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Molecular Pharmacology|April 18, 2001
BAY36-7620: a potent non-competitive mGlu1 receptor antagonist with inverse agonist activityF Y Carroll, A Stolle, P M Beart, et al.Genes, Chromosomes & Cancer|March 18, 2011
Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndromeJihane N Benhammou, Cathy D Vocke, Avni Santani, et al.Journal of Medicinal Chemistry|April 16, 2004
Synthesis, biological activity, and quantitative structure-activity relationship study of azanaphthalimide and arylnaphthalimide derivativesMiguel F Braña, Ana Gradillas, Angel Gómez, et al.Nature Communications|March 12, 2022
Recurring adaptive introgression of a supergene variant that determines social organizationEckart Stolle, Rodrigo Pracana, Federico López-Osorio, et al.Langmuir : the ACS Journal of Surfaces and Colloids|January 17, 2012
Does shape matter? Bioeffects of gold nanomaterials in a human skin cell modelNicole M Schaeublin, Laura K Braydich-Stolle, Elizabeth I Maurer, et al.Journal of Medicinal Chemistry|December 13, 2002
Synthesis, antitumor activity, molecular modeling, and DNA binding properties of a new series of imidazonaphthalimidesMiguel F Braña, Mónica Cacho, Mario A García, et al.Clinical Ophthalmology (Auckland, N.Z.)|April 27, 2026
Effects of Multimodal and Unimodal Physical Training Interventions on Visual Function in Glaucoma and Elderly Controls - A Pilot StudyCynthia Moffack Djuloun, Khaldoon O Al-Nosairy, Rosalie Beyer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: fluorescence in situ hybridization and dosage-sensitive Southern blot analysisK W Gripp, V Kasparcova, D M McDonald-McGinn, et al.The New England Journal of Medicine|May 13, 2011
A hemoglobin variant associated with neonatal cyanosis and anemiaMoira A Crowley, Todd L Mollan, Osheisa Y Abdulmalik, et al.American Journal of Medical Genetics. Part A|December 11, 2012
Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP arrayKosuke Izumi, Avni B Santani, Matthew A Deardorff, et al.Pageof 50