The DOI matches its Crossref record; 231 of the 232 references it cites were found in a registry or an index.
Extracellular matrix and matrix receptors in blood–brain barrier formation and stroke
Open accessAbstract
The blood–brain barrier (BBB) is formed primarily to protect the brain microenvironment from the influx of plasma components, which may disturb neuronal functions. The BBB is a functional unit that consists mainly of specialized endothelial cells (ECs) lining the cerebral blood vessels, astrocytes, and pericytes. The BBB is a dynamic structure that is altered in neurologic diseases, such as stroke. ECs and astrocytes secrete extracellular matrix (ECM) proteins to generate and maintain the basement membranes (BMs). ECM receptors, such as integrins and dystroglycan, are also expressed at the brain microvasculature and mediate the connections between cellular and matrix components in physiology and disease. ECM proteins and receptors elicit diverse molecular signals that allow cell adaptation to environmental changes and regulate growth and cell motility. The composition of the ECM is altered upon BBB disruption and directly affects the progression of neurologic disease. The purpose of this review is to discuss the dynamic changes of ECM composition and integrin receptor expression that control BBB functions in physiology and pathology. © 2011 Wiley Periodicals, Inc. Develop Neurobiol 71: 1018‐1039, 2011
Overview
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
Cites
Statistics
Verification
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Integrins mediate cell signaling by activating ECM ligands, growth factors, and growth factor receptors, which regulates multiple endothelial cell functions including survival, migration, differentiation, adhesion, and polarity (35).”
From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [35]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Integrins: Versatility, modulation, and signaling in cell adhesion
Hynes, R. O. (1992) · Cell · doi:10.1016/0092-8674(92)90115-s · Cited by 9,857
Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827
Astrocyte-endothelial interactions at the blood-brain barrier
Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595
Astrocytes: Biology and pathology
Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196
Getting to the site of inflammation: the leukocyte adhesion cascade updated
Ley, K., Laudanna, C., Cybulsky, M. I., & Nourshargh, S. (2007) · Nature Reviews Immunology · doi:10.1038/nri2156 · Cited by 4,354
Giancotti, F. G., & Ruoslahti, E. (1999) · Science · doi:10.1126/science.285.5430.1028 · Cited by 3,869
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
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
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
Flagged first, then by citations
1 of the 232 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 301–397 of 397
Schofield, C. L., Rodrigo‐Navarro, A., Dalby, M. J., Agtmael, T. V., & Salmerón‐Sánchez, M. (2021) · Advanced NanoBiomed Research · doi:10.1002/anbr.202000068 · Cited by 5
Qi, Z., Yuan, S., Zhou, X., Ji, X., & Liu, K. J. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.710129 · Cited by 5
(2021) · Biointerface Research in Applied Chemistry · doi:10.33263/briac124.53475362 · Cited by 6
Role of Matrix Metalloproteinases in Brain Edema
Yang, C., & Candelario‐Jalil, E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803196-4.00011-4 · Cited by 5
Rapid loss of perihematomal cell viability in the collagenase intracerebral hemorrhage model
Chen‐Roetling, J., Cao, Y., Peng, D., & Regan, R. F. (2019) · Brain Research · doi:10.1016/j.brainres.2019.01.014 · Cited by 5
Chemokine receptors on T cells in multiple sclerosis
Sato, W. (2014) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12130 · Cited by 5
A dispensable role of mural cell-derived laminin- α 5 in intracerebral hemorrhage
