Cargando…

Quantifying endothelial cell proliferation in the zebrafish embryo

Introduction: Endothelial cell (EC) proliferation is a fundamental determinant of vascular development and homeostasis, and contributes to cardiovascular disease by increasing vascular permeability to blood-borne lipoproteins. Rodents have been traditionally used to analyse EC proliferation mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bowley, George, Chico, Timothy JA, Serbanovic-Canic, Jovana, Evans, Paul C
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	F1000 Research Limited 2021
Materias:	Method Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944168/ https://www.ncbi.nlm.nih.gov/pubmed/36846519 http://dx.doi.org/10.12688/f1000research.73130.1

Ejemplares similares

The effect of absent blood flow on the zebrafish cerebral and trunk vasculature
por: Kugler, Elisabeth, et al.
Publicado: (2021)

EVA1A (Eva-1 Homolog A) Promotes Endothelial Apoptosis and Inflammatory Activation Under Disturbed Flow Via Regulation of Autophagy
por: Canham, Lindsay, et al.
Publicado: (2023)

Automated staging of zebrafish embryos with deep learning
por: Jones, Rebecca A, et al.
Publicado: (2023)

Zebrafish Model for Functional Screening of Flow-Responsive Genes
por: Serbanovic-Canic, Jovana, et al.
Publicado: (2017)

TWIST1 Integrates Endothelial Responses to Flow in Vascular Dysfunction and Atherosclerosis
por: Mahmoud, Marwa M., et al.
Publicado: (2016)

Refinement of the zebrafish embryo developmental toxicity assay
por: Hoyberghs, Jente, et al.
Publicado: (2020)

Shear stress induces endothelial-to-mesenchymal transition via the transcription factor Snail
por: Mahmoud, Marwa M., et al.
Publicado: (2017)

Author Correction: Shear stress induces endothelial-to-mesenchymal transition via the transcription factor Snail
por: Mahmoud, Marwa M., et al.
Publicado: (2020)

An in vivo translation-reporter system for the study of protein synthesis in zebrafish embryos
por: Garcez Palha, Inês, et al.
Publicado: (2018)

Flat mount preparation for whole-mount fluorescent imaging of zebrafish embryos
por: Frommelt, Joseph, et al.
Publicado: (2023)

Quantifying similarity between motifs
por: Gupta, Shobhit, et al.
Publicado: (2007)

A versatile, automated and high-throughput drug screening platform for zebrafish embryos
por: Lubin, Alexandra, et al.
Publicado: (2021)

Zebrafish promoter microarrays identify actively transcribed embryonic genes
por: Wardle, Fiona C, et al.
Publicado: (2006)

Homeobox B9 integrates bone morphogenic protein 4 with inflammation at atheroprone sites
por: Souilhol, Celine, et al.
Publicado: (2020)

Image-based characterization of thrombus formation in time-lapse DIC microscopy
por: Brieu, Nicolas, et al.
Publicado: (2012)

Novel liquid chromatography–mass spectrometry method shows that vitamin E deficiency depletes arachidonic and docosahexaenoic acids in zebrafish (Danio rerio) embryos()
por: Lebold, Katie M., et al.
Publicado: (2013)

A Loss of Function Screen of Identified Genome-Wide Association Study Loci Reveals New Genes Controlling Hematopoiesis
por: Bielczyk-Maczyńska, Ewa, et al.
Publicado: (2014)

Correlative Light and Electron Microscopy of Rare Cell Populations in Zebrafish Embryos Using Laser Marks
por: Goudarzi, Mohammad, et al.
Publicado: (2015)

Quantifying Position-Dependent Codon Usage Bias
por: Hockenberry, Adam J., et al.
Publicado: (2014)

A FIJI macro for quantifying pattern in extracellular matrix
por: Wershof, Esther, et al.
Publicado: (2021)

Phylodynamics with Migration: A Computational Framework to Quantify Population Structure from Genomic Data
por: Kühnert, Denise, et al.
Publicado: (2016)

Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos
por: Gurung, Suman, et al.
Publicado: (2022)

Targeted chromosomal deletions and inversions in zebrafish
por: Gupta, Ankit, et al.
Publicado: (2013)

Automated measurement of the spontaneous tail coiling of zebrafish embryos as a sensitive behavior endpoint using a workflow in KNIME
por: Ogungbemi, Afolarin O., et al.
Publicado: (2021)

A Fast, Simple, and Affordable Technique to Measure Oxygen Consumption in Living Zebrafish Embryos
por: Somkhit, Julie, et al.
Publicado: (2020)

Quantifying full-length circular RNAs in cancer
por: Yu, Ken Hung-On, et al.
Publicado: (2021)

An automated approach to quantify chemotaxis index in C. elegans
por: Crombie, Timothy A, et al.
Publicado: (2022)

SCoPE-MS: mass spectrometry of single mammalian cells quantifies proteome heterogeneity during cell differentiation
por: Budnik, Bogdan, et al.
Publicado: (2018)

Quantifying Transmission Heterogeneity Using Both Pathogen Phylogenies and Incidence Time Series
por: Li, Lucy M., et al.
Publicado: (2017)

Information theoretic measures for quantifying sequence–ensemble relationships of intrinsically disordered proteins
por: Cohan, Megan C, et al.
Publicado: (2019)

Quantifying compartment‐associated variations of protein abundance in proteomics data
por: Parca, Luca, et al.
Publicado: (2018)

ZebIAT, an image analysis tool for registering zebrafish embryos and quantifying cancer metastasis
por: Annila, Teppo, et al.
Publicado: (2013)

A major zebrafish polymorphism resource for genetic mapping
por: Bradley, Kevin M, et al.
Publicado: (2007)

Efficient knock-in method enabling lineage tracing in zebrafish
por: Mi, Jiarui, et al.
Publicado: (2023)

Single-cell RNA-seq transcriptome analysis of linear and circular RNAs in mouse preimplantation embryos
por: Fan, Xiaoying, et al.
Publicado: (2015)

OTTER, a new method for quantifying absolute amounts of tRNAs
por: Nagai, Akihisa, et al.
Publicado: (2021)

SPACE: an algorithm to predict and quantify alternatively spliced isoforms using microarrays
por: Anton, Miguel A, et al.
Publicado: (2008)

A novel approach to quantify random error explicitly in epidemiological studies
por: Janszky, Imre, et al.
Publicado: (2011)

SVFX: a machine learning framework to quantify the pathogenicity of structural variants
por: Kumar, Sushant, et al.
Publicado: (2020)

Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair
por: Auer, Thomas O., et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_hae64qbt459nbta61ph4d3kikf