Showing results (41-50 of 109) with videos related to

Sort By:
Pageof 11
Nature|July 7, 2009
miR-145 and miR-143 regulate smooth muscle cell fate and plasticityKimberly R Cordes, Neil T Sheehy, Mark P White, et al.
Cold Spring Harbor Molecular Case Studies|March 17, 2017
AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infantSarah U Morton, Sanjay P Prabhu, Hart G W Lidov, et al.
Pediatric Blood & Cancer|July 25, 2026
Bleeding and Thromboembolic Events With Antiplatelet Agents in Pediatric Heart Disease-An Exploratory Study of the Role of PharmacogenomicsPaul Esteso, Bryan Siegel, Hyun Kim, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 12, 2026
Quality improvement initiative to optimize use of rapid genomic sequencing in a level IV NICUAlissa M D'Gama, Rachel S Hu, Maya C Del Rosario, et al.
Pediatric Quality & Safety|May 20, 2020
Screening With Reticulocyte Hemoglobin Increased Iron Sufficiency Among NICU PatientsSarah U Morton, Jenny Chan Yuen, Henry A Feldman, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|March 19, 2024
Genomic testing and molecular diagnosis among infants with congenital heart disease in the neonatal intensive care unitErica E D'Souza, Tina O Findley, Rachel Hu, et al.
Eclinicalmedicine|January 7, 2025
Detection of neurologic changes in critically ill infants using deep learning on video data: a retrospective single center cohort studyAlec Gleason, Florian Richter, Nathalia Beller, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Structural variants in human congenital heart disease disrupt distal genomic regulatory contacts of developmental genesJodi Lee, Jingshing Wu, Maureen Pittman, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Accurate prediction of neurologic changes in critically ill infants using pose AIAlec Gleason, Florian Richter, Nathalia Beller, et al.
Human Molecular Genetics|September 16, 2017
Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early deathSiqi Cao, Laura L Smith, Sergio R Padilla-Lopez, et al.
Pageof 11