Central nervous system pericytes in health and disease

The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders

Zlokovic, B. V. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.003 · Cited by 3,280 · see citing works

Pericytes regulate the blood–brain barrier

Armulik, A., Genové, G., Mäe, M., Nisancioglu, M. H., Wallgard, E., Niaudet, C., He, L., Norlin, J., Lindblom, P., Strittmatter, K., et al. (2010) · Nature · doi:10.1038/nature09522 · Cited by 2,843 · see citing works

Role of platelet-derived growth factors in physiology and medicinePreprint

Andræ, J., Gallini, R., & Betsholtz, C. (2008) · Genes & Development · doi:10.1101/gad.1653708 · Cited by 2,444 · see citing works

Pericyte Loss and Microaneurysm Formation in PDGF-B-Deficient Mice

Lindahl, P., Johansson, B. R., Levéen, P., & Betsholtz, C. (1997) · Science · doi:10.1126/science.277.5323.242 · Cited by 2,226 · see citing works

Neurovascular regulation in the normal brain and in Alzheimer's disease

Iadecola, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1387 · Cited by 2,213 · see citing works

Pericytes are required for blood–brain barrier integrity during embryogenesis

Daneman, R., Zhou, L., Kebede, A. A., & Barres, B. A. (2010) · Nature · doi:10.1038/nature09513 · Cited by 2,128 · see citing works

The Science of Stroke: Mechanisms in Search of Treatments

Moskowitz, M. A., Lo, E. H., & Iadecola, C. (2010) · Neuron · doi:10.1016/j.neuron.2010.07.002 · Cited by 1,930 · see citing works

Role of PDGF-B and PDGFR-β in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse

Hellström, M., Kalén, M., Lindahl, P., Abramsson, A., & Betsholtz, C. (1999) · Development · doi:10.1242/dev.126.14.3047 · Cited by 1,702 · see citing works

Pericytes Control Key Neurovascular Functions and Neuronal Phenotype in the Adult Brain and during Brain Aging

Bell, R. D., Winkler, E. A., Sagare, A. P., Singh, I., LaRue, B., Deane, R., & Zlokovic, B. V. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.043 · Cited by 1,448 · see citing works

Bidirectional control of CNS capillary diameter by pericytes

Peppiatt, C. M., Howarth, C., Mobbs, P., & Attwell, D. (2006) · Nature · doi:10.1038/nature05193 · Cited by 1,150 · see citing works

Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities.Preprint

Levéen, P., Pekny, M., Gebré‐Medhin, S., Swolin, B., Larsson, E., & Betsholtz, C. (1994) · Genes & Development · doi:10.1101/gad.8.16.1875 · Cited by 1,130 · see citing works

Balancing the activation state of the endothelium via two distinct TGF‐β type I receptors

Goumans, M., Valdimarsdóttir, G., Itoh, S., Rosendahl, A., Sideras, P., & ten Dijke, P. (2002) · The EMBO Journal · doi:10.1093/emboj/21.7.1743 · Cited by 1,127 · see citing works

Lack of Pericytes Leads to Endothelial Hyperplasia and Abnormal Vascular Morphogenesis

Hellström, M., Gerhardt, H., Kalén, M., Li, X., Eriksson, U., Wolburg, H., & Betsholtz, C. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.3.543 · Cited by 1,103 · see citing works

Cerebral microvascular pathology in aging and Alzheimer's disease

Farkas, E., & Luiten, P. G. M. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00068-x · Cited by 1,102 · see citing works

Endothelial-pericyte interactions in angiogenesis

Gerhardt, H., & Betsholtz, C. (2003) · Cell and Tissue Research · doi:10.1007/s00441-003-0745-x · Cited by 1,060 · see citing works

Abnormal kidney development and hematological disorders in PDGF beta-receptor mutant mice.Preprint

Soriano, P. M. (1994) · Genes & Development · doi:10.1101/gad.8.16.1888 · Cited by 988 · see citing works

Endothelial-Mural Cell Signaling in Vascular Development and Angiogenesis

Gaengel, K., Genové, G., Armulik, A., & Betsholtz, C. (2009) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.107.161521 · Cited by 933 · see citing works

Neurovascular mechanisms of Alzheimer's neurodegeneration

Zloković, B. V. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.02.001 · Cited by 921 · see citing works

Intraventricular Hemorrhage in Premature Infants: Mechanism of Disease

Ballabh, P. (2009) · Pediatric Research · doi:10.1203/pdr.0b013e3181c1b176 · Cited by 784 · see citing works

Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery

Yemişçi, M., Özdemir, Y., Vural, A., Can, A., Topalkara, K., & Dalkara, T. (2009) · Nature Medicine · doi:10.1038/nm.2022 · Cited by 780 · see citing works

The Blood-Brain Barrier in Brain Homeostasis and Neurological Diseases

Weiss, N., Miller, F., Cazaubon, S., & Couraud, P.-O. (2009) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.10.022 · Cited by 731 · see citing works

Retinal angiogenesis in development and disease

Gariano, R. F., & Gardner, T. W. (2005) · Nature · doi:10.1038/nature04482 · Cited by 707 · see citing works

Endothelial PDGF-B retention is required for proper investment of pericytes in the microvessel wallPreprint

Lindblom, P., Gerhardt, H., Liebner, S., Abramsson, A., Enge, M., Hellström, M., Bäckström, G., Fredriksson, S., Landegren, U. D., Nyström, H. C., et al. (2003) · Genes & Development · doi:10.1101/gad.266803 · Cited by 659 · see citing works

The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain

Etchevers, H. C., Vincent, C., Douarin, N. M. L., & F. Couly, G. (2001) · Development · doi:10.1242/dev.128.7.1059 · Cited by 657 · see citing works