Ruan, J., Kang, M., Nirwane, A. M., & Yao, Y. (2024) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x241264083 · Cited by 4
Drug Repurposing to Circumvent Chemotherapy Resistance in Brain Tumours
Hill, R., Murray, S. A., Maherally, Z., Higgins, S. C., & Pilkington, G. J. (2016) · Resistance to targeted anti-cancer therapeutics · doi:10.1007/978-3-319-46505-0_6 · Cited by 4
Pathways Across the Blood-Brain Barrier
Abadier, M., & Lyck, R. (2017) · Springer eBooks · doi:10.1007/978-3-319-45514-3_9 · Cited by 4
Role of Aquaporins in the Formation and Resolution of Brain Edema
Rodriguez‐Grande, B., Konsman, J. P., & Badaut, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803196-4.00009-6 · Cited by 4
Neuroglia and the blood–brain barrier
Pinto, H. N., Zarekiani, P., & de Vries, H. E. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00014-0 · Cited by 3
Zhang, X., Ye, Z., Cui, S., Shmushkovich, T., Tani, H., Chen, Y., Coe, M., Arkhangelskiy, A., Arral, M. L., Savvidou, M. G., et al. (2026) · Biomaterials · doi:10.1016/j.biomaterials.2026.124202 · Cited by 3
RETRACTED: Physical activity and glioblastoma: a paradigm shift in neuro-oncology therapy
Xie, L., & Wang, F. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1638060 · Cited by 5
RetractedApplication of Organ-on-Chip in Blood Brain Barrier Model
Vatsa, P., & Pant, A. B. (2022) · Springer eBooks · doi:10.1007/978-981-19-1379-2_24 · Cited by 3
Toutouna, L., Beck‐Woedl, S., Feige, U., Gläser, B., Komlósi, K., Eckenweiler, M., Lützen, N., Haack, T. B., Fischer, J., Bader, I., et al. (2023) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.63349 · Cited by 3
Samadzadeh, S., Olesen, M. N., Wirenfeldt, M., Möller, S., Misu, T., Soelberg, K. K., Frederiksen, J. L., Heegaard, S., Mariotto, S., Fujihara, K., et al. (2023) · Multiple Sclerosis Journal · doi:10.1177/13524585231200720 · Cited by 4
Edema and BBB Breakdown in Stroke
Salmeron, K., Edwards, D. N., Fraser, J. F., & Bix, G. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803196-4.00012-6 · Cited by 3
Disease Influence on BBB Transport in Neurodegenerative Disorders
de Lange, E. C. M. (2013) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-1-4614-9105-7_22 · Cited by 3
Adesse, D., Marcos, A. C., Siqueira, M., Cascabulho, C. M., Waghabi, M. C., Barbosa, H. S., & Stipursky, J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/378588 · Cited by 3
Maes, M. H. J., Nikiforov, N. G., Plaimas, K., Suratanee, A., & Reiche, E. M. V. (2021) · Preprints.org · doi:10.20944/preprints202109.0070.v1 · Cited by 2
Yin, H., Lu, Z., Deng, Y., Tian, X., & Gong, Q. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102952 · Cited by 6
Paradisi, G., Bonavolontà, V., Venditti, M., Fasano, G., Pedalino, C., Bene, F. D., Tartaglia, M., & Lauri, A. (2025) · Matrix Biology · doi:10.1016/j.matbio.2025.11.004 · Cited by 2
Kim, I., Griffith, K. R., Brockway, D. F., Crowley, N. A., & Medina, S. H. (2025) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2025.139466 · Cited by 2
Lynch, W. B., Miracle, S. A., Goldstein, S. I., Beierle, J. A., Bhandari, R., Gerhardt, E., Farnan, A. D., Nguyen, B.-M., Wingfield, K. K., Kazerani, I., et al. (2024) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/j.jpet.2025.103557 · Cited by 2
Ligand–Receptor Analysis of Brain Cell Type Marker Data Reveals Intricate Endothelial Interaction
Mishra, A., & Kumar, G. (2025) · Annals of Neurosciences · doi:10.1177/09727531251343254 · Cited by 3
Spray, S., Johansson, S. E., Edwards, A. V. G., Larsen, M. R., Radziwon‐Balicka, A., Povlsen, G. K., & Edvinsson, L. I. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0875-8 · Cited by 2
Extracellular Matrix in Stroke
Yao, Y. (2018) · Springer series in translational stroke research · doi:10.1007/978-3-319-90194-7_8 · Cited by 2
Ishikawa, M., Hamada, K., Yamada, Y., Kumai, J., Katagiri, F., Kikkawa, Y., & Nomizu, M. (2020) · Journal of Peptide Science · doi:10.1002/psc.3284 · Cited by 2
