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The desmosomal cadherin Desmogon is necessary for the structural integrity of the Medaka notochord

https://doi.org/10.1101/620070

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.21184openalex-snapshot

Ascidian notochord morphogenesis

inferredcites →https://doi.org/10.1002/dvdy.24154openalex-snapshot

Differential reparative phenotypes between zebrafish and medaka after cardiac injury

inferredcites →https://doi.org/10.1006/dbio.1996.8495openalex-snapshot

Vessel Patterning in the Embryo of the Zebrafish: Guidance by Notochord

inferredcites →https://doi.org/10.1007/978-3-642-83631-2_19openalex-snapshot

Mechanical Development of the Notochord in Xenopus Early Tail-Bud Embryos

inferredcites →https://doi.org/10.1007/s00018-015-1897-zopenalex-snapshot

The notochord: structure and functions

inferredcites →https://doi.org/10.1016/0092-8674(91)90247-vopenalex-snapshot

Control of cell pattern in the developing nervous system: Polarizing activity of the floor plate and notochord

inferredcites →https://doi.org/10.1016/0092-8674(93)90248-oopenalex-snapshot

Control of cell pattern in the neural tube: Motor neuron induction by diffusible factors from notochord and floor plate

inferredcites →https://doi.org/10.1016/j.bbamem.2007.07.014openalex-snapshot

Desmosome structure, composition and function

inferredcites →https://doi.org/10.1016/j.celrep.2018.01.084openalex-snapshot

Spine Patterning Is Guided by Segmentation of the Notochord Sheath

inferredcites →https://doi.org/10.1016/j.cub.2004.09.065openalex-snapshot

The notochord

inferredcites →https://doi.org/10.1016/j.cub.2017.05.035openalex-snapshot

Sheath Cell Invasion and Trans-differentiation Repair Mechanical Damage Caused by Loss of Caveolae in the Zebrafish Notochord

inferredcites →https://doi.org/10.1016/j.cub.2017.05.067openalex-snapshot

Caveolae Protect Notochord Cells against Catastrophic Mechanical Failure during Development

inferredcites →https://doi.org/10.1016/j.devcel.2017.02.002openalex-snapshot

Eye Absence Does Not Regulate Planarian Stem Cells during Eye Regeneration

inferredcites →https://doi.org/10.1016/j.devcel.2018.06.003openalex-snapshot

A Rapid Method for Directed Gene Knockout for Screening in G0 Zebrafish

inferredcites →https://doi.org/10.1016/j.jcpa.2013.03.008openalex-snapshot

Immunohistochemical Characterization of the Hepatic Progenitor Cell Compartment in Medaka (Oryzias latipes) following Hepatic Injury

inferredcites →https://doi.org/10.1016/j.mod.2004.03.012openalex-snapshot

Stages of normal development in the medaka Oryzias latipes

inferredcites →https://doi.org/10.1016/j.mod.2004.03.015openalex-snapshot

Large-scale analysis of the genes involved in fin regeneration and blastema formation in the medaka, Oryzias latipes

inferredcites →https://doi.org/10.1016/j.ydbio.2011.06.020openalex-snapshot

Identification of an evolutionarily conserved regulatory element of the zebrafish col2a1a gene

inferredcites →https://doi.org/10.1016/j.ydbio.2013.11.028openalex-snapshot

Loss of col8a1a function during zebrafish embryogenesis results in congenital vertebral malformations

inferredcites →https://doi.org/10.1038/378150a0openalex-snapshot

A homeobox gene essential for zebrafish notochord development

inferredcites →https://doi.org/10.1038/nature17644openalex-snapshot

Modulation of tissue repair by regeneration enhancer elements

inferredcites →https://doi.org/10.1038/nmeth.2064openalex-snapshot

Multiview light-sheet microscope for rapid in toto imaging

inferredcites →https://doi.org/10.1038/nprot.2006.165openalex-snapshot

Transgenesis in fish: efficient selection of transgenic fish by co-injection with a fluorescent reporter construct

inferredcites →https://doi.org/10.1038/s41598-018-24036-4openalex-snapshot

A Rapid CRISPR/Cas-based Mutagenesis Assay in Zebrafish for Identification of Genes Involved in Thyroid Morphogenesis and Function

inferredcites →https://doi.org/10.1038/srep00019openalex-snapshot

Multicolor time-stamp reveals the dynamics and toxicity of amyloid deposition

inferredcites →https://doi.org/10.1073/pnas.0306512101openalex-snapshot

Reactivation of developmental programs: The cAMP-response element-binding protein pathway is involved in hydra head regeneration

inferredcites →https://doi.org/10.1073/pnas.90.11.5242openalex-snapshot

Control of dorsoventral patterning of somitic derivatives by notochord and floor plate.

