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Biology Open|February 18, 2016
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defectsBrian C Gibbs, Rama Rao Damerla, Eszter K Vladar, et al.Nature Biotechnology|November 18, 2025
Extensive restoration of forelimb function in primates with spinal cord injury by neural stem cell transplantationEleni Sinopoulou, Ephron S Rosenzweig, John H Brock, et al.Development (Cambridge, England)|September 6, 2021
Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strengthJennifer H Kong, Cullen B Young, Ganesh V Pusapati, et al.Human Molecular Genetics|April 17, 2015
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesRama Rao Damerla, Cheng Cui, George C Gabriel, et al.Nature Neuroscience|June 26, 2019
Chondroitinase improves anatomical and functional outcomes after primate spinal cord injuryEphron S Rosenzweig, Ernesto A Salegio, Justine J Liang, et al.Brain Research|December 3, 2014
Leveraging biomedical informatics for assessing plasticity and repair in primate spinal cord injuryJessica L Nielson, Jenny Haefeli, Ernesto A Salegio, et al.Frontiers in Neuroscience|December 5, 2022
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart diseaseJodie K Votava-Smith, Jenna Gaesser, Anna Lonyai Harbison, et al.Nature Communications|January 21, 2015
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterningPeter G Czarnecki, George C Gabriel, Danielle K Manning, et al.Leukemia|June 18, 2011
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratoriesA Kohlmann, H-U Klein, S Weissmann, et al.Tissue Antigens|February 9, 2011
A multi-site study using high-resolution HLA genotyping by next generation sequencingC L Holcomb, B Höglund, M W Anderson, et al.Pageof 43