Pericyte physiology

Sheṕro, D., & Morel-Laurens, N. (1993) · The FASEB Journal · doi:10.1096/fasebj.7.11.8370472 · Cited by 652 · see citing works

Neuronal Death in the Hippocampus Is Promoted by Plasmin-Catalyzed Degradation of Laminin

Chen, Z.-L., & Strickland, S. (1997) · Cell · doi:10.1016/s0092-8674(00)80483-3 · Cited by 632 · see citing works

Pericyte recruitment during vasculogenic tube assembly stimulates endothelial basement membrane matrix formation

Stratman, A. N., Malotte, K. M., Mahan, R. D., Davis, M. J., & Davis, G. E. (2009) · Blood · doi:10.1182/blood-2009-05-222364 · Cited by 581 · see citing works

Correlations of Neuronal and Microvascular Densities in Murine Cortex Revealed by Direct Counting and Colocalization of Nuclei and Vessels

Tsai, P. S., Kaufhold, J. P., Blinder, P., Friedman, B., Drew, P. J., Karten, H. J., Lyden, P. D., & Kleinfeld, D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3287-09.2009 · Cited by 575 · see citing works

Pericytes. Morphofunction, interactions and pathology in a quiescent and activated mesenchymal cell niche.

Díaz‐Flores, L., Gutiérrez, R., Madrid, J. F., Varela, H., Valladares, F., Acosta, E., Martı́n-Vasallo, P., & Díaz-Flores, L. (2009) · PubMed · doi:10.14670/hh-24.909 · Cited by 547 · see citing works

Diverse roles of matrix metalloproteinases and tissue inhibitors of metalloproteinases in neuroinflammation and cerebral ischemia

Candelario‐Jalil, E., Yang, Y., & Rosenberg, G. A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.06.025 · Cited by 524 · see citing works

TGF-? receptor function in the endothelium

Lebrin, F., Deckers, M., Bertolino, P., & ten Dijke, P. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.10.036 · Cited by 514 · see citing works

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease

Hamilton, N. B. (2010) · Frontiers in Neuroenergetics · doi:10.3389/fnene.2010.00005 · Cited by 513 · see citing works

Endothelial and nonendothelial sources of PDGF-B regulate pericyte recruitment and influence vascular pattern formation in tumors

Abramsson, A., Lindblom, P., & Betsholtz, C. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200318549 · Cited by 479 · see citing works

Endothelial and nonendothelial sources of PDGF-B regulate pericyte recruitment and influence vascular pattern formation in tumors

Abramsson, A., Lindblom, P., & Betsholtz, C. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18549 · Cited by 478 · see citing works

ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration

Zhong, Z., Deane, R., Ali, Z., Parisi, M., Shapovalov, Y., O'Banion, M. K., Stojanovic, K., Sagare, A., Boillee, S., Cleveland, D. W., et al. (2008) · Nature Neuroscience · doi:10.1038/nn2073 · Cited by 476 · see citing works

Angiopoietin-1 is essential in mouse vasculature during development and in response to injury

Jeansson, M., Gawlik, A., Anderson, G. A., Li, C., Kerjaschki, D., Henkelman, R. M., & Quaggin, S. E. (2011) · Journal of Clinical Investigation · doi:10.1172/jci46322 · Cited by 458 · see citing works

Activation of PKC-δ and SHP-1 by hyperglycemia causes vascular cell apoptosis and diabetic retinopathy

Geraldes, P., Hiraoka‐Yamamoto, J., Matsumoto, M., Clermont, A. C., Leitges, M., Marette, A., Aiello, L. P., Kern, T. S., & King, G. L. (2009) · Nature Medicine · doi:10.1038/nm.2052 · Cited by 424 · see citing works

Angiopoietins assemble distinct Tie2 signalling complexes in endothelial cell–cell and cell–matrix contacts

Saharinen, P., Eklund, L., Miettinen, J., Wirkkala, R., Anisimov, A., Winderlich, M., Nottebaum, A., Vestweber, D., Deutsch, U., Koh, G. Y., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1715 · Cited by 415 · see citing works

CNS Microvascular Pericytes Exhibit Multipotential Stem Cell Activity

Dore-Duffy, P., Katychev, A., Wang, X., & Van Buren, E. (2006) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600272 · Cited by 414 · see citing works

Endothelium‐specific platelet‐derived growth factor‐B ablation mimics diabetic retinopathy

Enge, M., Bjarnegård, M., Gerhardt, H., Gustafsson, E., Kalén, M., Asker, N., Hammes, H., Shani, M., Fässler, R., & Betsholtz, C. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf418 · Cited by 402 · see citing works

SOD1 rescues cerebral endothelial dysfunction in mice overexpressing amyloid precursor protein

Iadecola, C., Zhang, F., Niwa, K., Eckman, C., Turner, S. K., Fischer, E., Younkin, S., Borchelt, D. R., Hsiao, K. K., & Carlson, G. A. (1999) · Nature Neuroscience · doi:10.1038/5715 · Cited by 399 · see citing works

Pericytes in capillaries are contractile in vivo, but arterioles mediate functional hyperemia in the mouse brain

Fernández-Klett, F., Offenhauser, N., Dirnagl, U., Priller, J., & Lindauer, U. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011321108 · Cited by 399 · see citing works

Pericyte production of cell-associated VEGF is differentiation-dependent and is associated with endothelial survival

Darland, D. C., Massingham, L. J., Smith, S. R., Piek, E., Saint‐Geniez, M., & D'Amore, P. A. (2003) · Developmental Biology · doi:10.1016/j.ydbio.2003.08.015 · Cited by 383 · see citing works

Endothelium-specific ablation of PDGFB leads to pericyte loss and glomerular, cardiac and placental abnormalities

