The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
BACE1 inhibitors: Current status and future directions in treating Alzheimer's disease
Abstract
Alzheimer's disease (AD) is an irreversible, progressive neurodegenerative brain disorder with no current cure. One of the important therapeutic approaches of AD is the inhibition of β‐site APP cleaving enzyme‐1 (BACE1), which is involved in the rate‐limiting step of the cleavage process of the amyloid precursor protein (APP) leading to the generation of the neurotoxic amyloid β (Aβ) protein after the γ‐secretase completes its function. The produced insoluble Aβ aggregates lead to plaques deposition and neurodegeneration. BACE1 is, therefore, one of the attractive targets for the treatment of AD. This approach led to the development of potent BACE1 inhibitors, many of which were advanced to late stages in clinical trials. Nonetheless, the high failure rate of lead drug candidates targeting BACE1 brought to the forefront the need for finding new targets to uncover the mystery behind AD. In this review, we aim to discuss the most promising classes of BACE1 inhibitors with a description and analysis of their pharmacodynamic and pharmacokinetic parameters, with more focus on the lead drug candidates that reached late stages of clinical trials, such as MK8931, AZD‐3293, JNJ‐54861911, E2609, and CNP520. In addition, the manuscript discusses the safety concerns and insignificant physiological effects, which were highlighted for the most successful BACE1 inhibitors. Furthermore, the review demonstrates with increasing evidence that despite tremendous efforts and promising results conceived with BACE1 inhibitors, the latest studies suggest that their clinical use for treating Alzheimer's disease should be reconsidered. Finally, the review sheds light on alternative therapeutic options for targeting AD.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
Several BACE1 inhibitory drugs have been developed, yet despite progression to phase 3 clinical trials, none have made it to wide clinical use.
“Several BACE1 inhibitory drugs have been developed, yet despite progression to phase 3 clinical trials, none have made it to wide clinical use.”
From BACE1: More than just a β‐secretase (2022) · cites this paper as [185]
Citations
Cites
The antibody aducanumab reduces Aβ plaques in Alzheimer’s disease
Sevigny, J., Chiao, P., Bussière, T., Weinreb, P. H., Williams, L., Maier, M., Dunstan, R., Salloway, S., Chen, T., Ling, Y., et al. (2016) · Nature · doi:10.1038/nature19323 · Cited by 3,059
Bard, F., Cannon, C., Barbour, R., Burke, R.-L., Games, D., Grajeda, H., Guido, T., Hu, K., Huang, J., Johnson-Wood, K., et al. (2000) · Nature Medicine · doi:10.1038/78682 · Cited by 2,012
2018 Alzheimer's disease facts and figures
Alzheimer's Association (2018) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2018.02.001 · Cited by 1,912
Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers
Laurén, J., Gimbel, D. A., Nygaard, H. B., Gilbert, J. W., & Strittmatter, S. M. (2009) · Nature · doi:10.1038/nature07761 · Cited by 1,560
Clinical effects of Aβ immunization (AN1792) in patients with AD in an interrupted trial
Gilman, S., Koller, M., Black, R. S., Jenkins, L., Griffith, S. G., Fox, N. C., Eisner, L., Kirby, L., Rovira, M. B., Forette, F., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000159740.16984.3c · Cited by 1,329
Correlation Between Elevated Levels of Amyloid β-Peptide in the Brain and Cognitive Decline
Näslund, J. (2000) · JAMA · doi:10.1001/jama.283.12.1571 · Cited by 1,268
Tau-targeting therapies for Alzheimer disease
Congdon, E. E., & Sigurdsson, E. M. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0013-z · Cited by 1,113 · cited 27×
“GSK‐3 is a kinase that keeps glycogen synthase inactive via phosphorylation, whereas insulin tends to activate glycogen synthetase by dephosphorylation on the same sites.153 Therefore, in that manner insulin can act to block GSK‐3 thereby tackling AD.”
ResultInfluentialTrial of Solanezumab for Mild Dementia Due to Alzheimer’s Disease
Honig, L. S., Vellas, B., Woodward, M., Boada, M., Bullock, R., Borrie, M., Hager, K., Andreasen, N., Scarpini, E., Liu-Seifert, H., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1705971 · Cited by 1,049 · cited 1×
“treatment in mild patients with AD, however, solanezumab failed to meet the primary outcomes and studies have recently discontinued.(122) Nonetheless, the good safety profile of solanezumab was the main courage to currently run prevention trials.”
