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BMC Biology|August 1, 2017
The house spider genome reveals an ancient whole-genome duplication during arachnid evolutionEvelyn E Schwager, Prashant P Sharma, Thomas Clarke, 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.
BMC Genomics|November 23, 2018
The genome of the water strider Gerris buenoi reveals expansions of gene repertoires associated with adaptations to life on the waterDavid Armisén, Rajendhran Rajakumar, Markus Friedrich, et al.
The Journal of Experimental Medicine|October 12, 2019
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 functionMichael T Lam, Simona Coppola, Oliver H F Krumbach, et al.
Nature|November 19, 2015
Hemichordate genomes and deuterostome originsOleg Simakov, Takeshi Kawashima, Ferdinand Marlétaz, 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.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
The Western Journal of Emergency Medicine|August 12, 2025
Letter of Concern from the Association of Academic Chairs of Emergency Medicine Regarding ACGME Proposed ChangesRichard J Hamilton, Lance B Becker, Richard E Wolfe, et al.
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