Bjarnegård, M., Enge, M., Norlin, J., Gustafsdottir, S., Fredriksson, S., Abramsson, A., Takemoto, M., Gustafsson, E., Fässler, R., & Betsholtz, C. (2004) · Development · doi:10.1242/dev.01080 · Cited by 368 · see citing works

Brain pericytes contribute to the induction and up-regulation of blood–brain barrier functions through transforming growth factor-β production

Dohgu, S., Takata, F., Yamauchi, A., Nakagawa, S., Egawa, T., Naito, M., Tsuruo, T., Sawada, Y., Niwa, M., & Kataoka, Y. (2005) · Brain Research · doi:10.1016/j.brainres.2005.01.027 · Cited by 350 · see citing works

Pericyte-specific expression of PDGF beta receptor in mouse models with normal and deficient PDGF beta receptor signaling

Winkler, E. A., Bell, R. D., & Zloković, B. V. (2010) · Molecular Neurodegeneration · doi:10.1186/1750-1326-5-32 · Cited by 346 · see citing works

Diabetic Retinopathy: Targeting Vasoregression

Hammes, H., Feng, Y., Pfister, F., & Brownlee, M. (2010) · Diabetes · doi:10.2337/db10-0454 · Cited by 345 · see citing works

Angiopoietin-2 Causes Pericyte Dropout in the Normal Retina

Hammes, H., Lin, J., Wagner, P., Feng, Y., Hagen, F. V., Krzizok, T. H., Renner, O., Breier, G., Brownlee, M., & Deutsch, U. (2004) · Diabetes · doi:10.2337/diabetes.53.4.1104 · Cited by 341 · see citing works

Fibrin deposition accelerates neurovascular damage and neuroinflammation in mouse models of Alzheimer's disease

Paul, J., Strickland, S., & Melchor, J. P. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070304 · Cited by 319 · see citing works

Pericyte Migration from the Vascular Wall in Response to Traumatic Brain Injury

Dore-Duffy, P., Owen, C., Balabanov, R., Murphy, S., Beaumont, T., & Rafols, J. A. (2000) · Microvascular Research · doi:10.1006/mvre.2000.2244 · Cited by 304 · see citing works

Coregulation of vascular tube stabilization by endothelial cell TIMP-2 and pericyte TIMP-3

Saunders, W. B., Bohnsack, B. L., Faske, J. B., Anthis, N. J., Bayless, K. J., Hirschi, K. K., & Davis, G. E. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200603176 · Cited by 296 · see citing works

Endothelial-derived PDGF-BB and HB-EGF coordinately regulate pericyte recruitment during vasculogenic tube assembly and stabilization

Stratman, A. N., Schwindt, A. E., Malotte, K. M., & Davis, G. E. (2010) · Blood · doi:10.1182/blood-2010-05-286872 · Cited by 290 · see citing works

NOTCH3 Expression Is Induced in Mural Cells Through an Autoregulatory Loop That Requires Endothelial-Expressed JAGGED1

Liu, H., Kennard, S., & Lilly, B. (2009) · Circulation Research · doi:10.1161/circresaha.108.184846 · Cited by 286 · see citing works

Role of the MEOX2 homeobox gene in neurovascular dysfunction in Alzheimer disease

Wu, Z., Guo, H., Chow, N., Sallstrom, J., Bell, R. D., Deane, R., Brooks, A. I., Kanagala, S., Rubio, A., Sagare, A., et al. (2005) · Nature Medicine · doi:10.1038/nm1287 · Cited by 280 · see citing works

Sphingosine 1-phosphate receptor regulation of N-cadherin mediates vascular stabilizationPreprint

Paik, J., Skoura, A., Chae, S., Cowan, A. E., Han, D. K. M., Proia, R. L., & Hla, T. (2004) · Genes & Development · doi:10.1101/gad.1227804 · Cited by 278 · see citing works

Early Contribution of Pericytes to Angiogenic Sprouting and Tube Formation

Özerdem, U., & Stallcup, W. B. (2003) · Angiogenesis · doi:10.1023/b:agen.0000021401.58039.a9 · Cited by 263 · see citing works

SRF and myocardin regulate LRP-mediated amyloid-β clearance in brain vascular cells

Bell, R. D., Deane, R., Chow, N., Long, X., Sagare, A., Singh, I., Streb, J. W., Guo, H., Rubio, A., Van Nostrand, W., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1819 · Cited by 261 · see citing works

Endothelial Smad4 Maintains Cerebrovascular Integrity by Activating N-Cadherin through Cooperation with Notch

Li, F., Lan, Y., Wang, Y., Wang, J., Yang, G., Meng, F., Han, H., Meng, A., Wang, Y., & Yang, X. Y. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.01.011 · Cited by 259 · see citing works

Aβ1–40-related reduction in functional hyperemia in mouse neocortex during somatosensory activation

Niwa, K., Younkin, L. H., Ebeling, C., Turner, S. K., Westaway, D. A., Younkin, S. G., Ashe, K. H., Carlson, G. A., & Iadecola, C. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.17.9735 · Cited by 244 · see citing works

Notch Signaling in Blood Vessels

Hofmann, J. J., & Iruela‐Arispe, M. L. (2007) · Circulation Research · doi:10.1161/01.res.0000266408.42939.e4 · Cited by 225 · see citing works

Ultrastructural studies of the cells forming amyloid in the cortical vessel wall in Alzheimer's disease

Wisniewski, H. M., Wegiel, J., Wang, K. C., & Lach, B. (1992) · Acta Neuropathologica · doi:10.1007/bf00311383 · Cited by 221 · see citing works

Neural Crest–Derived Pericytes Promote Egress of Mature Thymocytes at the Corticomedullary Junction

Zachariah, M. A., & Cyster, J. G. (2010) · Science · doi:10.1126/science.1188222 · Cited by 209 · see citing works

