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European Journal of Human Genetics : EJHG|June 14, 2012
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole bloodDivya Mehta, Katharina Heim, Christian Herder, et al.
Thyroid : Official Journal of the American Thyroid Association|October 25, 2014
Translating pharmacological findings from hypothyroid rodents to euthyroid humans: is there a functional role of endogenous 3,5-T2?Maik Pietzner, Ina Lehmphul, Nele Friedrich, et al.
Scientific Reports|November 2, 2017
Helicobacter pylori colonization and obesity - a Mendelian randomization studyWouter J den Hollander, Linda Broer, Claudia Schurmann, et al.
Methods (San Diego, Calif.)|May 7, 2013
A proteomics workflow for quantitative and time-resolved analysis of adaptation reactions of internalized bacteriaHenrike Pförtner, Juliane Wagner, Kristin Surmann, et al.
BMC Medical Genetics|August 25, 2017
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsSteffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, et al.
American Journal of Hematology|June 16, 2018
Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE StudyChani Jo Hodonsky, Claudia Schurmann, Ursula M Schick, et al.
Journal of the American College of Cardiology|March 25, 2017
Apolipoprotein L1 Variants and Blood Pressure Traits in African AmericansGirish N Nadkarni, Geneviève Galarneau, Stephen B Ellis, et al.
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