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Micropublication Biology|December 22, 2025
Isolation and Characterization of the subcluster L2 Mycobacteriophage Underpass and its lysogenKiley R Toth, Alexa R Rogers, Emma R Wenzel, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Journal of Inherited Metabolic Disease|December 6, 2013
Update on transcobalamin deficiency: clinical presentation, treatment and outcomeY J Trakadis, A Alfares, O A Bodamer, et al.
Molecular Genetics and Metabolism|February 17, 2015
Disease specific therapies in leukodystrophies and leukoencephalopathiesGuy Helman, Keith Van Haren, Joshua L Bonkowsky, et al.
The New England Journal of Medicine|August 25, 2006
Aneurysm syndromes caused by mutations in the TGF-beta receptorBart L Loeys, Ulrike Schwarze, Tammy Holm, et al.
Journal of the American College of Cardiology|June 18, 2025
Differences in Arterial Events in Vascular Ehlers-Danlos, Loeys-Dietz, and Marfan SyndromeErnesto Calderon-Martinez, Walter V Velasco, Dongchuan Guo, et al.
Gene & Protein in Disease|August 1, 2025
Exploring dopamine as the master regulator of brain circuitry and mental health genomeKenneth Blum, Eric R Braverman, Alireza Sharafshah, et al.
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