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Westerfield

Showing results (251-260 of 290) with videos related to

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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|April 20, 2026
A 3D In Vitro Model of the Human Hepatobiliary JunctionAshley D Westerfield, Katarzyna A Grzelak, Katie Katsuyama, et al.
Development (Cambridge, England)|October 25, 2002
A zebrafish sox9 gene required for cartilage morphogenesisYi-Lin Yan, Craig T Miller, Robert M Nissen, et al.
Prenatal Diagnosis|April 27, 2022
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomaliesCatherine G Kernie, Julia Wynn, Allison Rosenbaum, et al.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
Experimental Eye Research|May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafishMargo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Methods in Cell Biology|July 23, 2016
A scientist's guide for submitting data to ZFIND G Howe, Y M Bradford, A Eagle, et al.
The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Plos One|December 20, 2012
A unified anatomy ontology of the vertebrate skeletal systemWasila M Dahdul, James P Balhoff, David C Blackburn, et al.
Nucleic Acids Research|November 10, 2020
The Zebrafish Information Network: major gene page and home page updatesDouglas G Howe, Sridhar Ramachandran, Yvonne M Bradford, et al.
Nucleic Acids Research|December 1, 2016
The Zebrafish Model Organism Database: new support for human disease models, mutation details, gene expression phenotypes and searchingDouglas G Howe, Yvonne M Bradford, Anne Eagle, et al.
Pageof 29

Showing results (251-260 of 290) with videos related to

Sort By:
Pageof 29
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|April 20, 2026
A 3D In Vitro Model of the Human Hepatobiliary JunctionAshley D Westerfield, Katarzyna A Grzelak, Katie Katsuyama, et al.
Development (Cambridge, England)|October 25, 2002
A zebrafish sox9 gene required for cartilage morphogenesisYi-Lin Yan, Craig T Miller, Robert M Nissen, et al.
Prenatal Diagnosis|April 27, 2022
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomaliesCatherine G Kernie, Julia Wynn, Allison Rosenbaum, et al.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
Experimental Eye Research|May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafishMargo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Methods in Cell Biology|July 23, 2016
A scientist's guide for submitting data to ZFIND G Howe, Y M Bradford, A Eagle, et al.
The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Plos One|December 20, 2012
A unified anatomy ontology of the vertebrate skeletal systemWasila M Dahdul, James P Balhoff, David C Blackburn, et al.
Nucleic Acids Research|November 10, 2020
The Zebrafish Information Network: major gene page and home page updatesDouglas G Howe, Sridhar Ramachandran, Yvonne M Bradford, et al.
Nucleic Acids Research|December 1, 2016
The Zebrafish Model Organism Database: new support for human disease models, mutation details, gene expression phenotypes and searchingDouglas G Howe, Yvonne M Bradford, Anne Eagle, et al.
Pageof 29