The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Cerebral amyloid-β proteostasis is regulated by the membrane transport protein ABCC1 in mice
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In addition to APP, there was an increase in the surface expression of several proteins involved in APP processing and amyloid-β response in VPS35-suppressed neuronal cultures, including BACE1, APLP1, APLP2, ABCC1, EPHA4, IGFR1, and SYP.
“In addition to APP, we found an increase in the surface expression of several proteins involved in APP processing and amyloid-β response in the VPS35 suppressed neuronal cultures.These included βsecretase 1 (BACE1), [92], APP-like β-secretase substrates APLP1 and APLP2 [93], transporter ABCC1 [94][95][96], ephrin type-A receptor 4 (EPHA4) [97,98], and insulin-like growth factor-1 (IGFR1) [99], and”
From Global identification of neuronal and astrocytic integral membrane proteins that require Retromer for their endosomal recycling (2026) · cites this paper as [96]
Some studies have reported a role for ABCB1 in Aβ peptide elimination from the brain.
“Whereas some studies have reported a role for ABCB1 in A peptide elimination from the brain [37,67]”
ABCB1 and probably ABCC1 restrict Aβ re-entry into the brain.
“whereas ABCB1 and probably ABCC1 restrict A re-entry into the brain [25,37,38].”
ABCB1 is involved in Aβ peptide transport across the BBB.
“but it is now clear that ABCB1 is also involved in A peptide transport across the BBB.”
ABCC1 mediates Aβ peptide transport across the BBB.
“More recently, it has been suggested that ABCC1 (another efflux pump expressed by BBB cells) mediates A peptide transport across the BBB [37].”
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1 retracted
RETRACTED ARTICLE: A specific amyloid-β protein assembly in the brain impairs memory
Lesné, S., Koh, M. T., Kotilinek, L., Kayed, R., Glabe, C. G., Yang, A., Gallagher, M., & Ashe, K. H. (2006) · Nature · doi:10.1038/nature04533 · Cited by 2,769
RetractedQuerfurth, H. W., & LaFerla, F. M. (2010) · New England Journal of Medicine · doi:10.1056/nejmra0909142 · Cited by 4,569
Decreased Clearance of CNS β-Amyloid in Alzheimer’s Disease
Mawuenyega, K. G., Sigurdson, W., Ovod, V., Munsell, L., Kasten, T., Morris, J. C., Yarasheski, K. E., & Bateman, R. J. (2010) · Science · doi:10.1126/science.1197623 · Cited by 2,078
RAGE mediates amyloid-β peptide transport across the blood-brain barrier and accumulation in brain
Deane, R., Du Yan, S., Submamaryan, R. K., LaRue, B., Jovanovic, S., Hogg, E., Welch, D., Manness, L., Lin, C., Yu, J., et al. (2003) · Nature Medicine · doi:10.1038/nm890 · Cited by 1,426
Self-citationShibata, M., Yamada, S., Kumar, S. R., Calero, M., Bading, J., Frangione, B., Holtzman, D. M., Miller, C. A., Strickland, D. K., Ghiso, J., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10498 · Cited by 1,413
Aβ42‐driven cerebral amyloidosis in transgenic mice reveals early and robust pathology
Radde, R., Bolmont, T., Kaeser, S. A., Coomaraswamy, J., Lindau, D., Stoltze, L., Calhoun, M. E., Jäggi, F., Wolburg, H., Gengler, S., et al. (2006) · The EMBO Reports · doi:10.1038/sj.embor.7400784 · Cited by 986
Cirrito, J. R. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25247 · Cited by 660
Deane, R., Wu, Z., & Zlokovic, B. V. (2004) · Stroke · doi:10.1161/01.str.0000143452.85382.d1 · Cited by 392
Herzig, M. C., Winkler, D. T., Burgermeister, P., Pfeifer, M., Kohler, E., Schmidt, S. D., Danner, S., Abramowski, D., Stürchler-Pierrat, C., Bürki, K., et al. (2004) · Nature Neuroscience · doi:10.1038/nn1302 · Cited by 391
Lack of ABCA1 Considerably Decreases Brain ApoE Level and Increases Amyloid Deposition in APP23 Mice
Koldamova, R., Staufenbiel, M., & Lefterov, I. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504513200 · Cited by 350
Studies on the first described Alzheimer's disease amyloid β mutant, the Dutch variant
Levy, E., Prelli, F., & Frangione, B. (2006) · Journal of Alzheimer's Disease · doi:10.3233/jad-2006-9s337 · Cited by 24
Flagged first, then by citations
Research works printed but not linked: 29
- 10.1126/science.1141448 · DOI · Paper page
- 10.1016/S0896-6273(01)00475-5 · DOI · Paper page
- 10.1038/nn.2575 · DOI · Paper page
- 10.1073/pnas.1009485107 · DOI · Paper page
- 10.1111/j.1750-3639.2008.00133.x · DOI
- 10.1016/j.neubiorev.2009.05.006 · DOI
- 10.1111/j.1750-3639.2007.00075.x · DOI
- 10.1046/j.1471-4159.2001.00113.x · DOI
- 10.1124/mol.109.061754 · DOI
- 10.2174/1567205043332225 · DOI
- 10.1523/JNEUROSCI.5103-08.2009 · DOI
- 10.2174/156720508785132262 · DOI
- 10.2217/14622416.9.1.105 · DOI
- 10.1007/s00401-010-0787-6 · DOI
- Scheffler K, et al. Determination of spatial and temporal distribution of microglia by 230nm-high-resolution, high-throughput automated analysis reveals different amyloid plaque populations in an APP/PS1 mouse model of Alzheimer’s disease [published online ahead of print January 19, 2011].Curr Alzheimer Res . PMID: 21244350.
