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Yu-Ri Lee

Showing results (61-70 of 67) with videos related to

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Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 5, 2024
RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish modelJi-Won Park, Tae-Ik Choi, Tae-Yoon Kim, et al.
Cell Stem Cell|November 29, 2023
VEGFA mRNA-LNP promotes biliary epithelial cell-to-hepatocyte conversion in acute and chronic liver diseases and reverses steatosis and fibrosisFatima Rizvi, Yu-Ri Lee, Ricardo Diaz-Aragon, et al.
Zebrafish|May 11, 2017
Zebrafish as a Screening Model for Testing the Permeability of Blood-Brain Barrier to Small MoleculesSeong Soon Kim, So Hee Im, Jung Yoon Yang, et al.
Research Square|March 30, 2023
Eye movement defects in KO zebrafish reveals <i>SRPK3</i> 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 Communications|July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathyYu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, 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.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 5, 2024
RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish modelJi-Won Park, Tae-Ik Choi, Tae-Yoon Kim, et al.
Cell Stem Cell|November 29, 2023
VEGFA mRNA-LNP promotes biliary epithelial cell-to-hepatocyte conversion in acute and chronic liver diseases and reverses steatosis and fibrosisFatima Rizvi, Yu-Ri Lee, Ricardo Diaz-Aragon, et al.
Zebrafish|May 11, 2017
Zebrafish as a Screening Model for Testing the Permeability of Blood-Brain Barrier to Small MoleculesSeong Soon Kim, So Hee Im, Jung Yoon Yang, et al.
Research Square|March 30, 2023
Eye movement defects in KO zebrafish reveals <i>SRPK3</i> 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 Communications|July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathyYu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, 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.
Pageof 7