Cited by 297

The DOI matches its Crossref record; 113 of the 113 references it cites were found in a registry or an index.

Mechanisms of Vessel Pruning and Regression

Open access

Korn, Claudia, Augustin, Hellmut G.·2015·Developmental Cell

DOI 10.1016/j.devcel.2015.06.004

Open this paper in CoChat — free account

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1016/j.devcel.2015.06.004

Cites

113 of 113 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Tumor angiogenesis: therapeutic implications
Sherwood, L. M., Parris, E. E., & Folkman, J. (1971) · New England Journal of Medicine · doi:10.1056/nejm197111182852108 · Cited by 10,187
Wnt/β-catenin signaling and disease
Clevers, H., & Nusse, R. (2012) · Cell · doi:10.1016/j.cell.2012.05.012 · Cited by 5,554
VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia
Gerhardt, H., Golding, M., Fruttiger, M., Ruhrberg, C., Lundkvist, A., Abramsson, A., Jeltsch, M., Mitchell, C., Alitalo, K., Shima, D., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200302047 · Cited by 2,894
Requisite Role of Angiopoietin-1, a Ligand for the TIE2 Receptor, during Embryonic Angiogenesis
Suri, C., Jones, P. F., Patan, S., Bartunkova, S., Maisonpierre, P. C., Davis, S., Sato, T. N., & Yancopoulos, G. D. (1996) · Cell · doi:10.1016/s0092-8674(00)81813-9 · Cited by 2,847
Basic and Therapeutic Aspects of Angiogenesis
Potente, M., Gerhardt, H., & Carmeliet, P. (2011) · Cell · doi:10.1016/j.cell.2011.08.039 · Cited by 2,771
A mechanosensory complex that mediates the endothelial cell response to fluid shear stress
Tzima, E., Irani-Tehrani, M., Kiosses, W. B., Dejana, E., Schultz, D. A., Engelhardt, B., Cao, G., DeLisser, H., & Schwartz, M. A. (2005) · Nature · doi:10.1038/nature03952 · Cited by 1,711
Principles and mechanisms of vessel normalization for cancer and other angiogenic diseases
Carmeliet, P., & Jain, R. K. (2011) · Nature Reviews Drug Discovery · doi:10.1038/nrd3455 · Cited by 1,675
Vascular endothelial growth factor acts as a survival factor for newly formed retinal vessels and has implications for retinopathy of prematurity
Alon, T., Hemo, I., Itin, A., Pe'er, J., Stone, J., & Keshet, E. (1995) · Nature Medicine · doi:10.1038/nm1095-1024 · Cited by 1,604
Control of vascular morphogenesis and homeostasis through the angiopoietin–Tie system
Augustin, H. G., Young Koh, G., Thurston, G., & Alitalo, K. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2639 · Cited by 1,465
Self-citation
Age-related macular degeneration
Jager, R. D., Mieler, W. F., & Miller, J. W. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0801537 · Cited by 1,379
Retinopathy of prematurity
Hellström, A., Smith, L. E., & Dammann, O. (2013) · The Lancet · doi:10.1016/s0140-6736(13)60178-6 · Cited by 1,304
A plasticity window for blood vessel remodelling is defined by pericyte coverage of the preformed endothelial network and is regulated by PDGF-B and VEGF
Benjamin, L. E., Hemo, I., & Keshet, E. (1998) · Development · doi:10.1242/dev.125.9.1591 · Cited by 1,265
Selective ablation of immature blood vessels in established human tumors follows vascular endothelial growth factor withdrawal
Benjamin, L. E., Golijanin, D., Itin, A., Pode, D., & Keshet, E. (1999) · Journal of Clinical Investigation · doi:10.1172/jci5028 · Cited by 1,241
Angiopoietin-2 Is Required for Postnatal Angiogenesis and Lymphatic Patterning, and Only the Latter Role Is Rescued by Angiopoietin-1
Gale, N. W., Thurston, G., Hackett, S. F., Renard, R., Wang, Q., McClain, J., Martin, C., Witte, C., Witte, M. H., Jackson, D., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00217-4 · Cited by 1,018
Dominant-negative and targeted null mutations in the endothelial receptor tyrosine kinase, tek, reveal a critical role in vasculogenesis of the embryo.
Dumont, D. J., Gradwohl, G., Fong, G. H., Puri, M. C., Gertsenstein, M., Auerbach, A., & Breitman, M. L. (1994) · Genes & Development · doi:10.1101/gad.8.16.1897 · Cited by 985
Identification of vascular endothelial genes differentially responsive to fluid mechanical stimuli: cyclooxygenase-2, manganese superoxide dismutase, and endothelial cell nitric oxide synthase are selectively up-regulated by steady laminar shear stress.