BackgroundStructure and regulation of Src family kinases
Boggon, T. J., & Eck, M. J. (2004) · Oncogene · doi:10.1038/sj.onc.1208081 · Cited by 712
Alzheimer's disease drug development pipeline: 2018
Cummings, J., Lee, G., Ritter, A., & Zhong, K. (2018) · Alzheimer's & Dementia: Translational Research & Clinical Interventions · doi:10.1016/j.trci.2018.03.009 · Cited by 697
Randomized trial of verubecestat for mild-to-moderate Alzheimer's disease
Egan, M. F., Kost, J., Tariot, P. N., Aisen, P. S., Cummings, J. L., Vellas, B., Sur, C., Mukai, Y., Voss, T., Furtek, C., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1706441 · Cited by 685
Tau deficiency induces parkinsonism with dementia by impairing APP-mediated iron export
Lei, P., Ayton, S., Finkelstein, D. I., Spoerri, L., Ciccotosto, G. D., Wright, D. K., Wong, B. X. W., Adlard, P. A., Cherny, R. A., Lam, L. Q., et al. (2012) · Nature Medicine · doi:10.1038/nm.2613 · Cited by 594
CD22 blockade restores homeostatic microglial phagocytosis in ageing brains
Pluvinage, J. V., Haney, M. S., Smith, B. A. H., Sun, J., Iram, T., Bonanno, L., Li, L., Lee, D. P., Morgens, D. W., Yang, A. C., et al. (2019) · Nature · doi:10.1038/s41586-019-1088-4 · Cited by 459
Bohrmann, B., Baumann, K., Benz, J., Gerber, F., Huber, W., Knoflach, F., Messer, J., Oroszlan, K., Rauchenberger, R., Richter, W. F., et al. (2012) · Journal of Alzheimer's Disease · doi:10.3233/jad-2011-110977 · Cited by 448
Mechanism of amyloid removal in patients with Alzheimer disease treated with gantenerumab
Ostrowitzki, S. (2012) · Archives of Neurology · doi:10.1001/archneurol.2011.1538 · Cited by 431 · cited 1×
“Gantenerumab underwent phase I and II clinical trials in patients with prodromal AD and was relatively safe, but small group experienced signs of ARIA in a dose and APOE‐ε4 phenotype dependent manner.(127) Up to date, a phase III randomized trial of gantenerumab in prodromal AD is still ongoing.”
BackgroundNixon, R. A. (2017) · The FASEB Journal · doi:10.1096/fj.201700359 · Cited by 400 · cited 27×
“GSK‐3 is a kinase that keeps glycogen synthase inactive via phosphorylation, whereas insulin tends to activate glycogen synthetase by dephosphorylation on the same sites.153 Therefore, in that manner insulin can act to block GSK‐3 thereby tackling AD.”
BackgroundInfluentialFerreira, S. T., Lourenco, M. V., Oliveira, M. M., & De Felice, F. G. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00191 · Cited by 373
Intraneuronal β-amyloid accumulation and synapse pathology in Alzheimer’s disease
Gouras, G. K., Tampellini, D., Takahashi, R. H., & Capetillo-Zarate, E. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0679-9 · Cited by 372
Oda, T., Wals, P., Osterburg, H. H., Johnson, S. A., Pasinetti, G. M., Morgan, T. E., Rozovsky, I., Stine, W. B., Snyder, S. W., Holzman, T. F., et al. (1995) · Experimental Neurology · doi:10.1006/exnr.1995.1080 · Cited by 352
Adolfsson, O., Pihlgren, M., Toni, N., Varisco, Y., Buccarello, A. L., Antoniello, K., Lohmann, S., Piorkowska, K., Gafner, V., Atwal, J. K., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4742-11.2012 · Cited by 317
