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Nature|March 26, 2025
Long-term impact and biological recovery in a deep-sea mining trackDaniel O B Jones, Maria Belen Arias, Loïc Van Audenhaege, et al.
Human Molecular Genetics|March 29, 2012
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosisJulien Couthouis, Michael P Hart, Renske Erion, et al.
Orphanet Journal of Rare Diseases|February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlationsVeerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2023
First observations of core-transiting seismic phases on MarsJessica C E Irving, Vedran Lekić, Cecilia Durán, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-DyskinesiaKathleen M Gorman, Esther Meyer, Detelina Grozeva, et al.
The Review of Scientific Instruments|October 1, 2022
Fusion product measurements by nuclear diagnostics in the Joint European Torus deuterium-tritium 2 campaign (invited)M Nocente, V Kiptily, M Tardocchi, et al.
The Journal of Clinical Investigation|August 2, 2022
GIGYF1 disruption associates with autism and impaired IGF-1R signalingGuodong Chen, Bin Yu, Senwei Tan, et al.
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