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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 20, 2026
A 3D In Vitro Model of the Human Hepatobiliary Junction
Ashley D Westerfield, Katarzyna A Grzelak, Katie Katsuyama, et al.
Development (Cambridge, England)
|
October 25, 2002
A zebrafish sox9 gene required for cartilage morphogenesis
Yi-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 anomalies
Catherine 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 Disorders
Justin O Szot, Carla Campagnolo, Ye Cao, et al.
Experimental Eye Research
|
May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafish
Margo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Methods in Cell Biology
|
July 23, 2016
A scientist's guide for submitting data to ZFIN
D 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 syndrome
Inga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Plos One
|
December 20, 2012
A unified anatomy ontology of the vertebrate skeletal system
Wasila 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 updates
Douglas 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 searching
Douglas G Howe, Yvonne M Bradford, Anne Eagle, et al.
Page
of 29
Search research articles
Search
Showing results (251-260 of 290) with videos related to
Sort By:
Page
of 29
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 20, 2026
A 3D In Vitro Model of the Human Hepatobiliary Junction
Ashley D Westerfield, Katarzyna A Grzelak, Katie Katsuyama, et al.
Development (Cambridge, England)
|
October 25, 2002
A zebrafish sox9 gene required for cartilage morphogenesis
Yi-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 anomalies
Catherine 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 Disorders
Justin O Szot, Carla Campagnolo, Ye Cao, et al.
Experimental Eye Research
|
May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafish
Margo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Methods in Cell Biology
|
July 23, 2016
A scientist's guide for submitting data to ZFIN
D 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 syndrome
Inga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Plos One
|
December 20, 2012
A unified anatomy ontology of the vertebrate skeletal system
Wasila 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 updates
Douglas 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 searching
Douglas G Howe, Yvonne M Bradford, Anne Eagle, et al.
Page
of 29