Matrix Metalloproteinases in Fragile X Syndrome
Ethell, D. W., & Sidhu, H. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804461-2.00015-9 · Cited by 2
Vascular Dysfunction and Neurodegenerative Disease
Gao, Z., Cilento, E. M., Stewart, T., & Zhang, J. (2019) · Springer eBooks · doi:10.1007/978-3-030-25249-6_1 · Cited by 2
Singh, A., & Vellapandian, C. (2022) · Qeios · doi:10.32388/5giw6a · Cited by 2
Wegener, M. A. B., Möller, S., Olesen, M. N., Madsen, J. S., Sørensen, G. L., Voss, A., & Asgari, N. (2024) · Frontiers in Lupus · doi:10.3389/flupu.2024.1386256 · Cited by 1
Shirvani, A., Shirvani, P., Jonah, U., Moore, B. E., & Holick, M. F. (2025) · Biomedicines · doi:10.3390/biomedicines13020469 · Cited by 2
Brown, S., Shallie, P. D., Sierra, C. A., Nayak, N., Odibo, A. O., Monaghan‐Nichols, P., & Nayak, N. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083862 · Cited by 3
Impact of HIV-1 TAT activation on retinal Müller glia: Implications for barrier properties
Khatak, K., Sankaranarayanan, K., & Chatterjee, N. (2025) · Journal of Biosciences · doi:10.1007/s12038-025-00507-5 · Cited by 1
Yang, J., Tang, N., Dai, R., Chen, J., Li, Z., Jiang, F., Li, S., & Meng, Q. (2025) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2025.09.008 · Cited by 1
Szecskó, A., Párdi, K., Cui, Z., Porkoláb, G., Hoyk, Z., Kovács, C., Adegbite, J. F., Fodor, V., Cser, N. M., Dér, L., et al. (2026) · British Journal of Pharmacology · doi:10.1111/bph.70568 · Cited by 1
Biomedical Materials and Fabrication Methods for Construction of In Vitro Neurovascular Unit Models
Xu, Y., Yu, W., Li, Y., & Zhang, L. (2026) · Materials · doi:10.3390/ma19173590 · Cited by 1
Castro, V., & Toborek, M. J. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1071-7_1 · Cited by 1
The Role of the Brain Extracellular Matrix in Synaptic Plasticity After Brain Injuries (Review)
Dembitskaya, Y., Tyurikova, O., & Semyanov, A. V. (2016) · Современные технологии в медицине · doi:10.17691/stm2016.8.4.31 · Cited by 1
Magnetic Nanocarrier Based Drug Targeting: Emerging Trend for the Treatment of Glioma
Satapathy, B. S., Panda, J., Biswal, B., Mishra, A., Pattnaik, S., Sahoo, P. K., & Gouda, A. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1002069 · Cited by 1
Evaluation of F3S4-m loaded liposomes as anti-AChE and its cytotoxic activity in PC12 and HMC3 cells
Camarillo-López, R. H., Morales, L. G. F., Cárdenas, L. F. D., Rivera-Antonio, A. M., Téllez, M. D. L. L. C., Macías, J. I. S., Valdez, M. O., & Rosales‐Hernández, M. C. (2023) · SN Applied Sciences · doi:10.1007/s42452-023-05583-6 · Cited by 1
Yang, J., Chen, S., Wang, Y.-F., Chang, C.-H., Chang, K.-H., Fuh, J., Chow, L., Han, C., Chen, Y., & Wang, S. (2024) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2024.100794 · Cited by 1
Koliaskin, L. Y., & Shibeko, A. M. (2024) · Российский физиологический журнал им И М Сеченова · doi:10.31857/s0869813924010021 · Cited by 1
Gelatinase-Mediated Impairment of Microvascular Beds in Cerebral Ischemia and Reperfusion Injury
Chen, S., Song, H., Cui, J., Shenker, J. I., Chen, Y., Sun, G. Y., Feng, H., & Gu, Z. (2018) · Springer series in translational stroke research · doi:10.1007/978-3-319-90194-7_1 · Cited by 1
Broekaart, D. W. M., Korotkov, A., Gorter, J. A., & van Vliet, E. A. (2021) · Progress in inflammation research · doi:10.1007/978-3-030-67403-8_4 · Cited by 1
Okamoto, L., Watanabe, S., Deno, S., Nie, X., Maruyama, J., Tomita, M., Hatano, A., & Yugi, K. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.12.006 · Cited by 1
Lubin, K. E., & Knipp, G. T. (2021) · Research Square · doi:10.21203/rs.3.rs-592200/v1 · Cited by 1
Recycling as a mechanism for extracellular matrix remodeling at the synapse
Dankovich, T. M. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8998 · Cited by 1
Mechanisms for Extracellular Matrix-Dependent Blood-Brain Barrier Dysfunction
