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Journal of Environmental Management|February 15, 2021
Ecosystem services consideration in the remediation process for contaminated sitesMatthew C Harwell, Chloe Jackson, Michael Kravitz, et al.Psychological Medicine|August 1, 2019
Evidence of shared familial factors influencing neurocognitive endophenotypes in adult- and childhood-onset schizophreniaTim B Bigdeli, Keith H Nuechterlein, Catherine A Sugar, et al.Mutation Research|September 3, 1998
A human lymphoid leukemia cell line with a V(D)J recombinase-mediated deletion of hprtC L Chen, M H Woo, G A Neale, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 16, 2004
Efficacy and safety of a new, chromatographically purified rhesus (D) immunoglobulinIan Z MacKenzie, Johann Bichler, Gerald C Mason, et al.Biological Psychiatry|February 8, 2008
Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density familiesAyman H Fanous, Michael C Neale, Bradley T Webb, et al.Journal of Food Protection|February 20, 2025
An outbreak of Shiga Toxin-producing Escherichia coli Serotype O145:H28 Associated with Domestic Travel and Consumption of Unpasteurized Cheese, UK, 2023Orlagh I Quinn, Claire Jenkins, David R Greig, et al.The Journal of Ambulatory Care Management|September 18, 2007
Healthcare utilization among veterans undergoing chemotherapy: the impact of a cancer care coordination/home-telehealth programNeale R Chumbler, Rita Kobb, Linda Harris, et al.The Journal of Investigative Dermatology|August 1, 2008
Incidence of basal cell carcinoma multiplicity and detailed anatomic distribution: longitudinal study of an Australian populationNaomi M Richmond-Sinclair, Nirmala Pandeya, Robert S Ware, et al.Experimental and Molecular Pathology|November 4, 2008
Promoter hypermethylation leads to decreased APC mRNA expression in familial polyposis and sporadic colorectal tumours, but does not substitute for truncating mutationsStefania Segditsas, Oliver M Sieber, Andrew Rowan, et al.Nature Genetics|September 22, 2022
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.Pageof 400