Fyn inhibition rescues established memory and synapse loss in Alzheimer mice
Kaufman, A. C., Salazar, S. V., Haas, L. T., Yang, J., Kostylev, M. A., Jeng, A. T., Robinson, S. A., Gunther, E. C., van Dyck, C. H., Nygaard, H. B., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24394 · Cited by 314
Bapineuzumab for mild to moderate Alzheimer’s disease in two global, randomized, phase 3 trials
Vandenberghe, R., Rinne, J. O., Boada, M., Katayama, S., Scheltens, P., Vellas, B., Tuchman, M., Gass, A., Fiebach, J. B., Hill, D., et al. (2016) · Alzheimer's Research & Therapy · doi:10.1186/s13195-016-0189-7 · Cited by 304
Lauritzen, I., Pardossi-Piquard, R., Bourgeois, A., Pagnotta, S., Biferi, M.-G., Barkats, M., Lacor, P., Klein, W., Bauer, C., & Checler, F. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1577-6 · Cited by 219
RGD peptide-based non-viral gene delivery vectors targeting integrin α v β 3 for cancer therapy
Fu, S., Xu, X., Ma, Y., Zhang, S., & Zhang, S. (2019) · Journal of drug targeting · doi:10.1080/1061186x.2018.1455841 · Cited by 139
Yuan, J., Venkatraman, S., Zheng, Y., McKeever, B. M., Dillard, L. W., & Singh, S. B. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm301659n · Cited by 135
Zhao, L., Mao, Z., Woody, S. K., & Brinton, R. D. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.011 · Cited by 132
BACE inhibition-dependent repair of Alzheimer’s pathophysiology
Keskin, A. D., Kekuš, M., Adelsberger, H., Neumann, U., Shimshek, D. R., Song, B., Zott, B., Peng, T., Förstl, H., Staufenbiel, M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1708106114 · Cited by 125
Structure of Crenezumab Complex with Aβ Shows Loss of β-Hairpin
Ultsch, M., Li, B., Maurer, T., Mathieu, M., Adolfsson, O., Muhs, A., Pfeifer, A., Pihlgren, M., Bainbridge, T. W., Reichelt, M., et al. (2016) · Scientific Reports · doi:10.1038/srep39374 · Cited by 124
Jiang, X.-Y., Chen, T.-K., Zhou, J.-T., He, S.-Y., Yang, H.-Y., Chen, Y., Qu, W., Feng, F., & Sun, H.-P. (2018) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.7b00463 · Cited by 122
The potential therapeutic effects of THC on Alzheimer’s disease
Cao, C., Li, Y., Liu, H., Bai, G., Mayl, J., Lin, X., Sutherland, K., Nabar, N., & Cai, J. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-140093 · Cited by 121
Alzheimer’s Disease: Advances in Drug Development
Piton, M., Hirtz, C., Desmetz, C., Milhau, J., Lajoix, A. D., Bennys, K., Lehmann, S., & Gabelle, A. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180145 · Cited by 60 · cited 3×
“clinical effects, however, none have passed the final stages of clinical trials yet to receive final FDA approval and reach the market.(8) 346 | MOUSSA‐PACHA ET AL.”
BackgroundAl-Tel, T. H., Semreen, M. H., Al-Qawasmeh, R. A., Schmidt, M. F., El-Awadi, R., Ardah, M., Zaarour, R., Rao, S. N., & El-Agnaf, O. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm201181f · Cited by 53 · cited 2×
“The traditional medicinal chemistry strategies followed in this study, such as rigidification, contraction, and bioisostere replacement led to the development of BACE1 inhibitors with high potencies.(39,63) Scheme 1 illustrates the main strategies utilized to design and develop a series of BACE1 inhibitors with improv…”
