pages. Lien externe

Dumont, J., Ionescu, M., Reiner, A., Poole, A. R., Tran-Khanh, N., Hoemann, C. D., McKee, M. D., & Buschmann, M. D. (1999). Mature Full-Thickness Articular Cartilage Explants Attached to Bone Are Physiologically Stable Over Long-Term Culture in Serum-Free Media. Connective Tissue Research, 40(4), 259-272. Lien externe

G

Gao, C., Seuntjens, J. A. N., Kaufman, G. N., Tran-Khanh, N., Butler, A., Li, A., Wang, H., Buschmann, M. D., Harvey, E. J., & Henderson, J. E. (2012). Mesenchymal Stem Cell Transplantation to Promote Bone Healing. Journal of Orthopaedic Research, 30(8), 1183-1189. Lien externe

Guzmán-Morales, J., El-Gabalawy, H., Pham, M. H., Tran-Khanh, N., McKee, M. D., Wu, W., Centola, M., & Hoemann, C. D. (2009). Effect of Chitosan Particles and Dexamethasone on Human Bone Marrow Stromal Cell Osteogenesis and Angiogenic Factor Secretion. Bone, 45(4), 617-626. Lien externe

H

Hoemann, C. D., Tran-Khanh, N., Chevrier, A., Chen, G., Lascau-Coman, V., Mathieu, C., Changoor, A., Yaroshinsky, A., McCormack, R. G., Stanish, W. D., & Buschmann, M. D. (2015). Chondroinduction Is the Main Cartilage Repair Response to Microfracture and Microfracture With BST-CarGel: Results as Shown by ICRS-II Histological Scoring and a Novel Zonal Collagen Type Scoring Method of Human Clinical Biopsy Specimens. American Journal of Sports Medicine, 43(10), 2469-2480. Lien externe

Hoemann, C. D., Guzmán-Morales, J., Tran-Khanh, N., Lavallée, G., Jolicoeur, M., & Lavertu, M. (2013). Chitosan rate of uptake in HEK293 cells is influenced by soluble versus microparticle state and enhanced by serum-induced cell metabolism and lactate-based media acidification. Molecules, 18(1), 1015-1035. Disponible

Hoemann, C. D., Chen, G., Marchand, C., Tran-Khanh, N., Thibault, M., Chevrier, A., Sun, J., Shive, M. S., Fernandes, M. J. G., Poubelle, P. E., Centola, M., & El-Gabalawy, H. (2010). Scaffold-Guided Subchondral Bone Repair Implication of Neutrophils and Alternatively Activated Arginase-1+Macrophages. American Journal of Sports Medicine, 38(9), 1845-1856. Lien externe

L

Lavertu, M., Méthot, S., Tran-Khanh, N., & Buschmann, M. D. (2006). High Efficiency Gene Transfer Using Chitosan/DNA Nanoparticles With Specific Combinations of Molecular Weight and Degree of Deacetylation. Biomaterials, 27(27), 4815-4824. Lien externe

M

Méthot, S., Changoor, A., Tran-Khanh, N., Hoemann, C. D., Stanish, W. D., Restrepo, A., Shive, M. S., & Buschmann, M. D. (2016). Osteochondral Biopsy Analysis Demonstrates That BST-CarGel Treatment Improves Structural and Cellular Characteristics of Cartilage Repair Tissue Compared With Microfracture. CARTILAGE, 7(1), 16-28. Lien externe

Marchand, C., Chen, G., Tran-Khanh, N., Sun, J., Chen, H., Buschmann, M. D., & Hoemann, C. D. (2012). Microdrilled Cartilage Defects Treated With Thrombin-Solidified Chitosan/Blood Implant Regenerate a More Hyaline, Stable, and Structurally Integrated Osteochondral Unit Compared to Drilled Controls. Tissue Engineering Part A, 18(5-6), 508-519. Lien externe

N

Nada, O., Marian, A., Tran-Khanh, N., Buschmann, M. D., Podtetenev, M., Vidal, F., Costantino, S., & Brunette, I. (2014). Effect of Corneal Hydration on the Quality of the Femtosecond Laser Anterior Lamellar Cut. PLOS One, 9(6). Disponible

T

Thibault, M., Astolfi, M., Tran-Khanh, N., Lavertu, M., Darras, V., Merzouki, A., & Buschmann, M. D. (2011). Excess polycation mediates efficient chitosan-based gene transfer by promoting lysosomal release of the polyplexes. Biomaterials, 32(20), 4639-4646. Lien externe

Tran-Khanh, N., Chevrier, A., Lascau-Coman, V., Hoemann, C. D., & Buschmann, M. D. (2010). Young Adult Chondrocytes Proliferate Rapidly and Produce a Cartilaginous Tissue at the Gel-Media Interface in Agarose Cultures. Connective Tissue Research, 51(3), 216-223. Lien externe

Tran-Khanh, N. (2007). Culture de chondrocytes en agarose : dépendance avec l'âge et caractérisation de la croissance en interface [Thèse de doctorat, École Polytechnique de Montréal]. Disponible

Tran-Khanh, N., Hoemann, C. D., McKee, M. D., Henderson, J. E., & Buschmann, M. D. (2005). Aged Bovine Chondrocytes Display a Diminished Capacity to Produce a Collagen-Rich, Mechanically Functional Cartilage Extracellular Matrix. Journal of Orthopaedic Research, 23(6), 1354-1362. Lien externe

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