Hoettles, B. A. (2021) · doi:10.18122/td/1903/boisestate · Cited by 1
Ahmadpour, D. (2021) · theses.fr (ABES) · doi:10.70675/cf02a85cz66d4z4c79za98czb8e4497ad04c · Cited by 1
Effects of cancer therapies on the brain : from molecular mechanisms to behavioral outcomes
Kovalchuk, A. (2015) · Open ULeth Scholarship (OPUS) (University of Lethbridge)
Investigating breast cancer metastasis to brain in pre-clinical mouse models of metastasis
Kim, S. (2015) · Minerva Access (University of Melbourne)
Blood Vessel Remodeling After Stroke
Moralı́, G., & Cervantes, M. (2015) · CRC Press eBooks · doi:10.1201/b18028-9
Laminin-511: a key regulator of breast cancer metastasis
Star, S. (2018) · Minerva Access (University of Melbourne)
The potential role of collagens in congenital Zika syndrome: A systems biology approachPreprint
Aguiar, R. S., Pohl, F. B., de Morais, G. L., Nogueira, F. C. S., de Carvalho, J. B., Guida, L. D. C., Arge, L. W., Melo, A., Moreira, M. E., Cunha, D. P., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/541268
Matrix metalloproteinases in stroke
Paltsyn, A. A. (2017) · Zhurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia» · doi:10.25557/0031-2991.2017.03.110-115
Shivappagowdar, A., Garg, S., Srivastava, A., Hada, R. S., Pati, S., Garg, L. C., & Singh, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.01.230623
Immune-to-Brain Signaling in Fever : The Brain Endothelium as Interface
Mirrasekhian, E. (2020) · Linköping University medical dissertations · doi:10.3384/diss.diva-168711
Cholesterol metabolism in mouse models of Multiple Sclerosis
Berghoff, S. A. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8239
Fibrinogen Level Predicts Prognosis of Patients with Acute Ischemic Stroke or TIAPreprint
Hou, H., Xiang, X., Pan, Y., Li, H., Meng, X., & Wang, Y. (2020) · Research Square · doi:10.21203/rs.3.rs-64098/v1
Mural norrin/β-catenin signaling regulates Lama2 expression to promote neurovascular unit assemblyPreprint
Biswas, S., Shahriar, S., Giangreco, N., Arvanitis, P., Winkler, M., Tatonetti, N. P., Brunken, W. J., Cutforth, T., & Agalliu, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.18.481046
Trends, technology, and future prospects of bioceramic materials
Kumar, A., Kumar, D., Goyal, A., Manhas, S., Kumar, A., & Sharma, A. K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89952-9.00017-8
Disease Influence on BBB Transport in Neurodegeneration
de Lange, E. C. M. (2022) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-030-88773-5_22
Bhuiyan, P., Khan, M. A., Sun, Z., & Qian, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-2070137/v1
The matrisome of the murine and human dorsal root ganglion: a transcriptomal approachPreprint
Vroman, R., Hunter, R. S., Wood, M. J., Davis, O., Malfait, Z., George, D., Ren, D., Tavares‐Ferreira, D., Price, T. J., Malfait, A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.22.513341
Configurable Models of the Neurovascular Unit
Mishra, Y., Sáez, J., & Owens, R. M. (2022) · Springer eBooks · doi:10.1007/978-3-031-11409-0_1
Wendt, T. S., & Gonzales, R. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.01.526738
Samadzadeh, S., Olesen, M. N., Wirenfeldt, M., Möller, S., Misu, T., Soelberg, K. K., Frederiksen, J. L., Heegaard, S., Mariotto, S., Fujihara, K., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2787239/v1
Molecular Biology and Treatment Strategies for Gliomas
Lichtor, T. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.110956
Koliaskin, L. Y., & Shibeko, A. M. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024010162
Whitehead, B. J. (2024) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.12326
Biomaterial for treating hemorrhagic stroke
Singh, D., & Dromel, P. C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-19085-8.00007-2
Control of Neuroinflammation and Protecting the Integrity of the Blood-Brain Barrier
Rom, S., & Persidsky, Y. (2024) · Springer eBooks · doi:10.1007/978-3-031-68237-7_42