Topper, J. N., Cai, J., Falb, D., & Gimbrone, M. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.19.10417 · Cited by 843
Rapid vascular regrowth in tumors after reversal of VEGF inhibition
Mancuso, M. R., Davis, R., Norberg, S. M., O'Brien, S., Sennino, B., Nakahara, T., Yao, V. J., Inai, T., Brooks, P., Freimark, B., et al. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24612 · Cited by 809
Delta-like ligand 4 (Dll4) is induced by VEGF as a negative regulator of angiogenic sprouting
Lobov, I. B., Renard, R. A., Papadopoulos, N., Gale, N. W., Thurston, G., Yancopoulos, G. D., & Wiegand, S. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611206104 · Cited by 774
Inhibition of Vascular Endothelial Growth Factor (VEGF) Signaling in Cancer Causes Loss of Endothelial Fenestrations, Regression of Tumor Vessels, and Appearance of Basement Membrane Ghosts
Inai, T., Mancuso, M., Hashizume, H., Baffert, F., Haskell, A., Baluk, P., Hu-Lowe, D. D., Shalinsky, D. R., Thurston, G., Yancopoulos, G. D., et al. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63273-7 · Cited by 757
Canonical Wnt Signaling Regulates Organ-Specific Assembly and Differentiation of CNS Vasculature
Stenman, J. M., Rajagopal, J., Carroll, T. J., Ishibashi, M., McMahon, J., & McMahon, A. P. (2008) · Science · doi:10.1126/science.1164594 · Cited by 641
Retinopathy of prematurity
Chen, J., & Smith, L. E. H. (2007) · Angiogenesis · doi:10.1007/s10456-007-9066-0 · Cited by 602
The receptor tyrosine kinase TIE is required for integrity and survival of vascular endothelial cells.
Puri, M. C., Rossant, J., Alitalo, K., Bernstein, A., & Partanen, J. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00276.x · Cited by 519
Development of the retinal vasculature
Fruttiger, M. (2007) · Angiogenesis · doi:10.1007/s10456-007-9065-1 · Cited by 505
Vascular remodeling of the mouse yolk sac requires hemodynamic force
Lucitti, J. L., Jones, E. A. V., Huang, C., Chen, J., Fraser, S. E., & Dickinson, M. E. (2007) · Development · doi:10.1242/dev.02883 · Cited by 483
Flow regulates arterial-venous differentiation in the chick embryo yolk sac
le Noble, F., Moyon, D., Pardanaud, L., Yuan, L., Djonov, V., Matthijsen, R., Bréant, C., Fleury, V., & Eichmann, A. (2004) · Development · doi:10.1242/dev.00929 · Cited by 483
Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signaling
Felcht, M., Luck, R., Schering, A., Seidel, P., Srivastava, K., Hu, J., Bartol, A., Kienast, Y., Vettel, C., Loos, E. K., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci58832 · Cited by 479
Self-citation
Endothelial Cilia Are Fluid Shear Sensors That Regulate Calcium Signaling and Nitric Oxide Production Through Polycystin-1
Nauli, S. M., Kawanabe, Y., Kaminski, J. J., Pearce, W. J., Ingber, D. E., & Zhou, J. (2008) · Circulation · doi:10.1161/circulationaha.107.710111 · Cited by 466
Angiopoietin-1 is essential in mouse vasculature during development and in response to injury
Jeansson, M., Gawlik, A., Anderson, G., Li, C., Kerjaschki, D., Henkelman, M., & Quaggin, S. E. (2011) · Journal of Clinical Investigation · doi:10.1172/jci46322 · Cited by 457
Pathophysiology of Diabetic Retinopathy
Tarr, J. M., Kaul, K., Chopra, M., Kohner, E. M., & Chibber, R. (2013) · ISRN Ophthalmology · doi:10.1155/2013/343560 · Cited by 455
WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature
Lobov, I. B., Rao, S., Carroll, T. J., Vallance, J. E., Ito, M., Ondr, J. K., Kurup, S., Glass, D. A., Patel, M. S., Shu, W., et al. (2005) · Nature · doi:10.1038/nature03928 · Cited by 430
Endothelial Cell Apoptosis in Angiogenesis and Vessel Regression
Dimmeler, S., & Zeiher, A. M. (2000) · Circulation Research · doi:10.1161/01.res.87.6.434 · Cited by 425
Signals Transduced by Ca2+/Calcineurin and NFATc3/c4 Pattern the Developing Vasculature
Graef, I. A., Chen, F., Chen, L., Kuo, A., & Crabtree, G. R. (2001) · Cell · doi:10.1016/s0092-8674(01)00396-8 · Cited by 417
