Basal lamina changes in neurodegenerative disorders

Regional differences in the morphological and functional effects of aging on cerebral basement membranes and perivascular drainage of amyloid‐β from the mouse brain

Hawkes, C. A., Gatherer, M., Sharp, M. M., Dorr, A. E., Yuen, H. M., Kalaria, R. N., Weller, R. O., & Carare, R. O. (2013) · Aging Cell · doi:10.1111/acel.12045 · Cited by 157

DECREASED mRNA EXPRESSION OF TIGHT JUNCTION PROTEINS IN LUMBAR SPINAL CORDS OF PATIENTS WITH ALS

Henkel, J. S., Beers, D. R., Wen, S., Bowser, R., & Appel, S. H. (2009) · Neurology · doi:10.1212/wnl.0b013e3181a41228 · Cited by 153

Perlecan a multifunctional extracellular proteoglycan scaffold

Farach‐Carson, M. C., & Carson, D. D. (2007) · Glycobiology · doi:10.1093/glycob/cwm043 · Cited by 153

Molecular and Genetic Analyses of Collagen Type IV Mutant Mouse Models of Spontaneous Intracerebral Hemorrhage Identify Mechanisms for Stroke Prevention

Jeanne, M., Jorgensen, J., & Gould, D. B. (2015) · Circulation · doi:10.1161/circulationaha.114.013395 · Cited by 153

A critical appraisal of the premotor symptoms of Parkinson's disease: Potential usefulness in early diagnosis and design of neuroprotective trials

Lang, A. E. (2011) · Movement Disorders · doi:10.1002/mds.23609 · Cited by 152

Blood-CNS Barrier Impairment in ALS patients versus an animal model

Garbuzova-Davis, S. N., & Sanberg, P. R. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00021 · Cited by 152

Incidence of cerebral microbleeds in preclinical Alzheimer disease

Yates, P. A., Desmond, P. M., Phal, P. M., Steward, C., Szoeke, C., Salvado, O., Ellis, K. A., Martins, R. N., Masters, C. L., Ames, D., et al. (2014) · Neurology · doi:10.1212/wnl.0000000000000285 · Cited by 150

Mechanism of depression as a risk factor in the development of Alzheimer’s disease: the function of AQP4 and the glymphatic system

Xia, M., Yang, L., Sun, G., Qi, S., & Li, B. (2017) · Psychopharmacology · doi:10.1007/s00213-016-4473-9 · Cited by 149

Thickening of the basement membrane of cortical capillaries in Alzheimer's disease

Mancardi, G., Perdelli, F., Rivano, C., Leonardi, A., & Bugiani, O. (1980) · Acta Neuropathologica · doi:10.1007/bf00692225 · Cited by 147

Blood–brain barrier disruption induces in vivo degeneration of nigral dopaminergic neurons

Rite, I., Machado, A., Cano, J., & Venero, J. L. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04567.x · Cited by 147

Blood–brain barrier dysfunction–induced inflammatory signaling in brain pathology and epileptogenesis

Kim, S. Y., Buckwalter, M., Soreq, H., Vezzani, A., & Kaufer, D. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03701.x · Cited by 145

The role of pericytic laminin in blood brain barrier integrity maintenance

Gautam, J., Zhang, X., & Yao, Y. (2016) · Scientific Reports · doi:10.1038/srep36450 · Cited by 144

Agrin Is a Major Heparan Sulfate Proteoglycan Accumulating in Alzheimer's Disease Brain

Verbeek, M. M., Otte‐Höller, I., van den Born, J., van den Heuvel, L. P. W. J., David, G., Wesseling, P., & de Waal, R. M. W. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65529-0 · Cited by 141

Organization and Expression of Basement Membrane Collagen IV Genes and Their Roles in Human Disorders

Sado, Y., Kagawa, M., Naito, I., Ueki, Y., Seki, T., Momota, R., Oohashi, T., & Ninomiya, Y. (1998) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a022003 · Cited by 140

Gene Structure and Functional Analysis of the Mouse Nidogen-2 Gene: Nidogen-2 Is Not Essential for Basement Membrane Formation in Mice

