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Neurology. Genetics|January 31, 2018
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 functionNatalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, et al.
Journal of Molecular and Cellular Cardiology|February 7, 2021
Phosphoproteomics of the developing heart identifies PERM1 - An outer mitochondrial membrane proteinSriram Aravamudhan, Clara Türk, Theresa Bock, et al.
Archives of Virology|July 26, 2012
Novel serological tools for detection of Thottapalayam virus, a Soricomorpha-borne hantavirusMathias Schlegel, Erdenesaikhan Tegshduuren, Kumiko Yoshimatsu, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 9, 2016
Efficacy of High-Intensity Local Treatment for Metastatic Urothelial Carcinoma of the Bladder: A Propensity Score-Weighted Analysis From the National Cancer Data BaseThomas Seisen, Maxine Sun, Jeffrey J Leow, et al.
Frontiers in Microbiology|April 12, 2019
Von Willebrand Factor Mediates Pneumococcal Aggregation and Adhesion in Blood FlowHilger Jagau, Ina-Kristin Behrens, Karen Lahme, et al.
Development (Cambridge, England)|December 1, 1996
Neural degeneration mutants in the zebrafish, Danio rerioM Furutani-Seiki, Y J Jiang, M Brand, et al.
Scientific Reports|December 6, 2016
Modular Architecture and Unique Teichoic Acid Recognition Features of Choline-Binding Protein L (CbpL) Contributing to Pneumococcal PathogenesisJavier Gutiérrez-Fernández, Malek Saleh, Martín Alcorlo, et al.
EMBO Molecular Medicine|March 21, 2014
Mild expression differences of MECP2 influencing aggressive social behaviorMartesa Tantra, Christian Hammer, Anne Kästner, et al.
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