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Toxicology and Applied Pharmacology|September 1, 2009
Toxicogenomic analysis of N-nitrosomorpholine induced changes in rat liver: comparison of genomic and proteomic responses and anchoring to histopathological parametersA Oberemm, H-J Ahr, P Bannasch, et al.European Journal of Nuclear Medicine and Molecular Imaging|June 30, 2019
[18F]GTP1 (Genentech Tau Probe 1), a radioligand for detecting neurofibrillary tangle tau pathology in Alzheimer's diseaseSandra Sanabria Bohórquez, Jan Marik, Annie Ogasawara, et al.Transplantation|March 14, 2015
Association of Kidney Graft Loss With De Novo Produced Donor-Specific and Non-Donor-Specific HLA Antibodies Detected by Single Antigen TestingCaner Süsal, Daniel Wettstein, Bernd Döhler, et al.Biorxiv : the Preprint Server for Biology|June 25, 2024
The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell statesElisabeth Rebboah, Narges Rezaie, Brian A Williams, et al.Infection and Immunity|June 8, 2011
Direct evaluation of Pseudomonas aeruginosa biofilm mediators in a chronic infection modelMatthew S Byrd, Bing Pang, Wenzhou Hong, et al.Nature Communications|October 26, 2021
Bone marrow derived stromal cells from myelodysplastic syndromes are altered but not clonally mutated in vivoJohann-Christoph Jann, Maximilian Mossner, Vladimir Riabov, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 9, 2014
Genetic analysis reveals that amyloid precursor protein and death receptor 6 function in the same pathway to control axonal pruning independent of β-secretaseOlav Olsen, Dara Y Kallop, Todd McLaughlin, et al.Mbio|February 23, 2017
Fallacy of the Unique Genome: Sequence Diversity within Single Helicobacter pylori StrainsJenny L Draper, Lori M Hansen, David L Bernick, et al.Journal of Palliative Medicine|September 6, 2022
Top Ten Tips Palliative Care Clinicians Should Know About BuprenorphineKyle J Neale, Melissa B Weimer, Mellar P Davis, et al.Frontiers in Genetics|April 10, 2023
Early postnatal administration of an AAV9 gene therapy is safe and efficacious in CLN3 diseaseTyler B Johnson, Jon J Brudvig, Shibi Likhite, et al.Pageof 160