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Pediatric Transplantation|November 25, 2011
Variable disease progression after successful stem cell transplantation: prospective follow-up investigations in eight patients with Hurler syndromeLorenz Grigull, Karl-Walter Sykora, Andreas Tenger, et al.Nature Communications|October 7, 2024
Mechanochemically responsive polymer enables shockwave visualizationPolette J Centellas, Kyle D Mehringer, Andrew L Bowman, et al.Journal of Pain and Symptom Management|April 14, 2009
Atropine, hyoscine butylbromide, or scopolamine are equally effective for the treatment of death rattle in terminal careHans Wildiers, Chris Dhaenekint, Peter Demeulenaere, et al.Journal of Molecular Biology|September 20, 2023
Analysis of Reconstituted Tripartite Complex Supports Avidity-based Recruitment of Hsp70 by Substrate Bound J-domain ProteinMarcin Jelen, Igor Grochowina, Aneta Grabinska-Rogala, et al.Proceedings of the National Academy of Sciences of the United States of America|January 9, 2026
Origin of class B J-domain proteins involved in amyloid transactionsPrzemyslaw Domanski, Milena Stolarska, Katarzyna Kalinowska, et al.Scientific Reports|July 1, 2015
Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC methodLieselot Deleye, Dieter De Coninck, Christodoulos Christodoulou, et al.Journal of Acquired Immune Deficiency Syndromes (1999)|May 12, 2006
The added value of a CD4 count to identify patients eligible for highly active antiretroviral therapy among HIV-positive adults in CambodiaLut Lynen, Sopheak Thai, Paul De Munter, et al.Fertility and Sterility|April 9, 2021
Low feasibility of in vitro matured oocytes originating from cumulus complexes found during ovarian tissue preparation at the moment of gender confirmation surgery and during testosterone treatment for fertility preservation in transgender menSylvie Lierman, Annelies Tolpe, Ilse De Croo, et al.Fertility and Sterility|August 19, 2015
Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocystsLieselot Deleye, Annelies Dheedene, Dieter De Coninck, et al.Clinical Epigenetics|December 19, 2024
Advancing diagnosis and early risk assessment of preeclampsia through noninvasive cell-free DNA methylation profilingMachteld Baetens, Bram Van Gaever, Stephanie Deblaere, et al.Pageof 86