Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Matthew W. C. Chan"'
Autor:
Brenda Lara, Enrique Gutierrez, Ricardo Balderrama, Conrad J. Villafuerte, Matthew W. C. Chan, Irving Sánchez, Luis H. Bayardo, Jerusha Padayachee, Omar Díaz, Víctor Manuel Cambero Ruiz, Alexander Sun, Cipatli Olimón, Jesús Guillermo Becerra Fuentes, José Rodríguez, Adrián Valles
Publikováno v:
Current Oncology
Current Oncology, Vol 28, Iss 233, Pp 2560-2578 (2021)
Current Oncology, Vol 28, Iss 233, Pp 2560-2578 (2021)
Lung metastases are the second most common malignant neoplasms of the lung. It is estimated that 20–54% of cancer patients have lung metastases at some point during their disease course, and at least 50% of cancer-related deaths occur at this stage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420e3161a326e5fa13ebe0e97556b841
https://pubmed.ncbi.nlm.nih.gov/34287274
https://pubmed.ncbi.nlm.nih.gov/34287274
Autor:
Melissa O'Neil, Devin Schellenberg, Andrew Hope, Matthew W. C. Chan, David A. Palma, Aisling Barry, Richard Moore, C. Jillian Tsai, Tony Tadic, Janet Papadakos, Meredith Giuliani
Publikováno v:
Advances in Radiation Oncology, Vol 6, Iss 1, Pp 100499-(2021)
Advances in Radiation Oncology
Advances in Radiation Oncology
Purpose With multiple phase 2 trials supporting the use of stereotactic body radiation therapy (SBRT) in oligo-metastatic disease, we evaluated practices that could inform effective implementation of an oligo-metastasis SBRT program. Methods and Mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed63ff3cfec790a9f5c91a39cdb1111
http://www.sciencedirect.com/science/article/pii/S2452109420301524
http://www.sciencedirect.com/science/article/pii/S2452109420301524
Autor:
Devin Schellenberg, Matthew W. C. Chan, Meredith Giuliani, Richard Moore, Melissa O'Neil, Aisling Barry, Andrew Hope, David A. Palma, C. Jillian Tsai, Janet Papadakos
Publikováno v:
Radiotherapy and Oncology. 150:S88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9b8369abd1b097df4643e52fb5b49b
https://doi.org/10.1016/s0167-8140(20)31099-9
https://doi.org/10.1016/s0167-8140(20)31099-9
Autor:
Craig A. Simmons, Matthew W. C. Chan, Edmond W. K. Young, Wilson Lee, Carol Laschinger, Konesh Sivagurunathan, Juliana Birek, Amy Yuen, Ilana Talior, Christopher A. McCulloch, Emily Won
Publikováno v:
Matrix Biology. 29:537-548
Fibrosis is a frequent complication of diabetes mellitus in many organs and tissues but the mechanism of how diabetes-induced glycation of extracellular matrix proteins impacts the formation of fibrotic lesions is not defined. As fibrosis is mediated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c0051a2a70654a1da3b3af1d8d5a632
https://doi.org/10.1016/j.matbio.2010.04.004
https://doi.org/10.1016/j.matbio.2010.04.004
Publikováno v:
Journal of Cell Science. 122:2769-2781
During the development of pressure-induced cardiac hypertrophy, fibroblasts are activated to become myofibroblasts, which exhibit actin-cytoskeletal remodeling and express alpha-smooth muscle actin (SMA; encoded by ACTA2). Currently, the mechanosensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77bec73774235813600a738ae66bdee8
https://doi.org/10.1242/jcs.044008
https://doi.org/10.1242/jcs.044008
Publikováno v:
American Journal of Physiology-Cell Physiology. 293:C1049-C1058
Cyclosporin A (CsA) inhibits collagen remodeling by interfering with the collagen-binding step of phagocytosis. In rapidly remodeling connective tissues such as human periodontium this interference manifests as marked tissue overgrowth and loss of fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::957fa891905229a481fd49deb4b724a4
https://doi.org/10.1152/ajpcell.00027.2007
https://doi.org/10.1152/ajpcell.00027.2007
Publikováno v:
Methods in cell biology. 98
The extracellular matrices of mammals undergo coordinated synthesis and degradation, dynamic remodeling processes that enable tissue adaptations to a broad range of environmental factors, including applied mechanical forces. The soft and mineralized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6fa5aa15dd953191b302a01f0d98728
https://pubmed.ncbi.nlm.nih.gov/20816235
https://pubmed.ncbi.nlm.nih.gov/20816235
Autor:
Wilson Lee, Faiza F. Chaudary, Christopher A. McCulloch, John W. Copeland, Matthew W. C. Chan
Publikováno v:
The Journal of biological chemistry. 285(12)
The development of fibrosis promotes the differentiation of myofibroblasts, pro-fibrotic cells, which contribute to tissue dysfunction. Myofibroblast differentiation is dependent on actin assembly, which in response to force, is mediated by various a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0bb9416e93cb8efe98e04a1b465e571
https://pubmed.ncbi.nlm.nih.gov/20071339
https://pubmed.ncbi.nlm.nih.gov/20071339
The extracellular matrices of mammals undergo coordinated synthesis and degradation, dynamic remodeling processes that enable tissue adaptations to a broad range of environmental factors, including applied mechanical forces. The soft and mineralized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ac8e71289a53c2edec8536360b44f90
https://doi.org/10.1016/s0091-679x(10)98008-4
https://doi.org/10.1016/s0091-679x(10)98008-4
Autor:
Carol Laschinger, Matthew W. C. Chan, Christopher A. McCulloch, Pamela D. Arora, Charlotte J. Morrison, Tarek Y. El Sayegh, Christopher M. Overall
Publikováno v:
The Journal of biological chemistry. 279(39)
The regulation of adherens junction formation in cells of mesenchymal lineage is of critical importance in tumorigenesis but is poorly characterized. As actin filaments are crucial components of adherens junction assembly, we studied the role of gels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d44c6f8b1911d6ccaea862987a29c0f
https://pubmed.ncbi.nlm.nih.gov/15247242
https://pubmed.ncbi.nlm.nih.gov/15247242