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Biorxiv : the Preprint Server for Biology|September 24, 2024
A Comprehensive Atlas of AAV Tropism in the MouseChristopher J Walkey, Kathy J Snow, Jote Bulcha, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Uncovering Phenotypic Expansion in AXIN2-Related Disorders through Precision Animal ModelingNathalie M Aceves-Ewing, Denise G Lanza, Paul C Marcogliese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 10, 2026
Uncovering Phenotypic Expansion in AXIN2-Related Disorders through Precision Animal ModelingNathalie M Aceves-Ewing, Denise G Lanza, Paul C Marcogliese, et al.
Scientific Reports|September 30, 2024
Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse linesHillary Elrick, Kevin A Peterson, Brandon J Willis, et al.
Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
American Journal of Human Genetics|August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.
Physical Review Letters|July 18, 2014
Isospin character of low-lying pygmy dipole states in 208Pb via inelastic scattering of 17O ionsF C L Crespi, A Bracco, R Nicolini, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Bioinformatics (Oxford, England)|October 9, 2019
Soft windowing application to improve analysis of high-throughput phenotyping dataHamed Haselimashhadi, Jeremy C Mason, Violeta Munoz-Fuentes, et al.
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