Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Craig Wooliver"'
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:
Emily B Martin, Angela Williams, Craig Wooliver, R Eric Heidel, Sarah Adams, John Dunlap, Marina Ramirez-Alvarado, Luis M Blancas-Mejia, Ronald H Lands, Stephen J Kennel, Jonathan S Wall
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0174152 (2017)
BACKGROUND:Monoclonal free light chain (LC) proteins are present in the circulation of patients with immunoproliferative disorders such as light chain (AL) amyloidosis and multiple myeloma (MM). Light chain-associated amyloid is a complex pathology c
Externí odkaz:
https://doaj.org/article/70a1e18a6c244bd991809094f706fbdf
Autor:
Helen P McWilliams-Koeppen, James S Foster, Nicole Hackenbrack, Marina Ramirez-Alvarado, Dallas Donohoe, Angela Williams, Sallie Macy, Craig Wooliver, Dale Wortham, Jennifer Morrell-Falvey, Carmen M Foster, Stephen J Kennel, Jonathan S Wall
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137716 (2015)
Light chain (AL) amyloidosis is the most common form of systemic amyloid disease, and cardiomyopathy is a dire consequence, resulting in an extremely poor prognosis. AL is characterized by the production of monoclonal free light chains that deposit a
Externí odkaz:
https://doaj.org/article/7182f06f22c546f9ac3476127cafd2be
Autor:
Jonathan S Wall, Angela Williams, Tina Richey, Alan Stuckey, Ying Huang, Craig Wooliver, Sallie Macy, Eric Heidel, Neil Gupta, Angela Lee, Brianna Rader, Emily B Martin, Stephen J Kennel
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66181 (2013)
Amyloid is a complex pathology associated with a growing number of diseases including Alzheimer's disease, type 2 diabetes, rheumatoid arthritis, and myeloma. The distribution and extent of amyloid deposition in body organs establishes the prognosis
Externí odkaz:
https://doaj.org/article/0b5f2c1bf4a044cbb5c5cf4fa589166e
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd06c6460612ca06556a2071d6bbb6f9
https://doi.org/10.1080/13506129.2022.2155133
https://doi.org/10.1080/13506129.2022.2155133
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::264c1f99489876c1c8a39db2c41244c5
https://doi.org/10.1016/j.ajpath.2019.01.011
https://doi.org/10.1016/j.ajpath.2019.01.011
Autor:
Tina Richey, Alan Stuckey, Emily B. Martin, Angela Williams, James S. Foster, Craig Wooliver, Jonathan S. Wall, Stephen J. Kennel
Publikováno v:
Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-11 (2017)
Journal of Translational Medicine
Journal of Translational Medicine
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 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9323e925034fdb7f8db19e05584f8987
http://link.springer.com/article/10.1186/s12967-017-1351-0
http://link.springer.com/article/10.1186/s12967-017-1351-0