Schymeinsky, J., Nedbal, S., Miosge, N., Pöschl, E., Rao, C., Beier, D. R., Skarnes, W. C., Timpl, R., & Bader, B. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.19.6820-6830.2002 · Cited by 140

Expression and adhesive properties of basement membrane proteins in cerebral capillary endothelial cell cultures

Tilling, T., Engelbertz, C. M., Decker, S., Korte, D., Hüwel, S., & Galla, H. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0604-1 · Cited by 138

Blood–Brain Barrier Dysfunction as a Hallmark Pathology in Chronic Traumatic Encephalopathy

Doherty, C. P., O’Keefe, E., Wallace, E., Loftus, T., Keaney, J., Kealy, J., Humphries, M. M., Molloy, M. G., Meaney, J. F., Farrell, M., et al. (2016) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlw036 · Cited by 135

Mesenchymal stem cell transplantation attenuates blood brain barrier damage and neuroinflammation and protects dopaminergic neurons against MPTP toxicity in the substantia nigra in a model of Parkinson's disease.

Chao, Y.-X., He, B., & Tay, S. (2009) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2009.09.003 · Cited by 133

Cerebral Microbleeds: Different Prevalence, Topography, and Risk Factors Depending on Dementia Diagnosis—The Karolinska Imaging Dementia Study

Shams, S., Martola, J., Granberg, T., Li, X., Shams, M., Fereshtehnejad, S. M., Cavallin, L., Aspelin, P., Kristoffersen-Wiberg, M., & Wahlund, L. O. (2015) · American Journal of Neuroradiology · doi:10.3174/ajnr.a4176 · Cited by 132

Heparan sulfate proteoglycan in diffuse plaques of hippocampus but not of cerebellum in Alzheimer's disease brain.

Snow, A. D., Sekiguchi, R., Nochlin, D., Kalaria, R. N., & Kimata, K. (1994) · PubMed Central · Cited by 132

Neurologic Defects and Selective Disruption of Basement Membranes in Mice Lacking Entactin-1/Nidogen-1

Dong, L., Chen, Y., Lewis, M. E., Hsieh, J.-C., Reing, J. E., Chaillet, J. R., Howell, C. Y., Melhem, M. F., Inoué, S., Kuszak, J. R., et al. (2002) · Laboratory Investigation · doi:10.1097/01.lab.0000042240.52093.0f · Cited by 132

Vascular Basement Membrane Thickening in Diabetic Retinopathy

Roy, S., Ha, J., Trudeau, K. M., & Beglova, E. (2010) · Current Eye Research · doi:10.3109/02713683.2010.514659 · Cited by 132

Endothelial LRP1 protects against neurodegeneration by blocking cyclophilin A

Nikolakopoulou, A. M., Wang, Y., Ma, Q., Sagare, A. P., Montagne, A., Huuskonen, M. T., Rege, S. V., Kisler, K., Dai, Z., Körbelin, J., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20202207 · Cited by 131

Microangiopathy and the colocalization of heparan sulfate proteoglycan with amyloid in senile plaques of Alzheimer's disease

Perlmutter, L. S., Chui, H. C., Saperia, D., & Athanikar, J. N. (1990) · Brain Research · doi:10.1016/0006-8993(90)91111-s · Cited by 131

Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles

Favor, J., Gloeckner, C. J., Janik, D., Klempt, M., Neuhäuser-Klaus, A., Pretsch, W., Schmahl, W., & Quintanilla-Fend, L. (2006) · Genetics · doi:10.1534/genetics.106.064733 · Cited by 129

Characterization of high affinity binding between laminin and Alzheimer's disease amyloid precursor proteins.

