Mechanisms of normal and tumor-derived angiogenesis.
By M. Papetti, I. Herman. American Journal of Physiology - Cell Physiology, 2002
846 citations recorded by the source corpus.
Subfields: Cancer Research, Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/77c0f84256df4bf51001f1835042b98b3cfee006
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
In Molecular Biology
- Uzoagu A Okonkwo
- Peter L. Choyke
- Hisataka Kobayashi
- L. DiPietro
- R. Watanabe
- T. Mabuchi
- G. D. del Zoppo
Citations in the corpus
- Improving Conventional Enhanced Permeability and Retention (EPR) Effects; What Is the Appropriate Target? (2013, background): “(17-19) Unlike the microvasculature of normal tissue, which has an organized and regular branching order, tumor microvasculature shows disorganization and lack of the conventional hierarchy of blood vessels.”
- Cerebral Microvessel Responses to Focal Ischemia (2003, background): “The formation of new microvessels from existing vessels (angiogenesis) is a hallmark tissue response to injury (Dvorak et al., 1995; Carmeliet, 2000; Papetti and Herman, 2002; Hynes, 2002).”
- Therapeutic targeting of the tumor microenvironment. (2005, neutral): “A plethora of antiangiogenic agents inhibiting either angiogenic growth fac tors or their receptors have been developed (see Table 1 for examples) and tested in preclinical experiments (Papetti and Herman, 2002).”
- Diabetes and Wound Angiogenesis (2017, background): “While basal levels of pro-angiogenic factors and the expression of their corresponding receptors are maintained during the healthy state of homeostasis, the diseased state exhibits upregulated expression of pro-angiogenic factors such as VEGF, fibroblast growth factor (FGF), and others to promote un”