Showing results (1721-1730 of 2,117) with videos related to

Sort By:
Pageof 212
Genome Medicine|November 7, 2024
Curating genomic disease-gene relationships with Gene2Phenotype (G2P)T Michael Yates, Morad Ansari, Louise Thompson, et al.
Biochemical Pharmacology|January 29, 2013
Tamoxifen magnifies therapeutic impact of ceramide in human colorectal cancer cells independent of p53Samy A F Morad, James P Madigan, Jonathan C Levin, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|September 21, 2017
Canadian benchmarks for acute injury careLynne Moore, David Evans, Natalie L Yanchar, et al.
Biosensors|May 15, 2023
The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological NanoparticlesNour Sharar, Konstantin Wüstefeld, Rahat Morad Talukder, et al.
Frontiers in Aging Neuroscience|February 6, 2019
Less Is More - Estimation of the Number of Strides Required to Assess Gait Variability in Spatially Confined SettingsDaniel Kroneberg, Morad Elshehabi, Anne-Christiane Meyer, et al.
European Journal of Medical Genetics|October 2, 2014
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 geneHanna Mandel, Ksenya Cohen Katsanelson, Morad Khayat, et al.
Journal of the American College of Surgeons|September 18, 2017
Impact of the Acute Care Surgery Model on Disease- and Patient-Specific Outcomes in Appendicitis and Biliary Disease: A Meta-AnalysisPatrick B Murphy, Kristin DeGirolamo, Theunis Jean Van Zyl, et al.
Zhonghua Yi Xue Za Zhi|December 6, 2005
[Mesenchymal stem cells from human proximal femurs possess immunosuppressive activity]Yi-zhuo Zhang, Loic Fouillard, Alain Chapel, et al.
International Journal of Ophthalmology|July 1, 2026
Factors affecting color vision: a systematic reviewFaezeh Fayaz, Ebrahim Jafarzadehpur, Morad Amir Ahmad, et al.
The Journal of Biological Chemistry|December 23, 2000
Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathyB C Knollmann, S A Blatt, K Horton, et al.
Pageof 212