Narindrasorasak, S., Lowery, D. E., Altman, R. A., Gonzalez‐DeWhitt, P. A., Greenberg, B. D., & Kisilevsky, R. (1992) · PubMed · Cited by 128

Increased intrathecal inflammatory activity in frontotemporal dementia: pathophysiological implications

Sjogren, M. (2004) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.019422 · Cited by 125

Where are we? The anatomy of the murine cortical meninges revisited for intravital imaging, immunology, and clearance of waste from the brain

Coles, J. A., Myburgh, E., Brewer, J. M., & McMenamin, P. G. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.05.002 · Cited by 123

The Natural History of Alzheimer's Disease: A Brain Bank Study

Jost, B. C., & Grossberg, G. T. (1995) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1995.tb07401.x · Cited by 123

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 & Metabolism · doi:10.1038/jcbfm.2015.76 · Cited by 122

Recommendations of the Alzheimer's Disease–Related Dementias Conference

Montine, T. J., Koroshetz, W. J., Babcock, D., Dickson, D. W., Galpern, W. R., Glymour, M. M., Greenberg, S. M., Hutton, M. L., Knopman, D. S., Kuzmichev, A. N., et al. (2014) · Neurology · doi:10.1212/wnl.0000000000000733 · Cited by 122

Changes in vascularization in substantia nigra pars compacta of monkeys rendered parkinsonian

Barcia, C., Bautista‐Hernández, V., Sánchez-Bahíllo, A., Fernández‐Villalba, E., Faucheux, B. A., Poza, M., Barreiro, A. F., Hirsch, É. C., & Herrero, M. T. (2005) · Journal of Neural Transmission · doi:10.1007/s00702-004-0256-2 · Cited by 120

Ablation of astrocytic laminin impairs vascular smooth muscle cell function and leads to hemorrhagic stroke

Chen, Z.-L., Yao, Y., Norris, E. H., Kruyer, A., Jno-Charles, O. C., Akhmerov, A., & Strickland, S. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201212032 · Cited by 120

Deposits of IgG and C3 in the spinal cord and motor cortex of ALS patients

Donnenfeld, H., Kascsak, R. J., & Bartfeld, H. (1984) · Journal of Neuroimmunology · doi:10.1016/0165-5728(84)90042-0 · Cited by 119

Identification of Sites in Domain I of Perlecan That Regulate Heparan Sulfate Synthesis

Dolan, M. A., Horchar, T., Rigatti, B. W., & Hassell, J. R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.7.4316 · Cited by 119

Laminin: loss-of-function studies

Yao, Y. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2381-0 · Cited by 118

Alzheimer's disease and soluble Aβ

Wısnıewskı, T., Ghiso, J. A., & Frangione, B. (1994) · Neurobiology of Aging · doi:10.1016/0197-4580(94)90105-8 · Cited by 112

A critical analysis of the ‘amyloid cascade hypothesis’

A. Armstrong, R. (2014) · Folia Neuropathologica · doi:10.5114/fn.2014.45562 · Cited by 110

In vivo dynamics of innate immune sentinels in the CNS

Nayak, D., Zinselmeyer, B. H., Corps, K. N., & McGavern, D. B. (2012) · IntraVital · doi:10.4161/intv.22823 · Cited by 109

Laminin and its neurite outgrowth‐promoting domain in the brain in Alzheimer's disease and Down's syndrome patients

Murtomäki, S., Risteli, J., Risteli, L., Koivisto, U., Johansson, S., & Liesi, P. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490320216 · Cited by 109

Fluid-Based Biomarkers for Amyotrophic Lateral Sclerosis

Vu, L. T., & Bowser, R. P. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0503-x · Cited by 108

Reduction of the cerebrovascular volume in a transgenic mouse model of Alzheimer's disease

Bourasset, F., Ouellet, M., Tremblay, C., Julien, C., Do, T. M., Oddo, S., LaFerla, F., & Calon, F. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.01.006 · Cited by 106

Blood-brain barrier dysfunction in Binswanger’s disease; an immunohistochemical study

Akiguchi, I., Tomimoto, H., Suenaga, T., Wakita, H., & Budka, H. (1998) · Acta Neuropathologica · doi:10.1007/s004010050768 · Cited by 104

Agrin in Alzheimer’s disease: Altered solubility and abnormal distribution within microvasculature and brain parenchyma

Donahue, J. E., Berzin, T. M., Rafii, M. S., Glass, D. J., Yancopoulos, G. D., Fallon, J. R., & Stopa, E. G. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6468 · Cited by 103