Serum response factor and myocardin mediate arterial hypercontractility and cerebral blood flow dysregulation in Alzheimer's phenotype

Chow, N., Bell, R. D., Deane, R., Streb, J. W., Chen, J., Brooks, A., Van Nostrand, W., Miano, J. M., & Zlokovic, B. V. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608251104 · Cited by 209 · see citing works

Neuroectodermal origin of brain pericytes and vascular smooth muscle cells

Korn, J., Christ, B., & Kurz, H. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.1423 · Cited by 208 · see citing works

TGF-β Is Required for Vascular Barrier Function, Endothelial Survival and Homeostasis of the Adult Microvasculature

Walshe, T. E., Saint‐Geniez, M., Maharaj, A. S. R., Sekiyama, E., Maldonado, A. E., & D'Amore, P. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005149 · Cited by 207 · see citing works

Notch Signaling Regulates Platelet-Derived Growth Factor Receptor-β Expression in Vascular Smooth Muscle Cells

Jin, S., Hansson, E. M., Tikka, S., Lanner, F., Sahlgren, C., Farnebo, F. A., Baumann, M., Kalimo, H., & Lendahl, U. (2008) · Circulation Research · doi:10.1161/circresaha.107.167965 · Cited by 197 · see citing works

Defective N -sulfation of heparan sulfate proteoglycans limits PDGF-BB binding and pericyte recruitment in vascular developmentPreprint

Abramsson, A., Kurup, S., Busse, M., Yamada, S., Lindblom, P., Schallmeiner, E., Stenzel, D., Sauvaget, D., Ledin, J., Ringvall, M., et al. (2007) · Genes & Development · doi:10.1101/gad.398207 · Cited by 195 · see citing works

Additive Effects of PDGF Receptor β Signaling Pathways in Vascular Smooth Muscle Cell Development

Tallquist, M. D., French, W. J., & Soriano, P. (2003) · PLoS Biology · doi:10.1371/journal.pbio.0000052 · Cited by 192 · see citing works

Pathological angiogenesis is reduced by targeting pericytes via the NG2 proteoglycan

Özerdem, U., & Stallcup, W. B. (2004) · Angiogenesis · doi:10.1007/s10456-004-4182-6 · Cited by 188 · see citing works

Notch3 Is Critical for Proper Angiogenesis and Mural Cell Investment

Liu, H., Zhang, W., Kennard, S., Caldwell, R. B., & Lilly, B. (2010) · Circulation Research · doi:10.1161/circresaha.110.218271 · Cited by 188 · see citing works

An intimate interplay between precocious, migrating pericytes and endothelial cells governs human fetal brain angiogenesis

Virgintino, D., Girolamo, F., Errede, M., Capobianco, C., Robertson, D., Stallcup, W. B., Perris, R., & Roncali, L. (2007) · Angiogenesis · doi:10.1007/s10456-006-9061-x · Cited by 184 · see citing works

Activated protein C therapy slows ALS-like disease in mice by transcriptionally inhibiting SOD1 in motor neurons and microglia cells

Zhong, Z., Ilieva, H., Hallagan, L., Bell, R., Singh, I., Paquette, N., Thiyagarajan, M., Deane, R., Fernandez, J. A., Lane, S., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38476 · Cited by 176 · see citing works

New Therapeutic Targets in the Neurovascular Pathway in Alzheimer's Disease

Zloković, B. V. (2008) · Neurotherapeutics · doi:10.1016/j.nurt.2008.05.011 · Cited by 149 · see citing works

Paucity of Pericytes in Germinal Matrix Vasculature of Premature Infants

Braun, A., Xu, H., Hu, F., Kocherlakota, P., Siegel, D. S., Chander, P. N., Ungvari, Z. I., Csiszár, A., Nedergaard, M., & Ballabh, P. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3281-07.2007 · Cited by 141 · see citing works

Angiogenic Recruitment of Pericytes from Bone Marrow after Stroke

Kokovay, E., Li, L., & Cunningham, L. A. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600214 · Cited by 139 · see citing works

Localization of Ang-1, -2, Tie-2, and VEGF expression at endothelial-pericyte interdigitation in rat angiogenesis

Wakui, S., Yokoo, K., Muto, T., Suzuki, Y., Takahashi, H., Furusato, M., Hano, H., Endou, H., & Kanai, Y. (2006) · Laboratory Investigation · doi:10.1038/labinvest.3700476 · Cited by 139 · see citing works

Lipoprotein Receptor-Related Protein-1 Mediates Amyloid-β-Mediated Cell Death of Cerebrovascular Cells

Wilhelmus, M. M. M., Otte-Höller, I., van Triel, J. J. J., Veerhuis, R., Maat-Schieman, M. L. C., Bu, G., de Waal, R. M. W., & Verbeek, M. M. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.070050 · Cited by 138 · see citing works

Thrombin Mediates Severe Neurovascular Injury During Ischemia

Chen, B., Cheng, Q., Yang, K., & Lyden, P. D. (2010) · Stroke · doi:10.1161/strokeaha.110.584920 · Cited by 135 · see citing works

The bone marrow constitutes a reservoir of pericyte progenitors

Lamagna, C., & Bergers, G. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0506309 · Cited by 131 · see citing works

Microvasculature in brain biopsy specimens from patients with Alzheimer's disease: an immunohistochemical and ultrastructural study.

