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Communications Biology|July 11, 2023
Architectural basis for cylindrical self-assembly governing Plk4-mediated centriole duplication in human cellsJong Il Ahn, Liang Zhang, Harsha Ravishankar, et al.
Research Square|March 30, 2023
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disabilityYu-Ri Lee, Mervyn G Thomas, Arkaprava Roychaudhury, et al.
Human Molecular Genetics|January 31, 2021
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafishYu-Ri Lee, Se Hee Kim, Afif Ben-Mahmoud, et al.
Nature Structural & Molecular Biology|July 7, 2014
Molecular basis for unidirectional scaffold switching of human Plk4 in centriole biogenesisSuk-Youl Park, Jung-Eun Park, Tae-Sung Kim, et al.
Annals of Neurology|July 29, 2024
SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual DisabilityArkaprava Roychaudhury, Yu-Ri Lee, Tae-Ik Choi, et al.
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