Showing results (101-110 of 117) with videos related to
Sort By:
Pageof 12
Human Mutation|July 29, 2018
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypesJorge Oliveira, Angela Gruber, Márcio Cardoso, et al.American Journal of Respiratory Cell and Molecular Biology|February 25, 2026
Altered cholesterol immunometabolism activates the macrophage NLRP3-inflammasome in lung fibrosisMariza Vaso, Matija Dukic, Peter Pennitz, et al.Annals of Clinical and Translational Neurology|September 12, 2019
Dominant collagen XII mutations cause a distal myopathyPayam Mohassel, Teerin Liewluck, Ying Hu, et al.Journal of Dental Education|December 16, 2006
The dental education environmentN Karl Haden, Sandra C Andrieu, D Gregory Chadwick, et al.Journal of Dental Education|September 7, 2006
The case for change in dental educationMarsha Pyle, Sandra C Andrieu, D Gregory Chadwick, et al.Journal of Dental Education|September 7, 2006
Educational strategies associated with development of problem-solving, critical thinking, and self-directed learningWilliam D Hendricson, Sandra C Andrieu, D Gregory Chadwick, et al.Journal of Dental Education|December 22, 2007
Does faculty development enhance teaching effectiveness?William D Hendricson, Eugene Anderson, Sandra C Andrieu, et al.Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.FEBS Letters|July 9, 2013
A model of yeast glycolysis based on a consistent kinetic characterisation of all its enzymesKieran Smallbone, Hanan L Messiha, Kathleen M Carroll, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 2, 2023
Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesisSafoora B Syeda, Museer A Lone, Payam Mohassel, et al.Pageof 12