Mechanotransduction, PROX1, and FOXC2 cooperate to control connexin37 and calcineurin during lymphatic-valve formation
Sabine, A., Agalarov, Y., Maby-El Hajjami, H., Jaquet, M., Hägerling, R., Pollmann, C., Bebber, D., Pfenniger, A., Miura, N., Dormond, O., et al. (2012) · Developmental Cell · doi:10.1016/j.devcel.2011.12.020 · Cited by 411
Cellular changes in normal blood capillaries undergoing regression after inhibition of VEGF signaling
Baffert, F., Le, T., Sennino, B., Thurston, G., Kuo, C. J., Hu-Lowe, D., & McDonald, D. M. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00616.2005 · Cited by 374
Vascular Mechanobiology Endothelial Cell Responses to Fluid Shear Stress
Ando, J., & Yamamoto, K. (2009) · Circulation Journal · doi:10.1253/circj.cj-09-0583 · Cited by 372
Targeted disruption of the Wnt2 gene results in placentation defects
Monkley, S. J., Delaney, S. J., Pennisi, D. J., Christiansen, J. H., & Wainwright, B. J. (1996) · Development · doi:10.1242/dev.122.11.3343 · Cited by 357
Endothelial KLF2 Links Local Arterial Shear Stress Levels to the Expression of Vascular Tone-Regulating Genes
Dekker, R. J., van Thienen, J. V., Rohlena, J., de Jager, S. C., Elderkamp, Y. W., Seppen, J., de Vries, C. J. M., Biessen, E. A. L., van Berkel, T. J. C., Pannekoek, H., et al. (2005) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63002-7 · Cited by 355
Wnt7b regulates mesenchymal proliferation and vascular development in the lung
Shu, W., Jiang, Y. Q., Lu, M. M., & Morrisey, E. E. (2002) · Development · doi:10.1242/dev.129.20.4831 · Cited by 354
Nrarp Coordinates Endothelial Notch and Wnt Signaling to Control Vessel Density in Angiogenesis
Phng, L.-K., Potente, M., Leslie, J. D., Babbage, J., Nyqvist, D., Lobov, I., Ondr, J. K., Rao, S., Lang, R. A., Thurston, G., et al. (2009) · Developmental Cell · doi:10.1016/j.devcel.2008.12.009 · Cited by 349
The conditional inactivation of the β-catenin gene in endothelial cells causes a defective vascular pattern and increased vascular fragility
Cattelino, A., Liebner, S., Gallini, R., Zanetti, A., Balconi, G., Corsi, A., Bianco, P., Wolburg, H., Moore, R., Oreda, B., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212157 · Cited by 323
The Wnt/β-Catenin Pathway Modulates Vascular Remodeling and Specification by Upregulating Dll4/Notch Signaling
Corada, M., Nyqvist, D., Orsenigo, F., Caprini, A., Giampietro, C., Taketo, M. M., Iruela-Arispe, M. L., Adams, R. H., & Dejana, E. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.05.006 · Cited by 318
Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis
Ishikawa, T.-O., Tamai, Y., Zorn, A. M., Yoshida, H., Seldin, M. F., Nishikawa, S.-I., & Taketo, M. M. (2001) · Development · doi:10.1242/dev.128.1.25 · Cited by 311
Angiopoietin-2 at high concentration can enhance endothelial cell survival through the phosphatidylinositol 3′-kinase/Akt signal transduction pathway
Kim, I., Kim, J.-H., Moon, S.-O., Kwak, H. J., Kim, N.-G., & Koh, G. Y. (2000) · Oncogene · doi:10.1038/sj.onc.1203800 · Cited by 306
Analysis of blood vessel maturation processes during cyclic ovarian angiogenesis.
Goede, V., Schmidt, T., Kimmina, S., Kozian, D. H., & Augustin, H. G. (1998) · PubMed · Cited by 299
Self-citation
Adaptations of carotid arteries of young and mature rabbits to reduced carotid blood flow
Langille, B. L., Bendeck, M. P., & Keeley, F. W. (1989) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1989.256.4.h931 · Cited by 296
Dynamic Endothelial Cell Rearrangements Drive Developmental Vessel Regression
Franco, C. A., Jones, M. L., Bernabeu, M. O., Geudens, I., Mathivet, T., Rosa, A., Lopes, F. M., Lima, A. P., Ragab, A., Collins, R. T., et al. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002125 · Cited by 295
Beyond VEGF: Inhibition of the Fibroblast Growth Factor Pathway and Antiangiogenesis
Lieu, C., Heymach, J., Overman, M., Tran, H., & Kopetz, S. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-0659 · Cited by 286
Regulation of angiogenesis by a non-canonical Wnt–Flt1 pathway in myeloid cells
