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The Journal of Investigative Dermatology|July 13, 2004
A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutationMaurice A M van Steensel, Peter M Steijlen, Reno S Bladergroen, et al.AIDS Research and Therapy|April 14, 2005
Monitoring processed, mature Human Immunodeficiency Virus type 1 particles immediately following treatment with a protease inhibitor-containing treatment regimenHeather A Baird, Andre J Marozsan, Michael M Lederman, et al.The Journal of Cardiovascular Surgery|June 5, 2004
In vivo transluminal microvascular endothelial cell seeding on balloon injured rabbit arteriesC H Arts, P G De Groot, N Attevelt, et al.Toxicology|March 5, 2008
The contact allergen dinitrochlorobenzene (DNCB) and respiratory allergy in the Th2-prone Brown Norway ratC Frieke Kuper, Rob H Stierum, Andre Boorsma, et al.Integrated Environmental Assessment and Management|August 16, 2024
Incorporating a weight-of-evidence approach into a tiered assessment for chemicals management, with emphasis on program development and applications in developing countries and emerging economiesCharles A Menzie, Patrick D Guiney, Scott E Belanger, et al.Nucleic Acids Research|November 28, 2018
An ultra-high affinity ligand of HIV-1 TAR reveals the RNA structure recognized by P-TEFbMatthew D Shortridge, Paul T Wille, Alisha N Jones, et al.Journal of the American Medical Directors Association|September 6, 2015
Physical Frailty and Cognitive Functioning in Depressed Older Adults: Findings From the NESDO StudyMatheus H L Arts, Rose M Collard, Hannie C Comijs, et al.Frontiers in Cellular and Infection Microbiology|December 12, 2025
Silver multilayer coating on orthopedic implant material of different alloys and surfaces significantly reduces bacterial colonizationLydia T D Speijker, Janine Fechter, Rainer Bargon, et al.Journal of Chemical Theory and Computation|September 9, 2023
Two for One: Diffusion Models and Force Fields for Coarse-Grained Molecular DynamicsMarloes Arts, Victor Garcia Satorras, Chin-Wei Huang, et al.Journal of Neurodevelopmental Disorders|April 28, 2016
Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 childrenRenée J Zwanenburg, Selma A J Ruiter, Edwin R van den Heuvel, et al.Pageof 203