Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Erica Modeste"'
Autor:
Caroline M. Watson, Eric B. Dammer, Lingyan Ping, Duc M. Duong, Erica Modeste, E. Kathleen Carter, Erik C. B. Johnson, Allan I. Levey, James J. Lah, Blaine R. Roberts, Nicholas T. Seyfried
Publikováno v:
Scientific Data, Vol 10, Iss 1, Pp 1-14 (2023)
Abstract Alzheimer’s disease (AD) is the most common form of dementia, with cerebrospinal fluid (CSF) β-amyloid (Aβ), total Tau, and phosphorylated Tau (pTau) providing the most sensitive and specific biomarkers for diagnosis. However, these diag
Externí odkaz:
https://doaj.org/article/d97c5b22ae5b4d2d8393e0db80f48464
Autor:
Shannon Jones, Alexis Blake, Lesly Corado-Santiago, Jasmine Crenshaw, Emma Goldman, Fernando Gomez, Chelsea Hall, Harry Hoke, Stephen Holmes, Benjamin Kornegay, Priscilla Kwarteng, Barry Lawson, Meghan Leber, Georges Leconte, Erica Modeste, Kristine Nolin, Michael Norris, Jose Santinni Roma, Addison Swackhammer, Marcella Torres, Joanna Wares, Dominique Ebony Williams, April Hill, Kathy Hoke, Carol Parish, B. Daniel Pierce
Publikováno v:
Frontiers in Education, Vol 8 (2023)
In the early 2000s, our primarily undergraduate, white institution (PUI/PWI), began recruiting and enrolling higher numbers of students of color and first-generation college students. However, like many of our peer institutions, our established pedag
Externí odkaz:
https://doaj.org/article/02e44c416ed645aa8b3e41222dd98ef7
Autor:
Meixiang Huang, Erica Modeste, Eric Dammer, Paola Merino, Georgia Taylor, Duc M. Duong, Qiudong Deng, Christopher J. Holler, Marla Gearing, Dennis Dickson, Nicholas T. Seyfried, Thomas Kukar
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-25 (2020)
Abstract Heterozygous, loss-of-function mutations in the granulin gene (GRN) encoding progranulin (PGRN) are a common cause of frontotemporal dementia (FTD). Homozygous GRN mutations cause neuronal ceroid lipofuscinosis-11 (CLN11), a lysosome storage
Externí odkaz:
https://doaj.org/article/ddd6ed1211be478aa3e32f948993154b
Autor:
Erica Modeste, Lingyan Ping, Caroline M. Watson, Duc M. Duong, Eric B. Dammer, Erik C.B. Johnson, Blaine R. Roberts, James J. Lah, Allan I. Levey, Nicholas T. Seyfried
Despite being twice as likely to get Alzheimer’s disease (AD), African Americans have been grossly underrepresented in AD research. While emerging evidence indicates that African Americans with AD have lower cerebrospinal fluid (CSF) levels of Tau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59becd123d28247f0884719b92d9b0f0
https://doi.org/10.1101/2022.12.07.519393
https://doi.org/10.1101/2022.12.07.519393
Autor:
Caroline M. Watson, Eric B. Dammer, Lingyan Ping, Duc M. Duong, Erica Modeste, E. Kathleen Carter, Erik C. B. Johnson, Allan I. Levey, James J. Lah, Blaine R. Roberts, Nicholas T. Seyfried
Alzheimer’s disease (AD) is the most common form of dementia, with cerebrospinal fluid (CSF) β-amyloid (Aβ), total Tau, and phosphorylated Tau (pTau) providing the most sensitive and specific biomarkers for diagnosis. However, these diagnostic bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03655077e4cd492a3e6515f848ac35d2
https://doi.org/10.1101/2022.08.30.22279370
https://doi.org/10.1101/2022.08.30.22279370
Autor:
Lenora Higginbotham, Eric B. Dammer, Duc M. Duong, Erica Modeste, Thomas J. Montine, James J. Lah, Allan I. Levey, Nicholas T. Seyfried
Publikováno v:
Proteomes, Vol 7, Iss 3, p 30 (2019)
Previous systems-based proteomic approaches have characterized alterations in protein co-expression networks of unfractionated asymptomatic (AsymAD) and symptomatic Alzheimer’s disease (AD) brains. However, it remains unclear how sample fractionati
Externí odkaz:
https://doaj.org/article/664703ef1e824e1892db36ae0f1eed16
Autor:
Pedro L. Valenzuela, Alejandro Lucia, Harald Hampel, Massimo Corbo, Mark Mapstone, Nicholas T. Seyfried, Giulia Maria Sancesario, Pablo Lemercier, Enzo Emanuele, Francesco Garaci, Andrea Urbani, Simone Lista, George Perry, Filippo Baldacci, Nicola Toschi, Erica Modeste, Allan I. Levey, Andrea Vergallo, Robert Nisticò
Alzheimer's disease (AD) is characterized by non-linear, genetic-driven pathophysiological dynamics with high heterogeneity in biological alterations and disease spatial-temporal progression. Human in-vivo and post-mortem studies point out a failure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9a30be6c33fdb5aab207c5c6c792615
https://hdl.handle.net/2108/325544
https://hdl.handle.net/2108/325544
Publikováno v:
Journal of Chemical Information and Modeling. 59:2423-2431
DNA polymerase I from Thermus aquaticus ( Taq DNA polymerase) is useful for polymerase chain reactions because of its exceptional thermostability; however, its activity at low temperatures can cause amplification of unintended products. Mutation of i
Autor:
Meixiang Huang, Thomas Kukar, Paola Merino, Eric B. Dammer, Christopher J. Holler, Qiudong Deng, Nicholas T. Seyfried, Erica Modeste, Georgia L Taylor
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Qiudong Deng, Duc M. Duong, Thomas Kukar, Paola Merino, Georgia Taylor, Nicholas T. Seyfried, Christopher J. Holler, Dennis W. Dickson, Eric B. Dammer, Meixiang Huang, Erica Modeste, Marla Gearing
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-25 (2020)
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-25 (2020)
Heterozygous, loss-of-function mutations in the granulin gene (GRN) encoding progranulin (PGRN) are a common cause of frontotemporal dementia (FTD). Homozygous GRN mutations cause neuronal ceroid lipofuscinosis-11 (CLN11), a lysosome storage disease.