Stefater III, J. A., Lewkowich, I., Rao, S., Mariggi, G., Carpenter, A. C., Burr, A. R., Fan, J., Ajima, R., Molkentin, J. D., Williams, B. O., et al. (2011) · Nature · doi:10.1038/nature10085 · Cited by 274
The Endothelial Transcription Factor ERG Promotes Vascular Stability and Growth through Wnt/β-Catenin Signaling
Birdsey, G. M., Shah, A. V., Dufton, N., Reynolds, L. E., Osuna Almagro, L., Yang, Y., Aspalter, I. M., Khan, S. T., Mason, J. C., Dejana, E., et al. (2015) · Developmental Cell · doi:10.1016/j.devcel.2014.11.016 · Cited by 267
Complementary Actions of Inhibitors of Angiopoietin-2 and VEGF on Tumor Angiogenesis and Growth
Hashizume, H., Falcón, B. L., Kuroda, T., Baluk, P., Coxon, A., Yu, D., Bready, J. V., Oliner, J. D., & McDonald, D. M. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-1977 · Cited by 251
Neurovascular Dysfunction and Faulty Amyloid -Peptide Clearance in Alzheimer Disease
Sagare, A. P., Bell, R. D., & Zlokovic, B. V. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a011452 · Cited by 251
Haemodynamics-Driven Developmental Pruning of Brain Vasculature in Zebrafish
Chen, Q., Jiang, L., Li, C., Hu, D., Bu, J.-W., Cai, D., & Du, J.-L. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001374 · Cited by 250
The neurovascular link in health and disease: molecular mechanisms and therapeutic implications
Quaegebeur, A., Lange, C., & Carmeliet, P. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.013 · Cited by 247
A direct and melanopsin-dependent fetal light response regulates mouse eye development
Rao, S., Chun, C., Fan, J., Kofron, J. M., Yang, M. B., Hegde, R. S., Ferrara, N., Copenhagen, D. R., & Lang, R. A. (2013) · Nature · doi:10.1038/nature11823 · Cited by 240
Notch controls retinal blood vessel maturation and quiescence
Ehling, M., Adams, S., Benedito, R., & Adams, R. H. (2013) · Development · doi:10.1242/dev.093351 · Cited by 231
Angiopoietin-2 Functions as a Tie2 Agonist in Tumor Models, Where It Limits the Effects of VEGF Inhibition
Daly, C., Eichten, A., Castanaro, C., Pasnikowski, E., Adler, A., Lalani, A. S., Papadopoulos, N., Kyle, A. H., Minchinton, A. I., Yancopoulos, G. D., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-2064 · Cited by 230
Leukocytes mediate retinal vascular remodeling during development and vaso-obliteration in disease
Ishida, S., Yamashiro, K., Usui, T., Kaji, Y., Ogura, Y., Hida, T., Honda, Y., Oguchi, Y., & Adamis, A. P. (2003) · Nature Medicine · doi:10.1038/nm877 · Cited by 229
Wnt5a Signaling Induces Proliferation and Survival of Endothelial Cells In Vitro and Expression of MMP-1 and Tie-2
Masckauchán, T. N. H., Agalliu, D., Vorontchikhina, M., Ahn, A., Parmalee, N. L., Li, C.-M., Khoo, A., Tycko, B., Brown, A. M. C., & Kitajewski, J. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-04-0320 · Cited by 223
Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch
Yashiro, K., Shiratori, H., & Hamada, H. (2007) · Nature · doi:10.1038/nature06254 · Cited by 218
Regression of the hyaloid vessels and pupillary membrane of the mouse
Ito, M., & Yoshioka, M. (1999) · Anatomy and Embryology · doi:10.1007/s004290050289 · Cited by 216
Flow detection and calcium signalling in vascular endothelial cells
Ando, J., & Yamamoto, K. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt084 · Cited by 203
Angiopoietin-2: An Attractive Target for Improved Antiangiogenic Tumor Therapy
Gerald, D., Chintharlapalli, S., Augustin, H. G., & Benjamin, L. E. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4697 · Cited by 202
Self-citation
Angiopoietin‐2 plays an important role in retinal angiogenesis
Hackett, S. F., Wiegand, S., Yancopoulos, G., & Campochiaro, P. A. (2002) · Journal of Cellular Physiology · doi:10.1002/jcp.10128 · Cited by 199
Pulsatile shear and Gja5 modulate arterial identity and remodeling events during flow-driven arteriogenesis
Buschmann, I., Pries, A., Styp-Rekowska, B., Hillmeister, P., Loufrani, L., Henrion, D., Shi, Y., Duelsner, A., Hoefer, I., Gatzke, N., et al. (2010) · Development · doi:10.1242/dev.045351 · Cited by 191
Untersuchungen über die Histogenese und Histomechanik des Gefässsystems
