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Frontiers in Cell and Developmental Biology|November 11, 2021
Loss of Function Glucose-Dependent Insulinotropic Polypeptide Receptor Variants Are Associated With Alterations in BMI, Bone Strength and Cardiovascular OutcomesHüsün Sheyma Kizilkaya, Kimmie Vestergaard Sørensen, Camilla J Kibsgaard, et al.Cold Spring Harbor Molecular Case Studies|July 14, 2017
Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathyDale L Bodian, Thierry Vilboux, Suchitra K Hourigan, et al.Journal of Paediatrics and Child Health|February 13, 2001
Bone mineral density in prepubertal asthmatics receiving corticosteroid treatmentM Harris, S Hauser, T V Nguyen, et al.Metabolism: Clinical and Experimental|January 10, 2026
Global glucagon-like peptide-2 receptor activation linked to increased obesity risk in the UK BiobankPeter A Gerlach, Sarina Gadgaard, Jakob S Madsen, et al.American Journal of Public Health|August 10, 2013
Assessment of genetic and nongenetic interactions for the prediction of depressive symptomatology: an analysis of the Wisconsin Longitudinal Study using machine learning algorithmsNicholas S Roetker, C David Page, James A Yonker, et al.BMJ Open|July 5, 2012
Multigene interactions and the prediction of depression in the Wisconsin Longitudinal StudyNicholas S Roetker, James A Yonker, Chee Lee, et al.Schizophrenia Research|July 20, 2022
Psychopharmacological treatment patterns prior to a schizophrenia diagnosis: A Danish nationwide studyChristopher Rohde, Mikkel Højlund, Christiane Gasse, et al.Microbiology Spectrum|October 27, 2023
A metagenomics method for the quantitative detection of bacterial pathogens causing hospital-associated and ventilator-associated pneumoniaS Hauser, V Lazarevic, M Tournoud, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 3, 2019
Receptor selectivity between the G proteins Gα12 and Gα13 is defined by a single leucine-to-isoleucine variationAmanda E Mackenzie, Tezz Quon, Li-Chiung Lin, et al.Molecular Genetics & Genomic Medicine|March 5, 2019
Rett syndrome (MECP2) and succinic semialdehyde dehydrogenase (ALDH5A1) deficiency in a developmentally delayed femaleMadalyn Brown, Paula Ashcraft, Erland Arning, et al.Pageof 30