Heparan sulfate proteoglycan expression in cerebrovascular amyloid β deposits in Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis (Dutch) brains

van Horssen, J., Otte‐Höller, I., David, G., Maat–Schieman, M. L. C., van den Heuvel, L. P., Wesseling, P., de Waal, R. M., & Verbeek, M. M. (2001) · Acta Neuropathologica · doi:10.1007/s004010100414 · Cited by 103

Multiple Microbleeds are Related to Cerebral Network Disruptions in Patients with Early Alzheimer's Disease

Heringa, S. M., on behalf of the Utrecht Vascular Cognitive Impairment (VCI) Study Group, Reijmer, Y. D., Leemans, A., Koek, H. L., Kappelle, L. J., & Biessels, G. J. (2013) · Journal of Alzheimer's Disease · doi:10.3233/jad-130542 · Cited by 100

High Prevalence of Cerebral Microbleeds at 7Tesla MRI in Patients with Early Alzheimer's Disease

Brundel, M., Heringa, S. M., de Bresser, J., Koek, H. L., Zwanenburg, J. J. M., Kappelle, L. J., Luijten, P. R., & Biessels, G. J. (2012) · Journal of Alzheimer's Disease · doi:10.3233/jad-2012-120364 · Cited by 97

Nidogen Is Nonessential and Not Required for Normal Type IV Collagen Localization inCaenorhabditis elegans

Kang, S. H., & Kramer, J. M. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.11.3911 · Cited by 96

Mapping of binding sites for nidogens, fibulin-2, fibronectin and heparin to different IG modules of perlecan

Hopf, M., Göhring, W., Mann, K., & Timpl, R. (2001) · Journal of Molecular Biology · doi:10.1006/jmbi.2001.4878 · Cited by 95

Laminin α5 Is Required for Lobar Septation and Visceral Pleural Basement Membrane Formation in the Developing Mouse Lung

Nguyen, N. M., Miner, J. H., Pierce, R. A., & Senior, R. M. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0658 · Cited by 94

Perlecan regulates pericyte dynamics in the maintenance and repair of the blood–brain barrier

Nakamura, K., Ikeuchi, T., Nara, K., Rhodes, C. S., Zhang, P., Chiba, Y., Kazuno, S., Miura, Y., Ago, T., Arikawa‐Hirasawa, E., et al. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201807178 · Cited by 93

The effects of cerebral amyloid angiopathy on integrity of the blood-brain barrier

Magaki, S., Tang, Z., Tung, S., Williams, C. K., Lo, D., Yong, W. H., Khanlou, N., & Vinters, H. V. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.06.004 · Cited by 93

Evidence of nidogen-2 compensation for nidogen-1 deficiency in transgenic mice

Miosge, N., Sasaki, T., & Timpl, R. (2002) · Matrix Biology · doi:10.1016/s0945-053x(02)00070-7 · Cited by 93

Age-Related Vascular Pathology in Transgenic Mice Expressing Presenilin 1-Associated Familial Alzheimer's Disease Mutations

Gama Sosa, M. A., Gasperi, R. D., Rocher, A. B., Wang, A. C.-J., Janssen, W. G. M., Flores, T., Perez, G. M., Schmeidler, J., Dickstein, D. L., Hof, P. R., et al. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.090482 · Cited by 92

Loss of Nidogen-1 and -2 Results in Syndactyly and Changes in Limb Development

Böse, K., Nischt, R., Page, A. M., Bader, B., Paulsson, M., & Smyth, N. R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607886200 · Cited by 92

Aging is associated with increased collagen type IV accumulation in the basal lamina of human cerebral microvessels

Uspenskaya, O., Martin Liebetrau, A., Herms, J. W., Danek, A., & Hamann, G. F. (2004) · BMC Neuroscience · doi:10.1186/1471-2202-5-37 · Cited by 89

Laminins and their receptors in the CNS

Nirwane, A. M., & Yao, Y. (2018) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12454 · Cited by 88

Extracellular matrix of secondary lymphoid organs impacts on B-cell fate and survival