Thoma, R. (1893) · In-house reproduction eBooks · Cited by 187
The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease
Ye, X., Wang, Y., & Nathans, J. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.07.003 · Cited by 182
The Effects of Hemodynamic Force on Embryonic Development
CULVER, J. C., & DICKINSON, M. E. (2010) · Microcirculation · doi:10.1111/j.1549-8719.2010.00025.x · Cited by 173
The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development
Kazanskaya, O., Ohkawara, B., Heroult, M., Wu, W., Maltry, N., Augustin, H. G., & Niehrs, C. (2008) · Development · doi:10.1242/dev.027284 · Cited by 173
Self-citation
Regulation of the endothelin system by shear stress in human endothelial cells
Morawietz, H., Talanow, R., Szibor, M., Rueckschloss, U., Schubert, A., Bartling, B., Darmer, D., & Holtz, J. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00761.x · Cited by 168
Endothelial Wnt/β-catenin signaling inhibits glioma angiogenesis and normalizes tumor blood vessels by inducing PDGF-B expression
Reis, M., Czupalla, C. J., Ziegler, N., Devraj, K., Zinke, J., Seidel, S., Heck, R., Thom, S., Macas, J., Bockamp, E., et al. (2012) · Journal of Experimental Medicine · doi:10.1084/jem.20111580 · Cited by 167
Apoptosis during macrophage-dependent ocular tissue remodelling
Lang, R., Lustig, M., Francois, F., Sellinger, M., & Plesken, H. (1994) · Development · doi:10.1242/dev.120.12.3395 · Cited by 165
Dynamic responses of endothelial cells to changes in blood flow during vascular remodeling of the mouse yolk sac
Udan, R. S., Vadakkan, T. J., & Dickinson, M. E. (2013) · Development · doi:10.1242/dev.096255 · Cited by 161
Astrocyte-Derived Vascular Endothelial Growth Factor Stabilizes Vessels in the Developing Retinal Vasculature
Scott, A., Powner, M. B., Gandhi, P., Clarkin, C., Gutmann, D. H., Johnson, R. S., Ferrara, N., & Fruttiger, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011863 · Cited by 153
VEGF deprivation-induced apoptosis is a component of programmed capillary regression
Meeson, A. P., Argilla, M., Ko, K. A., Witte, L., & Lang, R. A. (1999) · Development · doi:10.1242/dev.126.7.1407 · Cited by 149
A relationship between apoptosis and flow during programmed capillary regression is revealed by vital analysis
Meeson, A. P., Palmer, M. A. J., Calfon, M. A., & Lang, R. A. (1996) · Development · doi:10.1242/dev.122.12.3929 · Cited by 139
IP-10 induces dissociation of newly formed blood vessels
Bodnar, R. J., Yates, C. C., Rodgers, M. E., Du, X., & Wells, A. H. (2009) · Journal of Cell Science · doi:10.1242/jcs.048793 · Cited by 138
Endothelial Cell Self-fusion during Vascular Pruning
Lenard, A., Daetwyler, S., Betz, C., Ellertsdóttir, E., Belting, H., Huisken, J., & Affolter, M. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002126 · Cited by 137
Shear Stress Regulates Forward and Reverse Planar Cell Polarity of Vascular Endothelium In Vivo and In Vitro
McCue, S., Dajnowiec, D., Xu, F., Zhang, M., Jackson, M. R., & Langille, B. L. (2006) · Circulation Research · doi:10.1161/01.res.0000216595.15868.55 · Cited by 137
Cyclic angiogenesis and blood vessel regression in the ovary: blood vessel regression during luteolysis involves endothelial cell detachment and vessel occlusion.
Modlich, U., Kaup, F. ‐., & Augustin, H. G. (1996) · PubMed · Cited by 135
Self-citation
Embryonic atrial function is essential for mouse embryogenesis, cardiac morphogenesis and angiogenesis
Huang, C., Sheikh, F., Hollander, M. S., Cai, C.-L., Becker, D. L., Chu, P., Evans, S. Μ., & Chen, J. (2003) · Development · doi:10.1242/dev.00831 · Cited by 134
Endothelial cell-derived non-canonical Wnt ligands control vascular pruning in angiogenesis
Korn, C., Scholz, B., Hu, J., Srivastava, K., Wojtarowicz, J., Arnsperger, T., Adams, R. H., Boutros, M., Augustin, H. G., & Augustin, I. (2014) · Development · doi:10.1242/dev.104422 · Cited by 133
Self-citation
Notch as a hub for signaling in angiogenesis
Benedito, R., & Hellström, M. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.01.010 · Cited by 131