Vinters, H., Secor, D. L., Read, S., Frazee, J., Tomiyasu, U., Stanley, T., Ferreiro, J., & Akers, M.-A. (1994) · Ultrastructural Pathology · doi:10.3109/01913129409023202 · Cited by 126 · see citing works

Compensatory signalling induced in the yolk sac vasculature by deletion of TGFβ receptors in mice

Carvalho, R. L. C., Itoh, F., Goumans, M., et al. (2007) · Journal of Cell Science · doi:10.1242/jcs.013169 · Cited by 113 · see citing works

Role of connexin43 in central nervous system injury

Chew, S. S. L., Johnson, C. S., Green, C. R., & Danesh-Meyer, H. V. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.07.014 · Cited by 113 · see citing works

Reduced Connexin 43 Expression and Its Effect on the Development of Vascular Lesions in Retinas of Diabetic Mice

Bobbie, M., Roy, S., Trudeau, K. M., et al. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4489 · Cited by 106 · see citing works

Thrombin, a mediator of neurotoxicity and memory impairment

Mhatre, M., Nguyen, A., Kashani, S., Pham, T., Adesina, A., & Grammas, P. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.07.007 · Cited by 105 · see citing works

T lymphocyte adhesion to human brain pericytes is mediated via very late antigen-4/vascular cell adhesion molecule-1 interactions.

Verbeek, M. M., Westphal, J. R., Ruiter, D. J., & de Waal, R. M. W. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.154.11.5876 · Cited by 103 · see citing works

Neurovascular development

Bautch, V. L., & James, J. M. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.2.8397 · Cited by 92 · see citing works

Differential TGF-β Signaling in Retinal Vascular Cells: A Role in Diabetic Retinopathy?

van Geest, R. J., Klaassen, I., Vogels, I. M. C., Noorden, C. J. F. V., & Schlingemann, R. O. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4181 · Cited by 88 · see citing works

Pericytes: Blood-Brain Barrier Safeguards against Neurodegeneration?

Quaegebeur, A., Segura, I., & Carmeliet, P. (2010) · Neuron · doi:10.1016/j.neuron.2010.10.024 · Cited by 86 · see citing works

Effect of Prenatal Glucocorticoids on Cerebral Vasculature of the Developing Brain

Vinukonda, G., Dummula, K., Malik, S., Hu, F.-R., Thompson, C. I., Csiszar, A., Ungvari, Z., & Ballabh, P. (2010) · Stroke · doi:10.1161/strokeaha.110.588400 · Cited by 85 · see citing works

Retinal overexpression of angiopoietin-2 mimics diabetic retinopathy and enhances vascular damages in hyperglycemia

Pfister, F., Wang, Y., Schreiter, K., et al. (2009) · Acta Diabetologica · doi:10.1007/s00592-009-0099-2 · Cited by 78 · see citing works

TGF-β1 signaling controls retinal pericyte contractile protein expression

Sieczkiewicz, G. J., & Herman, I. M. (2003) · Microvascular Research · doi:10.1016/s0026-2862(03)00055-4 · Cited by 71 · see citing works

Calcium influx pathways in rat CNS pericytes

Kamouchi, M., Kitazono, T., Ago, T., Wakisaka, M., Ooboshi, H., Ibayashi, S., & Iida, M. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.03.008 · Cited by 58 · see citing works

Cell lineages and early patterns of embryonic CNS vascularization

Kurz, H. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.2.7855 · Cited by 48 · see citing works

Delta-like ligand 4–Notch signaling regulates bone marrow–derived pericyte/vascular smooth muscle cell formation

Stewart, K. S., Zhou, Z., Zweidler‐McKay, P. A., & Kleinerman, E. S. (2010) · Blood · doi:10.1182/blood-2010-05-284869 · Cited by 41 · see citing works

Peripheral mural cell recruitment requires cell-autonomous heparan sulfate

Stenzel, D., Nye, E. L., Nisancioglu, M. H., Adams, R. H., Yamaguchi, Y., & Gerhardt, H. (2009) · Blood · doi:10.1182/blood-2008-10-186239 · Cited by 41 · see citing works

Two‐photon imaging of brain pericytes in vivo using dextran‐conjugated dyes

Hirase, H., Creso, J., Singleton, M. K., Barthó, P., & Buzsáki, G. (2004) · Glia · doi:10.1002/glia.10295 · Cited by 38 · see citing works

Microvascular Retinal Endothelial and Pericyte Cell Apoptosis In Vitro: Role of Hedgehog and Notch Signaling

Walshe, T. E., Connell, P., Cryan, L. M., et al. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-7061 · Cited by 37 · see citing works

Cell Fusion Contributes to Pericyte Formation after Stroke

Piquer‐Gil, M., García‐Verdugo, J. M., Zipančić, I., et al. (2008) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2008.150 · Cited by 36 · see citing works

Lack of Smad or Notch Leads to a Fatal Game of Brain Pericyte Hopscotch

Winkler, E. A., Bell, R. D., & Zloković, B. V. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.03.002 · Cited by 25 · see citing works

Building a Vessel Wall With Notch Signaling

Regan, J. N., & Majesky, M. W. (2009) · Circulation Research · doi:10.1161/circresaha.109.194233 · Cited by 19 · see citing works

Untitled work

(2000) · doi:10.1002/1097-0177(200007)218:3

Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders

Sweeney, M. D., Sagare, A. P., & Zlokovic, B. V. (2018) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.188 · Cited by 3,076 · see citing works

Development, maintenance and disruption of the blood-brain barrier

Obermeier, B., Daneman, R., & Ransohoff, R. M. (2013) · Nature Medicine · doi:10.1038/nm.3407 · Cited by 2,452 · see citing works

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 2,294 · see citing works

Blood-brain barrier breakdown in the aging human hippocampus

Montagne, A., Barnes, S. R., Sweeney, M. D., Halliday, M. R., Sagare, A. P., Zhao, Z., Toga, A. W., Jacobs, R. E., Liu, C. Y., Amezcua, L., et al. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.032 · Cited by 2,102 · see citing works

A blood–brain barrier overview on structure, function, impairment, and biomarkers of integrity

Kadry, H., Noorani, B., & Cucullo, L. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00230-3 · Cited by 1,853 · see citing works

