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Development (Cambridge, England)|May 30, 2020
The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryosHelen Rankin Willsey, Yuxiao Xu, Amanda Everitt, et al.Environmental Science & Technology|March 19, 2024
Enrichment of Geogenic Organoiodine Compounds in Alluvial-Lacustrine Aquifers: Molecular Constraints by Organic MatterJiangkai Xue, Yamin Deng, Kunfu Pi, et al.Biorxiv : the Preprint Server for Biology|April 2, 2026
Transient activation of potent progenitor cells is required for spinal cord regenerationChase A Weinholtz, Lili Zhou, Vishnu Muraleedharan Saraswathy, et al.Cell Systems|August 19, 2021
A convergent molecular network underlying autism and congenital heart diseaseSara Brin Rosenthal, Helen Rankin Willsey, Yuxiao Xu, et al.Development (Cambridge, England)|June 27, 2023
Pleiotropy of autism-associated chromatin regulatorsMicaela Lasser, Nawei Sun, Yuxiao Xu, et al.Development (Cambridge, England)|November 5, 2021
Deep learning is widely applicable to phenotyping embryonic development and diseaseThomas Naert, Özgün Çiçek, Paulina Ogar, et al.Neuron|January 26, 2021
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilienceHelen Rankin Willsey, Cameron R T Exner, Yuxiao Xu, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2019
Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tractAlexandria T M Blackburn, Nasim Bekheirnia, Vanessa C Uma, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2019
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tractAlexandria T M Blackburn, Nasim Bekheirnia, Vanessa C Uma, et al.Pageof 3