Sandra W Curtiss
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Explore the profile of Sandra W Curtiss including associated specialties, affiliations and a list of published articles.
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12
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1005
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Recent Articles
1.
Elam J, Glasser M, Harms M, Sotiropoulos S, Andersson J, Burgess G, et al.
Neuroimage
. 2021 Sep;
244:118543.
PMID: 34508893
The Human Connectome Project (HCP) was launched in 2010 as an ambitious effort to accelerate advances in human neuroimaging, particularly for measures of brain connectivity; apply these advances to study...
2.
Bookheimer S, Salat D, Terpstra M, Ances B, Barch D, Buckner R, et al.
Neuroimage
. 2018 Oct;
185:335-348.
PMID: 30332613
The original Human Connectome Project yielded a rich data set on structural and functional connectivity in a large sample of healthy young adults using improved methods of data acquisition, analysis,...
3.
Somerville L, Bookheimer S, Buckner R, Burgess G, Curtiss S, Dapretto M, et al.
Neuroimage
. 2018 Aug;
183:456-468.
PMID: 30142446
Recent technological and analytical progress in brain imaging has enabled the examination of brain organization and connectivity at unprecedented levels of detail. The Human Connectome Project in Development (HCP-D) is...
4.
Hodge M, Horton W, Brown T, Herrick R, Olsen T, Hileman M, et al.
Neuroimage
. 2015 May;
124(Pt B):1102-1107.
PMID: 25934470
ConnectomeDB is a database for housing and disseminating data about human brain structure, function, and connectivity, along with associated behavioral and demographic data. It is the main archive and dissemination...
5.
Marcus D, Harms M, Snyder A, Jenkinson M, Wilson J, Glasser M, et al.
Neuroimage
. 2013 May;
80:202-19.
PMID: 23707591
The Human Connectome Project (HCP) has developed protocols, standard operating and quality control procedures, and a suite of informatics tools to enable high throughput data collection, data sharing, automated data...
6.
Marcus D, Harwell J, Olsen T, Hodge M, Glasser M, Prior F, et al.
Front Neuroinform
. 2011 Jul;
5:4.
PMID: 21743807
The Human Connectome Project (HCP) is a major endeavor that will acquire and analyze connectivity data plus other neuroimaging, behavioral, and genetic data from 1,200 healthy adults. It will serve...
7.
Morris D, ONeil S, Devraj R, Portanova J, Gilles R, Gross C, et al.
Toxicol Pathol
. 2010 May;
38(4):606-18.
PMID: 20448081
Exposure to moderately selective p38alpha mitogen-activated protein kinase (MAPK) inhibitors in the Beagle dog results in an acute toxicity consisting of mild clinical signs (decreased activity, diarrhea, and fever), lymphoid...
8.
Hughes R, Rogier D, Jacobsen E, Walker J, Macinnes A, Bond B, et al.
J Med Chem
. 2010 Mar;
53(6):2656-60.
PMID: 20196613
We recently described a novel series of aminopyridopyrazinones as PDE5 inhibitors. Efforts toward optimization of this series culminated in the identification of 3-[4-(2-hydroxyethyl)piperazin-1-yl]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one, which possessed an excellent potency and selectivity...
9.
Elrick M, Kramer J, Alden C, Blomme E, Bunch R, Cabonce M, et al.
Toxicol Pathol
. 2005 Apr;
33(1):118-26.
PMID: 15805063
Hepatic enzyme inducers such as phenobarbital are often nongenotoxic rodent hepatocarcinogens. Currently, nongenotoxic hepatocarcinogens can only be definitively identified through costly and extensive long-term, repeat-dose studies (e.g., 2-year rodent carcinogenicity...
10.
Kramer J, Curtiss S, Kolaja K, Alden C, Blomme E, Curtiss W, et al.
Chem Res Toxicol
. 2004 Apr;
17(4):463-70.
PMID: 15089088
Currently, the only way to identify nongenotoxic hepatocarcinogens is through long-term repeat dose studies such as the 2 year rodent carcinogenicity assay. Such assays are both time consuming and expensive...