The Dll4/Notch pathway controls postangiogenic blood vessel remodeling and regression by modulating vasoconstriction and blood flow
Lobov, I. B., Cheung, E., Wudali, R., Cao, J., Halász, G., Wei, Y., Economides, A. N., Lin, H. C., Papadopoulos, N. J., Yancopoulos, G. D., et al. (2011) · Blood · doi:10.1182/blood-2010-08-302067 · Cited by 125
Regulated Angiogenesis and Vascular Regression in Mice Overexpressing Vascular Endothelial Growth Factor in Airways
Bałuk, P., Lee, C. G., Link, H., Ator, E., Haskell, A., Elias, J. A., & McDonald, D. M. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63369-x · Cited by 125
Regression of vessels in the tunica vasculosa lentis is initiated by coordinated endothelial apoptosis: A role for vascular endothelial growth factor as a survival factor for endothelium
Mitchell, C. A., Risau, W., & Drexler, H. C. A. (1998) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199811)213:3<322::aid-aja8>3.0.co;2-e · Cited by 117
Obligatory participation of macrophages in an angiopoietin 2-mediated cell death switch
Rao, S., Lobov, I. B., Vallance, J. E., Tsujikawa, K., Shiojima, I., Akunuru, S., Walsh, K. X., Benjamin, L. E., & Lang, R. A. (2007) · Development · doi:10.1242/dev.012187 · Cited by 116
Radial Glial Neural Progenitors Regulate Nascent Brain Vascular Network Stabilization Via Inhibition of Wnt Signaling
Ma, S., Kwon, H. J., Johng, H., Zang, K., & Huang, Z. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001469 · Cited by 116
Blood Flow Changes Coincide with Cellular Rearrangements during Blood Vessel Pruning in Zebrafish Embryos
Kochhan, E., Lenard, A., Ellertsdóttir, E., Herwig, L., Affolter, M., Belting, H., & Siekmann, A. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075060 · Cited by 116
Angiopoietin-2 Impairs Revascularization After Limb Ischemia
Reiss, Y., Droste, J., Heil, M., Tribulova, S., Schmidt, M. H. H., Schaper, W. K. A., Dumont, D., & Plate, K. H. (2007) · Circulation Research · doi:10.1161/circresaha.106.143594 · Cited by 111
Mechanisms of Vessel Regression: Toward an Understanding of the Resolution of Angiogenesis
Wietecha, M. S., Cerny, W. L., & DiPietro, L. A. (2012) · Current topics in microbiology and immunology · doi:10.1007/82_2012_287 · Cited by 109
Angiopoietin‐2 enhances retinal vessel sensitivity to vascular endothelial growth factor
Oshima, Y., Deering, T. G., Oshima, S. M., Nambu, H., Reddy, P. S., Kaleko, M., Connelly, S., Hackett, S. F., & Campochiaro, P. A. (2004) · Journal of Cellular Physiology · doi:10.1002/jcp.10442 · Cited by 108
The Endothelial Receptor Tyrosine Kinase Tie1 Activates Phosphatidylinositol 3-Kinase and Akt To Inhibit Apoptosis
Kontos, C. D., Cha, E. H., York, J. D., & Peters, K. G. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.6.1704-1713.2002 · Cited by 107
Systemic Overexpression of Angiopoietin-2 Promotes Tumor Microvessel Regression and Inhibits Angiogenesis and Tumor Growth
Cao, Y., Sonveaux, P., Liu, S., Zhao, Y., Mi, J., Clary, B. M., Li, C., Kontos, C. D., & Dewhirst, M. W. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4056 · Cited by 101
The Noncanonical WNT Pathway Is Operative in Idiopathic Pulmonary Arterial Hypertension
Laumanns, I. P., Fink, L., Wilhelm, J., Wolff, J.-C., Mitnacht‐Kraus, R., Graef-Hoechst, S., Stein, M. M., Bohle, R. M., Klepetko, W., Hoda, M. A. R., et al. (2008) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0153oc · Cited by 94
Tie1 attenuation reduces murine atherosclerosis in a dose-dependent and shear stress–specific manner
Woo, K. V., Qu, X., Babaev, V. R., Linton, M. F., Guzman, R. J., Fazio, S., & Baldwin, H. S. (2011) · Journal of Clinical Investigation · doi:10.1172/jci42040 · Cited by 92
Specific Induction of tie1 Promoter by Disturbed Flow in Atherosclerosis-Prone Vascular Niches and Flow-Obstructing Pathologies
Porat, R. M., Grunewald, M., Globerman, A., Itin, A., Barshtein, G., Alhonen, L. I., Alitalo, K. K., & Keshet, E. (2003) · Circulation Research · doi:10.1161/01.res.0000111803.92923.d6 · Cited by 89
A role for planar cell polarity signaling in angiogenesis