Clearance systems in the brain—implications for Alzheimer disease

Tarasoff-Conway, J. M., Carare, R. O., Osorio, R. S., Glodzik, L., Butler, T., Fieremans, E., Axel, L., Rusinek, H., Nicholson, C., Zlokovic, B. V., et al. (2015) · Nature Reviews Neurology · doi:10.1038/nrneurol.2015.119 · Cited by 1,678 · see citing works

Establishment and Dysfunction of the Blood-Brain Barrier

Zhao, Z., Nelson, A. R., Betsholtz, C., & Zlokovic, B. V. (2015) · Cell · doi:10.1016/j.cell.2015.10.067 · Cited by 1,670 · see citing works

Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging

Wardlaw, J. M., Smith, C., & Dichgans, M. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70060-7 · Cited by 1,657 · see citing works

Pericytes of the neurovascular unit: key functions and signaling pathways

Sweeney, M. D., Ayyadurai, S., & Zlokovic, B. V. (2016) · Nature Neuroscience · doi:10.1038/nn.4288 · Cited by 1,125 · see citing works

The role of brain vasculature in neurodegenerative disorders

Sweeney, M. D., Kisler, K., Montagne, A., Toga, A. W., & Zlokovic, B. V. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0234-x · Cited by 998 · see citing works

Glioblastoma Stem Cells Generate Vascular Pericytes to Support Vessel Function and Tumor Growth

Cheng, L., Huang, Z., Zhou, W., Wu, Q., Donnola, S., Liu, J. K., Fang, X., Sloan, A. E., Mao, Y., Lathia, J. D., et al. (2013) · Cell · doi:10.1016/j.cell.2013.02.021 · Cited by 905 · see citing works

The blood-brain barrier in aging and neurodegeneration

Knox, E. G., Aburto, M. R., Clarke, G., Cryan, J. F., & O’Driscoll, C. M. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01511-z · Cited by 738 · see citing works

3D self-organized microvascular model of the human blood-brain barrier with endothelial cells, pericytes and astrocytes

Campisi, M., Shin, Y., Osaki, T., Hajal, C., Chiono, V., & Kamm, R. D. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.07.014 · Cited by 718 · see citing works

Brain metastatic cancer cells release microRNA-181c-containing extracellular vesicles capable of destructing blood-brain barrier

Tominaga, N., Kosaka, N., Ono, M., Katsuda, T., Yoshioka, Y., Tamura, K., Lötvall, J., Nakagama, H., & Ochiya, T. (2015) · Nature Communications · doi:10.1038/ncomms7716 · Cited by 724 · see citing works

The blood-brain barrier: an engineering perspective

Wong, A. D., Ye, M., Levy, A. F., Rothstein, J. D., Bergles, D. E., & Searson, P. C. (2013) · Frontiers in Neuroengineering · doi:10.3389/fneng.2013.00007 · Cited by 662 · see citing works

Accelerated pericyte degeneration and blood–brain barrier breakdown in apolipoprotein E4 carriers with Alzheimer’s disease

Halliday, M. R., Rege, S. V., Ma, Q., Zhao, Z., Miller, C. A., Winkler, E. A., & Zlokovic, B. V. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.44 · Cited by 649 · see citing works

Brain Tissue Responses to Neural Implants Impact Signal Sensitivity and Intervention Strategies

Kozai, T. D. Y., Jaquins-Gerstl, A. S., Vazquez, A. L., Michael, A. C., & Cui, X. T. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500256e · Cited by 622 · see citing works

Deficiency in Mural Vascular Cells Coincides with Blood–Brain Barrier Disruption in <scp>A</scp> lzheimer's Disease

Sengillo, J. D., Winkler, E. A., Walker, C. T., Sullivan, J. S., Johnson, M., & Zlokovic, B. V. (2013) · Brain Pathology · doi:10.1111/bpa.12004 · Cited by 553 · see citing works

Hypertension-induced cognitive impairment: From pathophysiology to public health

Ungvari, Z., Toth, P., Tarantini, S., Prodan, C. I., Sorond, F., Merkely, B., & Csiszar, A. (2021) · Nature Reviews Nephrology · doi:10.1038/s41581-021-00430-6 · Cited by 544 · see citing works

A retinoic acid-enhanced, multicellular human blood-brain barrier model derived from stem cell sources

Lippmann, E. S., Al-Ahmad, A., Azarin, S. M., Palecek, S. P., & Shusta, E. V. (2014) · Scientific Reports · doi:10.1038/srep04160 · Cited by 508 · see citing works

Functional vascular contributions to cognitive impairment and dementia: mechanisms and consequences of cerebral autoregulatory dysfunction, endothelial impairment, and neurovascular uncoupling in aging

Toth, P., Tarantini, S., Csiszar, A., & Ungvari, Z. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00581.2016 · Cited by 522 · see citing works

Pericyte degeneration leads to neurovascular uncoupling and limits oxygen supply to brain

Kisler, K., Nelson, A. R., Rege, S. V., Ramanathan, A., Wang, Y., Ahuja, A., Lazic, D., Tsai, P. S., Zhao, Z., Zhou, Y., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4489 · Cited by 497 · see citing works

Brain Pericytes As Mediators of Neuroinflammation

Rustenhoven, J., Jansson, D., Smyth, L. C., & Dragunow, M. (2017) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2016.12.001 · Cited by 371 · see citing works

Vascular, glial, and lymphatic immune gateways of the central nervous system

Engelhardt, B., Carare, R. O., Bechmann, I., Flügel, A., Laman, J. D., & Weller, R. O. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1606-5 · Cited by 362 · see citing works

Vascular remodeling after ischemic stroke: mechanisms and therapeutic potentials.