BackgroundSelf-citationMignon, L., Kordasiewicz, H., Lane, R., Smith, A., Miller, T., Narayanan, P., Swayze, E., Norris, D., Fitzsimmons, B., & Bennett, F. (2018) · Neurology · doi:10.1212/wnl.90.15_supplement.s2.006 · Cited by 29
Koynova, R., & Tenchov, B. (2018) · Recent Patents on Drug Delivery & Formulation · doi:10.2174/1872211312666171207152326 · Cited by 25 · cited 1×
“Moreover, management of complicated diseases such as AD may require natural materials that contain various natural compounds with targeting multiple proteins rather than a single‐target synthetic compound.(75) Therefore, phytochemicals enjoy high 3D‐content and diverse molecular”
Background
Flagged first, then by citations
Research works printed but not linked: 165
- 10.1021/jm0004897 · DOI
- 10.1126/science.275.5300.630 · DOI
- 10.1039/C3CS60460H · DOI
- 10.3233/JAD-143060 · DOI
- Prince M, 2015, The epidemiology and impact of dementia: current state and future trends
- Mullard A, 2017, BACE inhibitor bust in Alzheimer trial, Nat Rev Drug Discov, 16, 155, 10.1038/nrd.2017.43 · DOI
- 10.2217/nmt-2018-0029 · DOI
- 10.3233/JAD-180514 · DOI
- 10.1111/bpa.12717 · DOI
- 10.1111/jnc.12715 · DOI · Paper page
- 10.1186/1750-1326-2-22 · DOI · Paper page
- 10.1016/j.brainresbull.2016.04.007 · DOI
- 10.3233/JAD-181198 · DOI
- 10.1096/fj.04-1764com · DOI
- 10.1523/JNEUROSCI.21-15-05703.2001 · DOI
- 10.1016/j.bbrc.2012.10.129 · DOI
- 10.15252/emmm.201809717 · DOI
- 10.1515/revneuro-2017-0063 · DOI · Paper page
- 10.1111/febs.14004 · DOI · Paper page
- 10.1016/j.neurobiolaging.2018.06.038 · DOI
- 10.2174/1567205016666190325092841 · DOI
- 10.1186/s40035-016-0061-5 · DOI
- 10.1016/S0197-4580(02)00122-7 · DOI
- 10.1038/sj.emboj.7600061 · DOI
- 10.1186/s40035-017-0093-5 · DOI
- 10.1186/s13024-015-0033-8 · DOI · Paper page
- Volloch V, 2018, Results of Beta Secretase‐Inhibitor Clinical Trials Support Amyloid Precursor Protein‐Independent Generation of Beta Amyloid in Sporadic Alzheimer's Disease, Med Sci, 6
- 10.1080/13543784.2017.1369527 · DOI
- 10.1016/j.pharmthera.2012.07.001 · DOI
- 10.3389/fchem.2018.00178 · DOI
- 10.1186/s13195-014-0089-7 · DOI
- 10.1111/j.1745-7254.2006.00432.x · DOI
- 10.1126/science.290.5489.150 · DOI
- 10.1155/2014/482463 · DOI
- 10.1021/acsomega.6b00482 · DOI
- 10.1107/S0907444911047251 · DOI
- Barman A, 2014, Computational insights into substrate and site specificities, catalytic mechanism, and protonation states of the catalytic Asp Dyad of beta ‐secretase, Scientifica (Cairo), 2014, 598728
- 10.1016/j.jmb.2004.08.018 · DOI
- 10.3389/fnagi.2014.00165 · DOI
- 10.1080/713609213 · DOI
- Luo X, 2010, Inhibition of BACE1 for therapeutic usein Alzheimer's disease, Int J Clin Exp Pathol, 3, 618
- 10.1021/ja058636j · DOI
- 10.1021/jm061338s · DOI
- 10.2174/1874104501307010001 · DOI
- 10.1096/fj.10-167213 · DOI
- 10.1016/j.bmcl.2007.12.028 · DOI
- 10.1016/j.bmcl.2007.12.020 · DOI
- 10.1016/j.bmcl.2013.07.071 · DOI
- 10.1021/jm049379g · DOI · Paper page
- 10.1016/j.bmcl.2007.03.096 · DOI