Cirone, P., Lin, S., Griesbach, H. L., Zhang, Y., Slusarski, D. C., & Crews, C. M. (2008) · Angiogenesis · doi:10.1007/s10456-008-9116-2 · Cited by 87
The Absence of Pericytes Does Not Increase the Sensitivity of Tumor Vasculature to Vascular Endothelial Growth Factor-A Blockade
Nisancioglu, M. H., Betsholtz, C., & Genové, G. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-4245 · Cited by 87
PDGF-CC blockade inhibits pathological angiogenesis by acting on multiple cellular and molecular targets
Hou, X., Kumar, A., Lee, C., Wang, B., Arjunan, P., Dong, L., Maminishkis, A., Tang, Z., Yang, L., Zhang, F., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004143107 · Cited by 83
Roles of Endothelial Cell Migration and Apoptosis in Vascular Remodeling during Development of the Central Nervous System
Hughes, S., & Chan‐Ling, T. (2000) · Microcirculation · doi:10.1111/j.1549-8719.2000.tb00131.x · Cited by 82
Frizzled 4 Regulates Arterial Network Organization Through Noncanonical Wnt/Planar Cell Polarity Signaling
Descamps, B., Sewduth, R. N., Tojais, N. F., Jaspard‐Vinassa, B., Reynaud, A., Sohet, F., Lacolley, P. J., Allières, C., Lamazière, J. D., Moreau, C., et al. (2011) · Circulation Research · doi:10.1161/circresaha.111.250936 · Cited by 78
c-mycin the hematopoietic lineage is crucial for its angiogenic function in the mouse embryo
He, C., Hu, H., Braren, R., Fong, S.-Y., Trumpp, A., Carlson, T. R., & Wang, R. A. (2008) · Development · doi:10.1242/dev.020131 · Cited by 76
Wntless is required for peripheral lung differentiation and pulmonary vascular development
Cornett, B., Snowball, J. M., Varisco, B. M., Lang, R. A., Whitsett, J. A., & Sinner, D. I. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.03.010 · Cited by 72
Endothelial Cell–Specific FGD5 Involvement in Vascular Pruning Defines Neovessel Fate in Mice
Cheng, C., Haasdijk, R. A., Tempel, D., van de Kamp, E. H. M., Herpers, R., Bos, F. L., den Dekker, W. K., Blonden, L. A. J., de Jong, R., Bürgisser, P. E., et al. (2012) · Circulation · doi:10.1161/circulationaha.111.064030 · Cited by 71
Vascular development and hemodynamic force in the mouse yolk sac
Garcia, M. D., & Larina, I. V. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00308 · Cited by 69
Angiopoietin-2-Driven Vascular Remodeling in Airway Inflammation
Tabruyn, S. P., Colton, K., Morisada, T., Fuxe, J., Wiegand, S. J., Thurston, G., Coyle, A. J., Connor, J. R., & McDonald, D. M. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.100059 · Cited by 67
In Vivo Immunostaining Demonstrates Macrophages Associate with Growing and Regressing Vessels
Shen, J., Xie, B., Dong, A., Swaim, M., Hackett, S. F., & Campochiaro, P. A. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0113 · Cited by 65
Polarizing pathways: Balancing endothelial polarity, permeability, and lumen formation
Lizama, C. O., & Zovein, A. C. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.03.028 · Cited by 57
Crim1 maintains retinal vascular stability during development by regulating endothelial cell Vegfa autocrine signaling
Fan, J., Ponferrada, V. G., Sato, T., Vemaraju, S., Fruttiger, M., Gerhardt, H., Ferrara, N., & Lang, R. A. (2013) · Development · doi:10.1242/dev.097949 · Cited by 47
Macrophages engulf endothelial cell membrane particles preceding pupillary membrane capillary regression
Poché, R. A., Hsu, C., McElwee, M. L., Burns, A. R., & Dickinson, M. E. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.03.017 · Cited by 41
Length of Day during Early Gestation as a Predictor of Risk for Severe Retinopathy of Prematurity
Yang, M. B., Rao, S., Copenhagen, D. R., & Lang, R. A. (2013) · Ophthalmology · doi:10.1016/j.ophtha.2013.07.051 · Cited by 33
An Inducible Hepatocellular Carcinoma Model for Preclinical Evaluation of Antiangiogenic Therapy in Adult Mice
Runge, A., Hu, J., Wieland, M. J., Bergeest, J.-P., Mogler, C., Neumann, A., Géraud, C., Arnold, B., Rohr, K., Komljenovic, D., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-2311 · Cited by 28
Self-citation
Born to Die
Korn, C., & Augustin, H. G. (2012) · Circulation · doi:10.1161/circulationaha.112.112755 · Cited by 10
Self-citation