inferredcites →https://doi.org/10.1083/jcb.201212095openalex-snapshot

Notochord vacuoles are lysosome-related organelles that function in axis and spine morphogenesis

inferredcites →https://doi.org/10.1093/icb/40.1.28openalex-snapshot

Mechanical Design of Fiber-Wound Hydraulic Skeletons: The Stiffening and Straightening of Embryonic Notochords

inferredcites →https://doi.org/10.1093/nar/gku936openalex-snapshot

Easy quantitative assessment of genome editing by sequence trace decomposition

inferredcites →https://doi.org/10.1101/cshperspect.a002543openalex-snapshot

The Desmosome

inferredcites →https://doi.org/10.1101/gad.12.11.1705openalex-snapshot

Notochord repression of endodermal Sonic hedgehog permits pancreas development

inferredcites →https://doi.org/10.1111/j.1525-142x.2011.00522.xopenalex-snapshot

How was the notochord born?

inferredcites →https://doi.org/10.1126/science.aar3131openalex-snapshot

Single-cell reconstruction of developmental trajectories during zebrafish embryogenesis

inferredcites →https://doi.org/10.1126/science.aar5780openalex-snapshot

The dynamics of gene expression in vertebrate embryogenesis at single-cell resolution

inferredcites →https://doi.org/10.1186/1471-213x-12-1openalex-snapshot

Desmosomal cadherins in zebrafish epiboly and gastrulation

inferredcites →https://doi.org/10.1242/dev.00952openalex-snapshot

A central role for the notochord in vertebral patterning

inferredcites →https://doi.org/10.1242/dev.01812openalex-snapshot

Structure and function of the notochord: an essential organ for chordate development

inferredcites →https://doi.org/10.1242/dev.031682openalex-snapshot

Triggering the regeneration and tissue repair programs

inferredcites →https://doi.org/10.1242/dev.051011openalex-snapshot

Mib-Jag1-Notch signalling regulates patterning and structural roles of the notochord by controlling cell-fate decisions

inferredcites →https://doi.org/10.1242/dev.073007openalex-snapshot

Convergent extension: using collective cell migration and cell intercalation to shape embryos

inferredcites →https://doi.org/10.1242/dev.114629openalex-snapshot

Cavefish eye loss in response to an early block in retinal differentiation progression

inferredcites →https://doi.org/10.1242/dev.122.7.2225openalex-snapshot

Specification of cell fates at the dorsal margin of the zebrafish gastrula

inferredcites →https://doi.org/10.1242/dev.123.1.117openalex-snapshot

Mutations affecting development of the notochord in zebrafish

inferredcites →https://doi.org/10.1242/dev.142752openalex-snapshot

Sequential organogenesis sets two parallel sensory lines in medaka

inferredcites →https://doi.org/10.1242/jcs.003830openalex-snapshot

Caveolin-1 is required for lateral line neuromast and notochord development

inferredcites →https://doi.org/10.1371/journal.pbio.2006643openalex-snapshot

Large-scale investigation of the reasons why potentially important genes are ignored

inferredcites →https://doi.org/10.1371/journal.pone.0124633openalex-snapshot

CCTop: An Intuitive, Flexible and Reliable CRISPR/Cas9 Target Prediction Tool

inferredcites →https://doi.org/10.1371/journal.pone.0212956openalex-snapshot

Enhanced in vivo-imaging in medaka by optimized anaesthesia, fluorescent protein selection and removal of pigmentation

inferredcites →https://doi.org/10.1668/0003-1569(2000)040[0028:mdofwh]2.0.co;2openalex-snapshot

Mechanical Design of Fiber-Wound Hydraulic Skeletons: The Stiffening and Straightening of Embryonic Notochords1

inferredcites →https://doi.org/10.4161/bioa.25503openalex-snapshot

The vacuole within

inferredcites →https://doi.org/10.7554/elife.10230openalex-snapshot

Planar cell polarity-mediated induction of neural stem cell expansion during axolotl spinal cord regeneration

inferredcites →https://doi.org/10.7554/elife.25605openalex-snapshot

Reciprocal analyses in zebrafish and medaka reveal that harnessing the immune response promotes cardiac regeneration

inferredcites →https://doi.org/10.7554/elife.29173openalex-snapshot

Neural stem cells induce the formation of their physical niche during organogenesis

inferredcites →https://doi.org/10.7554/elife.30657openalex-snapshot

Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair

inferredcites →https://doi.org/10.7554/elife.32319openalex-snapshot

Activating the regenerative potential of Müller glia cells in a regeneration-deficient retina

inferredcites →https://doi.org/10.7554/elife.33843openalex-snapshot

Segmentation of the zebrafish axial skeleton relies on notochord sheath cells and not on the segmentation clock

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