- 10.1038/nm1197-1275 · DOI
- 10.1016/S0197-4580(01)00317-7 · DOI · Paper page
- WesoBowska, 2009, In Vivo., 23, 943
- 10.1073/pnas.96.7.3900 · DOI
- 10.1172/JCI8267 · DOI
- 10.2741/1085 · DOI
- 10.1016/j.parkreldis.2007.11.007 · DOI
- 10.1016/j.neuroscience.2003.10.012 · DOI
- Lee, 2010, Methods Mol Biol., 596, 325, 10.1007/978-1-60761-416-6_14 · DOI
- 10.1073/pnas.202607599 · DOI · Paper page
- 10.1016/0092-8674(94)90212-7 · DOI
- 10.1038/nprot.2006.273 · DOI · Paper page
- 10.1038/labinvest.3700281 · DOI
- 10.1016/0026-2862(88)90023-4 · DOI
Cited by
Sorted by citations
Role of Blood-Brain Barrier in Alzheimer’s Disease
Cai, Z., Qiao, P.-F., Wan, C.-Q., Cai, M., Zhou, N.-K., & Li, Q. (2018) · Journal of Alzheimer's Disease · doi:10.3233/jad-180098 · Cited by 370
Regulation of ABC efflux transporters at blood-brain barrier in health and neurological disorders
Qosa, H., Miller, D. S., Pasinelli, P., & Trotti, D. (2015) · Brain Research · doi:10.1016/j.brainres.2015.07.005 · Cited by 249
Blood–Brain Barrier Breakdown in Alzheimer’s Disease: Mechanisms and Targeted Strategies
Alkhalifa, A. E., Al-Ghraiybah, N. F., Odum, J., Shunnarah, J. G., Austin, N., & Kaddoumi, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216288 · Cited by 212
Dysfunction of ABC transporters at the blood-brain barrier: Role in neurological disorders
Gil-Martins, E., Barbosa, D. J., Silva, V., Remião, F., & Silva, R. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107554 · Cited by 152
The relationship between amyloid-beta and brain capillary endothelial cells in Alzheimer’s disease
Su, Q., Guo, J.-H., Zhang, Y.-L., Wang, J., & Zhang, Z.-N. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.335829 · Cited by 91
Revisiting rodent models: Octodon degus as Alzheimer’s disease model?
Steffen, J., Krohn, M., Paarmann, K., Schwitlick, C., Brüning, T., Marreiros, R., Müller-Schiffmann, A., Korth, C., Braun, K., & Pahnke, J. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0363-y · Cited by 62
Self-citationKuntz, M., Candela, P., Saint-Pol, J., Lamartinière, Y., Boucau, M.-C., Sevin, E., Fenart, L., & Gosselet, F. (2015) · Journal of Alzheimer's Disease · doi:10.3233/jad-150469 · Cited by 55
Matsumoto, K., Chiba, Y., Fujihara, R., Kubo, H., Sakamoto, H., & Ueno, M. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1366-7 · Cited by 46
Molecular mechanisms of Alzheimer’s disease: From therapeutic targets to promising drugs
Alan, E., Kerry, Z., & Sevin, G. (2023) · Fundamental & Clinical Pharmacology · doi:10.1111/fcp.12861 · Cited by 17
Li, X., Initiative, O. B. O. A. D. N., Chu, S.-G., Shen, X.-N., Hou, X.-H., Xu, W., Ou, Y.-N., Dong, Q., Tan, L., & Yu, J.-T. (2019) · Aging · doi:10.18632/aging.102435 · Cited by 7
Jones, E., Adams, H., Chen, K.-E., Maroof, F., Ibbotson, T. M., Nakamura, Y., Banks, P. J., Healy, M. D., Lewis, P. A., Heesom, K. J., et al. (2026) · doi:10.64898/2026.05.14.724903
Metadata
- Authors
- Krohn, M., Lange, C., Hofrichter, J., Scheffler, K., Stenzel, J., Steffen, J., Schumacher, T., Brüning, T., Plath, A.-S., Alfen, F., Schmidt, A., Winter, F., Rateitschak, K., Wree, A., Gsponer, J., Walker, L. C., & Pahnke, J.
- Venue
- Journal of Clinical Investigation
- Published
- 2011-10-03
- Volume
- 121
- Issue
- 10
- Pages
- 3924-3931
- ISSN
- 0021-9738
- Cited by
- 183
- References
- 11
- Language
- en
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