Liu, J., Wang, Y., Akamatsu, Y., Lee, C. C., Stetler, R. A., Lawton, M. T., & Yang, G.-Y. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.11.004 · Cited by 335 · see citing works

Blood−brain barrier breakdown and neovascularization processes after stroke and traumatic brain injury

Prakash, R., & Carmichael, S. T. (2015) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000248 · Cited by 296 · see citing works

Factors influencing the blood-brain barrier permeability

Zhao, Y., Gan, L., Ren, L., Lin, Y., Ma, C., & Lin, X. (2022) · Brain Research · doi:10.1016/j.brainres.2022.147937 · Cited by 291 · see citing works

Blood-brain barrier permeability and physical exercise

Małkiewicz, M. A., Szarmach, A., Sabisz, A., Cubała, W. J., Szurowska, E., & Winklewski, P. J. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1403-x · Cited by 276 · see citing works

Cerebrovascular Effects of Apolipoprotein E: Implications for Alzheimer Disease

Zlokovic, B. V. (2013) · JAMA Neurology · doi:10.1001/jamaneurol.2013.2152 · Cited by 263 · see citing works

Microglia in the developing brain: a potential target with lifetime effects

Harry, G. J., & Kraft, A. D. (2012) · NeuroToxicology · doi:10.1016/j.neuro.2012.01.012 · Cited by 250 · see citing works

Brain and Retinal Pericytes: Origin, Function and Role

Trost, A., Lange, S., Schroedl, F., Bruckner, D., Motloch, K. A., Bogner, B., Kaser-Eichberger, A., Strohmaier, C., Runge, C., Aigner, L., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00020 · Cited by 244 · see citing works

Gut reactions: how the blood-brain barrier connects the microbiome and the brain

Logsdon, A. F., Erickson, M. A., Rhea, E. M., Salameh, T. S., & Banks, W. A. (2018) · Experimental Biology and Medicine · doi:10.1177/1535370217743766 · Cited by 235 · see citing works

Development and Function of the Blood-Brain Barrier in the Context of Metabolic Control

Haddad-Tóvolli, R., Dragano, N. R. V., Ramalho, A. F. S., & Velloso, L. A. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00224 · Cited by 226 · see citing works

Neurovascular Dysfunction in Vascular Dementia, Alzheimer's and Atherosclerosis

Shabir, O., Berwick, J., & Francis, S. E. (2018) · BMC Neuroscience · doi:10.1186/s12868-018-0465-5 · Cited by 191 · see citing works

Pericytes impair capillary blood flow and motor function after chronic spinal cord injury

Li, Y., Lucas-Osma, A. M., Black, S., Bandet, M. V., Stephens, M. J., Vavrek, R., Sanelli, L., Fenrich, K. K., Di Narzo, A. F., Dracheva, S., et al. (2017) · Nature Medicine · doi:10.1038/nm.4331 · Cited by 164 · see citing works

Engineering of a Biomimetic Pericyte-Covered 3D Microvascular Network

Kim, J., Chung, M., Kim, S., Jo, D. H., Kim, J. H., & Jeon, N. L. (2015) · PLOS ONE · doi:10.1371/journal.pone.0133880 · Cited by 160 · see citing works

The perivascular origin of pathological fibroblasts

Di Carlo, S. E., & Peduto, L. (2018) · Journal of Clinical Investigation · doi:10.1172/jci93558 · Cited by 164 · see citing works

Mfsd2a is a transporter for the essential ω-3 fatty acid docosahexaenoic acid (DHA) in Eye and is important for photoreceptor cell development

Wong, B. H., Chan, J. P., Cazenave-Gassiot, A., Poh, R. W., Foo, J. C., Galam, D. L. A., Ghosh, S., Nguyen, L. N., Barathi, V. A., Yeo, S. W., et al. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.721340 · Cited by 155 · see citing works

Benchmarking in vitro tissue-engineered blood–brain barrier models

DeStefano, J. G., Jamieson, J. J., Linville, R. M., & Searson, P. C. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0117-2 · Cited by 142 · see citing works

Shedding of soluble platelet-derived growth factor receptor-β from human brain pericytes

Sagare, A. P., Sweeney, M. D., Makshanoff, J., & Zlokovic, B. V. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.09.025 · Cited by 142 · see citing works

APOE Stabilization by Exercise Prevents Aging Neurovascular Dysfunction and Complement Induction

Soto, I., Graham, L. C., Richter, H. J., Simeone, S. N., Radell, J. E., Grabowska, W., Funkhouser, W. K., Howell, M. C., & Howell, G. R. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002279 · Cited by 140 · see citing works

Three-dimensional biomimetic vascular model reveals a RhoA, Rac1, and <i>N</i> -cadherin balance in mural cell–endothelial cell-regulated barrier function

Alimperti, S., Mirabella, T., Bajaj, V., Polacheck, W., Pirone, D. M., Duffield, J., Eyckmans, J., Assoian, R. K., & Chen, C. S. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618333114 · Cited by 122 · see citing works

Induction of Mesoderm and Neural Crest-Derived Pericytes from Human Pluripotent Stem Cells to Study Blood-Brain Barrier Interactions

Faal, T., Phan, D. T. T., Davtyan, H., Scarfone, V. M., Varady, E., Blurton-Jones, M., Hughes, C. C. W., & Inlay, M. A. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.01.005 · Cited by 124 · see citing works

Cerebrospinal Fluid Biomarkers of Neurovascular Dysfunction in Mild Dementia and Alzheimer'S Disease

Sweeney, M. D., Sagare, A. P., & Zlokovic, B. V. (2015) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1038/jcbfm.2015.76 · Cited by 122 · see citing works

Increased Nanoparticle Delivery to Brain Tumors by Autocatalytic Priming for Improved Treatment and Imaging

Han, L., Kong, D. K., Zheng, M.-Q., Murikinati, S., Ma, C., Yuan, P., Li, L., Tian, D., Cai, Q., Ye, C., et al. (2016) · ACS Nano · doi:10.1021/acsnano.5b07573 · Cited by 122 · see citing works

