Xenopus: Experimental Access to Cardiovascular Development, Regeneration Discovery, and Cardiovascular Heart-Defect Modeling
Author:
Publisher
Cold Spring Harbor Laboratory
Subject
General Biochemistry, Genetics and Molecular Biology
Reference78 articles.
1. Afouda BA . 2012. Stem-cell-like embryonic explants to study cardiac development, pp. 515–523. Humana, Totowa, NJ.
2. Genome-wide transcriptomics analysis identifies sox7 and sox18 as specifically regulated by gata4 in cardiomyogenesis
3. High efficiency non-mosaic CRISPR mediated knock-in and mutations in F0 Xenopus
4. Transient early embryonic expression of Nkx2-5 mutations linked to congenital heart defects in human causes heart defects inXenopus laevis
5. Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development.
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1. Fbrsl1 is required for heart development in Xenopus laevis and de novo variants in FBRSL1 can cause human heart defects;Disease Models & Mechanisms;2024-05-14
2. Modelling human genetic disorders in Xenopus tropicalis;Disease Models & Mechanisms;2024-05-01
3. Preclinical Models of Cardiac Disease: A Comprehensive Overview for Clinical Scientists;Cardiovascular Engineering and Technology;2024-01-16
4. Xenopus laevis (Daudin, 1802) as a Model Organism for Bioscience: A Historic Review and Perspective;Biology;2023-06-20
5. Recessive aminoacyl-tRNA synthetase disorders: lessons learned from in vivo disease models;Frontiers in Neuroscience;2023-05-09
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