Drelich, A. K., Saenkham, P., Wang, Y.-H., Xie, X., Judy, B. M., Ksiazek, T. G., Peng, B., & Tseng, C.-T. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.03.646981
Toxicology of the Brain Barrier System in Brain’s Health and Diseases
Liu, L. L., & Zheng, W. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00225-4
The Blood-Brain Barrier Disruption Methods for Drug Delivery
Amini, M., & Banu, M. A. (2025) · Springer eBooks · doi:10.1007/978-3-031-80173-0_5
Tang, Y., Zhang, Q., Yuan, Z., Yin, D., Zhang, S., Sun, Y., Mo, C., Tang, Z., Zhao, J., & Tang, Y. (2025) · Cell Cycle · doi:10.1080/15384101.2025.2539645
Aoki, H., Yamashita, M., Hashita, T., Iwao, T., & Matsunaga, T. (2020) · Figshare · doi:10.6084/m9.figshare.12050235
Uzunallı, G., Herr, S., Dieterly, A. M., Shi, R., & Lyle, L. T. (2021) · Figshare · doi:10.6084/m9.figshare.13545920
藤居, 貴., ARIMA, H., Miyamatsu, N., 漆谷, 真., Miura, K., 野﨑, 和., FUJII, T., Takashima, N., Kita, Y., Tanaka‐Mizuno, S., et al. (n.d.) · Institutional Repositories DataBase (IRDB)
Marqueurs périphériques de l'inflammation et déclin cognitif au cours de la maladie d'Alzheimer
Julian, A. (2018) · theses.fr (ABES) · doi:10.70675/0f58e0a1z28d9z40b7z886fz752caf42c261
Neurovascular unit changes after juvenile traumatic brain injury
Ichkova, A. (2019) · theses.fr (ABES) · doi:10.70675/7dacb9e2z3b14z4c14zbdafzbdcfad78c341
Gal, R. L. (2019) · theses.fr (ABES) · doi:10.70675/34274846z9781z4412za206zf4744182aea5
Contribution of astrocytes in brain vulnerability after juvenile mild traumatic brain injury
Clément, T. (2020) · theses.fr (ABES) · doi:10.70675/2892171fzc838z4d9azbf65zf208dafdf173
Impact cérébral précoce de l'inhalation chez le rat, le tungstène comme contaminant émergent
Macé, L. (2021) · theses.fr (ABES) · doi:10.70675/c7da5a7czefe9z4aa7zaa25z91a53cbb43b9
Role of extracellular space in neurodegenerative diseases
Estaún‐Panzano, J. (2024) · theses.fr (ABES) · doi:10.70675/98d1d96eza025z406ezba93z33e0820c3cf3
Oommen, A. M., Morel, M., Cunningham, S., Seoighe, C., & Joshi, L. (2026) · Genes · doi:10.3390/genes17040486
Hintze, M., Chunder, R., Schwarz, P. M., Nurmatov, Z., Lorke, M., Baecker, J., Holzbauer, K. L., Brockmann, E. M., Ekici, A. B., Boccaccini, A. R., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.23.734091
Mutant huntingtin in the extracellular matrix: A new perspective on Huntington's disease pathology
Trabolsi, C., & Cicchetti, F. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107502
Exploring immune-endothelial interactions in neuroinflammation and vascular dysfunction
Wang, Z., Kang, Z., Wu, L., Hu, J., Chen, X., & Tang, T. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1978704
Metadata
- Authors
- Baeten, K. M., & Akassoglou, K.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Akassoglou, Katerina
- Venue
- Developmental Neurobiology
- Publisher
- Wiley
- Published
- 2011-10-11
- Volume
- 71
- Issue
- 11
- Pages
- 1018-1039
- ISSN
- 1932-8451 (ISSN-L)
- 1932-846X
- PMC
- PMC3482610
- OpenAlex
- W2067935721
- Cited by
- 397
- References
- 232
- Citations by year
- 2026: 8 · 2025: 27 · 2024: 32 · 2023: 48 · 2022: 38 · 2021: 44 · 2020: 39 · 2019: 32 · 2018: 38 · 2017: 22 · 2016: 20 · 2015: 11 · 2014: 14 · 2013: 13 · 2012: 7
- FWCI
- 1.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Developmental Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS066361, R01NS052189, R01NS051470)
- National Center for Research Resources (P41RR004050)
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- blood-brain barrier, extracellular matrix, integrins, dystroglycan, basement membrane, endothelial cells, astrocytes, pericytes, stroke, blood-brain barrier disruption, ECM receptors, cell motility, neurovascular unit
- MeSH terms
- Animals, Blood-Brain Barrier, Brain, Humans, Microcirculation, Receptors, Cell Surface, Extracellular Matrix Proteins, Stroke
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