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The Science of the Total Environment|February 15, 2020
Technetium immobilization by materials through sorption and redox-driven processes: A literature reviewCarolyn I Pearce, Robert C Moore, Joseph W Morad, et al.
Journal of Medical Genetics|June 22, 2012
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesisYifat Zivony-Elboum, Wendy Westbroek, Nehama Kfir, et al.
Iscience|February 25, 2025
The bacterial microbiome modulates the initiation of brain metastasis by impacting the gut-to-brain axisMatteo Massara, Michelle Ballabio, Bastien Dolfi, et al.
The Journal of Experimental Medicine|March 7, 2022
FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse modelMaxence Cornille, Stéphanie Moriceau, Roman H Khonsari, et al.
International Journal of Environmental Research and Public Health|March 8, 2020
Serum Ghrelin Levels in Saudi Obese Asthmatic School-Children-Correlation with Interleukin-4, Interleukin-5, and Interleukin-21Mohammed Saeed Al-Ayed, Khaled Sadeq Al-Shaibari, Dhafer Alshehri, et al.
Journal of Medical Internet Research|January 6, 2026
Correction: Combining Artificial Intelligence and Human Support in Mental Health: Digital Intervention With Comparable Effectiveness to Human-Delivered CareClare E Palmer, Emily Marshall, Edward Millgate, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Journal of Lipid Research|May 4, 2016
Ceramide-tamoxifen regimen targets bioenergetic elements in acute myelogenous leukemiaSamy A F Morad, Terence E Ryan, P Darrell Neufer, et al.
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