Zobrazeno 1 - 10
of 78
pro vyhledávání: '"James S. Foster"'
Autor:
James S. Foster, Manasi Balachandran, Trevor J. Hancock, Emily B. Martin, Sallie Macy, Craig Wooliver, Tina Richey, Alan Stuckey, Angela D. Williams, Joseph W. Jackson, Stephen J. Kennel, Jonathan S. Wall
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionSystemic amyloidosis is a progressive disorder characterized by the extracellular deposition of amyloid fibrils and accessory proteins in visceral organs and tissues. Amyloid accumulation causes organ dysfunction and is not generally clea
Externí odkaz:
https://doaj.org/article/3ce636148a204e3aafd0f0efaec0fd54
Autor:
Emily B. Martin, Alan Stuckey, Dustin Powell, Ronald Lands, Bryan Whittle, Craig Wooliver, Sallie Macy, James S. Foster, Spencer Guthrie, Stephen J. Kennel, Jonathan S. Wall
Publikováno v:
Pharmaceuticals, Vol 16, Iss 4, p 629 (2023)
There are at least 20 distinct types of systemic amyloidosis, all of which result in the organ-compromising accumulation of extracellular amyloid deposits. Amyloidosis is challenging to diagnose due to the heterogeneity of the clinical presentation,
Externí odkaz:
https://doaj.org/article/0c7a66e5b85e4db4a58eeeaf99099fad
Autor:
Emily B. Martin, Angela Williams, Tina Richey, Craig Wooliver, Alan Stuckey, James S. Foster, Stephen J. Kennel, Jonathan S. Wall
Publikováno v:
Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-11 (2017)
Abstract Background Systemic amyloidoses comprise diseases characterized by the deposition of proteinaceous material known as amyloid. Currently, without performing multiple biopsies, there is no way to ascertain the extent of amyloid deposition in p
Externí odkaz:
https://doaj.org/article/557423129c224980958d264ad5096d06
Autor:
Jonathan S. Wall, Emily B. Martin, Tina Richey, Alan C. Stuckey, Sallie Macy, Craig Wooliver, Angela Williams, James S. Foster, Penney McWilliams-Koeppen, Ed Uberbacher, Xiaolin Cheng, Stephen J. Kennel
Publikováno v:
Molecules, Vol 20, Iss 5, Pp 7657-7682 (2015)
Amyloid is a complex pathologic matrix comprised principally of paracrystalline protein fibrils and heparan sulfate proteoglycans. Systemic amyloid diseases are rare, thus, routine diagnosis is often challenging. The glycosaminoglycans ubiquitously p
Externí odkaz:
https://doaj.org/article/599fcb02977e46dc8ccd340512015f8d
Autor:
James S. Foster, Angela D. Williams, Sallie Macy, Tina Richey, Alan Stuckey, Daniel Craig Wooliver, Richa Koul-Tiwari, Emily B. Martin, Stephen J. Kennel, Jonathan S. Wall
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
There is a continuing need for therapeutic interventions for patients with the protein misfolding disorders that result in systemic amyloidosis. Recently, specific antibodies have been employed to treat AL amyloidosis by opsonizing tissue amyloid dep
Externí odkaz:
https://doaj.org/article/77898dc3ab4441cdbcb2ebfc9ee72ae6
Autor:
Daniel P. Kestler, James S. Foster, Charles T. Bruker, John W. Prenshaw, Stephen J. Kennel, Jonathan S. Wall, Deborah T. Weiss, Alan Solomon
Publikováno v:
Breast Cancer: Basic and Clinical Research, Vol 2011, Iss 5, Pp 73-85 (2011)
Externí odkaz:
https://doaj.org/article/34a2130841fe4947b3ca3f8b9a166bc6
Autor:
Stephen J Kennel, Joseph W Jackson, Alan Stuckey, Tina Richey, James S Foster, Jonathan S Wall
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0301756 (2024)
IntroductionAmyloid deposition is a cause of restrictive cardiomyopathy. Patients who present with cardiac disease can be evaluated for transthyretin (TTR)-associated cardiac amyloidosis using nuclear imaging with 99mTc-labeled pyrophosphate (PYP); h
Externí odkaz:
https://doaj.org/article/ae00333921e540a68f07fb68eada90da
Autor:
Joseph W. Jackson, James S. Foster, Emily B. Martin, Sallie Macy, Craig Wooliver, Manasi Balachandran, Tina Richey, R. Eric Heidel, Angela D. Williams, Stephen J. Kennel, Jonathan S. Wall
Publikováno v:
Amyloid. :1-12
Autor:
James S. Foster, Anna B. Williams, Dianne J. Trent, Tina Richey, Emily B. Martin, Siva Karthik Varanasi, Alexa Stroh, Stephen A. Kania, Jonathan S. Wall, Craig Wooliver, Sallie Macy, Elizabeth N. Ergen, Stephen J. Kennel, Angela Williams, R. Eric Heidel
Publikováno v:
Am J Pathol
Light chain–associated amyloidosis is characterized by the extracellular deposition of amyloid fibrils in abdominothoracic organs, skin, soft tissue, and peripheral nerves. Phagocytic cells of the innate immune system appear to be ineffective at cl
Autor:
James S. Foster, Spencer D. Guthrie, Sébastien Bender, Frank Bridoux, Suganya Selvarajah, Jonathan S. Wall, Arnaud Jaccard, Angela Williams, Christophe Sirac, Gemma Martinez-Rivas, Gregory D Bell, Stephen J. Kennel, Roussine Codo
Publikováno v:
Blood. 138:1207-1207
Background: Amyloidosis is characterized by extracellular deposition of protein fibrils that can involve any organ or tissue in the body. It is a severe, progressive and often lethal disorder. There are approximately seventeen different systemic amyl