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Nature Genetics|July 14, 1998
Identification of the gene responsible for Best macular dystrophyK Petrukhin, M J Koisti, B Bakall, et al.
Journal of Lipid Research|October 16, 2014
Deletion of CGI-58 or adipose triglyceride lipase differently affects macrophage function and atherosclerosisMadeleine Goeritzer, Stefanie Schlager, Branislav Radovic, et al.
Plos One|October 11, 2018
Apolipoprotein E is a pancreatic extracellular factor that maintains mature β-cell gene expressionAhmed I Mahmoud, Francisco X Galdos, Katherine A Dinan, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 31, 2003
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosisAnnalisa Frattini, Alessandra Pangrazio, Lucia Susani, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 6, 2025
Loss of RET-ROS at complex I induces diastolic dysfunction in mice that is reversed by aerobic exerciseAna Vujic, Amy Koo, Guillaume Bidault, et al.
BMC Biology|March 5, 2017
Structural basis for potency differences between GDF8 and GDF11Ryan G Walker, Magdalena Czepnik, Erich J Goebel, et al.
Nature Communications|November 12, 2017
Novel genetically encoded fluorescent probes enable real-time detection of potassium in vitro and in vivoHelmut Bischof, Markus Rehberg, Sarah Stryeck, et al.
Circulation Research|March 11, 2018
Lysosomal Cholesterol Hydrolysis Couples Efferocytosis to Anti-Inflammatory Oxysterol ProductionManon Viaud, Stoyan Ivanov, Nemanja Vujic, et al.
American Journal of Human Genetics|February 3, 2009
Mutations in SPINT2 cause a syndromic form of congenital sodium diarrheaPeter Heinz-Erian, Thomas Müller, Birgit Krabichler, et al.
JAAD International|August 19, 2021
Effectiveness and clinical predictors of drug survival in psoriasis patients receiving apremilast: A registry analysisThomas Graier, Wolfgang Weger, Paul-Gunther Sator, et al.
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