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Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.Nature Neuroscience|March 3, 2017
Video-rate volumetric functional imaging of the brain at synaptic resolutionRongwen Lu, Wenzhi Sun, Yajie Liang, et al.Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.Nature Genetics|February 5, 2013
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomasMiriam J Smith, James O'Sullivan, Sanjeev S Bhaskar, et al.Journal of Neurosurgery|February 7, 2025
Outcomes following stereotactic radiosurgery for high-grade brain arteriovenous malformations: a systematic review and meta-analysisImran Farhad, Adam Ridzuan-Allen, Saniya Ansari, et al.Current Biology : CB|February 5, 2025
Eye saccades align optic flow with retinal specializations during object pursuit in freely moving ferretsDamian J Wallace, Kay-Michael Voit, Daniela Martin Machado, et al.American Journal of Human Genetics|January 25, 2003
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathyKristien Verhoeven, Peter De Jonghe, Katrien Coen, et al.Nature Communications|July 28, 2025
Suppression of ERK signalling promotes pluripotent epiblast in the human blastocystClaire S Simon, Afshan McCarthy, Laura Woods, et al.Resuscitation|March 19, 2018
Out-of-hospital cardiac arrest survival in international airportsSiobhán Masterson, Bryan McNally, John Cullinan, et al.American Journal of Human Genetics|August 2, 2007
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosumElena Boland, Jill Clayton-Smith, Victoria G Woo, et al.Pageof 17