Role of iPSC-derived pericytes on barrier function of iPSC-derived brain microvascular endothelial cells in 2D and 3D

Jamieson, J. J., Linville, R. M., Ding, Y. Y., Gerecht, S., & Searson, P. C. (2019) · Fluids and Barriers of the CNS · doi:10.1186/s12987-019-0136-7 · Cited by 117 · see citing works

3D Biomimetic Models to Reconstitute Tumor Microenvironment In Vitro: Spheroids, Organoids, and Tumor‐on‐a‐Chip

Li, W., Zhou, Z., Zhou, X., Khoo, B. L., Gunawan, R., Chin, Y. R., Zhang, L., Yi, C., Guan, X., & Yang, M. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202202609 · Cited by 109 · see citing works

Regional early and progressive loss of brain pericytes but not vascular smooth muscle cells in adult mice with disrupted platelet-derived growth factor receptor-β signaling

Nikolakopoulou, A. M., Zhao, Z., Montagne, A., & Zlokovic, B. V. (2017) · PLOS ONE · doi:10.1371/journal.pone.0176225 · Cited by 109 · see citing works

Hypoxia Pretreatment of Bone Marrow Mesenchymal Stem Cells Facilitates Angiogenesis by Improving the Function of Endothelial Cells in Diabetic Rats with Lower Ischemia

Liu, J., Hao, H., Xia, L., Ti, D., Huang, H., Dong, L., Tong, C., Hou, Q., Zhao, Y., Liu, H., et al. (2015) · PLOS ONE · doi:10.1371/journal.pone.0126715 · Cited by 101 · see citing works

Aberrant astrocytes impair vascular reactivity in <scp>H</scp>untington disease

Hsiao, H., Chen, Y., Huang, C., Chen, C., Hsu, Y., Chen, H., Chiu, F., Kuo, H., Chang, C., & Chern, Y. (2015) · Annals of Neurology · doi:10.1002/ana.24428 · Cited by 99 · see citing works

Hypertension impairs neurovascular coupling and promotes microvascular injury: role in exacerbation of Alzheimer’s disease

Csiszar, A., Tarantini, S., Fülöp, G. A., Kiss, T., Valcarcel-Ares, M. N., Galvan, V., Ungvari, Z., & Yabluchanskiy, A. (2017) · GeroScience · doi:10.1007/s11357-017-9991-9 · Cited by 93 · see citing works

ApoE (Apolipoprotein E) in brain pericytes regulates endothelial function in an isoform-dependent manner by modulating basement membrane components

Yamazaki, Y., Shinohara, M., Yamazaki, A., Ren, Y., Asmann, Y. W., Kanekiyo, T., & Bu, G. (2020) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.119.313169 · Cited by 89 · see citing works

Gamma interferon alters junctional integrity via rho kinase, resulting in blood-brain barrier leakage in experimental viral encephalitis.

Bonney, S., Seitz, S., Ryan, C. A., Jones, K. L., Clarke, P., Tyler, K. L., & Siegenthaler, J. A. (2019) · mBio · doi:10.1128/mbio.01675-19 · Cited by 79 · see citing works

Basal lamina changes in neurodegenerative disorders

Nguyen, B., Bix, G., & Yao, Y. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00502-y · Cited by 75 · see citing works

Role of P2X7 Receptors in Immune Responses During Neurodegeneration

Oliveira-Giacomelli, Á., Petiz, L. L., Andrejew, R., Turrini, N., Silva, J. B., Sack, U., & Ulrich, H. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.662935 · Cited by 68 · see citing works

Regenerative effects of heme oxygenase metabolites on neuroinflammatory diseases

Lee, H., & Choi, Y. K. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms20010078 · Cited by 47 · see citing works

Transgenic animal models to explore and modulate the blood brain and blood retinal barriers of the CNS

Goncalves, A., & Antonetti, D. A. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00386-0 · Cited by 22 · see citing works

Cerebral Pericytes and Endothelial Cells Communicate through Inflammasome-Dependent Signals

Kozma, M., Mészáros, Á., Nyúl-Tóth, Á., Molnár, K., Costea, L., Hernádi, Z., Fazakas, C., Farkas, A. E., Wilhelm, I., & Krizbai, I. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116122 · Cited by 21 · see citing works

Decoding Blood-Brain Barrier Dysfunction in Alzheimer's Disease: Innovations and Challenges in Multimodal MRI and PET Imaging Biomarkers.

Yin, H., Lu, Z., Deng, Y., Tian, X., & Gong, Q. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102952 · Cited by 6 · see citing works

[Angiogenesis and arteriogenesis; the long road from concept to clinical application].

Voskuil, M., van Royen, N., Hoefer, I. E., et al. (2001) · PubMed · Cited by 7 · see citing works

Insights into mechanisms behind arteriogenesis: what does the future hold?

van Oostrom, M. C., van Oostrom, O., Quax, P. H. A., et al. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0508281 · Cited by 45 · see citing works

Importance of c-Kit Signaling In Arteriogenesis

Lassance‐Soares, R. M., Hernandez, D. R., Artiles-Valor, A., et al. (2018) · Annals of Vascular Surgery · doi:10.1016/j.avsg.2017.11.010

Mechanisms of arteriogenesis

Cai, W., & Schaper, W. K. A. (2008) · Acta Biochimica et Biophysica Sinica · doi:10.1111/j.1745-7270.2008.00436.x · Cited by 131 · see citing works

Arteriogenesis: Mechanisms and modulation of collateral artery development

van Royen, N., Piek, J. J., Schaper, W., et al. (2001) · Journal of Nuclear Cardiology · doi:10.1067/mnc.2001.118924 · Cited by 76 · see citing works