Song, J., Lokmic‐Tomkins, Z., Lämmermann, T., Rolf, J., Wu, C., Zhang, X., Hallmann, R., Hannocks, M., Horn, N., Rüegg, M. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218131110 · Cited by 86

Abnormal Expression of Collagen IV in Lens Activates Unfolded Protein Response Resulting in Cataract

Karagonlar, Z. F., Danysh, B. P., Bai, X., Gould, D. B., Kobayashi, T., & Duncan, M. K. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.060384 · Cited by 86

Subtle blood‐brain barrier leakage rate and spatial extent: Considerations for dynamic contrast‐enhanced MRI

van de Haar, H. J., Jansen, J. F. A., Jeukens, C. R. L. P. N., Burgmans, S., van Buchem, M. A., Muller, M., Hofman, P. A. M., Verhey, F. R. J., van Osch, M. J. P., & Backes, W. H. (2017) · Medical Physics · doi:10.1002/mp.12328 · Cited by 85

Vascular Basement Membrane Pathology and Alzheimer's Disease

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Primary structure and high expression of human agrin in basement membranes of adult lung and kidney

Groffen, A. J. A., Buskens, C. A. F., Kuppevelt, T. H. V., Veerkamp, J. H., Monnens, L. A. H., & van den Heuvel, L. P. W. J. (1998) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.1998.2540123.x · Cited by 85

Basement membrane and stroke

Yao, Y. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18801467 · Cited by 84

Role of clusterin in the brain vascular clearance of amyloid-β

Nelson, A. R., Sagare, A. P., & Zloković, B. V. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1711357114 · Cited by 79

Laminin α2 is a component of brain capillary basement membrane: Reduced expression in dystrophic dy mice

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String Vessel Formation is Increased in the Brain of Parkinson Disease

Yang, P., Pavlovic, D., Waldvogel, H. J., Dragunow, M., Synek, B. J., Turner, C. P., Faull, R. L. M., & Guan, J. (2015) · Journal of Parkinson s Disease · doi:10.3233/jpd-140454 · Cited by 77

Niche-derived laminin-511 promotes midbrain dopaminergic neuron survival and differentiation through YAP

Zhang, D., Yang, S., Toledo, E. M., Gyllborg, D., Saltó, C., Villaescusa, J. C., & Arenas, E. (2017) · Science Signaling · doi:10.1126/scisignal.aal4165 · Cited by 76

Altered microglia and neurovasculature in the Alzheimer's disease cerebellum

Singh‐Bains, M. K., Linke, V., Austria, M. D. R., Tan, A. Y. S., Scotter, E. L., Mehrabi, N. F., Faull, R. L. M., & Dragunow, M. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104589 · Cited by 74

Microvascular pathology and vascular basement membrane components in Alzheimer's disease

Perlmutter, L. S. (1994) · Molecular Neurobiology · doi:10.1007/bf02816103 · Cited by 73

An interaction between basement membrane and Alzheimer amyloid precursor proteins suggests a role in the pathogenesis of Alzheimer's disease.

Narindrasorasak, S., Altman, R. A., Gonzalez‐DeWhitt, P. A., Greenberg, B. D., & Kisilevsky, R. (1995) · PubMed · Cited by 73

Acute Ablation of Cortical Pericytes Leads to Rapid Neurovascular Uncoupling

Kisler, K., Nikolakopoulou, A. M., Sweeney, M. D., Lazić, D., Zhao, Z., & Zloković, B. V. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00027 · Cited by 73

Glymphatic fluid transport controls paravascular clearance of AAV vectors from the brain

Murlidharan, G., Crowther, A., Reardon, R. A., Song, J., & Asokan, A. (2016) · JCI Insight · doi:10.1172/jci.insight.88034 · Cited by 72

Reduced perlecan in mice results in chondrodysplasia resembling Schwartz–Jampel syndrome

Bungartz, K. D., Sasaki, T., Aszódi, A., & Jacenko, O. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddl484 · Cited by 72

Cooperative effect of heparan sulfate and laminin mimetic peptide nanofibers on the promotion of neurite outgrowth