- 10.1007/s00044-012-0277-6 · DOI
- 10.1021/jm9008482 · DOI
- 10.1016/j.ejmech.2016.11.021 · DOI
- 10.1021/jm901168f · DOI
- 10.1007/7355_2016_16 · DOI
- 10.1016/j.nurt.2008.05.007 · DOI
- 10.1016/j.bmcl.2015.10.031 · DOI
- 10.1126/scitranslmed.aad9704 · DOI
- 10.1016/j.bmcl.2012.02.013 · DOI
- 10.1021/ml500458t · DOI
- 10.1021/jm400225m · DOI
- 10.1021/acs.jnatprod.5b01055 · DOI · Paper page
- 10.7150/ijbs.23247 · DOI
- 10.1016/j.jff.2014.12.029 · DOI
- 10.1016/j.jff.2015.10.036 · DOI
- 10.2174/156720510791050812 · DOI
- 10.1016/j.jep.2012.03.023 · DOI
- 10.1016/j.phytochem.2016.11.011 · DOI
- 10.2174/1381612824666181106111020 · DOI
- 10.1155/2012/164689 · DOI
- Kaundal M, 2017, Lupeol isolated from Betula alnoides ameliorates amyloid beta induced neuronal damage via targeting various pathological events and alteration in neurotransmitter levels in rat's brain, Neurol Neurosci, 08, 195
- 10.3390/md16030094 · DOI
- 10.1021/acs.jnatprod.6b00235 · DOI
- 10.1016/j.jmgm.2017.07.010 · DOI
- 10.1007/s10822-011-9443-z · DOI
- 10.1128/MCB.02185-07 · DOI · Paper page
- 10.1016/j.jmgm.2016.10.013 · DOI
- 10.1186/1750-1326-7-46 · DOI
- 10.1016/j.ejmech.2016.08.028 · DOI
- 10.1016/j.celrep.2016.01.076 · DOI
- 10.1038/nn1797 · DOI · Paper page
- 10.2174/156720512799361637 · DOI
- 10.1126/science.1156609 · DOI
- 10.1083/jcb.200207113 · DOI · Paper page
- 10.1016/j.jalz.2010.11.007 · DOI
- 10.1007/s12035-012-8281-x · DOI
- 10.1002/ana.24135 · DOI · Paper page
- 10.1371/journal.pone.0032737 · DOI
- 10.1016/j.neuroscience.2018.11.031 · DOI
- 10.1101/cshperspect.a006270 · DOI · Paper page
- 10.1016/j.neures.2016.02.002 · DOI
- 10.1016/j.biopsych.2014.10.013 · DOI
- 10.1016/j.biopsych.2016.12.023 · DOI · Paper page
- 10.1016/j.neuron.2007.09.018 · DOI · Paper page
- 10.1016/j.neuroscience.2015.08.037 · DOI
- 10.1016/j.coche.2017.12.006 · DOI
- 10.1016/j.biopsych.2017.08.010 · DOI · Paper page
- 10.1177/1073858410381532 · DOI
- Cehlar O, 2018, Structural aspects of Alzheimer's disease immunotherapy targeted against amyloid‐beta peptide, Bratisl Lek Listy, 119, 201
- 10.1016/j.jalz.2017.04.015 · DOI
- 10.3233/JAD-2008-15202 · DOI · Paper page
- 10.3389/fnins.2018.00254 · DOI · Paper page
- 10.1002/cpdd.584 · DOI
- 10.5772/intechopen.76299 · DOI
- 10.1097/WNF.0b013e31827db49b · DOI
- 10.1016/j.trci.2017.05.003 · DOI
- 10.1186/s13195-017-0318-y · DOI · Paper page
- 10.1016/j.jalz.2018.06.2339 · DOI
- 10.1021/acs.jmedchem.7b00393 · DOI
- 10.3389/fnins.2018.00025 · DOI · Paper page
- 10.1038/nrd.2018.65 · DOI
- 10.1073/pnas.1714175114 · DOI · Paper page
- 10.1038/nchembio.83 · DOI · Paper page
- 10.1016/j.bmcl.2005.07.077 · DOI
- 10.1038/cddis.2012.176 · DOI · Paper page
- Mullard A, 2018, BACE failures lower AD expectations, again, Nat Rev Drug Discov, 17, 385, 10.1038/nrd.2018.94 · DOI
- 10.1016/j.pestbp.2018.08.008 · DOI
- 10.1111/j.1471-4159.2004.02422.x · DOI
- 10.1111/j.1471-4159.2007.05194.x · DOI · Paper page
- 10.1016/j.ejmech.2015.10.018 · DOI
- 10.1273/cbij.10.1 · DOI
- 10.1016/j.bmcl.2015.03.046 · DOI
- Lao K, 2018, Drug development for Alzheimer's disease: review, J Drug Target, 27, 1
- 10.1055/s-0044-100186 · DOI
