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Journal of Biomolecular Screening|August 28, 2012
A selective ATP-binding cassette subfamily G member 2 efflux inhibitor revealed via high-throughput flow cytometryJ Jacob Strouse, Irena Ivnitski-Steele, Hadya M Khawaja, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 10, 2024
Identification of a cell-active chikungunya virus nsP2 protease inhibitor using a covalent fragment-based screening approachEric M Merten, John D Sears, Tina M Leisner, et al.
Cerebrovascular Diseases (Basel, Switzerland)|May 26, 2025
Assessing the Quality of Stroke Services in Brazil Using the World Stroke Organization RoadmapAline Palmeira Pires, Kelin Cristine Martin, Thaís L Secchi, et al.
Nature Immunology|August 7, 2024
Age-related epithelial defects limit thymic function and regenerationAnastasia I Kousa, Lorenz Jahn, Kelin Zhao, et al.
Frontiers in Genetics|September 23, 2022
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomesCaio Robledo D' Angioli Costa Quaio, Antonio Victor Campos Coelho, Livia Maria Silva Moura, et al.
ACS Infectious Diseases|February 22, 2022
Identification of β-Lactams Active against <i>Mycobacterium tuberculosis</i> by a Consortium of Pharmaceutical Companies and Academic InstitutionsBen Gold, Jun Zhang, Landys Lopez Quezada, et al.
Nature Biotechnology|June 2, 2022
Expanding RNAi therapeutics to extrahepatic tissues with lipophilic conjugatesKirk M Brown, Jayaprakash K Nair, Maja M Janas, et al.
Human Genomics|November 16, 2023
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023Caio Robledo D'Angioli Costa Quaio, José Ricardo Magliocco Ceroni, Michele Araújo Pereira, et al.
Pediatric Research|May 8, 2026
Assessment of diagnostic yield and clinical utility of genome sequencing in critically ill infantsCarolina A Moreno, Marina de França, Joana R M Prota, et al.
HGG Advances|May 5, 2026
Genome Sequencing for the Diagnosis of Rare Disorders: The Brazilian Rare Genomes Project, Antonio Victor Campos Coelho, Rafael Sales de Albuquerque, et al.
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