Blood-Brain Barrier: From Physiology to Disease and Back
Sweeney, M. D., Zhao, Z., Montagne, A., Nelson, A. R., & Zlokovic, B. V. (2019) · Physiological Reviews · doi:10.1152/physrev.00050.2017 · Cited by 2,312
Vascular heterogeneity and specialization in development and disease
Potente, M., & Mäkinen, T. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.36 · Cited by 653
Diabetic retinopathy: hyperglycaemia, oxidative stress and beyond
Hammes, H.-P. (2018) · Diabetologia · doi:10.1007/s00125-017-4435-8 · Cited by 357
Plastic roles of pericytes in the blood–retinal barrier
Park, D. Y., Lee, J., Kim, J., Kim, K., Hong, S., Han, S., Kubota, Y., Augustin, H. G., Ding, L., Kim, J. W., et al. (2017) · Nature Communications · doi:10.1038/ncomms15296 · Cited by 322
Self-citation
Macrophages of diverse phenotypes drive vascularization of engineered tissues
Graney, P. L., Ben-Shaul, S., Landau, S., Bajpai, A., Singh, B., Eager, J., Cohen, A., Levenberg, S., & Spiller, K. L. (2020) · Science Advances · doi:10.1126/sciadv.aay6391 · Cited by 281

See all 297

Authors: Korn, C., & Augustin, H. G.
Venue: Developmental Cell
Publisher: Elsevier BV
Published: 2015-07
Volume: 34
Issue: 1
Pages: 5-17
ISSN: 1534-5807 (ISSN-L)
DOI: 10.1016/j.devcel.2015.06.004
OpenAlex: W1607213229
Cited by: 297
References: 113
FWCI: 9.52
Type: journal article
Language: en
Open access: bronze

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Mechanisms of Vessel Pruning and Regression

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks

Data sources