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Human Molecular Genetics|March 8, 2008
C3 R102G polymorphism increases risk of age-related macular degenerationKylee L Spencer, Lana M Olson, Brent M Anderson, et al.
BMC Medical Genetics|November 22, 2013
Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III)Robert Goodloe, Kristin Brown-Gentry, Niloufar B Gillani, et al.
Molecular Pharmacology|February 1, 2024
Discovery and Characterization of VU0542270, the First Selective Inhibitor of Vascular Kir6.1/SUR2B KATP ChannelsKangjun Li, Samantha J McClenahan, Changho Han, et al.
Biochemistry|June 8, 2001
Characterization of the lysyl adducts of prostaglandin H-synthases that are derived from oxygenation of arachidonic acidO Boutaud, C J Brame, P Chaurand, et al.
Genes, Brain, and Behavior|August 14, 2009
Examination of tetrahydrobiopterin pathway genes in autismN C Schnetz-Boutaud, B M Anderson, K D Brown, et al.
Zookeys|October 3, 2022
The ground beetle tribe Platynini Bonelli, 1810 (Coleoptera, Carabidae) in the southern Levant: dichotomous and interactive identification tools, ecological traits, and distributionThorsten Assmann, Esteve Boutaud, Jörn Buse, et al.
ACS Bio & Med Chem Au|April 27, 2023
Discovery of "Molecular Switches" within a Series of mGlu5 Allosteric Ligands Driven by a "Magic Methyl" Effect Affording Both PAMs and NAMs with In Vivo Activity, Derived from an M1 PAM ChemotypeLisa Barbaro, Alice L Rodriguez, Ashlyn N Blevins, et al.
Jvs-Vascular Insights|May 11, 2026
Platelet activation in patients with peripheral artery disease from 43 sites: Assessment of samples transported by overnight mailWilliam B Stubblefield, Alexander E Sullivan, Katherine N Cahill, et al.
Investigative Ophthalmology & Visual Science|December 31, 2005
Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6Jonathan L Haines, Nathalie Schnetz-Boutaud, Silke Schmidt, et al.
Human Mutation|June 19, 2007
Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer diseaseXueying Liang, Eden R Martin, Nathalie Schnetz-Boutaud, et al.
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