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Neuron|January 14, 2014
Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and miceLissandra Castellan Baldan, Kyle A Williams, Jean-Dominique Gallezot, et al.
Heart Rhythm O2|June 11, 2021
Catheter ablation of atrial fibrillation in patients with diabetes mellitusAllen Wang, Tracy Truong, Eric Black-Maier, et al.
Journal of Geophysical Research. Atmospheres : JGR|July 21, 2022
Increases in Future AR Count and Size: Overview of the ARTMIP Tier 2 CMIP5/6 ExperimentT A O'Brien, M F Wehner, A E Payne, et al.
Nature Genetics|February 7, 2018
CLCN2 chloride channel mutations in familial hyperaldosteronism type IIUte I Scholl, Gabriel Stölting, Julia Schewe, et al.
Stem Cells Translational Medicine|February 5, 2015
Enabling consistency in pluripotent stem cell-derived products for research and development and clinical applications through material standardsAnna French, Christopher Bravery, James Smith, et al.
Stem Cell Reports|December 31, 2021
Biomanufacturing in low Earth orbit for regenerative medicineArun Sharma, Rachel A Clemens, Orquidea Garcia, et al.
Genome Research|August 11, 2006
Human embryonic stem cells have a unique epigenetic signatureMarina Bibikova, Eugene Chudin, Bonnie Wu, et al.
Human Molecular Genetics|September 6, 2013
Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemiaYoung H Lim, Diana Ovejero, Jeffrey S Sugarman, et al.
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