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Nature Communications|October 2, 2020
Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipidsAdriaan van der Graaf, Annique Claringbould, Antoine Rimbert, et al.
European Journal of Human Genetics : EJHG|October 9, 2014
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designsGiorgio Pistis, Eleonora Porcu, Scott I Vrieze, et al.
Molecular Biology Reports|July 21, 2011
Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profileFrancesca Crobu, Veronica Latini, Maria Franca Marongiu, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2008
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemiaManuela Uda, Renzo Galanello, Serena Sanna, et al.
American Journal of Human Genetics|June 3, 2008
Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid functionLisette Arnaud-Lopez, Gianluca Usala, Graziano Ceresini, et al.
Frontiers in Immunology|April 17, 2024
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq datasetPaola Forabosco, Mauro Pala, Francesca Crobu, et al.
Developmental Biology|May 24, 2016
Novel action of FOXL2 as mediator of Col1a2 gene autoregulationMara Marongiu, Manila Deiana, Loredana Marcia, et al.
Human Molecular Genetics|January 7, 2011
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levelsIrene Pichler, Cosetta Minelli, Serena Sanna, et al.
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