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Journal of the Air & Waste Management Association (1995)|August 4, 2009
Methods for characterizing fine particulate matter using ground observations and remotely sensed data: potential use for environmental public health surveillanceMohammad Z Al-Hamdan, William L Crosson, Ashutosh S Limaye, et al.
The American Naturalist|June 27, 2025
Quantifying Phylogenetic and Nonphylogenetic Patterns in the Richness, Frequency, and Identity of Links in a Herbivore-Parasitoid Interaction NetworkFrazer H Sinclair, Chang-Ti Tang, Richard I Bailey, et al.
PNAS Nexus|February 10, 2025
Perceived self and social relevance of content motivates news sharing across cultures and topicsDanielle Cosme, Hang-Yee Chan, Alyssa H Sinclair, et al.
Genes|November 24, 2022
Integral Role of the Mitochondrial Ribosome in Supporting Ovarian Function: MRPS7 Variants in Syndromic Premature Ovarian InsufficiencyBrianna L Kline, Sylvie Jaillard, Katrina M Bell, et al.
Acta Pharmacologica Sinica|October 29, 2008
Pharmacokinetic and toxicity study of intravitreal erythropoietin in rabbitsJing-fa Zhang, Ya-lan Wu, Jing-ying Xu, et al.
Ecology and Evolution|December 7, 2018
Ice ages and butterflyfishes: Phylogenomics elucidates the ecological and evolutionary history of reef fishes in an endemism hotspotJoseph D DiBattista, Michael E Alfaro, Laurie Sorenson, et al.
European Journal of Human Genetics : EJHG|November 30, 2022
LARS2 variants can present as premature ovarian insufficiency in the absence of overt hearing lossAnne Sophie Neyroud, Joëlle Rudinger-Thirion, Magali Frugier, et al.
Frontiers in Immunology|April 29, 2021
Latent Cytomegalovirus-Driven Recruitment of Activated CD4+ T Cells Promotes Virus ReactivationSarah E Jackson, Kevin C Chen, Ian J Groves, et al.
Stem Cell Research|March 8, 2024
Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC linesLucas G A Ferreira, Mauricio C Cabral-da-Silva, Svenja Pachernegg, et al.
Molecular and Cellular Endocrinology|January 9, 2025
Functional analysis of SRY variants in individuals with 46,XY differences of sex developmentFirman P Idris, Jocelyn van den Bergen, Gorjana Robevska, et al.
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