- 10.1021/jm011020u · DOI
- 10.2174/1568026618666180112161406 · DOI
- 10.1007/s11910-012-0297-0 · DOI
- 10.1042/BST0320803 · DOI
- 10.3389/fnmol.2011.00032 · DOI
- 10.1016/j.biopsych.2017.06.004 · DOI · Paper page
- 10.1038/nn.3178 · DOI
- 10.3389/fcell.2014.00063 · DOI
- 10.1523/JNEUROSCI.4152-10.2011 · DOI · Paper page
- 10.2174/092986711796150531 · DOI
- 10.1186/alzrt238 · DOI
- 10.1016/j.bbi.2017.08.015 · DOI
- 10.1007/978-3-319-20825-1_3 · DOI
- 10.3389/fnins.2016.00243 · DOI
- 10.1111/j.1476-5381.2010.00729.x · DOI
- 10.1007/s40263-018-0515-7 · DOI
- 10.1016/j.plipres.2011.01.001 · DOI
- 10.1016/j.neurobiolaging.2012.06.005 · DOI
- 10.1002/glia.22988 · DOI · Paper page
- 10.3233/JAD-180230 · DOI
- 10.1016/S0968-0896(02)00331-0 · DOI
- 10.3233/JAD-130137 · DOI
- 10.1016/j.neuropharm.2012.05.013 · DOI
- 10.1124/mol.111.071290 · DOI
- 10.1002/ejp.1148 · DOI
- 10.1038/npjamd.2016.12 · DOI
- 10.1097/YCO.0000000000000399 · DOI
- 10.1111/jnc.13230 · DOI
- 10.1097/NEN.0000000000000030 · DOI · Paper page
- 10.1016/S1474-4422(13)70090-5 · DOI · Paper page
- 10.1186/s40478-019-0664-z · DOI
- 10.1084/jem.20161731 · DOI · Paper page
- 10.1038/nrd.2017.155 · DOI · Paper page
- 10.3389/fnmol.2017.00447 · DOI
- 10.1021/acschemneuro.5b00121 · DOI
- 10.1021/jm401824w · DOI
- 10.1016/j.jalz.2017.02.001 · DOI
- 10.1002/anie.201605460 · DOI
- 10.1073/pnas.1015253108 · DOI
- 10.1002/med.21563 · DOI
- 10.1002/med.21434 · DOI
Cited by
Sorted by citations
BACE1: More than just a β‐secretase
Taylor, H. A., Przemylska, L., Clavane, E. M., & Meakin, P. J. (2022) · Obesity Reviews · doi:10.1111/obr.13430 · Cited by 107
Ferreira, J. P. S., Albuquerque, H. M. T., Cardoso, S. M., Silva, A. M. S., & Silva, V. L. M. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113492 · Cited by 96
Qu, L., Li, S., Ji, L., Luo, S., Ding, M., Yin, F., Wang, C., Luo, H., Lu, D., Liu, X., et al. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113889 · Cited by 61
Pan-SHIP1/2 inhibitors promote microglia effector functions essential for CNS homeostasis
Pedicone, C., Fernandes, S., Dungan, O. M., Dormann, S. M., Viernes, D. R., Adhikari, A. A., Choi, L. B., De Jong, E. P., Chisholm, J. D., & Kerr, W. G. (2020) · Journal of Cell Science · doi:10.1242/jcs.238030 · Cited by 61
Zhao, Z., Liu, Y., Ruan, S., & Hu, Y. (2023) · International Journal of Nanomedicine · doi:10.2147/ijn.s444115 · Cited by 49
Gardenia jasminoides J.Ellis extract GJ-4 alleviated cognitive deficits of APP/PS1 transgenic mice
Zang, C., Liu, H., Shang, J., Yang, H., Wang, L., Sheng, C., Zhang, Z., Bao, X., Yu, Y., Yao, X., et al. (2021) · Phytomedicine · doi:10.1016/j.phymed.2021.153780 · Cited by 22
Metadata
- Authors
- Moussa‐Pacha, N. M., Abdin, S. M., Omar, H. A., Alniss, H., & Al‐Tel, T. H.
- Affiliations
- Sharjah Institute for Medical Research University of Sharjah Sharjah United Arab Emirates
- Venue
- Medicinal Research Reviews
- Publisher
- Wiley
- Published
- 2019-07-26
- Volume
- 40
- Issue
- 1
- Pages
- 339-384
- ISSN
- 0198-6325
- 1098-1128
- Cited by
- 274
- References
- 34
- Language
- en
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