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American Journal of Physiology. Renal Physiology|October 5, 2020
Afferent renal innervation in anti-Thy1.1 nephritis in ratsKristina Rodionova, Roland Veelken, Karl F Hilgers, et al.Journal of the American Society of Nephrology : JASN|March 20, 2010
CCR6 recruits regulatory T cells and Th17 cells to the kidney in glomerulonephritisJan-Eric Turner, Hans-Joachim Paust, Oliver M Steinmetz, et al.Kidney International|October 15, 2015
Treg17 cells are programmed by Stat3 to suppress Th17 responses in systemic lupusMalte A Kluger, Simon Melderis, Anna Nosko, et al.Oncology Reports|November 6, 2007
Saliva as a biomarker for head and neck squamous cell carcinoma: in vitro detection of cytotoxic effects by using the plating efficiency indexMarc B Bloching, James Barnes, Wolfram Aust, et al.Journal of Communication Disorders|January 14, 2021
Speech restructuring group treatment for 6-to-9-year-old children who stutter: A therapeutic trialHarald A Euler, Anna Merkel, Katja Hente, et al.Hepatology (Baltimore, Md.)|February 21, 2013
Interstrain differences in chronic hepatitis and tumor development in a murine model of inflammation-mediated hepatocarcinogenesisTamara Potikha, Evgeniy Stoyanov, Orit Pappo, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|February 28, 2009
Computer-assisted documentation of the fiberoptic endoscopic evaluation of swallowingChristiane Hey, Robert A Sader, Dmitri Belogradski, et al.BMC Pediatrics|December 18, 2022
Comparison of cerebral oxygen desaturation events between children under general anesthesia and chloral hydrate sedation - a randomized controlled trialPhilipp Gude, Thomas P Weber, Stefan Dazert, et al.Stem Cell Research|August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.Stem Cell Research|September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.Pageof 23