Mammadov, B., Mammadov, R., Guler, M. O., & Tekinay, A. B. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2012.02.006 · Cited by 71

Common Binding Sites for β-Amyloid Fibrils and Fibroblast Growth Factor-2 in Heparan Sulfate from Human Cerebral Cortex

Lindahl, B., Westling, C., Giménez‐Gallego, G., Lindahl, U., & Salmivirta, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.43.30631 · Cited by 70

Trafficking of immune cells across the blood-brain barrier is modulated by neurofibrillary pathology in tauopathies

Majerová, P., Michalicová, A., Cente, M., Hanes, J., Vegh, J., Kittel, Á., Kosikova, N., Cigánková, V., Mihaljević, S., Jadhav, S., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217216 · Cited by 70

Comparison of gene expression of extracellular matrix molecules in brain microvascular endothelial cells and astrocytes

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Abnormalities in neural crest cell migration in laminin α5 mutant mice

Coles, E. G., Gammill, L. S., Miner, J. H., & Bronner-Fraser, M. E. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.10.031 · Cited by 69

Alpha-synuclein deregulates the expression of COL4A2 and impairs ER-Golgi function

Paiva, I., Jain, G., Lázaro, D. F., Gotovac, K., Hentrich, T., Kerimoglu, C., Pinho, R., Szegő, É. M., Burkhardt, S., Capece, V., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.08.001 · Cited by 68

Altered Brain Uptake of Therapeutics in a Triple Transgenic Mouse Model of Alzheimer’s Disease

Mehta, D. C., Short, J. L., & Nicolazzo, J. A. (2013) · Pharmaceutical Research · doi:10.1007/s11095-013-1116-2 · Cited by 68

Binding of vascular heparan sulfate proteoglycan to Alzheimer's amyloid precursor protein is mediated in part by the N-terminal region of A4 peptide

Buée, L., Ding, W., Anderson, J. P., Narindrasorasak, S., Kisilevsky, R., Boyle, N. J., Robakis, N. K. R. K., Delacourte, A., Greenberg, B., & Fillit, H. M. (1993) · Brain Research · doi:10.1016/0006-8993(93)90321-d · Cited by 66

Human Truncated Tau is Using a Different Mechanism from Amyloid-β to Damage the Blood-Brain Barrier

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Aging alters mRNA expression of amyloid transporter genes at the blood-brain barrier

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Differential distribution of laminins in Alzheimer disease and normal human brain tissue

Palu, E., & Liesi, P. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10292 · Cited by 63

Functional interactions of neuronal heparan sulphate proteoglycans with laminin

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Laminin inhibits amyloid-β-peptide fibrillation

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Loss of Endothelial Laminin α5 Exacerbates Hemorrhagic Brain Injury

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Aquaporin‐4 Overexpression in Rat ALS Model

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Pericytic Laminin Maintains Blood-Brain Barrier Integrity in an Age-Dependent Manner

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Basement Membranes in Skin Are Differently Affected by Lack of Nidogen 1 and 2

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The α1.α2 Network of Collagen IV

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Microvascular disturbance with decreased pericyte coverage is prominent in the ventral horn of patients with amyotrophic lateral sclerosis

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Upregulated Expression of Heparanase and Heparanase 2 in the Brains of Alzheimer’s Disease

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Laminin blocks the assembly of wild-type Aβ and the Dutch variant peptide into Alzheimer's fibrils

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Altered Expression of Basement Membrane-related Molecules in Rat Brain Pericyte, Endothelial, and Astrocyte Cell Lines after Transforming Growth Factor-β1 Treatment

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Amyloid Precursor-like Protein 2 Promotes Cell Migration toward Fibronectin and Collagen IV

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Decreased type IV collagen of skin and serum in patients with amyotrophic lateral sclerosis

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Different Impact of ALS on Laminin Isoforms in Human Extraocular Muscles versus Limb Muscles

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Basal Lamina of Abdominal Skeletal Muscle Capillaries in Diabetics and Nondiabetics

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Perlecan Domain V Inhibits Amyloid-β Induced Brain Endothelial Cell Toxicity and Restores Angiogenic Function

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Untitled work

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