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VEGF Signaling

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Cover of 'VEGF Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 VEGF Splicing and the Role of VEGF Splice Variants: From Physiological-Pathological Conditions to Specific Pre-mRNA Splicing.
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    Chapter 2 Detection and Quantification of VEGF Isoforms by ELISA
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    Chapter 3 Quantitation of Circulating Neuropilin-1 in Human, Monkey, Mouse, and Rat Sera by ELISA.
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    Chapter 4 Detection and Quantification of Vascular Endothelial Growth Factor Receptor Tyrosine Kinases in Primary Human Endothelial Cells
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    Chapter 5 Induction of VEGF Secretion in Cardiomyocytes by Mechanical Stretch
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    Chapter 6 Chromatin Immunoprecipitation Assay: Examining the Interaction of NFkB with the VEGF Promoter.
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    Chapter 7 An Overview of VEGF-Mediated Signal Transduction
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    Chapter 8 Identification of Receptor Tyrosine Kinase Inhibitors Using Cell Surface Biotinylation and Affinity Isolation
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    Chapter 9 VEGF Signaling
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    Chapter 10 In Vitro Angiogenesis Assays
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    Chapter 11 Chemotactic Migration of Endothelial Cells Towards VEGF-A 165
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    Chapter 12 Vasculogenesis and Angiogenesis in VEGF Receptor-1 Deficient Mice
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    Chapter 13 The Embryonic Mouse Hindbrain and Postnatal Retina as In Vivo Models to Study Angiogenesis
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    Chapter 14 VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Guinea Pigs to Enhance Fetal Growth
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    Chapter 15 VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Sheep to Enhance Fetal Growth
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    Chapter 16 Generation of Targeted Mutations in Zebrafish Using the CRISPR/Cas System.
Attention for Chapter 15: VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Sheep to Enhance Fetal Growth
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Chapter title
VEGF Gene Transfer to the Utero-Placental Circulation of Pregnant Sheep to Enhance Fetal Growth
Chapter number 15
Book title
VEGF Signaling
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2917-7_15
Pubmed ID
Book ISBNs
978-1-4939-2916-0, 978-1-4939-2917-7
Authors

David J. Carr, Vedanta Mehta, Jacqueline M. Wallace, Anna L. David, Carr, David J., Mehta, Vedanta, Wallace, Jacqueline M., David, Anna L.

Abstract

In this chapter, we describe a safe and effective approach to achieve local VEGF gene transfer to the uterine arteries in pregnant sheep using direct injection of viral vectors into the uterine arteries. This approach resulted in improved fetal growth in growth-restricted pregnancies. Adenoviral vectors encoding VEGF-A165 or a reporter gene β-galactosidase were dissolved in 10 mL normal saline shortly before administration. A midline laparotomy was performed and the course of the uterine artery identified. The main trunk (just prior to the first bifurcation) was mobilized by dissection and a vessel loop placed beneath it in order to elevate the artery, which was then occluded digitally just proximal to the planned injection site. The adenoviral solution was slowly injected over 1 min, and the occlusion was maintained for a further 4 min to maximize transduction of the downstream endothelium. After ensuring hemostasis, the abdomen was closed in layers.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 20%
Unknown 4 80%

Demographic breakdown

Readers by professional status Count As %
Professor > Associate Professor 2 40%
Researcher 1 20%
Lecturer 1 20%
Student > Master 1 20%
Readers by discipline Count As %
Medicine and Dentistry 3 60%
Pharmacology, Toxicology and Pharmaceutical Science 1 20%
Unknown 1 20%